CA2614526A1 - Benzimidazole formulation - Google Patents
Benzimidazole formulation Download PDFInfo
- Publication number
- CA2614526A1 CA2614526A1 CA002614526A CA2614526A CA2614526A1 CA 2614526 A1 CA2614526 A1 CA 2614526A1 CA 002614526 A CA002614526 A CA 002614526A CA 2614526 A CA2614526 A CA 2614526A CA 2614526 A1 CA2614526 A1 CA 2614526A1
- Authority
- CA
- Canada
- Prior art keywords
- alkaline substance
- dry
- benzimidazole
- alkaline
- formulation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000000203 mixture Substances 0.000 title claims description 89
- 238000009472 formulation Methods 0.000 title claims description 38
- 239000000126 substance Substances 0.000 claims abstract description 117
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 45
- 238000004519 manufacturing process Methods 0.000 claims abstract description 30
- IQPSEEYGBUAQFF-UHFFFAOYSA-N Pantoprazole Chemical group COC1=CC=NC(CS(=O)C=2NC3=CC=C(OC(F)F)C=C3N=2)=C1OC IQPSEEYGBUAQFF-UHFFFAOYSA-N 0.000 claims description 85
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 85
- 229960005019 pantoprazole Drugs 0.000 claims description 85
- 235000017550 sodium carbonate Nutrition 0.000 claims description 42
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 38
- 229940001593 sodium carbonate Drugs 0.000 claims description 37
- 238000007906 compression Methods 0.000 claims description 33
- 230000006835 compression Effects 0.000 claims description 33
- 238000007908 dry granulation Methods 0.000 claims description 31
- 239000002994 raw material Substances 0.000 claims description 30
- 150000003839 salts Chemical class 0.000 claims description 25
- 239000002702 enteric coating Substances 0.000 claims description 24
- 238000009505 enteric coating Methods 0.000 claims description 24
- 239000007884 disintegrant Substances 0.000 claims description 22
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 18
- 239000007916 tablet composition Substances 0.000 claims description 17
- 229910000406 trisodium phosphate Inorganic materials 0.000 claims description 17
- 235000019801 trisodium phosphate Nutrition 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 16
- -1 alkaline earth metal carbonate Chemical class 0.000 claims description 14
- 229960000913 crospovidone Drugs 0.000 claims description 10
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 claims description 10
- 239000011734 sodium Substances 0.000 claims description 10
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 claims description 9
- 229960000381 omeprazole Drugs 0.000 claims description 9
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 claims description 9
- 239000011777 magnesium Substances 0.000 claims description 8
- 150000007522 mineralic acids Chemical class 0.000 claims description 8
- 239000001488 sodium phosphate Substances 0.000 claims description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 210000002784 stomach Anatomy 0.000 claims description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 6
- 150000008041 alkali metal carbonates Chemical class 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 4
- SUBDBMMJDZJVOS-DEOSSOPVSA-N esomeprazole Chemical compound C([S@](=O)C1=NC2=CC=C(C=C2N1)OC)C1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-DEOSSOPVSA-N 0.000 claims description 4
- MJIHNNLFOKEZEW-UHFFFAOYSA-N lansoprazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1CS(=O)C1=NC2=CC=CC=C2N1 MJIHNNLFOKEZEW-UHFFFAOYSA-N 0.000 claims description 4
- YREYEVIYCVEVJK-UHFFFAOYSA-N rabeprazole Chemical compound COCCCOC1=CC=NC(CS(=O)C=2NC3=CC=CC=C3N=2)=C1C YREYEVIYCVEVJK-UHFFFAOYSA-N 0.000 claims description 4
- HBDKFZNDMVLSHM-UHFFFAOYSA-N 2-(pyridin-2-ylmethylsulfinyl)-1h-benzimidazole Chemical compound N=1C2=CC=CC=C2NC=1S(=O)CC1=CC=CC=N1 HBDKFZNDMVLSHM-UHFFFAOYSA-N 0.000 claims description 3
- 239000004475 Arginine Substances 0.000 claims description 3
- CEUORZQYGODEFX-UHFFFAOYSA-N Aripirazole Chemical compound ClC1=CC=CC(N2CCN(CCCCOC=3C=C4NC(=O)CCC4=CC=3)CC2)=C1Cl CEUORZQYGODEFX-UHFFFAOYSA-N 0.000 claims description 3
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004472 Lysine Substances 0.000 claims description 3
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 3
- 229960004372 aripiprazole Drugs 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims description 3
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- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
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- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 125000005587 carbonate group Chemical group 0.000 claims description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 claims description 2
- 235000019800 disodium phosphate Nutrition 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 238000007873 sieving Methods 0.000 claims description 2
- 229950011585 timoprazole Drugs 0.000 claims description 2
- 101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- 238000004090 dissolution Methods 0.000 abstract description 25
- 239000013618 particulate matter Substances 0.000 abstract description 12
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- 239000011230 binding agent Substances 0.000 abstract description 10
- 239000008194 pharmaceutical composition Substances 0.000 abstract description 10
- 239000007788 liquid Substances 0.000 abstract description 7
- 238000001035 drying Methods 0.000 abstract description 2
- 239000003826 tablet Substances 0.000 description 107
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 80
- 229960003563 calcium carbonate Drugs 0.000 description 40
- 229910000019 calcium carbonate Inorganic materials 0.000 description 40
- 235000010216 calcium carbonate Nutrition 0.000 description 39
- 238000002156 mixing Methods 0.000 description 27
- 238000009490 roller compaction Methods 0.000 description 23
- 239000002245 particle Substances 0.000 description 20
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- 239000008186 active pharmaceutical agent Substances 0.000 description 14
- 229940088679 drug related substance Drugs 0.000 description 14
- 238000012430 stability testing Methods 0.000 description 14
- 235000021186 dishes Nutrition 0.000 description 13
- 229940079593 drug Drugs 0.000 description 12
- 239000003814 drug Substances 0.000 description 12
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
- 239000008187 granular material Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- LQIAZOCLNBBZQK-UHFFFAOYSA-N 1-(1,2-Diphosphanylethyl)pyrrolidin-2-one Chemical compound PCC(P)N1CCCC1=O LQIAZOCLNBBZQK-UHFFFAOYSA-N 0.000 description 9
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 9
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- 238000009498 subcoating Methods 0.000 description 9
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 8
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- 235000019359 magnesium stearate Nutrition 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
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- 238000009491 slugging Methods 0.000 description 6
- 235000015424 sodium Nutrition 0.000 description 6
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- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 6
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 6
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
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- 150000001556 benzimidazoles Chemical class 0.000 description 4
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- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 3
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- A61K9/2886—Dragees; Coated pills or tablets, e.g. with film or compression coating having two or more different drug-free coatings; Tablets of the type inert core-drug layer-inactive layer
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Abstract
A dry manufacturing process for the production of a pharmaceutical formulation of a benzimidazole and an alkaline substance is described. A tablet is compressed directly from a dry powder or a dry particulate matter avoiding any liquid or excipient conventionally used as a wet binder. The manufacturing process has the advantage of being simple and cost efficient. At the same time an expensive drying step is superfluous. The resulting pharmaceutical formulation has a good stability and a good dissolution profile.
Description
BENZIMIDAZOLE FORMULATION
FIELD OF INVENTION
The present invention relates to the field of pharmaceutical formulation science. In particular, the present invention relates to pharmaceutical formulations comprising acid labile benzimidazoles. The invention provides cost-effective production methods providing stable formulations.
BACKGROUND
Due to the acid lablie nature of the benzimidazoles it is necessary to protect the drug substance from exposure to acids, especially in the presence of humidity. In the first stage, the benzimidazole has to be protected from acid attack during storage of the drug.
In the prior art, this is provided by contacting the benzimidazole with an alkaline substance present in the pharmaceutical formulation. In the next stage the benzimidazole must be protected from acid attack in the stomach. The person skilled in the art will realise that this -can be achieved by applying an enteric coating. It:is however acknowledged in the art that an enteric coating will introduce a stability problem in that commonly used enteric coatings are acidic by nature. This stability problem is described in EP 0244380 (Hassle). Applying a neutral subcoating for protection of the acid labile benzimidazole was suggested by EP 244 380 for solving the stability problem.
Wet granulation techniques are traditionally employed in such formulation approaches. EP
0244380 e.g. discloses use of conventional granulation process, wherein a wet binder is used as well as an aqueous granulation liquid. EP 0589981 e.g. discloses use of polyvinylpyrrolidone as a wet binder.
WO 05009410 (Dr. Reddy's) discloses an enteric coated benzimidazole formulation, wherein the tablets are arrived at via different combinations of wet mixing and dry mixing.
Example 7 e.g. discloses dry mixing and compression of esomeprazole and magnesium oxide.
WO 9850019 (Sage) discloses an enteric coated formulation comprising omeprazole or lanzoprazole. In Example 2C, ten grams of omeprazole were mixed with pharmaceutical excipient lactose anhydrous USP/NF and then passed through a screen to obtain a homogenous granule size. In Example 4, it is stated that "The individual core granulation was mixed with lactose and talc or magnesium stearate and compressed into tablets by known pharmaceutical techniques." No stability assays are disclosed with tablets according to Example 2C+4.
WO 04075881 (Ranbaxy) discloses an enteric coated formulation comprising rabeprazole and a low viscosity hyd roxypropyice flu lose optionally in combination with antioxidants produced by a method comprising dry granulation.
FIELD OF INVENTION
The present invention relates to the field of pharmaceutical formulation science. In particular, the present invention relates to pharmaceutical formulations comprising acid labile benzimidazoles. The invention provides cost-effective production methods providing stable formulations.
BACKGROUND
Due to the acid lablie nature of the benzimidazoles it is necessary to protect the drug substance from exposure to acids, especially in the presence of humidity. In the first stage, the benzimidazole has to be protected from acid attack during storage of the drug.
In the prior art, this is provided by contacting the benzimidazole with an alkaline substance present in the pharmaceutical formulation. In the next stage the benzimidazole must be protected from acid attack in the stomach. The person skilled in the art will realise that this -can be achieved by applying an enteric coating. It:is however acknowledged in the art that an enteric coating will introduce a stability problem in that commonly used enteric coatings are acidic by nature. This stability problem is described in EP 0244380 (Hassle). Applying a neutral subcoating for protection of the acid labile benzimidazole was suggested by EP 244 380 for solving the stability problem.
Wet granulation techniques are traditionally employed in such formulation approaches. EP
0244380 e.g. discloses use of conventional granulation process, wherein a wet binder is used as well as an aqueous granulation liquid. EP 0589981 e.g. discloses use of polyvinylpyrrolidone as a wet binder.
WO 05009410 (Dr. Reddy's) discloses an enteric coated benzimidazole formulation, wherein the tablets are arrived at via different combinations of wet mixing and dry mixing.
Example 7 e.g. discloses dry mixing and compression of esomeprazole and magnesium oxide.
WO 9850019 (Sage) discloses an enteric coated formulation comprising omeprazole or lanzoprazole. In Example 2C, ten grams of omeprazole were mixed with pharmaceutical excipient lactose anhydrous USP/NF and then passed through a screen to obtain a homogenous granule size. In Example 4, it is stated that "The individual core granulation was mixed with lactose and talc or magnesium stearate and compressed into tablets by known pharmaceutical techniques." No stability assays are disclosed with tablets according to Example 2C+4.
WO 04075881 (Ranbaxy) discloses an enteric coated formulation comprising rabeprazole and a low viscosity hyd roxypropyice flu lose optionally in combination with antioxidants produced by a method comprising dry granulation.
Several approaches of providing a stable pharmaceutical formulation of benzimidazoles are thus suggested in the art. The suggested manufacturing processes are however relatively laborious. There is thus a need in the art for simple and cost efficient manufacturing methods for producing benzimidazole formulations with good stability properties and good dissoiution profiles. There is furthermore a need in the art for .obtaining such tablets in a relatively small size for efficient passage and drug delivery in the intestinal tract.
SUMMARY OF INVENTION "
The object of the present invention thus to provide a stable and cost-efficient pharmaceutical formuiation intended for oral administration and subsequent efficient delivery of the active benzidimazole in the intestinal tract, wherein said formulation has a good shelf life stability and release profile.
In particular, the present invention relates to a method for producing a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granulating steps and dry compressing of tablets, wherein said formulation is further chaaracterized by one or more of the following features:
(i) the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (li) the alkaline substance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (iii) the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) the alkaline substance has a pKa of at least about 10 and a BET area of at least about .1 m2/g prior to any dry granulation and/or dry compression steps, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKa1-value of 6 or more and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vii) the alkaline substance has a BET-area of at least about 1 mZJg prior to any dry granulation and/or dry compression steps, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
The invention furthermore relates to a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is further characterized by one or more of the following features:
(P) the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 n-i2/g, (ii) the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 mz/g, (iii) the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 - 1:5, (v) the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 mZ/g, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about I mZ/g, (vii) the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30 lo by weight.
The manufacturing process involves only few production steps and the use of any liquid is avoided rendering an expensive drying step superFluous. A liquid can, however, be applicable in the subsequent coating steps providing an enteric coat and optionally a subcoat.
DETAILED DESCRIPTION OF THE INVENTION
In a ffrst aspect, the present invention relates to a pharmaceutical tablet formulation comprising a benzimidazole as the bioiogically active component, wherein:
said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is 'further characterized by one or more of the following features:
(i:) the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g, (if) the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g, (iii) the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 - 1:5, (v) the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 ma/g, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 mz/g, (vii) the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
SUMMARY OF INVENTION "
The object of the present invention thus to provide a stable and cost-efficient pharmaceutical formuiation intended for oral administration and subsequent efficient delivery of the active benzidimazole in the intestinal tract, wherein said formulation has a good shelf life stability and release profile.
In particular, the present invention relates to a method for producing a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granulating steps and dry compressing of tablets, wherein said formulation is further chaaracterized by one or more of the following features:
(i) the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (li) the alkaline substance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (iii) the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) the alkaline substance has a pKa of at least about 10 and a BET area of at least about .1 m2/g prior to any dry granulation and/or dry compression steps, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKa1-value of 6 or more and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vii) the alkaline substance has a BET-area of at least about 1 mZJg prior to any dry granulation and/or dry compression steps, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
The invention furthermore relates to a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is further characterized by one or more of the following features:
(P) the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 n-i2/g, (ii) the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 mz/g, (iii) the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 - 1:5, (v) the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 mZ/g, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about I mZ/g, (vii) the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30 lo by weight.
The manufacturing process involves only few production steps and the use of any liquid is avoided rendering an expensive drying step superFluous. A liquid can, however, be applicable in the subsequent coating steps providing an enteric coat and optionally a subcoat.
DETAILED DESCRIPTION OF THE INVENTION
In a ffrst aspect, the present invention relates to a pharmaceutical tablet formulation comprising a benzimidazole as the bioiogically active component, wherein:
said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is 'further characterized by one or more of the following features:
(i:) the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g, (if) the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g, (iii) the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 - 1:5, (v) the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 ma/g, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 mz/g, (vii) the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
In a second aspect, the present invention relates to a method for producing a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granutating steps and dry compressing of tabiets wherein said formulation is further characterized by one or more of the following features:
(i) the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about i m2/g prior to any dry granulation and/or dry compression steps, (ii) the alkaline subStance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about i m2/g prior to any dry granulation and/or dry compression steps, (iii) the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) the alkaline substance has a pKa of at least about 10 and a BET area of at least about 1 mz/g prior to any dry granulation and/or dry compression steps, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (vii) the alkaline substance has a BET-area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (viii) the tablet formufiation further comprises a disintegrant in an amount of about 1-30% by weight.
In a preferred embodiment the benzimidazole is pantoprazole such as pantoprazole sodium hydrate or pantoprazole sodium sesquihydrate. In other preferred embodiments the benzimidazole may be omeprazole or a salt and/or a hydrate thereof, lansoprazole or a salt and/or a hydrate thereof, esomeprazol or a salt and/or a hydrate thereof, aripiprazole or a salt and/or a hydrate thereof, rabeprazol or a salt and/or a hydrate thereof, or timoprazole or a salt and/or a hydrate thereof.
In another preferred embodiment, said formulation further comprises other pharmaceutically acceptable excipients such as fillers, dry binders, glidants and lubricants.
In a particularly preferred embodiment, said formulation comprises crospovidone as a disintegrant in an amount of from about 5-20%, preferably 7,5-15%, most preferably 10-13% by weight.
In yet another embodiment, said formulation comprises a subcoat. In a particularly preferred embodiment however, said formulation does not comprise a subcoat. in the Examples it is shown that it is possible according to the present invention to obtain tablet formulations with good stability properties and good dissolution profiles without the laborious steps of applying a subcoat.
In yet another preferred embodiment, the alkaline substance is a salt of an organic or an 5 inorganic acid where the anion of the salt is carbonate (C032"), hydrogenphosphate (HP042"
) or phosphate (P043"). The alkaline substance may also be a salt of an organic or an inorganic acid where the kation is sodium (Na}), caicium (CaZ+) or magnesium (Mg2+).
Preferably, the salt of the organic and/or inorganic acid according is sodiumcarbonate (NaZCO3), or Calciumcarbonate (CaCO3) trisodiumphosphate (Na3PO4), disodiumhydrogenphosphate (NazHPO4), hydrazine or derivatives thereof, lysine or a derivative thereof, arginine or a derivative thereof, or histidine or a derivative thereof.
In yet another preferred embodiment, dry granulation is provided by means of a roller compactor.
In a final preferred embodiment, the mixture has been subject to sieving prior to tablet compression with a sieve size (Roller compactor) of 1,25 mm or less. It is shown in the examples that relatively small and, relatively homogenous particles result in a more accurate dosing of the active compound. Doze accuracy is of particular importance in production of relatively small tablets.
In a final aspect, the present invention relates to products obtainable or.obtained by the methods disclosed herein.
Definitions Pharmaceutical tablet formulation:
A pharmaceutical tablet formulation according to the present invention is equivalent to a solid dosis form.
Druas:
According to the present invention, the drug substance belongs to the group of benzimidazoles or salts and/or hydrates thereof. The benzimidazole is preferably pantoprazole, omeprazole, lansoprazole, timoprazol, aripiprazole, rabeprazol or esomeprazole, as well as pharmaceutically acceptable salts, hydrates and mixtures thereof. Preferably, the benzimidazole is pantoprazole sodium sesquihydrate.
Any pharmaceutically acceptable salt can be used. Examples of conventionally used salts are sodium or potassium salts of the drug substance.
A pharmaceutical formulation according to the present invention comprises about 1 to 500 mg drug pr. dose; such as 1 to 200 mg; or 1 to 100 mg. Preferably, the unit dose comprises 10-120 mg; 15-100 mg; 15-80 mg, 15-70 mg; 15-60 mg; 15-50 mg; 15-45 mg; such as 20, 30, or 40 mg of benzimidazole, preferably pantoprazole.
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granutating steps and dry compressing of tabiets wherein said formulation is further characterized by one or more of the following features:
(i) the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about i m2/g prior to any dry granulation and/or dry compression steps, (ii) the alkaline subStance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about i m2/g prior to any dry granulation and/or dry compression steps, (iii) the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) the alkaline substance has a pKa of at least about 10 and a BET area of at least about 1 mz/g prior to any dry granulation and/or dry compression steps, (vi) if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (vii) the alkaline substance has a BET-area of at least about 1 mZ/g prior to any dry granulation and/or dry compression steps, (viii) the tablet formufiation further comprises a disintegrant in an amount of about 1-30% by weight.
In a preferred embodiment the benzimidazole is pantoprazole such as pantoprazole sodium hydrate or pantoprazole sodium sesquihydrate. In other preferred embodiments the benzimidazole may be omeprazole or a salt and/or a hydrate thereof, lansoprazole or a salt and/or a hydrate thereof, esomeprazol or a salt and/or a hydrate thereof, aripiprazole or a salt and/or a hydrate thereof, rabeprazol or a salt and/or a hydrate thereof, or timoprazole or a salt and/or a hydrate thereof.
In another preferred embodiment, said formulation further comprises other pharmaceutically acceptable excipients such as fillers, dry binders, glidants and lubricants.
In a particularly preferred embodiment, said formulation comprises crospovidone as a disintegrant in an amount of from about 5-20%, preferably 7,5-15%, most preferably 10-13% by weight.
In yet another embodiment, said formulation comprises a subcoat. In a particularly preferred embodiment however, said formulation does not comprise a subcoat. in the Examples it is shown that it is possible according to the present invention to obtain tablet formulations with good stability properties and good dissolution profiles without the laborious steps of applying a subcoat.
In yet another preferred embodiment, the alkaline substance is a salt of an organic or an 5 inorganic acid where the anion of the salt is carbonate (C032"), hydrogenphosphate (HP042"
) or phosphate (P043"). The alkaline substance may also be a salt of an organic or an inorganic acid where the kation is sodium (Na}), caicium (CaZ+) or magnesium (Mg2+).
Preferably, the salt of the organic and/or inorganic acid according is sodiumcarbonate (NaZCO3), or Calciumcarbonate (CaCO3) trisodiumphosphate (Na3PO4), disodiumhydrogenphosphate (NazHPO4), hydrazine or derivatives thereof, lysine or a derivative thereof, arginine or a derivative thereof, or histidine or a derivative thereof.
In yet another preferred embodiment, dry granulation is provided by means of a roller compactor.
In a final preferred embodiment, the mixture has been subject to sieving prior to tablet compression with a sieve size (Roller compactor) of 1,25 mm or less. It is shown in the examples that relatively small and, relatively homogenous particles result in a more accurate dosing of the active compound. Doze accuracy is of particular importance in production of relatively small tablets.
In a final aspect, the present invention relates to products obtainable or.obtained by the methods disclosed herein.
Definitions Pharmaceutical tablet formulation:
A pharmaceutical tablet formulation according to the present invention is equivalent to a solid dosis form.
Druas:
According to the present invention, the drug substance belongs to the group of benzimidazoles or salts and/or hydrates thereof. The benzimidazole is preferably pantoprazole, omeprazole, lansoprazole, timoprazol, aripiprazole, rabeprazol or esomeprazole, as well as pharmaceutically acceptable salts, hydrates and mixtures thereof. Preferably, the benzimidazole is pantoprazole sodium sesquihydrate.
Any pharmaceutically acceptable salt can be used. Examples of conventionally used salts are sodium or potassium salts of the drug substance.
A pharmaceutical formulation according to the present invention comprises about 1 to 500 mg drug pr. dose; such as 1 to 200 mg; or 1 to 100 mg. Preferably, the unit dose comprises 10-120 mg; 15-100 mg; 15-80 mg, 15-70 mg; 15-60 mg; 15-50 mg; 15-45 mg; such as 20, 30, or 40 mg of benzimidazole, preferably pantoprazole.
Unit dose is a pharmaceutically formulated unit comprising the dosage of drug substance intended for administration. The dosage unit can be a tablet.
Alkaline substance:
Due to the acid labile nature of the drug substance, the unit dose comprises an alkaline substance, or a mixture of two or more different alkaline substances, in the core to confer shelf life stability of the pharmaceutical formulation, The alkaline substance according to the present invention may be soluble in water or even practically insoluble in water. E.g., I part of water soluble alkaline substance might be dissolved in about e.g. 100, 50, 30, or 10 parts of water or less. 1 part of alkaline substance with low water solubility may be dissolved in at least about 100, 300, 500, 1000, 10,000 or even more than 10,000 parts of water. This is in contrast tc) conventional production methods employing wet granulation wherein water soluble alkaline substances are preferred. The rationale behind using water soluble alkaline substances in conventional methods is that water soluble alkaline substances are thought to generate a humid environment with an alkaline pH protecting the active drug substance during disintegration of the tabiet in the gastric system. In the present invention it is surprisingly demonstrated in the Examples 6, 8 og 15 that alkaline substances such as calcium carbonate which are practically insoluble in water (1 part in more than 10,000 parts of water according to handbook of Pharmaceutical Excipients, 5" ed.) may result in stable formulations with good dissolution profiles. It however appears that alkaiine substances with low water solubility should preferably have a relatively large BET area (about 1 mZ/g or more).
Generally, alkaline earth metal salts (such as e.g. calcium carbonate, magnesium oxide, magnesium carbonate) tend to have low water solubility. On the other hand, alkali metal ,. -salts (such as e.g. sodium carbonate and potassium carbonate) tend to be more water soluble.
According to the prior art such as e.g. W005009410 (Dr. Reddy's), ratios between benzimidazole and alkaline substance of about 1:0.17 are disclosed (Examples 1 and 2).
On basis of the existing knowledge in the art, the skilled man would thus not expect that it would be possible to use ratios of 1:0.2 and above and definitely not ratios of about 1:0.5 or 1:1 or more since increasing amounts of base would be expected to result in slow ' dissolution profiles of the active compound. According to the present invention however, the weight ratio between the drug substance and the alkaline substance ranges between 1:0.2 to 1:10, preferably between 1:0.5 and 1:5, and most preferably between 1:1 to 1:5 while surprisingly still providing formulations with a combination of good shelf life stabilities and good dissolution profiles (examples 6, 8, and 15). The weight ratio between the drug and the alkaline substance may thus be about 1:0.2, or 1:0.3, or 1:0.4, or 1:0.5, or 1:0.6, or 1: 0.7, or 1:
0.8,or1:0.9or1:1,or1:1.5,or1:2,or1:2.5,or1:3,or1:3.5, or1:4,or1:4.5,or1:5,or1:6,or1:7,or1:8,or1:9,or1:10.
It is preferred that the pKa of the chosen alkaline material is at least 10.
However, this alone is not sufficient. If the alkaiine material is polyvalent the pKal, (where pKaI is the most acidic pKa value) should be above 6. As shown in ex. 6 the use of tricalcium phosphate which has a pKal of 2.2 results in a poorer stability than if disodium carbonate (which has a pKal of 6.4) is used.
Alkaline substance preferably having a pKa value of 6 or above. The alkaline substance will typically provide an alkaline pH in the range of 7-12, when being dissolved and/or dispersed in water at room temperature in an amount of about 10-100 mg/mi.
Accordingly, the term alkaline substance includes the corresponding base of an organic or an inorganic acid, such as provided in the form of a pharmaceutically acceptable salt of an organic or inorganic acid and/or a mixture thereof, and some amino acids.
According to the present invention, it is understood that a pharmaceutical formulation may very well comprise more than one aikaline substance, if appropriate.
The alkaline substance raw material is understood to be the alkaline substance prior to any formulation processing steps.
Examples of alkaline substances are listed in the following table.
Alkaline substance:
Due to the acid labile nature of the drug substance, the unit dose comprises an alkaline substance, or a mixture of two or more different alkaline substances, in the core to confer shelf life stability of the pharmaceutical formulation, The alkaline substance according to the present invention may be soluble in water or even practically insoluble in water. E.g., I part of water soluble alkaline substance might be dissolved in about e.g. 100, 50, 30, or 10 parts of water or less. 1 part of alkaline substance with low water solubility may be dissolved in at least about 100, 300, 500, 1000, 10,000 or even more than 10,000 parts of water. This is in contrast tc) conventional production methods employing wet granulation wherein water soluble alkaline substances are preferred. The rationale behind using water soluble alkaline substances in conventional methods is that water soluble alkaline substances are thought to generate a humid environment with an alkaline pH protecting the active drug substance during disintegration of the tabiet in the gastric system. In the present invention it is surprisingly demonstrated in the Examples 6, 8 og 15 that alkaline substances such as calcium carbonate which are practically insoluble in water (1 part in more than 10,000 parts of water according to handbook of Pharmaceutical Excipients, 5" ed.) may result in stable formulations with good dissolution profiles. It however appears that alkaiine substances with low water solubility should preferably have a relatively large BET area (about 1 mZ/g or more).
Generally, alkaline earth metal salts (such as e.g. calcium carbonate, magnesium oxide, magnesium carbonate) tend to have low water solubility. On the other hand, alkali metal ,. -salts (such as e.g. sodium carbonate and potassium carbonate) tend to be more water soluble.
According to the prior art such as e.g. W005009410 (Dr. Reddy's), ratios between benzimidazole and alkaline substance of about 1:0.17 are disclosed (Examples 1 and 2).
On basis of the existing knowledge in the art, the skilled man would thus not expect that it would be possible to use ratios of 1:0.2 and above and definitely not ratios of about 1:0.5 or 1:1 or more since increasing amounts of base would be expected to result in slow ' dissolution profiles of the active compound. According to the present invention however, the weight ratio between the drug substance and the alkaline substance ranges between 1:0.2 to 1:10, preferably between 1:0.5 and 1:5, and most preferably between 1:1 to 1:5 while surprisingly still providing formulations with a combination of good shelf life stabilities and good dissolution profiles (examples 6, 8, and 15). The weight ratio between the drug and the alkaline substance may thus be about 1:0.2, or 1:0.3, or 1:0.4, or 1:0.5, or 1:0.6, or 1: 0.7, or 1:
0.8,or1:0.9or1:1,or1:1.5,or1:2,or1:2.5,or1:3,or1:3.5, or1:4,or1:4.5,or1:5,or1:6,or1:7,or1:8,or1:9,or1:10.
It is preferred that the pKa of the chosen alkaline material is at least 10.
However, this alone is not sufficient. If the alkaiine material is polyvalent the pKal, (where pKaI is the most acidic pKa value) should be above 6. As shown in ex. 6 the use of tricalcium phosphate which has a pKal of 2.2 results in a poorer stability than if disodium carbonate (which has a pKal of 6.4) is used.
Alkaline substance preferably having a pKa value of 6 or above. The alkaline substance will typically provide an alkaline pH in the range of 7-12, when being dissolved and/or dispersed in water at room temperature in an amount of about 10-100 mg/mi.
Accordingly, the term alkaline substance includes the corresponding base of an organic or an inorganic acid, such as provided in the form of a pharmaceutically acceptable salt of an organic or inorganic acid and/or a mixture thereof, and some amino acids.
According to the present invention, it is understood that a pharmaceutical formulation may very well comprise more than one aikaline substance, if appropriate.
The alkaline substance raw material is understood to be the alkaline substance prior to any formulation processing steps.
Examples of alkaline substances are listed in the following table.
Table 1: Examples of alkaline substances Substance Examples Structure pKa*
Saft of carbonic acid DiSodium carbonate Na2CO3 10.3 (carbonate) and phosphoric acid Sodium hydrogen NaHCO3 6.4 (phosphate). Soluble carbonate salts with pKa-values of 9 and above Trisodium phosphate Na3PO4 12.4 Disodium hydrogen Na2HPO4 7.2 phosphate Sodium dihydrogen NaH2PO4 2.2 phosphate Salt of carbonic acid Calcium carbonate CaCO3 10.3 (carbonate). Practically insoluble with pKa-value of 9 or above Amino acids with pKa3- Lysine C6H1402N2 pKa2: 8.9 Values of 9 or above pKa3: 10.3 Arginine C6H14N402 pKa2:9.1 pKa3: 13.2 pHz11.4 (100 g/L Hz0) Histidine - C6HgOZN3 pKa3:9.0 pH~z;7.7 (10 g/L HZO) * The pKa-values in this table are approximate values and refer to the pKa of the acid.
Only relevant pKa values are included.
A suitable disintegration time means that the pharmaceutical formulation must comply with the standards set up in the European Pharmacopoeia. Those skilled in the art will appreciate that it is desirable for compressed tablets to disintegrate within 30 minutes, most desirable within 15 minutes upon contact with an aqueous solution, provided that the enteric coating is absent or bursted. Disintegration is preferably performed in a dissolution apparatus such as the Ph.Eur. Basket method as disclosed in e.g. example 11.
Furthermore, it should be understood that the alkaline substance should be provided in solid form, such as in the form of a powder, granulate or the like.
In connection with the present invention (example 16) it has been demonstrated that different alkaline substances may have different surface areas (BET areas) and that the same compound purchased under different trade names (e.g. calcium carbonate -"Sturcal L" and "Scoralite") may have different BET areas (see the SEM pictures in the figures). It is furthermore demonstrated that alkaline substances with reiativeiy large BET
areas (at least about 0.5, 0.6, 0.7, 0.8, 0.9, preferably at least about 1.0, 1.1, 1.2, 1.3, 1.4, and most preferably 1.5 mZ/g or more) tend to result in tablets with improved stability properties while at the same time retaining good dissolution properties (example 15). A
plausible explanation for this finding is that porous alkaline substances with relatively large BET
areas used as a raw material tend to be crushed into fine particles upon mechanical pressure such.as e.g. dry granulation and/or dry compression. In contrast, substances with relatively small BET areas (such as e.g. calcium carbonate purchased under the trade name "Scora{ite") tends to either not being affected by mechanical pressure and/or to be crushed into relatively large particles and/or to show a slightly improved distribution of the particles around the drug substance. It is thus preferred to use porous and/or polycrystallic alkaline substances with relative large BET area having a tendency to be crushed into very fine particles upon mechanical pressure. Such alkaline substances in the form of very fine particles in the resulting tablet most likely provide a better "alkaline shield" against acid and humidity attacks of the active compound by providing a close physical contact between the drug and the protective alkaline substance. It is shown in Example 10 that a particularly preferred way of providing a close physical contact and thus a stable tablet with good dissolution profiles is to include a step wherein the two substances are mixed and subsequently dry granulated together prior to compression into a tablet.
Pharmaceutical excipients:
It is shown in the Examples that it is possible to compress tablets with good stability and dissolution profiles where the only pharmaceutical exciplent, apart from the alkaline substance, is minute amounts of MgStearate (example 5). When manufacturing tablets according to the invention in larger scale, such as in production scale, it can however be advantageous to add at least one of the following ingredients: a l~g_dant, a lubricant, a filler, a dry binder, a color, and a disinte rq ant to the formulation comprising alkaline substance and a benzimidazole. Preferably, the only additional pharmaceutical excipient is a glidant or a lubricant, preferably along with at least one disintegrant, thus providing a simple and cost efficient production method.
Examples of lig dant and lubricants are stearic acid, metallic stearates, talc, colloidal silica, sodium stearyl fumarate and alkyl sulphates.
In the present invention, a dry binder such as e.g. sorbitol, isomalt, or mixtures thereof may be used. The dry binder provides the effect of binding a material and thereby providing a powder that can be compressed into a tablet.
A ftller substance is any pharmaceutically acceptable substance that does not interact with the drug substance or with other excipients. Commonly used filler substances are:
mannitol, Dextrins, maltodextrins (e.g. Lodex 5 and Lodex 10), inositol, erythritol, isomalt, lactitol, maltitol, mannitol, xylitol, low-substituted hydroxypropylcellulose (e.g LH
Saft of carbonic acid DiSodium carbonate Na2CO3 10.3 (carbonate) and phosphoric acid Sodium hydrogen NaHCO3 6.4 (phosphate). Soluble carbonate salts with pKa-values of 9 and above Trisodium phosphate Na3PO4 12.4 Disodium hydrogen Na2HPO4 7.2 phosphate Sodium dihydrogen NaH2PO4 2.2 phosphate Salt of carbonic acid Calcium carbonate CaCO3 10.3 (carbonate). Practically insoluble with pKa-value of 9 or above Amino acids with pKa3- Lysine C6H1402N2 pKa2: 8.9 Values of 9 or above pKa3: 10.3 Arginine C6H14N402 pKa2:9.1 pKa3: 13.2 pHz11.4 (100 g/L Hz0) Histidine - C6HgOZN3 pKa3:9.0 pH~z;7.7 (10 g/L HZO) * The pKa-values in this table are approximate values and refer to the pKa of the acid.
Only relevant pKa values are included.
A suitable disintegration time means that the pharmaceutical formulation must comply with the standards set up in the European Pharmacopoeia. Those skilled in the art will appreciate that it is desirable for compressed tablets to disintegrate within 30 minutes, most desirable within 15 minutes upon contact with an aqueous solution, provided that the enteric coating is absent or bursted. Disintegration is preferably performed in a dissolution apparatus such as the Ph.Eur. Basket method as disclosed in e.g. example 11.
Furthermore, it should be understood that the alkaline substance should be provided in solid form, such as in the form of a powder, granulate or the like.
In connection with the present invention (example 16) it has been demonstrated that different alkaline substances may have different surface areas (BET areas) and that the same compound purchased under different trade names (e.g. calcium carbonate -"Sturcal L" and "Scoralite") may have different BET areas (see the SEM pictures in the figures). It is furthermore demonstrated that alkaline substances with reiativeiy large BET
areas (at least about 0.5, 0.6, 0.7, 0.8, 0.9, preferably at least about 1.0, 1.1, 1.2, 1.3, 1.4, and most preferably 1.5 mZ/g or more) tend to result in tablets with improved stability properties while at the same time retaining good dissolution properties (example 15). A
plausible explanation for this finding is that porous alkaline substances with relatively large BET
areas used as a raw material tend to be crushed into fine particles upon mechanical pressure such.as e.g. dry granulation and/or dry compression. In contrast, substances with relatively small BET areas (such as e.g. calcium carbonate purchased under the trade name "Scora{ite") tends to either not being affected by mechanical pressure and/or to be crushed into relatively large particles and/or to show a slightly improved distribution of the particles around the drug substance. It is thus preferred to use porous and/or polycrystallic alkaline substances with relative large BET area having a tendency to be crushed into very fine particles upon mechanical pressure. Such alkaline substances in the form of very fine particles in the resulting tablet most likely provide a better "alkaline shield" against acid and humidity attacks of the active compound by providing a close physical contact between the drug and the protective alkaline substance. It is shown in Example 10 that a particularly preferred way of providing a close physical contact and thus a stable tablet with good dissolution profiles is to include a step wherein the two substances are mixed and subsequently dry granulated together prior to compression into a tablet.
Pharmaceutical excipients:
It is shown in the Examples that it is possible to compress tablets with good stability and dissolution profiles where the only pharmaceutical exciplent, apart from the alkaline substance, is minute amounts of MgStearate (example 5). When manufacturing tablets according to the invention in larger scale, such as in production scale, it can however be advantageous to add at least one of the following ingredients: a l~g_dant, a lubricant, a filler, a dry binder, a color, and a disinte rq ant to the formulation comprising alkaline substance and a benzimidazole. Preferably, the only additional pharmaceutical excipient is a glidant or a lubricant, preferably along with at least one disintegrant, thus providing a simple and cost efficient production method.
Examples of lig dant and lubricants are stearic acid, metallic stearates, talc, colloidal silica, sodium stearyl fumarate and alkyl sulphates.
In the present invention, a dry binder such as e.g. sorbitol, isomalt, or mixtures thereof may be used. The dry binder provides the effect of binding a material and thereby providing a powder that can be compressed into a tablet.
A ftller substance is any pharmaceutically acceptable substance that does not interact with the drug substance or with other excipients. Commonly used filler substances are:
mannitol, Dextrins, maltodextrins (e.g. Lodex 5 and Lodex 10), inositol, erythritol, isomalt, lactitol, maltitol, mannitol, xylitol, low-substituted hydroxypropylcellulose (e.g LH
11, LH 20, LH 21, LH 22, LH 30, LH 31, LH 32 available from Shin-Etsu Chemical Co.), starches or modified starches (e.g potato starch, maize starch, rice starch, pre-gelatinised starch), polyvinylpyrrolidone, polyvinylpyrrolidone/vinyl acetate copolymer, agar (e.g.
sodium alginate), , carboxyalkylcellulose, dextrates, gelatine, gummi arabicum, hydroxypropyl cellulose, hydroxypropyimethylcellulose, methylceliulose, polyethylene glycol, polyethylene oxide, polysaccharides e.g. dextran, soy polysaccharide, sodium carbonate, and sodium chloride.
A wet binder is an excipient that in combination with water facilitates a powder to be =
5 compressed into coherent bodies such as tablets or facilitates a powder to be granulated into a paiticulate matter. A wet binder must, at least to some extent, be soluble in water.
Examples of wet binders are PVP (polyvinylpyrrolidone), HPMC
(hydroxymethylpropylcellulose) or getatine. If a wet binder is used according to the present invention, the wet binder will merely act as a filler and will not exhibit the binding 10 properties normally associated with such wet binders. It will therefore be understood that excipients conventionally regarded as wet binders might be used as mere fillers in the context of the present invention.
A disintegrant is a pharmaceutically acceptable substance that improves the disintegration of tablets without interacting with the drug substance or with any other exciplents. The disintegrant has the capability of swelling upon contact with water, causing the tablet to swell/disintegrate and thus releasing the active compound. This effect is shown in the Examples (example 18), where dissolution profiles are improved upon addition of disintegrant in the tablet. Traditional wet granulated benzimidazole formulations normally comprise large amounts of disintegrants (at least about 30%) since "wet"
production steps cause a significant proportion of the disintegrant to swell and thus irreversibly reducing its swelling capacity. However, in connection with the present invention it has surprisingly been shown that it is possible to obtain a good dissolution profile using relatively small amounts of disintegrant thus enabling production of smaller tablets using more cost-efficient methods (disintegrants are often relatively expensive ingredients).
Small tablets have the advantage of being easier to swallow, pack, store, transport, etc.
Small tablets furthermore improve movement through the gastric system and are less dependent on the gastric emptying. This effect is probably achieved because dry granulatian techniques do not result in unwanted preswelling of the disintegrant. It is furthermore shown that it is possible to use water in connection with the subcoating and/or the enteric coating process without causing unwanted preswelling and/or disintegration of the tablets (example 12, figure 8).
Examples of commonly used disintegrants are: Alginic acid - alginates, carboxymethylcellulose calcium, carboxymethylcellulose sodium, crospovidone, hydroxypropylcellulose, hydroxypropylmethylcel lu lose (HPMC), cellulose derivatives such as low-substituted hydroxypropylcellulose (e.g LH 11, LH 20, LH 21, LH 22, LH
30, LH 31, LH 32 available from Shin-Etsu Chemical Co.) and microcrystalline cellulose, polacrilin , potassium or sodium, polyacrylic acid, polycarbofif, polyethylene glycol, polyvinylacetate, crosslinked polyvinylpyrrolidone (e.g. Polyvidon(D CL, Polyvidon CL-M, Kollidon CL, Polyplasdone XL, Poiyplasdone XL-10); sodium carboxymethyl starch (e.g.
Primogel(D
and Explotabo), sodium croscarmellose (i.e. cross-linked carboxymethylcellulose sodium salt; e.g. Ac-Di-SalO), sodium starch glycolate, starches (e.g potato starch, maize starch, rice starch), and pre-gelatinised starch.
The disintegrant may be present in the tablet in an amount of about 1-30%, preferably 3-25%, more preferably 5-20% and most preferably 10-15 !0, and even most preferably about 8-14%.
Granulation and compression:
Powders comprising either the drug in question, the alkaline substance, the pharmaceutical excipient(-s), or any combination thereof are subjected to a dry granulation process. The dry granulation process causes the powder to agglomerate into larger particles having a size suitable for further processing. Dry granulation can 'thus be said to improve the flowability of a mixture in order to be able to produce tablets that comply with the demand of mass variation or content uniformity set out in the European Pharmacopoeia.
Formulations according to the invention may be produced using one or more mixing and dry granulations steps. The order and the number of the mixing and granulation steps do not seem to be critical. However, it seems to be of importance that at least one of the alkaline substance and the drug has been subject to dry granulation before compression into tablets. Dry granulation of drug and alkaline substance together prior to tablet compression seem, surprisingly, to be a simple, inexpensive and efficient way of providing close physical contact between the alkaline substance and the drug and thus a tablet formulation with good stability properties. Relatively large BET areas of the alkaline raw material do also have a beneficial effect on the stability properties.
Dry granulation is carried out by a mechanical process, which transfers energy to the mixture without any use of any liquid substances (neither in the form of aqueous solutions, solutions based on organic solutes, or mixtures thereof) in contrast to conventional wet granulation processes. Generally, the mechanical process requires compaction such as the one provided by roller compaction. An example of an alternative method for dry granulation is slugging.
Roller compaction is a process comprising highly intensive mechanical compacting of one or more substances. The powder is pressed, that is roller compacted, between 2 counter rotating rollers to make a solid sheet which is subsequently crushed in a sieve to form a particulate matter. In this particulate matter a close mechanical contact between the substance(-s) has been obtained. An example of equipment is Minipactoro or a Gerteis 3W-Polygran from Gerteis Maschinen + Processengineering AG.
Tablet comaression according to the present invention takes place without any use of any liquid substances (neither in the form of aqueous solutions, solutions based on organic solutes, or mixtures thereof). In a typical embodiment the resulting core or tablet must have a crushing strength in the range of 10 to 150 N; such as 15 to 125 N, preferably in the range of 20 to 100 N.
A core is thus provided by compression of a powder or a particulate matter.
Typically the core has a weight in the range of 75 mg to 2.5 g; such as 80 mg to 1 g; such as 80 mg to 500 mg; such as 100 mg to 300 mg. Preferably, the core is a tablet with a weight in the range of 75 mg to 2.5 g; such as 80 mg to 1 g; such as 80 mg to 500 mg; such as 100 mg to 300 mg. In the present invention, the core is further coated with an enteric coat and optionally a subcoat to obtain the desired tablet formulation.
Tablets according to the present invention may be smaller than conventional tablets, i.e.
having a diameter of about 7, preferably about 6 and most preferably about 5 mm or below. In contrast to tablets with a diameter of e.g. 7.S mm or above, tablets having a smaller diameter will be able to move freely through the pylorus sphincter into the small intestine and thus be less dependent on the gastric emptying.
Subcoatinci:
Any conventionally used water soluble film forming excipient can be used for subcoating such as a sugar, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, hydroxypropyl cellulose, methyl cellulose, hydroxymethyl cellulose, hydroxypropyl methylcellulose, polyvinyl acetal diethylenaminoacetate, "Kollicoat IR" (polyvinyl alcohol -polyethylene grycol graft copolymer), etc. Water or any conventionally used organic solvent or a mixture thereof is suitable as a subcoating solvent.
It is a general teaching within the field that the subcoat is critical to the stability of the entire formulation. In Sage (WO 9850019) it is e.g. disclosed that the enteric coating and the drug must be separated by a subcoat in order to avoid acid degradation of the drug (page 8, lines 16-30). Even though absence of a subcoat may be suggested in various patent documents (e.g. as a non-enabling statement in WO 04075881 on page 3, line 21) the existing knowledge leads the skilled person to the conclusion that tablets produced without subcoating have a poor drug stability. In contrast to the general teaching, the inventors of the present invention have surprisingly shown that is possible to produce tablets without subcoating having a drug stability compared with tablets with conventional subcoating (table 18 and figure 9). As the subcoating process is laborious and time consuming, a production process according to the present invention without laborious subcoating steps is thus far more cost-efficient while still obtaining a product with the desired stability and dissolution properties.
Enteric coating Any conventionally used enteric coating polymer can be used such as celiulose acetate phthalate such as Aquacoat CPD (FMC) or C-A-P NF (Eastman Chemical), polyvinyl acetate phthalate such as Sureteric (Colorcon), carboxymethylethylcellulose, co-polymerized methacrylic acid/methacrylic acid methyl esters such as Eudragit L 30 D, or Eudragit L 12.5 or Eudragit L 100 (Degussa - Rbhm Pharma Polymers) or Kollicoat MAE
30 DP or Kollicoat 1OOP (BASF) or Acryl-Eze (Colorcon) or Eastacryl 30 D
(Eastman Chemical) etc.
Preferred plasticizers include cetanol, triacetin, citric acid esters such as Citroflexo (Pfizer), phthalic acid esters, dibutyl succinate, acetylated monoglyceride, acetyltributyl, acetyltributyl citrate, acetyltriethyl citrate, benzyl benzoate, calcium stearate, castor oil, cetanot, chlorebutanol, colloidal silica dioxide, dibutyl phthalate, dibutyl sebacate, diethyl oxalate, diethyl malate, diethyl maleate, diethyl malonate, diethyl fumarate, diethyl phthalate, diethyl sebacate, diethyl succinate, dimethylphthalate, dioctyl phthalate, glycerin, glyceroltributyrate, glyceroltriacetate, glyceryl behanate, glyceryl monostearate, hydrogenated vegetable oil, lecithin, leucine, magnesium silicate, magnesium stearate, polyethylene glycol, propylene, glycol, polysorbate, silicone, stearic acid, talc, titanium dioxide, triacetin, tributyl citrate, triethyl citrate, zinc stearate, PEG
(polyethylene glycol), etc. Methods for enteric coating are well known in the art such as described in e.g. (Stuart C. Porter in Remmington 215t Ed. 2005, pp 929), hereby incorporated by reference.
Stability Preferably, at least 95% (w/w) of the declared content of drug substance remains in the tablet formulation according to the present invention after storage at 25C /60 %RH
(relative humidity) of a period of 2, 3, 4, or 5 years. Alternatively, the stability can be determined after storage at other conditions according to appropriate ICH
guidelines.
Methods of assessing stability are described in the Examples.
Brief description of drawings Flgure 1: Stability test of coated tablets containing Sodium Carbonate, Calcium Carbonate (Sturcal L), or Tri calcium phosphate. Test performed in open petri dishes at 70 and not more than (nmt) 10 % relative humidity. Example 6.
Figure 2: Stability test of coated tablets containing Sodium Carbonate or Calcium Carbonate (Sturcal L) in the mixing ratio's of 1:0.2 or 1:0.8. Test performed in open petri dishes at 700 and not more than (nmt) 10 % relative humidity. Example 8.
Figure 3: Stability test of coated tablets containing Sodium Carbonate (Sturcal L) 1:0.8 based on different sequential order of mixing and roller compaction. Test performed in open petri dishes at 70 and not more than (nmt) 10 %-relative humidity.
Example 10.
Figure 4: Particle size distribution using two different sieve sizes (1.25 mm and 1.0 mm) during roller compaction. Example 11.
Figure 5: Impact on dose variation of Roller compactor sieve size illustrated by tablet core dissolution. Example 11.
Figure 6: Impact on dissolution of amount of subcoat, HPMC E15, applied.
Example 12.
Figure 7: Impact on dissolution of type of subcoat, HPMC E 5 and HPMC E 15.
Evaluated on subcoated tablets. Example,12.
Figure 8: Impact on dissolution of type of subcoat, HPMC E 5 and HPMC E 15.
Evaluated for enteric coated tablets. Example 12.
sodium alginate), , carboxyalkylcellulose, dextrates, gelatine, gummi arabicum, hydroxypropyl cellulose, hydroxypropyimethylcellulose, methylceliulose, polyethylene glycol, polyethylene oxide, polysaccharides e.g. dextran, soy polysaccharide, sodium carbonate, and sodium chloride.
A wet binder is an excipient that in combination with water facilitates a powder to be =
5 compressed into coherent bodies such as tablets or facilitates a powder to be granulated into a paiticulate matter. A wet binder must, at least to some extent, be soluble in water.
Examples of wet binders are PVP (polyvinylpyrrolidone), HPMC
(hydroxymethylpropylcellulose) or getatine. If a wet binder is used according to the present invention, the wet binder will merely act as a filler and will not exhibit the binding 10 properties normally associated with such wet binders. It will therefore be understood that excipients conventionally regarded as wet binders might be used as mere fillers in the context of the present invention.
A disintegrant is a pharmaceutically acceptable substance that improves the disintegration of tablets without interacting with the drug substance or with any other exciplents. The disintegrant has the capability of swelling upon contact with water, causing the tablet to swell/disintegrate and thus releasing the active compound. This effect is shown in the Examples (example 18), where dissolution profiles are improved upon addition of disintegrant in the tablet. Traditional wet granulated benzimidazole formulations normally comprise large amounts of disintegrants (at least about 30%) since "wet"
production steps cause a significant proportion of the disintegrant to swell and thus irreversibly reducing its swelling capacity. However, in connection with the present invention it has surprisingly been shown that it is possible to obtain a good dissolution profile using relatively small amounts of disintegrant thus enabling production of smaller tablets using more cost-efficient methods (disintegrants are often relatively expensive ingredients).
Small tablets have the advantage of being easier to swallow, pack, store, transport, etc.
Small tablets furthermore improve movement through the gastric system and are less dependent on the gastric emptying. This effect is probably achieved because dry granulatian techniques do not result in unwanted preswelling of the disintegrant. It is furthermore shown that it is possible to use water in connection with the subcoating and/or the enteric coating process without causing unwanted preswelling and/or disintegration of the tablets (example 12, figure 8).
Examples of commonly used disintegrants are: Alginic acid - alginates, carboxymethylcellulose calcium, carboxymethylcellulose sodium, crospovidone, hydroxypropylcellulose, hydroxypropylmethylcel lu lose (HPMC), cellulose derivatives such as low-substituted hydroxypropylcellulose (e.g LH 11, LH 20, LH 21, LH 22, LH
30, LH 31, LH 32 available from Shin-Etsu Chemical Co.) and microcrystalline cellulose, polacrilin , potassium or sodium, polyacrylic acid, polycarbofif, polyethylene glycol, polyvinylacetate, crosslinked polyvinylpyrrolidone (e.g. Polyvidon(D CL, Polyvidon CL-M, Kollidon CL, Polyplasdone XL, Poiyplasdone XL-10); sodium carboxymethyl starch (e.g.
Primogel(D
and Explotabo), sodium croscarmellose (i.e. cross-linked carboxymethylcellulose sodium salt; e.g. Ac-Di-SalO), sodium starch glycolate, starches (e.g potato starch, maize starch, rice starch), and pre-gelatinised starch.
The disintegrant may be present in the tablet in an amount of about 1-30%, preferably 3-25%, more preferably 5-20% and most preferably 10-15 !0, and even most preferably about 8-14%.
Granulation and compression:
Powders comprising either the drug in question, the alkaline substance, the pharmaceutical excipient(-s), or any combination thereof are subjected to a dry granulation process. The dry granulation process causes the powder to agglomerate into larger particles having a size suitable for further processing. Dry granulation can 'thus be said to improve the flowability of a mixture in order to be able to produce tablets that comply with the demand of mass variation or content uniformity set out in the European Pharmacopoeia.
Formulations according to the invention may be produced using one or more mixing and dry granulations steps. The order and the number of the mixing and granulation steps do not seem to be critical. However, it seems to be of importance that at least one of the alkaline substance and the drug has been subject to dry granulation before compression into tablets. Dry granulation of drug and alkaline substance together prior to tablet compression seem, surprisingly, to be a simple, inexpensive and efficient way of providing close physical contact between the alkaline substance and the drug and thus a tablet formulation with good stability properties. Relatively large BET areas of the alkaline raw material do also have a beneficial effect on the stability properties.
Dry granulation is carried out by a mechanical process, which transfers energy to the mixture without any use of any liquid substances (neither in the form of aqueous solutions, solutions based on organic solutes, or mixtures thereof) in contrast to conventional wet granulation processes. Generally, the mechanical process requires compaction such as the one provided by roller compaction. An example of an alternative method for dry granulation is slugging.
Roller compaction is a process comprising highly intensive mechanical compacting of one or more substances. The powder is pressed, that is roller compacted, between 2 counter rotating rollers to make a solid sheet which is subsequently crushed in a sieve to form a particulate matter. In this particulate matter a close mechanical contact between the substance(-s) has been obtained. An example of equipment is Minipactoro or a Gerteis 3W-Polygran from Gerteis Maschinen + Processengineering AG.
Tablet comaression according to the present invention takes place without any use of any liquid substances (neither in the form of aqueous solutions, solutions based on organic solutes, or mixtures thereof). In a typical embodiment the resulting core or tablet must have a crushing strength in the range of 10 to 150 N; such as 15 to 125 N, preferably in the range of 20 to 100 N.
A core is thus provided by compression of a powder or a particulate matter.
Typically the core has a weight in the range of 75 mg to 2.5 g; such as 80 mg to 1 g; such as 80 mg to 500 mg; such as 100 mg to 300 mg. Preferably, the core is a tablet with a weight in the range of 75 mg to 2.5 g; such as 80 mg to 1 g; such as 80 mg to 500 mg; such as 100 mg to 300 mg. In the present invention, the core is further coated with an enteric coat and optionally a subcoat to obtain the desired tablet formulation.
Tablets according to the present invention may be smaller than conventional tablets, i.e.
having a diameter of about 7, preferably about 6 and most preferably about 5 mm or below. In contrast to tablets with a diameter of e.g. 7.S mm or above, tablets having a smaller diameter will be able to move freely through the pylorus sphincter into the small intestine and thus be less dependent on the gastric emptying.
Subcoatinci:
Any conventionally used water soluble film forming excipient can be used for subcoating such as a sugar, polyethylene glycol, polyvinylpyrrolidone, polyvinyl alcohol, hydroxypropyl cellulose, methyl cellulose, hydroxymethyl cellulose, hydroxypropyl methylcellulose, polyvinyl acetal diethylenaminoacetate, "Kollicoat IR" (polyvinyl alcohol -polyethylene grycol graft copolymer), etc. Water or any conventionally used organic solvent or a mixture thereof is suitable as a subcoating solvent.
It is a general teaching within the field that the subcoat is critical to the stability of the entire formulation. In Sage (WO 9850019) it is e.g. disclosed that the enteric coating and the drug must be separated by a subcoat in order to avoid acid degradation of the drug (page 8, lines 16-30). Even though absence of a subcoat may be suggested in various patent documents (e.g. as a non-enabling statement in WO 04075881 on page 3, line 21) the existing knowledge leads the skilled person to the conclusion that tablets produced without subcoating have a poor drug stability. In contrast to the general teaching, the inventors of the present invention have surprisingly shown that is possible to produce tablets without subcoating having a drug stability compared with tablets with conventional subcoating (table 18 and figure 9). As the subcoating process is laborious and time consuming, a production process according to the present invention without laborious subcoating steps is thus far more cost-efficient while still obtaining a product with the desired stability and dissolution properties.
Enteric coating Any conventionally used enteric coating polymer can be used such as celiulose acetate phthalate such as Aquacoat CPD (FMC) or C-A-P NF (Eastman Chemical), polyvinyl acetate phthalate such as Sureteric (Colorcon), carboxymethylethylcellulose, co-polymerized methacrylic acid/methacrylic acid methyl esters such as Eudragit L 30 D, or Eudragit L 12.5 or Eudragit L 100 (Degussa - Rbhm Pharma Polymers) or Kollicoat MAE
30 DP or Kollicoat 1OOP (BASF) or Acryl-Eze (Colorcon) or Eastacryl 30 D
(Eastman Chemical) etc.
Preferred plasticizers include cetanol, triacetin, citric acid esters such as Citroflexo (Pfizer), phthalic acid esters, dibutyl succinate, acetylated monoglyceride, acetyltributyl, acetyltributyl citrate, acetyltriethyl citrate, benzyl benzoate, calcium stearate, castor oil, cetanot, chlorebutanol, colloidal silica dioxide, dibutyl phthalate, dibutyl sebacate, diethyl oxalate, diethyl malate, diethyl maleate, diethyl malonate, diethyl fumarate, diethyl phthalate, diethyl sebacate, diethyl succinate, dimethylphthalate, dioctyl phthalate, glycerin, glyceroltributyrate, glyceroltriacetate, glyceryl behanate, glyceryl monostearate, hydrogenated vegetable oil, lecithin, leucine, magnesium silicate, magnesium stearate, polyethylene glycol, propylene, glycol, polysorbate, silicone, stearic acid, talc, titanium dioxide, triacetin, tributyl citrate, triethyl citrate, zinc stearate, PEG
(polyethylene glycol), etc. Methods for enteric coating are well known in the art such as described in e.g. (Stuart C. Porter in Remmington 215t Ed. 2005, pp 929), hereby incorporated by reference.
Stability Preferably, at least 95% (w/w) of the declared content of drug substance remains in the tablet formulation according to the present invention after storage at 25C /60 %RH
(relative humidity) of a period of 2, 3, 4, or 5 years. Alternatively, the stability can be determined after storage at other conditions according to appropriate ICH
guidelines.
Methods of assessing stability are described in the Examples.
Brief description of drawings Flgure 1: Stability test of coated tablets containing Sodium Carbonate, Calcium Carbonate (Sturcal L), or Tri calcium phosphate. Test performed in open petri dishes at 70 and not more than (nmt) 10 % relative humidity. Example 6.
Figure 2: Stability test of coated tablets containing Sodium Carbonate or Calcium Carbonate (Sturcal L) in the mixing ratio's of 1:0.2 or 1:0.8. Test performed in open petri dishes at 700 and not more than (nmt) 10 % relative humidity. Example 8.
Figure 3: Stability test of coated tablets containing Sodium Carbonate (Sturcal L) 1:0.8 based on different sequential order of mixing and roller compaction. Test performed in open petri dishes at 70 and not more than (nmt) 10 %-relative humidity.
Example 10.
Figure 4: Particle size distribution using two different sieve sizes (1.25 mm and 1.0 mm) during roller compaction. Example 11.
Figure 5: Impact on dose variation of Roller compactor sieve size illustrated by tablet core dissolution. Example 11.
Figure 6: Impact on dissolution of amount of subcoat, HPMC E15, applied.
Example 12.
Figure 7: Impact on dissolution of type of subcoat, HPMC E 5 and HPMC E 15.
Evaluated on subcoated tablets. Example,12.
Figure 8: Impact on dissolution of type of subcoat, HPMC E 5 and HPMC E 15.
Evaluated for enteric coated tablets. Example 12.
Figure 9: Stability of batches 13030634 and 31030634 (without the application of a sub coat) at 70 C in open petri dishes. Example 14.
Figure 10: Pantoprazole Sodium Sesquihydrate (SEM picture).
Figure 11: Calcium Carbonate (Sturcal L) (SEM picture).
Figure 12: Calcum Carbonate (Scoralite) (SEM picture).
Figure 13: Sodium Carbonate (SEM picture).
Figure 14: Sodium Carbonate (SEM picture).
Figure 15: Pantoprazole Sodium Sesquihydrate and Calcium Carbonate (Sturcal L);
Mixing followed by slugging (SEM picture).
Figure 16: Pantoprazole Sodium Sesquihydrate and Calcium Carbonate (Scoralite) Mixing followed by slugging (SEM picture).
Figure 17: Pantoprazole Sodium Sesquihydrate and Sodium Carbonate;
Mixing followed by slugging (SEM picture).
Figure 18: Pantoprazole Sodium Sesquihydrate and Sodium Carbonate Pre rollercompaction of Pantoprazole, mixing with sodium carbonate, and slugging (SEM
picture).
Figure 19: Impact of disintegrant on tablet core dissolution. Example 18.
It should be noted that, according to the present invention, embodiments and features described in the context of one of the aspects of the present invention also apply to the other aspects of the invention.
The following non-limiting examples are meant to illustrate the present invention.
EXAMPLES
Example 1 Dry manufacture of tablets containing pantoprazole or omeprazole. Dry granulation is followed by compressing the resulting particulate matter into tablets.
Table 2 Raw Manufactured bathes, no.
Materials * 1 2 3 4 5 6 L 8 9 10 11 12 a+b a+b 1 Pantoprazole 20,0 20.0 20.0 20.0 20.0 20.0 Na 1.51iz0 1 Omeprazole 20.0 20.0 20.0 20.0 20.0 20.0 Na 2 CaCO3 56.4 56.4 56.4 56.4 2 Na3PO4 56.4 56.4 56.4 56.4 2 NaZCO3 56.4 56.4 56.4 56.4 3 Sorbitok 17.6 17.6 17.6 17.6 17.6 17.6 3 Mannitol 17.6 17.6 17.6 17.6 17.6 17.6 4 MCC 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5 Mg-stearate 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 *: Amounts in % wjw Table 3: List of ingredients 1 PantoprazoEe sodium sesquihydrate 1 Omeprazole sodium 2 CaCO3 Sturcal L
2 Na3PO4 trisodium phosphate 2 Na2CO3 sodium carbonate 3 Sorbitol 3 Mannitol 4 MCC; Cellulose Microcrystalline type 1010 5 Mg-stearate; magnesium stearate The drug substance 1) (having a mean particle size of about 7 pm) was mixed by hand with the alkaline substance 2) and with 3).
10 The resulting mixture of the ingredients 1) to 3) was subjected to roller compaction by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm 15 Sieve size 1.25 mm Force 10 kN/cm The resulting particulate matter of the dry granulated ingredients 1) to 3) was admixed with 4) and 5). Thereafter, tablets were compressed of the mixture of ingredients 1) to 5) using a Diaf TM 20 press and 7.5 mm standard concave punch design. Unless otherwise stated, a relatively low compression force was used. ' Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 (n=6). Both tests were performed according to the European Pharmacopoeia.
Figure 10: Pantoprazole Sodium Sesquihydrate (SEM picture).
Figure 11: Calcium Carbonate (Sturcal L) (SEM picture).
Figure 12: Calcum Carbonate (Scoralite) (SEM picture).
Figure 13: Sodium Carbonate (SEM picture).
Figure 14: Sodium Carbonate (SEM picture).
Figure 15: Pantoprazole Sodium Sesquihydrate and Calcium Carbonate (Sturcal L);
Mixing followed by slugging (SEM picture).
Figure 16: Pantoprazole Sodium Sesquihydrate and Calcium Carbonate (Scoralite) Mixing followed by slugging (SEM picture).
Figure 17: Pantoprazole Sodium Sesquihydrate and Sodium Carbonate;
Mixing followed by slugging (SEM picture).
Figure 18: Pantoprazole Sodium Sesquihydrate and Sodium Carbonate Pre rollercompaction of Pantoprazole, mixing with sodium carbonate, and slugging (SEM
picture).
Figure 19: Impact of disintegrant on tablet core dissolution. Example 18.
It should be noted that, according to the present invention, embodiments and features described in the context of one of the aspects of the present invention also apply to the other aspects of the invention.
The following non-limiting examples are meant to illustrate the present invention.
EXAMPLES
Example 1 Dry manufacture of tablets containing pantoprazole or omeprazole. Dry granulation is followed by compressing the resulting particulate matter into tablets.
Table 2 Raw Manufactured bathes, no.
Materials * 1 2 3 4 5 6 L 8 9 10 11 12 a+b a+b 1 Pantoprazole 20,0 20.0 20.0 20.0 20.0 20.0 Na 1.51iz0 1 Omeprazole 20.0 20.0 20.0 20.0 20.0 20.0 Na 2 CaCO3 56.4 56.4 56.4 56.4 2 Na3PO4 56.4 56.4 56.4 56.4 2 NaZCO3 56.4 56.4 56.4 56.4 3 Sorbitok 17.6 17.6 17.6 17.6 17.6 17.6 3 Mannitol 17.6 17.6 17.6 17.6 17.6 17.6 4 MCC 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5.25 5 Mg-stearate 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 *: Amounts in % wjw Table 3: List of ingredients 1 PantoprazoEe sodium sesquihydrate 1 Omeprazole sodium 2 CaCO3 Sturcal L
2 Na3PO4 trisodium phosphate 2 Na2CO3 sodium carbonate 3 Sorbitol 3 Mannitol 4 MCC; Cellulose Microcrystalline type 1010 5 Mg-stearate; magnesium stearate The drug substance 1) (having a mean particle size of about 7 pm) was mixed by hand with the alkaline substance 2) and with 3).
10 The resulting mixture of the ingredients 1) to 3) was subjected to roller compaction by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm 15 Sieve size 1.25 mm Force 10 kN/cm The resulting particulate matter of the dry granulated ingredients 1) to 3) was admixed with 4) and 5). Thereafter, tablets were compressed of the mixture of ingredients 1) to 5) using a Diaf TM 20 press and 7.5 mm standard concave punch design. Unless otherwise stated, a relatively low compression force was used. ' Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 (n=6). Both tests were performed according to the European Pharmacopoeia.
Table 4: Crushing strength and disintegration time Batch no. Crushing strength Disintegration time in water [ N ] [sec. ]
1 39.5 291.0 2 39.5 151.0 3 41.3 520.0 4 39.9 457.8 41.1 496.5 6 42.1 523.0 7 32.4 281.8 8 30.9 477.5 9 36.0 300 38.0 284.7 11a 45.3 269.7 Low Comp.
Force lib 90.6 301.8 High Comp.
Force 12a 40.7 256.8 Low Comp.
Force 12b 61.7 271.2 High Comp.
Force The results from table 4 show that tablets containing pantoprazole or omeprazole having a 5 satisfactory crushing strength and disintegration time can be manufactured from a dry manufacturing process based on a particulate matter provided by dry granulation resulting from roller compaction.
Furthermore, batches 11a+b and 12 a+b illustrate that the crushing strength can be 10 increased without any significant influence on the disintegration time.
This means that the tablets are of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water-soluble film like HPMC (Hydroxypropyl methylcellulose) can be used to protect the enteric coat from the alkaline reacting core.
Example 2 Crushing strength and disintegration time resulting from compression of particulate matter based on roller compaction Table 5 Raw Materials 1 Manufactured batches, no.
1 Pantoprazole sodium 21.3 21.3 sesquihydrate (Mean particle size around 7pm) 2 Na3PO4 trisodium phosphate 60.0 60.0 3 Sorbitol 18.7 -3 Mannitol - 18.7 Amounts in % w/w 1) was mixed by hand with 2) and 3).
The resulting mixture of the ingredients 1) to 3) was roller compacted by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm Sieve size 1.25 mm Force 10 kN/cm The particulate matter resulting from roller compaction of the ingredients 1) to 3) was compressed into tablets using a Diaf TM 20 press and 7.5 mm standard concave punch design. Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 disintegrations tester (n=6).
Table 6: Crushing strength and disintegration time Batch no. Crushing strength [N] Disintegration time [sec.]
13 42.6 443.0 14 52.6 486.7 The results from table 6 show that tablets containing pantoprazole having a satisfactory crushing strength and disintegration time can be manufactured by compression of a particulate matter provided by a dry granulation process based on roller compacted granulates, without the addition of further excipients (apart from a dry binder). Addition of magnesium stearate could, however, be advantageous in production scale.
The tablets are thus of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water-soluble film like HPMC can be used to protect the enteric coat from the alkaline reacting core.
Example 3 Crushing strength and disintegration time of tablets resulting from direct compression of mixtures of pantoprazole and compactable alkaline excipient Table 7 Raw material D(v;0.5) 10060531 10060532 [pm]
1 Pantoprazole sodium 7 20.00 20.00 sesquihydrate 2 Trisodium phosphate, 203 79.26 71.34 coarse 2 Trisodium phosphate, 40 7.92 fine 3 Magnesium stearate - 0.74 0.74 *: Amounts in % w/w The drug substance 1) and the ingredient 2) were mixed by hand followed by admixing of 3). The mixture of ingredients 1) to 3) was compressed into tablets using a Diaf TM 20 press and 7.5 mm standard concave punch design.
Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 disintegration tester (n=6).
Table 8: Crushing strength and disintegration time Batch no. Crushing strength [N] Disintegration time Mass variation [sec.] [ s.rel - roj 10060531 37.4 657 0.96 10060532 41.2 631 The results shown in table 8 show that tablets containing pantoprazole having a satisfactory crushing strength and disintegration time result from direct compression of the compactable alkaline substance. The mass variation illustrates that the flowability of the mixture of ingredients 1) to 3) is acceptable. It is conceivable that the coarse alkaline substance functions both as a filler substance and an alkaline substance in this formulation.
The resulting tablets are of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water soluble film like HPMC can be used to protect the enteric coat from the alkaline reacting core.
Example 4 Manufacture of tablets having a diameter of 5 mm based on a particulate matter resulting from dry granulation in a roller compactor Table 9 Raw Materials * 1 2 3 4 5 6 7 8 1 Pantoprazole 40 40 40 40 sodium 1.5H20 1 Omeprazole 40 40 40 40 sodium 2 Na3PO4 40 40 40 40 2 Na2CO3 40 40 40 40 3 Sorbitol 18.25 18.25 18.25 18.25 3 Mannitol 18.25 18.25 18.25 18.25 4 Mg-stearate 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 Amounts in %w/w Table 10: List of ingredients 1 Pantoprazole sodium sesquihydrate 1 Omeprazole sodium 2 Na3PO4 trisodium phosphate 2 NaZCO3 sodium carbonate 3 Sorbitol 3 Mannitol 4 Mg-stearate; magnesium stearate The drug substance 1) was mixed by hand with 2) and 3).
The resulting mixture of the ingredients 1) to 3) was dry granulated by roller compaction by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm Sieve size 1.25 mm Force 10 kN/cm The resulting particulate matter of the dry granulated ingredients 1) to 3) was admixed with 4). The resulting mixture of the ingredients 1) to 4) was compressed into tablets using a 5.0 mm standard concave punch design. The resulting tablets are of a quality that allows applying a standard enteric coat using standard coating equipment and parameters.
Optionally a sub coat consisting of a standard water soluble film like FIPMC
can be used to protect the enteric coat from the alkaline reacting core.
Example 5:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of a sub coat and an enteric coating.
Table 11: Composition of tablet core % w/w:
Batch no. 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Granulate by roller compaction Pantoprazo{e, 11/z H20 13.3 11.7 14.1 12.9 Sodium carbonate 13.3 55.2 -Calcium carbonate - 54.9 - -(Sturcal L) TriCalciumPhosphate 60.6 Pantoprazole:alkaline excipient 1:1 1:4.7 1:3.9 1:4.7 Mannitol - 13.5 - 14.9 Crospovidone 0.4 1.1 1.1 1.2 Tablet core excipients DiCafos A 62.7 8.5 19.2 -Crospovidone 9.7 9.7 10.0 9.8 Mg Stearate 0.5 0.4 0.5 0.5 Table 12: Composition of sub coat [% w/w]:
Raw materials Coating liquid Dry film composition composition Hypromellose 15 5 55,60lo Propylenglycol 1 11,1%
Talc 3 33,3%
Water, purified 91 % Plasticizer of polymer 20,0%
5 Table 13: Composition of enteric coat [% w/w]::
Raw materials Coating -iquid Dry film composition composition Methacryl acid-acryl 41,76 62,49 Copolymer disp. 30%
Triethylcitrate 1,25 6,24 Talc 6,27 31,28 Water, purified 50,92 % Plasticizer of Polymer 10,0 Table 17: Approximately amount of film dry matter applied [% w/w]:
Coat 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Theoretical applied 9,7 10,3 10,9 9,0 amount of sub coat [mg polymer/cmz]
Theoretical applied 5,5 5,4 5,3 + 2 5,7 amount of enteric coat [mg polymer/cmZ]
Pantoprazole was mixed with the alkaline excipient in a tumble mixer together with Crosspovidone and mannitol followed by roller compaction as described in example 1.
The remaining tablet core excipients were admixed and tablets were compressed by use of a Korsch PH106 tablet press and 6 mm concave punches aiming at a mean weight of 160 mg and a crushing strength of 50 N. Thereafter the tablet cores were coated with the sub coat followed by the enteric coat by use of a lab-scale Combi Coata. The obtained coated tablets were used for stability testing as described in example 6.
Example 6 (stability testing) A stability testing program with batches obtained in example 5 was performed.
The batches were stored at accelerated stability testing conditions (open petri dishes at 70 C
and not more than 10% relative humidity for three months). Such conditions probably correspond to shelf life stability testing of at least two years.
The analytical method is as follows: 10 tablets are transferred to a 200 ml volumetric flask. 150 ml mobile phase (the initial composition) is added and sample is shaken for 90 minutes. After the solutions pH-values have been adjusted to 8.0, mobile phase is added to the mark. The sample solution is filtered through 0.45 m filter and analysed by reverse phase HPLC in order to quantify the amount of Pantoprazole as well as degradation products thereof. The amount is given in % of total area, see table 19.
Furthermore, in figure 1 is shown the amount of pantoprazole as a function of time.
Table 18: HPLC method parameters Mobile phase ammonium phosphate buffer: methanoi: acetonitril Time % Buffer % Methanol % Acetonitril 0 min 65 10 25 Gradient profile 25 min 30 10 60 min 30 10 60 31 min 65 10 25 Flow 1,0 mI/min Column Waters Spherisorb, 250X4,6 mm, 5 pm particle size Column temperature 30 C
Auto sampler temperature 4 C
Detection UV-290 nm Injection volume 10 ial Run time 40 min.
Pantoprazole 10,7 min Approx. Retention time Impurity B 6,6 min Impurity A 13,4 min Table 19: Results of stability study Batch 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Pantoprazole:sodium carbonate 1:1 1:3,9 Pantoprazole:calcium carbonate 1:4,7 Pantoprazole:calcium phosphate 1:4,7 Pantoprazole:DiCafos A 1:4,7 1:0;7 1:1,4 9 25160 C lmonth 99,7 99,7 99,7 99,2 ' 70110 OP 1 month 97,4 96,6 97,3 93,9 o ca 70/10 OP 2 months 96,4 95,5 96,1 91,9 70/10 OP 3 months 94,9 94,3 94,6 89,3 cu 40/75 3 months 99,4 99,4 99,5 97,2 25/60 C 1month 0,18 0,15 0,20 0,56 0- 70/10 OP lmonth 2,2 3,2 2,3 6,0 M
a) ~~~ 70/10 OP 2 months 3,3 4,0 3,6 7,6 70/10 OP 3 months 4,3 4,8 4,4 9,3 a 40175 3 months 0,5 0,5 0,5 2,6 70/10 OP: 70 C / 10 % RH in Open petri dishes 25/60: 25 C / 60% RH in closed containers 40/75: 40 C / 75% RH in closed containers According to table 19 and figure 1, use of Ca$(P04)3OH as alkaline substance result in a relatively larger degree of pantoprazole degradation compared with use of Na2CO3, CaCO3i and DiCafos A as alkaline excipients. The stability data for the stressed stability testing conditions (70 C open Petri dishes, 70/10 OP) probably corresponds to a shelf life of at least two years.
Example 7:
Dry manufacture of tablets containing pantoprazole and Sodium carbonate or calcium carbonate and a disintegrant followed by application of a sub coat and an enteric coating.
Table 20: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 H20 14.1 14.1 14.1 14.1 Sodium carbonate 2.82 11.3 Calcium carbonate 2.82 11.3 (Sturcal L) Pantoprazole: alkaline exciplent 1:0.2 1:0.8 1:0.2 1:0,8 Tabiet core excipients DlCafos A 69.6 61.1 69.6 61.1 Crosspovidone 13.0 13 13.0 13 Mg Stearate 0.5 0.5 0.5 0.5 Based on the tablet core compositions listed above coated tablets were manufactured as described in example 5 with the following exception:
The pantoprazole was pre-rollercompacted prior to mixing with the alkaline excipient by use of the following parameters Rpm: 2.0 Gap size: 1.0 mm Sieve size: 1.25 mm Force: 4 kfV/cm The pre-roller compaction leads to formation of pantoprazole granules.
The obtained coated tablets were used for stability testing with the purpose of investigating the impact of lower amounts of alkaline material than used in example 5 and the use of pre-roffercompaction of the pantoprazole. The stability testing is disclosed in example B.
ExampEe 8: stability testing A stability program, including batches obtained in example 7 was performed.
The batches were stored in open petri dishes at 70 C and not more than 10 % RH for up to six weeks.
The anaEytical method is as described in example 6 Table 21: Result of stability study batch 3F-C 2F-C 7F-C 8F-C
Pantoprazole:sodium carbonate 1:0.8 1:0.2 Pantoprazole:calcium carbonate 1:0.2 1:0.8 Pantoprazole:DiCafos A 1:5 1:4,3 1:5 1:4,3 Pantoprazole 25/60 C 2 weeks 99,7 99,8 99,8 99,1 in % area 70/10 OP 2weeks 98,3 97,9 98,3 98,1 70/10 OP 6weeks 97,5 97,2 Degradation 25/60 C 2 weeks 0,20 0,15 0,10 0,52 products in 70/10 OP 2weeks 1,2 1,6 1,4 1,2 % area 70/10 OP 6weeks 2,0 2,4 It appears in table 21 and figure 2 that use of sodium carbonate and calcium carbonate as alkaline excip9ent at the mixing ratios of 1:0.2 and 1:0.8 result in nearly identical and acceptable degradation ratios when tested at 70 C and not more than 10 % RH
for up to six weeks. It is surprising that the solubility of the alkaline material apparently does not affect stability of the benzimidazole composition (calcium carbonate is poorly soluble in water).
Example 9:
Dry manufacture of tablets containfng pantoprazole and alkaline excipients focusing on order of mixing and roller compaction followed by application of a sub coat and an enteric coating.
Table 22: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 1l/z H20 14.1 Sodium carbonate 11.3 Pantoprazole:alkafine excipient 1:0.8 Tablet core excipients DiCafos A 61.1 Crospovidone 13 Mg Stearate 0.5 The composition shown in table 22 was mixed and roller compacted in different sequential order as shown in table 23 Table 23: Sequential order of mixing and roller compaction:
Batch no. 1 2 3 4 (Of coated Mixing with Pre-roller Mixing with Roller tablets) alkaline compaction alkaline compaction excipient (solely excipient pantoprazole) 01050633 3F-C Not used X X X
05050635 X Not used Not used X
05050638 12F-C Not used X X Not used Mixing and roller compaction were carried out as described in example 5.
5 The remaining tablet core excipients (Dicafos A, Crosspovidone and Mg-stearate) were admixed and tablets were compressed and coated in accordance with example 5.
The batches 01050633 and 05050638 were used for stability testing in example 10 and 05050635 was used for comparison with batches of example 16 with the purpose of 10 evaluating excipient homogeneity of granules.
Example 10: stability testing A stability program, including batches mentioned in example 9 was performed.
The 15 batches were stored in open petri dishes at 70 C for 2 weeks.
The analytical method is as described in example 6 Table 24: Results of stability testing:
batch Pantoprazole:sodium carbonate 1:0.8 1:0.8 Pantoprazole:DiCafos A 1:5 1:4,3 Pre-rollercompacting, Pre-mixing, rollercompacting, - rollercompacting mixing Pantoprazole 25160 C 2 weeks 99,7 99,5 in % area 70/10 OP 2weeks 98,3 97,2 70/10 OP 6weeks 97,5 Degradation 25/60 C 2 weeks 0,20 0,33 products in 70/10 OP 2weeks 1,2 2,9 % area 70/10 OP 6weeks 2,0 It appears in table 24 and figure 3 that panoprazole degradation is relatively small when pantoprazole is pre-roller compacted, mixed with the alkaline excipient and then roller compacted again. The pantoprazole degradation is relatively high when pantoprazole is pre-roller compacted and mixed with the alkaline excipient without including a step of roller compacting pantoprazole and alkaline substance together. The impact on stability is seen already after two weeks.
Example 11:
Dry manufacture of tablets containing pantoprazole and alkaline excipients.
Roller compaction has been carried out using two different sieve sizes. Tableting was followed by application of a sub coat and an enteric coating.
Table 25: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 HZ0 14.1 Sodium carbonate 2.82 Pantoprazole:alkaline excipient 1:0.2 Tablet core excipients DiCaPos A 69.6 Crospovidone 13.0 Mg Stearate 0.5 Based on the tablet core compositions listed above coated tablets were manufactured as described in example 5 with the following exception:
The pantoprazole was pre-rollercompacted prior to mixing with the alkaline excipient by use of the following parameters Rpm: 2.0 Gap size: 1.0 mm Sieve size: 1.25 mm (used for batch 29050641) or 1.0 mm (used for batch 29050645) Force: 4 kN/cm The pre-roller compacted pantoprazole and the sodium carbonate were mixed by use of a tumble-mixer and roller compacted using the following parameters:
Rpm: 2.0 Gap size: 2.5 mm Sieve size: 1.25 mm (used for batch 29050641) or 1.0 mm (used for batch 29050645) Force: 10 kN/cm The remaining tablet core excipients were admixed and tablets were compressed and coated in accordance with example 5.
Evaluation of the impact of the sieve size was based on sieve analysis and dissolution testing. Dissolution was carried out by use of the following method:
Table 26: Dissolution method.
USP/Ph.Eur Dissolution apparatus 1 Spindle Basket Rotation 150 rpm Temperature 37 C 0,5 C
Filter Whatman GF/F (0.7 pm) Dissolution medium 0- 120 minutes 600 ml 0.1 N HC!
After 120 minutes the dissolution medium 200 ml 0.20 M Na3PO4 added to the is changed to pH 6.8 vessel (method A, USP) Detection, UV 288 nm Sampling time The absorbance is measured by each minutes at 288 nm From figure 4 it can be seen that the use of a sieve size of 1.0 mm results in a relatively narrow particle size distribution compared to sieve size 1.25. The narrow size distribution results in a better dose variation of pantoprazole as can be seen form figure S.
Example 12:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of different types and amounts of sub coat.
Table 27: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 H20 14,1 Sodium carbonate 55,2 Pantoprazole: allcaline excipient 1:3,9 Crospovidone 1,1 Tablet core excipients DlCafos A 19,2 Crospovidone 10,0 Mg Stearate 0,5 Tablet cores according to the above mentioned composition were manufactured as described in example S. Sub coat was applied as laid out in example 5 with the exception of variation in applied amount and type of polymer as shown En table 28:
Table 28: Amount (approximately) and type of sub coat applied:
Batch no. HPMC type Theoretical amount of HPMC
Cm9/cm2]
13030634 E15 10.9 (1/1 amount) 31030633 (C) E15 5.3 (1/2 amount) 21040634 E5 9.9 (1/1 amount) Enteric coat was applied as described in example 5.
Evaluation of the impact of amount and type of sub coat was based following dissolution results obtained obtained in example 11. However, tablets only coated with a sub coat were analysed solely in a dissolution medium with pH 6.8.
Figures 6, 7 and 8 disclose the impact of type of sub coat on the dissolution rate form both sub coated tabiets and sub + enteric coated tablets. A HPMC E5 based sub coat results in a relatively quick dissolution rate.
Example 13:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of an enteric coating.
Tablet cores of batch 13030634 and 31030634 were manufactured as described in example 12. The tablet cores of batch 13030634 were enteric coated as described in example S. Batch 31030634 was produced with an enteric coating but without the application of a sub coat. The enteric coated tablets were used for stability testing in example 14.
Example 14: stability testing A stability program, including batches mentioned in example 13 was performed.
The batches were stored in open petri dishes at 70 C for respectively 2 and 3 months.
The analytical method is as described in example 6 Table 29: Results of stability testing Batch 13030634 31030634 Without sub coat 1 month 99,7 99,7 Pantoprazole 70/10 OP 97,3 97,9 in % of area I month 2 months 96,1 97,4 1 month 0,20 0,22 Degradation products. 70/10 OP
in % of area 1 month 2,3 1,7 2 months 3,6 2,2 70/10 OP: 70 C / 10 % RH in Open petri dishes 25/60: 25 C / 60% RH in closed containers It appears from table 29 and figure 9 that the stability (70 C / 10 % RH in Open petri dishes and 25 C / 60% RH in closed containers) of sub-coated tablets is fully comparable with tablets which has not been sub-coated.
Example 15:
Impact of type and amount of alkaline excipient on deg'radation of pantoprazole in a stress test by the addition of a weakly acidic component (ibuprofen) Table 30: Composition of mixtures [gram]
Raw materials Amounts in gram Sodium carbonate 4 16 20 25 Calcium carbonate 4 16 20 25 (Sturcal L) Ibuprofen 0.8 0.8 0.8 0.8 0.8 0.8 0.8 0.8 Pantoprazole 11/2 H20 20 20 10 5 20 20 10 5 Pantoprazole:alkaline 10.2 1:0.8 1:2 1:5 1:0.2 1:0.8 1:2 1:5 excipient Table 31: Composition of mixtures [gram]
Raw materials Amounts in gram Calcium carbonate 4 16 20 25 (Scoralite) Tri calcium phosphate 4 16 20 25 Ibuprofen 0.8 0.8 0.8 0.8 0.8 0.8 0.8 0.8 Pantoprazole 11/2 HZO 20 20 10 5 20 20 10 5 Pantoprazole:alkaline 1:0.2 1:0.8 1:2 1:5 1:0.2 1:0.8 1:2 1:5 excipient Mixtures were made by grinding the raw materials in a steel bowl and subsequently placing the mixture in petri dishes in sealed alu-bags for two weeks at ambient conditions.
5 The evaluation of this stability test is shown in table 32 (pantoprazole degradation products are coloured). Discoloration is evaluated based on a scale ranging from 1 - 10 where "1" indicates no discoloration and "10" indicates a severe discoloration.
Table 32. Discoloration scale of powder mixtures of table 30 and 31:
Alkaline material Mixing ratio Mixing ratio Mixing ratio Mixing ratio 1:0.2 1:0.8 1:2 1:5 Sodium carbonate 9 8 4 1 Calcium carbonate 10 8 4 1 (Sturcal L) Calcium carbonate 10 10 7 7 (Scoralite) Tri calcium 9 6 - 1 phosphate The results in table 32 are discussed in example 16.
Example 16:
Characterisation of alkaline materials.
Alkaline materials:
* Calcium carbonate, Sturcal L
* Calcium carbonate, Scoralite * Sodium carbonate anhydrate Alkaline substance raw material particle sizes have. been measured by laser light scattering (Malvem) and BET area has been measured by use of a Micromeritics Gemini 2375 at relative target pressures (P/Po) of 0.1 and 0.2 and 0.3. Samples have been dried for minimum 12 hours at 40 C prior to the measurements.
Table 33: BET-areas Raw materials BET-area [mz/g] Particle size D(v 0,5) [pm]
Calcium carbonate, Sturcal L 3.0 9 Calcium carbonate, Scoralite 0.2-0.5 29 Sodium carbonate anhydrate 2.1 99 The SEM pictures (figures 10-18) illustrate considerable differences in size and morphology on the alkaline raw materials. It should be noted that even though Sodium carbonate anhydrate has a larger particle size than the Calcium carbonate (Scoralite), sodium carbonate anhydrate has the largest BET area. This difference is further illustrated in example 17 by use of Scanning Electron Microscope pictures. The impact of the BET area and particle size on stability was illustrated in example 15.
The discoloration shown in table 32 demonstrates the impact of BET area (see example 16, table 33) and mixing ratio on pantoprazole stability. A high BET area favours good stability results. It appears from example 16 that a relatively small particle size may not suffice to ensure a satisfactory stability. Relatively big particles can be useful, provided that their porosity leads to a sufficiently high BET area.
Furthermore, it is illustrated that a high amount of alkaline material is preferred.
However, the discoloration test cannot reveal smaller amount of degradation product as can be seen by comparison of the addition of tri calcium phosphate in example 6. This means that tri calclum phosphate is not as efficient as e.g. sodium carbonate and calcium carbonate (Sturcal L).
Example 17 Impact of type and amount of alkaline excipient on homogeneity of a mixture with pantoprazole with alkaline materials.
Composition of powder mixtures * Pantoprazole, 11/2 H20 : Calcium carbonate (Sturcal L), 1:0.8 * Pantoprazole, 11/z H20 : Calcium carbonate (Scoralite), 1:0.8 = Pantoprazole, 11I2 H20 (pre-roller compacted) : sodium carbonate, 1:0.8 Pantoprazole, 11/2 H20 : Calcium carbonate (Sturcal L) and Pantoprazole, 11/2 H20 :
Calcium carbonate (Scoralite) batches have been mixed in a lab. scale high shear mixer for 1 minute. The Pantoprazole, 11/7. H20 (pre-roller compacted) batch was manufactured as described in example 7 prior to mixing with sodium carbonate. The mixing was done as described above.
All the mixtures were slugged on a single punch tableting machine using 11.3 mm flat faced punches. The slugs were evaluated for mixture homogeneity by use of scanning electronic microscopy (SEM). For reference, SEM pictures of the individual raw materials were obtained.
The SEM pictures are shown in the figures 10 - 18. Figure 11 and 12 disclose a considerable difference between Calcium carbonate (Sturcal L) and Calcium carbonate (Scoralite). SEM appearances of Sturcal L and Scoralite are in full accordance with the BET
areas measured in example 16.
Figure 13 is a magnification of the particles shown in figure 14. The magnification showing the porosity of the particles clearly supports the finding of a high BET area of Sodium Carbonate is illustrated.
Figures 15 and 16 show that the use of Calcium carbonate (Sturcal L) leads to a much more homogeneous mixture than Calcium carbonate (Scoralite). The impact on stability of this difference was illustrated in example 15. Figure 17 shows that the sodium carbonate particles are crushed during manufacturing. The physical structure of Sturcal L results in an improved distribution of the particles during mechanical pressure. An acceptable stability is obtained as illustrated in examples 15 and 6, 8 and 10.
Figure 18 iliustrates the effect of pre-roller compacting pantoprazole prior to mixing with alkaline substance. Slugging (or roller compaction) of the mixture results in "coating" of the surface of the relative large pantoprazole granules with calcium carbonate particles (Sturcal L). This "coating" also leads to an acceptable stability as shown in example 6 and 8. The need for using roller compaction to apply this coat is indicated in example 9, which was based on the use of sodium carbonate.
Example 18.
Impact of disintegrant on dissolution rate.
Table 34: Composition of tablet core % w/w:
Pantoprazole, 1112 H20 14.1 14.1 Calcium carbonate 11.3 11.3 (Sturcal L) Pantoprazole:alkaiine 1,0 8 1=0,8 excipient ~ ' DiCafos A 74.1 61.1 Crospovidone - 13 Mg Stearate 0.5 0.5 Based on the tablet core compositions listed above tablets were manufactured as described in example 7 with the following exception that no coat has been applied.
The cores were tested with respect to dissolution rate as described in example 11 with the exception that tablet cores were analysed solely in a dissolution medium with pH 6.8.
The results shown in figure 19 illustrate the advantages of the incorporation a disintegra,nt as the presence of a disintegrant in the formulation significantly increases the dissolution rate.
1 39.5 291.0 2 39.5 151.0 3 41.3 520.0 4 39.9 457.8 41.1 496.5 6 42.1 523.0 7 32.4 281.8 8 30.9 477.5 9 36.0 300 38.0 284.7 11a 45.3 269.7 Low Comp.
Force lib 90.6 301.8 High Comp.
Force 12a 40.7 256.8 Low Comp.
Force 12b 61.7 271.2 High Comp.
Force The results from table 4 show that tablets containing pantoprazole or omeprazole having a 5 satisfactory crushing strength and disintegration time can be manufactured from a dry manufacturing process based on a particulate matter provided by dry granulation resulting from roller compaction.
Furthermore, batches 11a+b and 12 a+b illustrate that the crushing strength can be 10 increased without any significant influence on the disintegration time.
This means that the tablets are of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water-soluble film like HPMC (Hydroxypropyl methylcellulose) can be used to protect the enteric coat from the alkaline reacting core.
Example 2 Crushing strength and disintegration time resulting from compression of particulate matter based on roller compaction Table 5 Raw Materials 1 Manufactured batches, no.
1 Pantoprazole sodium 21.3 21.3 sesquihydrate (Mean particle size around 7pm) 2 Na3PO4 trisodium phosphate 60.0 60.0 3 Sorbitol 18.7 -3 Mannitol - 18.7 Amounts in % w/w 1) was mixed by hand with 2) and 3).
The resulting mixture of the ingredients 1) to 3) was roller compacted by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm Sieve size 1.25 mm Force 10 kN/cm The particulate matter resulting from roller compaction of the ingredients 1) to 3) was compressed into tablets using a Diaf TM 20 press and 7.5 mm standard concave punch design. Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 disintegrations tester (n=6).
Table 6: Crushing strength and disintegration time Batch no. Crushing strength [N] Disintegration time [sec.]
13 42.6 443.0 14 52.6 486.7 The results from table 6 show that tablets containing pantoprazole having a satisfactory crushing strength and disintegration time can be manufactured by compression of a particulate matter provided by a dry granulation process based on roller compacted granulates, without the addition of further excipients (apart from a dry binder). Addition of magnesium stearate could, however, be advantageous in production scale.
The tablets are thus of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water-soluble film like HPMC can be used to protect the enteric coat from the alkaline reacting core.
Example 3 Crushing strength and disintegration time of tablets resulting from direct compression of mixtures of pantoprazole and compactable alkaline excipient Table 7 Raw material D(v;0.5) 10060531 10060532 [pm]
1 Pantoprazole sodium 7 20.00 20.00 sesquihydrate 2 Trisodium phosphate, 203 79.26 71.34 coarse 2 Trisodium phosphate, 40 7.92 fine 3 Magnesium stearate - 0.74 0.74 *: Amounts in % w/w The drug substance 1) and the ingredient 2) were mixed by hand followed by admixing of 3). The mixture of ingredients 1) to 3) was compressed into tablets using a Diaf TM 20 press and 7.5 mm standard concave punch design.
Crushing strength and time of disintegration of the obtained tablets were measured by use of a Schleuniger E2 hardness tester (n=10) and a Sotax DT 2 disintegration tester (n=6).
Table 8: Crushing strength and disintegration time Batch no. Crushing strength [N] Disintegration time Mass variation [sec.] [ s.rel - roj 10060531 37.4 657 0.96 10060532 41.2 631 The results shown in table 8 show that tablets containing pantoprazole having a satisfactory crushing strength and disintegration time result from direct compression of the compactable alkaline substance. The mass variation illustrates that the flowability of the mixture of ingredients 1) to 3) is acceptable. It is conceivable that the coarse alkaline substance functions both as a filler substance and an alkaline substance in this formulation.
The resulting tablets are of a quality that allows the application of a standard enteric coating using standard coating equipment and parameters. Optionally a sub coat comprising a standard water soluble film like HPMC can be used to protect the enteric coat from the alkaline reacting core.
Example 4 Manufacture of tablets having a diameter of 5 mm based on a particulate matter resulting from dry granulation in a roller compactor Table 9 Raw Materials * 1 2 3 4 5 6 7 8 1 Pantoprazole 40 40 40 40 sodium 1.5H20 1 Omeprazole 40 40 40 40 sodium 2 Na3PO4 40 40 40 40 2 Na2CO3 40 40 40 40 3 Sorbitol 18.25 18.25 18.25 18.25 3 Mannitol 18.25 18.25 18.25 18.25 4 Mg-stearate 0.75 0.75 0.75 0.75 0.75 0.75 0.75 0.75 Amounts in %w/w Table 10: List of ingredients 1 Pantoprazole sodium sesquihydrate 1 Omeprazole sodium 2 Na3PO4 trisodium phosphate 2 NaZCO3 sodium carbonate 3 Sorbitol 3 Mannitol 4 Mg-stearate; magnesium stearate The drug substance 1) was mixed by hand with 2) and 3).
The resulting mixture of the ingredients 1) to 3) was dry granulated by roller compaction by use of the following set of parameters:
Rpm: 2.0 Gab size 2.5 mm Sieve size 1.25 mm Force 10 kN/cm The resulting particulate matter of the dry granulated ingredients 1) to 3) was admixed with 4). The resulting mixture of the ingredients 1) to 4) was compressed into tablets using a 5.0 mm standard concave punch design. The resulting tablets are of a quality that allows applying a standard enteric coat using standard coating equipment and parameters.
Optionally a sub coat consisting of a standard water soluble film like FIPMC
can be used to protect the enteric coat from the alkaline reacting core.
Example 5:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of a sub coat and an enteric coating.
Table 11: Composition of tablet core % w/w:
Batch no. 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Granulate by roller compaction Pantoprazo{e, 11/z H20 13.3 11.7 14.1 12.9 Sodium carbonate 13.3 55.2 -Calcium carbonate - 54.9 - -(Sturcal L) TriCalciumPhosphate 60.6 Pantoprazole:alkaline excipient 1:1 1:4.7 1:3.9 1:4.7 Mannitol - 13.5 - 14.9 Crospovidone 0.4 1.1 1.1 1.2 Tablet core excipients DiCafos A 62.7 8.5 19.2 -Crospovidone 9.7 9.7 10.0 9.8 Mg Stearate 0.5 0.4 0.5 0.5 Table 12: Composition of sub coat [% w/w]:
Raw materials Coating liquid Dry film composition composition Hypromellose 15 5 55,60lo Propylenglycol 1 11,1%
Talc 3 33,3%
Water, purified 91 % Plasticizer of polymer 20,0%
5 Table 13: Composition of enteric coat [% w/w]::
Raw materials Coating -iquid Dry film composition composition Methacryl acid-acryl 41,76 62,49 Copolymer disp. 30%
Triethylcitrate 1,25 6,24 Talc 6,27 31,28 Water, purified 50,92 % Plasticizer of Polymer 10,0 Table 17: Approximately amount of film dry matter applied [% w/w]:
Coat 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Theoretical applied 9,7 10,3 10,9 9,0 amount of sub coat [mg polymer/cmz]
Theoretical applied 5,5 5,4 5,3 + 2 5,7 amount of enteric coat [mg polymer/cmZ]
Pantoprazole was mixed with the alkaline excipient in a tumble mixer together with Crosspovidone and mannitol followed by roller compaction as described in example 1.
The remaining tablet core excipients were admixed and tablets were compressed by use of a Korsch PH106 tablet press and 6 mm concave punches aiming at a mean weight of 160 mg and a crushing strength of 50 N. Thereafter the tablet cores were coated with the sub coat followed by the enteric coat by use of a lab-scale Combi Coata. The obtained coated tablets were used for stability testing as described in example 6.
Example 6 (stability testing) A stability testing program with batches obtained in example 5 was performed.
The batches were stored at accelerated stability testing conditions (open petri dishes at 70 C
and not more than 10% relative humidity for three months). Such conditions probably correspond to shelf life stability testing of at least two years.
The analytical method is as follows: 10 tablets are transferred to a 200 ml volumetric flask. 150 ml mobile phase (the initial composition) is added and sample is shaken for 90 minutes. After the solutions pH-values have been adjusted to 8.0, mobile phase is added to the mark. The sample solution is filtered through 0.45 m filter and analysed by reverse phase HPLC in order to quantify the amount of Pantoprazole as well as degradation products thereof. The amount is given in % of total area, see table 19.
Furthermore, in figure 1 is shown the amount of pantoprazole as a function of time.
Table 18: HPLC method parameters Mobile phase ammonium phosphate buffer: methanoi: acetonitril Time % Buffer % Methanol % Acetonitril 0 min 65 10 25 Gradient profile 25 min 30 10 60 min 30 10 60 31 min 65 10 25 Flow 1,0 mI/min Column Waters Spherisorb, 250X4,6 mm, 5 pm particle size Column temperature 30 C
Auto sampler temperature 4 C
Detection UV-290 nm Injection volume 10 ial Run time 40 min.
Pantoprazole 10,7 min Approx. Retention time Impurity B 6,6 min Impurity A 13,4 min Table 19: Results of stability study Batch 07030631 10030631 13030634 13030636 "33C" "34C" "35C" "36C"
Pantoprazole:sodium carbonate 1:1 1:3,9 Pantoprazole:calcium carbonate 1:4,7 Pantoprazole:calcium phosphate 1:4,7 Pantoprazole:DiCafos A 1:4,7 1:0;7 1:1,4 9 25160 C lmonth 99,7 99,7 99,7 99,2 ' 70110 OP 1 month 97,4 96,6 97,3 93,9 o ca 70/10 OP 2 months 96,4 95,5 96,1 91,9 70/10 OP 3 months 94,9 94,3 94,6 89,3 cu 40/75 3 months 99,4 99,4 99,5 97,2 25/60 C 1month 0,18 0,15 0,20 0,56 0- 70/10 OP lmonth 2,2 3,2 2,3 6,0 M
a) ~~~ 70/10 OP 2 months 3,3 4,0 3,6 7,6 70/10 OP 3 months 4,3 4,8 4,4 9,3 a 40175 3 months 0,5 0,5 0,5 2,6 70/10 OP: 70 C / 10 % RH in Open petri dishes 25/60: 25 C / 60% RH in closed containers 40/75: 40 C / 75% RH in closed containers According to table 19 and figure 1, use of Ca$(P04)3OH as alkaline substance result in a relatively larger degree of pantoprazole degradation compared with use of Na2CO3, CaCO3i and DiCafos A as alkaline excipients. The stability data for the stressed stability testing conditions (70 C open Petri dishes, 70/10 OP) probably corresponds to a shelf life of at least two years.
Example 7:
Dry manufacture of tablets containing pantoprazole and Sodium carbonate or calcium carbonate and a disintegrant followed by application of a sub coat and an enteric coating.
Table 20: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 H20 14.1 14.1 14.1 14.1 Sodium carbonate 2.82 11.3 Calcium carbonate 2.82 11.3 (Sturcal L) Pantoprazole: alkaline exciplent 1:0.2 1:0.8 1:0.2 1:0,8 Tabiet core excipients DlCafos A 69.6 61.1 69.6 61.1 Crosspovidone 13.0 13 13.0 13 Mg Stearate 0.5 0.5 0.5 0.5 Based on the tablet core compositions listed above coated tablets were manufactured as described in example 5 with the following exception:
The pantoprazole was pre-rollercompacted prior to mixing with the alkaline excipient by use of the following parameters Rpm: 2.0 Gap size: 1.0 mm Sieve size: 1.25 mm Force: 4 kfV/cm The pre-roller compaction leads to formation of pantoprazole granules.
The obtained coated tablets were used for stability testing with the purpose of investigating the impact of lower amounts of alkaline material than used in example 5 and the use of pre-roffercompaction of the pantoprazole. The stability testing is disclosed in example B.
ExampEe 8: stability testing A stability program, including batches obtained in example 7 was performed.
The batches were stored in open petri dishes at 70 C and not more than 10 % RH for up to six weeks.
The anaEytical method is as described in example 6 Table 21: Result of stability study batch 3F-C 2F-C 7F-C 8F-C
Pantoprazole:sodium carbonate 1:0.8 1:0.2 Pantoprazole:calcium carbonate 1:0.2 1:0.8 Pantoprazole:DiCafos A 1:5 1:4,3 1:5 1:4,3 Pantoprazole 25/60 C 2 weeks 99,7 99,8 99,8 99,1 in % area 70/10 OP 2weeks 98,3 97,9 98,3 98,1 70/10 OP 6weeks 97,5 97,2 Degradation 25/60 C 2 weeks 0,20 0,15 0,10 0,52 products in 70/10 OP 2weeks 1,2 1,6 1,4 1,2 % area 70/10 OP 6weeks 2,0 2,4 It appears in table 21 and figure 2 that use of sodium carbonate and calcium carbonate as alkaline excip9ent at the mixing ratios of 1:0.2 and 1:0.8 result in nearly identical and acceptable degradation ratios when tested at 70 C and not more than 10 % RH
for up to six weeks. It is surprising that the solubility of the alkaline material apparently does not affect stability of the benzimidazole composition (calcium carbonate is poorly soluble in water).
Example 9:
Dry manufacture of tablets containfng pantoprazole and alkaline excipients focusing on order of mixing and roller compaction followed by application of a sub coat and an enteric coating.
Table 22: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 1l/z H20 14.1 Sodium carbonate 11.3 Pantoprazole:alkafine excipient 1:0.8 Tablet core excipients DiCafos A 61.1 Crospovidone 13 Mg Stearate 0.5 The composition shown in table 22 was mixed and roller compacted in different sequential order as shown in table 23 Table 23: Sequential order of mixing and roller compaction:
Batch no. 1 2 3 4 (Of coated Mixing with Pre-roller Mixing with Roller tablets) alkaline compaction alkaline compaction excipient (solely excipient pantoprazole) 01050633 3F-C Not used X X X
05050635 X Not used Not used X
05050638 12F-C Not used X X Not used Mixing and roller compaction were carried out as described in example 5.
5 The remaining tablet core excipients (Dicafos A, Crosspovidone and Mg-stearate) were admixed and tablets were compressed and coated in accordance with example 5.
The batches 01050633 and 05050638 were used for stability testing in example 10 and 05050635 was used for comparison with batches of example 16 with the purpose of 10 evaluating excipient homogeneity of granules.
Example 10: stability testing A stability program, including batches mentioned in example 9 was performed.
The 15 batches were stored in open petri dishes at 70 C for 2 weeks.
The analytical method is as described in example 6 Table 24: Results of stability testing:
batch Pantoprazole:sodium carbonate 1:0.8 1:0.8 Pantoprazole:DiCafos A 1:5 1:4,3 Pre-rollercompacting, Pre-mixing, rollercompacting, - rollercompacting mixing Pantoprazole 25160 C 2 weeks 99,7 99,5 in % area 70/10 OP 2weeks 98,3 97,2 70/10 OP 6weeks 97,5 Degradation 25/60 C 2 weeks 0,20 0,33 products in 70/10 OP 2weeks 1,2 2,9 % area 70/10 OP 6weeks 2,0 It appears in table 24 and figure 3 that panoprazole degradation is relatively small when pantoprazole is pre-roller compacted, mixed with the alkaline excipient and then roller compacted again. The pantoprazole degradation is relatively high when pantoprazole is pre-roller compacted and mixed with the alkaline excipient without including a step of roller compacting pantoprazole and alkaline substance together. The impact on stability is seen already after two weeks.
Example 11:
Dry manufacture of tablets containing pantoprazole and alkaline excipients.
Roller compaction has been carried out using two different sieve sizes. Tableting was followed by application of a sub coat and an enteric coating.
Table 25: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 HZ0 14.1 Sodium carbonate 2.82 Pantoprazole:alkaline excipient 1:0.2 Tablet core excipients DiCaPos A 69.6 Crospovidone 13.0 Mg Stearate 0.5 Based on the tablet core compositions listed above coated tablets were manufactured as described in example 5 with the following exception:
The pantoprazole was pre-rollercompacted prior to mixing with the alkaline excipient by use of the following parameters Rpm: 2.0 Gap size: 1.0 mm Sieve size: 1.25 mm (used for batch 29050641) or 1.0 mm (used for batch 29050645) Force: 4 kN/cm The pre-roller compacted pantoprazole and the sodium carbonate were mixed by use of a tumble-mixer and roller compacted using the following parameters:
Rpm: 2.0 Gap size: 2.5 mm Sieve size: 1.25 mm (used for batch 29050641) or 1.0 mm (used for batch 29050645) Force: 10 kN/cm The remaining tablet core excipients were admixed and tablets were compressed and coated in accordance with example 5.
Evaluation of the impact of the sieve size was based on sieve analysis and dissolution testing. Dissolution was carried out by use of the following method:
Table 26: Dissolution method.
USP/Ph.Eur Dissolution apparatus 1 Spindle Basket Rotation 150 rpm Temperature 37 C 0,5 C
Filter Whatman GF/F (0.7 pm) Dissolution medium 0- 120 minutes 600 ml 0.1 N HC!
After 120 minutes the dissolution medium 200 ml 0.20 M Na3PO4 added to the is changed to pH 6.8 vessel (method A, USP) Detection, UV 288 nm Sampling time The absorbance is measured by each minutes at 288 nm From figure 4 it can be seen that the use of a sieve size of 1.0 mm results in a relatively narrow particle size distribution compared to sieve size 1.25. The narrow size distribution results in a better dose variation of pantoprazole as can be seen form figure S.
Example 12:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of different types and amounts of sub coat.
Table 27: Composition of tablet core % w/w:
Granulate by roller compaction Pantoprazole, 11/2 H20 14,1 Sodium carbonate 55,2 Pantoprazole: allcaline excipient 1:3,9 Crospovidone 1,1 Tablet core excipients DlCafos A 19,2 Crospovidone 10,0 Mg Stearate 0,5 Tablet cores according to the above mentioned composition were manufactured as described in example S. Sub coat was applied as laid out in example 5 with the exception of variation in applied amount and type of polymer as shown En table 28:
Table 28: Amount (approximately) and type of sub coat applied:
Batch no. HPMC type Theoretical amount of HPMC
Cm9/cm2]
13030634 E15 10.9 (1/1 amount) 31030633 (C) E15 5.3 (1/2 amount) 21040634 E5 9.9 (1/1 amount) Enteric coat was applied as described in example 5.
Evaluation of the impact of amount and type of sub coat was based following dissolution results obtained obtained in example 11. However, tablets only coated with a sub coat were analysed solely in a dissolution medium with pH 6.8.
Figures 6, 7 and 8 disclose the impact of type of sub coat on the dissolution rate form both sub coated tabiets and sub + enteric coated tablets. A HPMC E5 based sub coat results in a relatively quick dissolution rate.
Example 13:
Dry manufacture of tablets containing pantoprazole and alkaline excipients followed by application of an enteric coating.
Tablet cores of batch 13030634 and 31030634 were manufactured as described in example 12. The tablet cores of batch 13030634 were enteric coated as described in example S. Batch 31030634 was produced with an enteric coating but without the application of a sub coat. The enteric coated tablets were used for stability testing in example 14.
Example 14: stability testing A stability program, including batches mentioned in example 13 was performed.
The batches were stored in open petri dishes at 70 C for respectively 2 and 3 months.
The analytical method is as described in example 6 Table 29: Results of stability testing Batch 13030634 31030634 Without sub coat 1 month 99,7 99,7 Pantoprazole 70/10 OP 97,3 97,9 in % of area I month 2 months 96,1 97,4 1 month 0,20 0,22 Degradation products. 70/10 OP
in % of area 1 month 2,3 1,7 2 months 3,6 2,2 70/10 OP: 70 C / 10 % RH in Open petri dishes 25/60: 25 C / 60% RH in closed containers It appears from table 29 and figure 9 that the stability (70 C / 10 % RH in Open petri dishes and 25 C / 60% RH in closed containers) of sub-coated tablets is fully comparable with tablets which has not been sub-coated.
Example 15:
Impact of type and amount of alkaline excipient on deg'radation of pantoprazole in a stress test by the addition of a weakly acidic component (ibuprofen) Table 30: Composition of mixtures [gram]
Raw materials Amounts in gram Sodium carbonate 4 16 20 25 Calcium carbonate 4 16 20 25 (Sturcal L) Ibuprofen 0.8 0.8 0.8 0.8 0.8 0.8 0.8 0.8 Pantoprazole 11/2 H20 20 20 10 5 20 20 10 5 Pantoprazole:alkaline 10.2 1:0.8 1:2 1:5 1:0.2 1:0.8 1:2 1:5 excipient Table 31: Composition of mixtures [gram]
Raw materials Amounts in gram Calcium carbonate 4 16 20 25 (Scoralite) Tri calcium phosphate 4 16 20 25 Ibuprofen 0.8 0.8 0.8 0.8 0.8 0.8 0.8 0.8 Pantoprazole 11/2 HZO 20 20 10 5 20 20 10 5 Pantoprazole:alkaline 1:0.2 1:0.8 1:2 1:5 1:0.2 1:0.8 1:2 1:5 excipient Mixtures were made by grinding the raw materials in a steel bowl and subsequently placing the mixture in petri dishes in sealed alu-bags for two weeks at ambient conditions.
5 The evaluation of this stability test is shown in table 32 (pantoprazole degradation products are coloured). Discoloration is evaluated based on a scale ranging from 1 - 10 where "1" indicates no discoloration and "10" indicates a severe discoloration.
Table 32. Discoloration scale of powder mixtures of table 30 and 31:
Alkaline material Mixing ratio Mixing ratio Mixing ratio Mixing ratio 1:0.2 1:0.8 1:2 1:5 Sodium carbonate 9 8 4 1 Calcium carbonate 10 8 4 1 (Sturcal L) Calcium carbonate 10 10 7 7 (Scoralite) Tri calcium 9 6 - 1 phosphate The results in table 32 are discussed in example 16.
Example 16:
Characterisation of alkaline materials.
Alkaline materials:
* Calcium carbonate, Sturcal L
* Calcium carbonate, Scoralite * Sodium carbonate anhydrate Alkaline substance raw material particle sizes have. been measured by laser light scattering (Malvem) and BET area has been measured by use of a Micromeritics Gemini 2375 at relative target pressures (P/Po) of 0.1 and 0.2 and 0.3. Samples have been dried for minimum 12 hours at 40 C prior to the measurements.
Table 33: BET-areas Raw materials BET-area [mz/g] Particle size D(v 0,5) [pm]
Calcium carbonate, Sturcal L 3.0 9 Calcium carbonate, Scoralite 0.2-0.5 29 Sodium carbonate anhydrate 2.1 99 The SEM pictures (figures 10-18) illustrate considerable differences in size and morphology on the alkaline raw materials. It should be noted that even though Sodium carbonate anhydrate has a larger particle size than the Calcium carbonate (Scoralite), sodium carbonate anhydrate has the largest BET area. This difference is further illustrated in example 17 by use of Scanning Electron Microscope pictures. The impact of the BET area and particle size on stability was illustrated in example 15.
The discoloration shown in table 32 demonstrates the impact of BET area (see example 16, table 33) and mixing ratio on pantoprazole stability. A high BET area favours good stability results. It appears from example 16 that a relatively small particle size may not suffice to ensure a satisfactory stability. Relatively big particles can be useful, provided that their porosity leads to a sufficiently high BET area.
Furthermore, it is illustrated that a high amount of alkaline material is preferred.
However, the discoloration test cannot reveal smaller amount of degradation product as can be seen by comparison of the addition of tri calcium phosphate in example 6. This means that tri calclum phosphate is not as efficient as e.g. sodium carbonate and calcium carbonate (Sturcal L).
Example 17 Impact of type and amount of alkaline excipient on homogeneity of a mixture with pantoprazole with alkaline materials.
Composition of powder mixtures * Pantoprazole, 11/2 H20 : Calcium carbonate (Sturcal L), 1:0.8 * Pantoprazole, 11/z H20 : Calcium carbonate (Scoralite), 1:0.8 = Pantoprazole, 11I2 H20 (pre-roller compacted) : sodium carbonate, 1:0.8 Pantoprazole, 11/2 H20 : Calcium carbonate (Sturcal L) and Pantoprazole, 11/2 H20 :
Calcium carbonate (Scoralite) batches have been mixed in a lab. scale high shear mixer for 1 minute. The Pantoprazole, 11/7. H20 (pre-roller compacted) batch was manufactured as described in example 7 prior to mixing with sodium carbonate. The mixing was done as described above.
All the mixtures were slugged on a single punch tableting machine using 11.3 mm flat faced punches. The slugs were evaluated for mixture homogeneity by use of scanning electronic microscopy (SEM). For reference, SEM pictures of the individual raw materials were obtained.
The SEM pictures are shown in the figures 10 - 18. Figure 11 and 12 disclose a considerable difference between Calcium carbonate (Sturcal L) and Calcium carbonate (Scoralite). SEM appearances of Sturcal L and Scoralite are in full accordance with the BET
areas measured in example 16.
Figure 13 is a magnification of the particles shown in figure 14. The magnification showing the porosity of the particles clearly supports the finding of a high BET area of Sodium Carbonate is illustrated.
Figures 15 and 16 show that the use of Calcium carbonate (Sturcal L) leads to a much more homogeneous mixture than Calcium carbonate (Scoralite). The impact on stability of this difference was illustrated in example 15. Figure 17 shows that the sodium carbonate particles are crushed during manufacturing. The physical structure of Sturcal L results in an improved distribution of the particles during mechanical pressure. An acceptable stability is obtained as illustrated in examples 15 and 6, 8 and 10.
Figure 18 iliustrates the effect of pre-roller compacting pantoprazole prior to mixing with alkaline substance. Slugging (or roller compaction) of the mixture results in "coating" of the surface of the relative large pantoprazole granules with calcium carbonate particles (Sturcal L). This "coating" also leads to an acceptable stability as shown in example 6 and 8. The need for using roller compaction to apply this coat is indicated in example 9, which was based on the use of sodium carbonate.
Example 18.
Impact of disintegrant on dissolution rate.
Table 34: Composition of tablet core % w/w:
Pantoprazole, 1112 H20 14.1 14.1 Calcium carbonate 11.3 11.3 (Sturcal L) Pantoprazole:alkaiine 1,0 8 1=0,8 excipient ~ ' DiCafos A 74.1 61.1 Crospovidone - 13 Mg Stearate 0.5 0.5 Based on the tablet core compositions listed above tablets were manufactured as described in example 7 with the following exception that no coat has been applied.
The cores were tested with respect to dissolution rate as described in example 11 with the exception that tablet cores were analysed solely in a dissolution medium with pH 6.8.
The results shown in figure 19 illustrate the advantages of the incorporation a disintegra,nt as the presence of a disintegrant in the formulation significantly increases the dissolution rate.
Claims (16)
1. A pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is further characterized by one or more of the following features:
(i) ~the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g, (ii) ~the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g, (iii) ~the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) ~the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) ~the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 m2/g, (vi) ~if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 m2/g, (vii) ~the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) ~the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, wherein said formulation is further characterized by one or more of the following features:
(i) ~the alkaline substance raw material is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g, (ii) ~the alkaline substance raw material is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g, (iii) ~the benzimidazole and the alkaline substance raw material have been mixed and dry granulated together prior to dry compression, (iv) ~the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) ~the alkaline substance raw material has a pKa of at least about 10 and a BET
area of at least about 1 m2/g, (vi) ~if the alkaline substance is polyvalent, said alkaline substance has a pKal-value of 6 or more and a BET area of at least about 1 m2/g, (vii) ~the alkaline substance raw material has a BET-area of at least about 1 m2/g, (viii) ~the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
2.A method for producing a pharmaceutical tablet formulation comprising a benzimidazole as the biologically active component, wherein:
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granulating steps and dry compressing of tablets, wherein said formulation is further characterized by one or more of the following features:
(i) ~the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (ii) ~the alkaline substance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (iii) ~the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) ~the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) ~the alkaline substance has a pKa of at least about 10 and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vi) ~if the alkaline substance is polyvalent, said alkaline substance has a pKa1-value of 6 or more and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vii) ~the alkaline substance has a BET-area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (viii) ~the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
- said formulation comprises an enteric coating for protection of the active component from acid attack in the stomach, - said benzimidazole is further stabilized by an alkaline substance in the tablet, - said method comprising dry granulating steps and dry compressing of tablets, wherein said formulation is further characterized by one or more of the following features:
(i) ~the alkaline substance is an alkali metal carbonate with high water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (ii) ~the alkaline substance is an alkaline earth metal carbonate with low water solubility and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (iii) ~the benzimidazole and the alkaline substance have been mixed and dry granulated together prior to dry compression, (iv) ~the weight ratio of benzimidazole and alkaline substance is from about 1:0.2 -1:5, (v) ~the alkaline substance has a pKa of at least about 10 and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vi) ~if the alkaline substance is polyvalent, said alkaline substance has a pKa1-value of 6 or more and a BET area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (vii) ~the alkaline substance has a BET-area of at least about 1 m2/g prior to any dry granulation and/or dry compression steps, (viii) ~the tablet formulation further comprises a disintegrant in an amount of about 1-30% by weight.
3. A method according to claim 2, wherein the benzimidazole is pantoprazole.
4. A method according to any one of claims 2-3, wherein the pantoprazole is pantoprazole sodium hydrate or pantoprazole sodium sesquihydrate.
5. A method according to any one of claims 2-4, wherein said formulation further comprises pharmaceutically acceptable excipients.
6. A method according to any one of claims 2-5, wherein said formulation comprises crospovidone in an amount of from about 5-15% by weight.
7. A method according to any one of claims 2-6, wherein said formulation further comprises a subcoat.
8. A method according to any one of claims 2-7, wherein said formulation is lacking a subcoat.
9. A method according to any one of claims 2-8, wherein the alkaline substance is a salt of an organic or an inorganic acid and the anion of the salt is carbonate (C032 ), hydrogenphosphate (HPO4 2-) or phosphate (PO4 3-).
10. A method according to any one of claims 2-9, wherein the alkaline substance is a salt of an organic or an inorganic acid and the kation is sodium (Na+), calcium (Ca2+) or magnesium (Mg2+).
11. A method according to claim 9 or 10, wherein the salt of the organic and/or inorganic acid according is sodiumcarbonate (Na2CO3), trisodiumphosphate (Na3PO4), disodiumhydrogenphosphate (Na2HPO4), hydrazine or derivatives thereof, lysine or a derivative thereof, arginine or a derivative thereof, or histidine or a derivative thereof.
12. A method according to any one of claims 2 and 5-11, wherein the benzimidazole is omeprazole or a salt and/or a hydrate thereof, lansoprazole or a salt and/or a hydrate thereof, esomeprazol or a salt and/or a hydrate thereof, aripiprazole or a salt and/or a hydrate thereof, rabeprazol or a salt and/or a hydrate thereof, timoprazole or a salt and/or a hydrate thereof.
13. A method according to any one of claims 2-12, wherein the tablet has a weight in the range of 75 mg to 2.5 g.
14. A method according to any one of claims 2-13, wherein the dry granulation is provided by means of a roller compactor.
15. A method according to any one of claims 2-14, wherein the mixture has been subject to sieving prior to tablet compression with a sieve size of 1,25 mm or less.
16. A product obtainable by a method according to any one of claims 2-15.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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DKPA200501019 | 2005-07-11 | ||
DKPA200501019 | 2005-07-11 | ||
US72785505P | 2005-10-19 | 2005-10-19 | |
US60/727,855 | 2005-10-19 | ||
PCT/DK2006/000409 WO2006105798A2 (en) | 2005-07-11 | 2006-07-11 | Benzimidazole formulation |
Publications (1)
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CA2614526A1 true CA2614526A1 (en) | 2006-10-12 |
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CA002614526A Abandoned CA2614526A1 (en) | 2005-07-11 | 2006-07-11 | Benzimidazole formulation |
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EP (1) | EP1901719A2 (en) |
AU (1) | AU2006230974C1 (en) |
CA (1) | CA2614526A1 (en) |
EA (1) | EA015535B1 (en) |
WO (1) | WO2006105798A2 (en) |
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JP5228359B2 (en) * | 2007-04-12 | 2013-07-03 | ニプロ株式会社 | Active ingredient particles, process for producing the same and orally disintegrating tablets |
BRPI0909439A2 (en) | 2008-03-11 | 2015-12-15 | Takeda Pharmaceutical | solid preparation for oral disintegration, and method for suppressing fine granule rupture |
TR201000948A1 (en) * | 2010-02-09 | 2011-08-22 | Sanovel İlaç San.Ve Ti̇c.A.Ş. | Aripiprazole formulations. |
JP6038128B2 (en) | 2011-06-03 | 2016-12-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | A biomarker for predicting and evaluating the reactivity of thyroid and renal cancer subjects to lenvatinib compounds |
CN103479593B (en) * | 2013-05-10 | 2014-10-08 | 青岛双鲸药业有限公司 | Preparation method for omeprazole enteric coated tablet |
CN103386133A (en) * | 2013-07-09 | 2013-11-13 | 重庆莱美药业股份有限公司 | Oral instant preparation of proton pump inhibitor and preparation method thereof |
HRP20221047T1 (en) | 2014-08-28 | 2022-11-11 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
HUE064614T2 (en) | 2015-02-25 | 2024-04-28 | Eisai R&D Man Co Ltd | Method for suppressing bitterness of quinoline derivative |
AU2015384801B2 (en) | 2015-03-04 | 2022-01-06 | Eisai R&D Management Co., Ltd. | Combination of a PD-1 antagonist and a VEGFR/FGFR/RET tyrosine kinase inhibitor for treating cancer |
CN104825414B (en) * | 2015-05-07 | 2018-11-16 | 山东新时代药业有限公司 | A kind of stable S-pantoprazole sodium enteric tablet |
US11369623B2 (en) | 2015-06-16 | 2022-06-28 | Prism Pharma Co., Ltd. | Anticancer combination of a CBP/catenin inhibitor and an immune checkpoint inhibitor |
CN113318079B (en) * | 2021-05-13 | 2024-01-09 | 江西博莱大药厂有限公司 | Method for improving dissolution rate of triclabendazole particles and dissolution rate detection method thereof |
CN115645373B (en) * | 2022-12-24 | 2024-01-30 | 山东理工职业学院 | Preparation method of omeprazole sodium tablet |
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US5433959A (en) * | 1986-02-13 | 1995-07-18 | Takeda Chemical Industries, Ltd. | Stabilized pharmaceutical composition |
TW550090B (en) * | 1997-05-09 | 2003-09-01 | Sage Pharmaceuticals Inc | Stable oral pharmaceutical dosage forms for acid-unstable drug |
KR100627614B1 (en) * | 1998-04-20 | 2006-09-25 | 에자이 가부시키가이샤 | Medicament comprising stabilized compositions containing benzimidazole-type compounds |
AU2001296908A1 (en) * | 2000-09-29 | 2002-04-08 | Geneva Pharmaceuticals, Inc. | Proton pump inhibitor formulation |
AR036354A1 (en) * | 2001-08-31 | 2004-09-01 | Takeda Chemical Industries Ltd | SOLID PREPARATION |
AU2004216405A1 (en) * | 2003-02-28 | 2004-09-10 | Ranbaxy Laboratories Limited | Stable pharmaceutical composition of rabeprazole and processes for their preparation |
WO2004112756A1 (en) * | 2003-06-26 | 2004-12-29 | Isa Odidi | Proton pump-inhibitor-containing capsules which comprise subunits differently structured for a delayed release of the active ingredient |
BRPI0412697A (en) * | 2003-07-17 | 2006-10-03 | Reddys Lab Inc Dr | pharmaceutical compositions having an expandable coating |
-
2006
- 2006-07-11 EA EA200800290A patent/EA015535B1/en not_active IP Right Cessation
- 2006-07-11 EP EP06753346A patent/EP1901719A2/en not_active Withdrawn
- 2006-07-11 AU AU2006230974A patent/AU2006230974C1/en not_active Ceased
- 2006-07-11 CA CA002614526A patent/CA2614526A1/en not_active Abandoned
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WO2006105798A2 (en) | 2006-10-12 |
EA200800290A1 (en) | 2008-08-29 |
AU2006230974B2 (en) | 2011-09-29 |
AU2006230974C1 (en) | 2012-02-02 |
WO2006105798A3 (en) | 2006-12-07 |
AU2006230974A1 (en) | 2006-10-12 |
EP1901719A2 (en) | 2008-03-26 |
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