[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US20130053440A1 - Self-Preserved Aqueous Pharmaceutical Compositions - Google Patents

Self-Preserved Aqueous Pharmaceutical Compositions Download PDF

Info

Publication number
US20130053440A1
US20130053440A1 US13/664,049 US201213664049A US2013053440A1 US 20130053440 A1 US20130053440 A1 US 20130053440A1 US 201213664049 A US201213664049 A US 201213664049A US 2013053440 A1 US2013053440 A1 US 2013053440A1
Authority
US
United States
Prior art keywords
concentration
composition
zinc
compositions
present
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
Application number
US13/664,049
Inventor
Bhagwati P. Kabra
Masood A. Chowhan
L. Wayne Schneider
Wesley Wehsin Han
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Alcon Research LLC
Original Assignee
Alcon Research LLC
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39156274&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20130053440(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Alcon Research LLC filed Critical Alcon Research LLC
Priority to US13/664,049 priority Critical patent/US20130053440A1/en
Publication of US20130053440A1 publication Critical patent/US20130053440A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/24Heavy metals; Compounds thereof
    • A61K33/30Zinc; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0048Eye, e.g. artificial tears
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/22Boron compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention is directed to self-preserved pharmaceutical compositions. More specifically, the invention is directed to the provision of aqueous, multi-dose pharmaceutical compositions that have been formulated so as to have sufficient antimicrobial activity to satisfy the preservation efficacy requirements of the United States Pharmacopeia (“USP”) and analogous guidelines in other countries, without requiring a conventional antimicrobial preservative, such as benzalkonium chloride, polyquaternium-1, hydrogen peroxide (e.g., sodium perborate), or chorine-containing agents.
  • USP United States Pharmacopeia
  • benzalkonium chloride polyquaternium-1
  • hydrogen peroxide e.g., sodium perborate
  • chorine-containing agents chorine-containing agents.
  • the ability to achieve self-preservation is based on a unique combination of formulation components and criteria.
  • compositions are required to be sterile (i.e., free of bacteria, fungi and other pathogenic microorganisms).
  • sterile i.e., free of bacteria, fungi and other pathogenic microorganisms.
  • examples of such compositions include: solutions and suspensions that are injected into the bodies of humans or other mammals; creams, lotions, solutions or other preparations that are topically applied to wounds, abrasions, burns, rashes, surgical incisions, or other conditions where the skin is not intact; and various types of compositions that are applied either directly to the eye (e.g., artificial tears, irrigating solutions, and drug products), or are applied to devices that will come into contact with the eye (e.g., contact lenses).
  • compositions can be manufactured under sterile conditions via procedures that are well known to those skilled in the art. However, once the packaging for a product is opened, such that the composition contained therein is exposed to the atmosphere and other sources of potential microbial contamination (e.g., the hands of a human patient), the sterility of the product may be compromised. Such products are typically utilized multiple times by the patient, and are therefore frequently referred to as being of a “multi-dose” nature.
  • the means employed may be: (i) a chemical agent that prevents the proliferation of microbes in a composition, which is referred to herein as an “antimicrobial preservative”; or (ii) a packaging system that prevents or reduces the risk of microbes reaching a pharmaceutical composition within a container.
  • Prior multi-dose ophthalmic compositions have generally contained one or more antimicrobial preservatives in order to prevent the proliferation of bacteria, fungi and other microbes. Such compositions may come into contact with the cornea either directly or indirectly.
  • the cornea is particularly sensitive to exogenous chemical agents. Consequently, in order to minimize the potential for harmful effects on the cornea, it is preferable to use anti-microbial preservatives that are relatively non-toxic to the cornea, and to use such preservatives at the lowest possible concentrations (i.e., the minimum amounts required in order to perform their anti-microbial functions).
  • the concentration of an antimicrobial agent necessary for the preservation of ophthalmic formulations from microbial contamination may create the potential for toxicological effects on the cornea and/or other ophthalmic tissues.
  • Using lower concentrations of the anti-microbial agents generally helps to reduce the potential for such toxicological effects, but the lower concentrations may be insufficient to achieve the required level of biocidal efficacy (i.e., antimicrobial preservation).
  • Ophthalmic compositions are generally formulated as isotonic, buffered solutions.
  • One approach to enhancing the anti-microbial activity of such compositions is to include multi-functional components in the compositions. In addition to performing their primary functions, these multi-functional components also serve to enhance the overall anti-microbial activity of the compositions.
  • compositions of the present invention are multi-dose products that do not require a conventional antimicrobial preservative (e.g., benzalkonium chloride), and yet are preserved from microbial contamination.
  • a conventional antimicrobial preservative e.g., benzalkonium chloride
  • Such compositions have been referred to in the art as being “preservative free” (see, e.g., U.S. Pat. No. 5,597,559 issued to Olejnik, et al.).
  • Compositions that are preserved from microbial contamination as a result of the inherent antimicrobial activity of one or more components of the compositions are also referred to in the art as being “self-preserved” (see, e.g., U.S. Pat. No. 6,492,361 issued to Muller, et al.).
  • compositions that are “preservative-free” or “self-preserving”: Kabara, et al., Preservative - Free and Self - Preserving Cosmetics and Drugs—Principles and Practice , Chapter 1, pages 1-14, Marcel Dekker, Inc. (1997).
  • compositions of the present invention which do not contain a conventional antimicrobial preservative, are referred to herein as being “self-preserved”.
  • the present invention is directed to the self-preservation of aqueous ophthalmic compositions via the use of very low concentration of zinc ions.
  • the present invention is based in part on the finding that in order to utilize low concentrations of zinc ions to self-preserve multi-dose ophthalmic compositions having ophthalmically acceptable pH and osmolality values, certain formulation parameters must be maintained. Specifically, the concentration of buffering anions utilized to maintain the pH within an ophthalmically acceptable range must be limited to an amount of 15 millimolar (“mM”) or less in order to avoid interfering with the anti-microbial activity of the zinc ions.
  • mM millimolar
  • the antimicrobial activity of the zinc-containing compositions of the present invention can be further enhanced by the use of zinc ions in combination with borate or a borate/polyol complex, and that if such a combination is utilized, the use of propylene glycol is strongly preferred, so as to avoid ionic interactions between anionic species generated by other polyols (e.g., sorbitol) and the zinc cations.
  • the performance of the zinc-based preservative systems of the present invention is further enhanced by: (i) limiting the amount of multivalent metal cations other than zinc (e.g., calcium and magnesium) in the compositions of the present invention; and (ii) limiting the amount of ionized salts (e.g., sodium chloride and potassium chloride) in said compositions.
  • the compositions of the present invention are preferably free of or substantially free of both ionized salts and multivalent metal cations other than zinc.
  • compositions of the present invention have several advantages over existing ophthalmic formulations that are either: (i) packaged as a “single dose” or “unit of use” product, so as to avoid the inclusion of any antimicrobial preservative (e.g., BION®TEARS Lubricant Eye Drops, which is marketed by Alcon Laboratories, Inc.), or (ii) preserved by means of a so-called “disappearing” preservatives, such as the chlorite-based system described in U.S. Pat. Nos.
  • antimicrobial preservative e.g., BION®TEARS Lubricant Eye Drops, which is marketed by Alcon Laboratories, Inc.
  • the multi-dose ophthalmic compositions of the present invention are able to satisfy the USP preservative efficacy requirements, as well as analogous requirements in other countries, including the Japanese Pharmacopoeia (“JP”) and European Pharmacopoeia (“EP”) preservative efficacy standards, without employing any conventional antimicrobial preservatives, such as chlorite or hydrogen peroxide.
  • JP Japanese Pharmacopoeia
  • EP European Pharmacopoeia
  • the present invention is particularly directed to the provision of aqueous ophthalmic solutions that are effective in preventing microbial contamination in the absence of conventional antimicrobial preservatives, such as benzalkonium chloride (“BAC”), polyquaternium-1, chlorite or hydrogen peroxide.
  • BAC benzalkonium chloride
  • polyquaternium-1 polyquaternium-1
  • chlorite hydrogen peroxide
  • FIGS. 1-3 are graphs showing the interaction of boric acid and various polyols.
  • the pharmaceutical compositions of the present invention contain zinc ions at a concentration of 0.04 to 0.9 millimoles/liter (“mM”), preferably 0.04 to 0.4 mM and most preferably 0.1 to 0.4 mM.
  • mM millimoles/liter
  • the use of this very low concentration is particularly desirable in ophthalmic pharmaceutical compositions containing therapeutically active agents, such as prostaglandin analogues used to control intraocular pressure (e.g., travoprost), because at higher concentrations the zinc ions may produce an astringent effect when applied to the eye.
  • the zinc ions are preferably provided in the form of zinc chloride, at a concentration of 0.0005 to 0.012 percent by weight/volume (“w/v %”), preferably 0.0005 to 0.005 w/v % and most preferably 0.001 to 0.005 w/v %.
  • the zinc may be provided in various forms, such as zinc chloride, zinc sulfate, zinc acetate or zinc carbonate.
  • zinc chloride is preferred.
  • the present invention is based on part on a finding that anionic agents utilized to buffer the compositions of the present invention may interfere with the ability of zinc to exert antimicrobial activity. Such interference can be very detrimental to the ability of the compositions to maintain sufficient antimicrobial activity to meet preservative efficacy standards, particularly in view of the very low concentrations of zinc utilized in the present invention. Accordingly, it has been determined that the total concentration of anionic species in the compositions of the present invention should be limited. Specifically, it is preferred that the total concentration of anionic species, particularly buffering anions, should be limited to an amount of less than 15 mM, more preferably less than 10 mM, and most preferably less than 5 mM. For simplicity and clarity, the concentration of buffering anionic species in this patent application will be represented by the concentration of monovalent cations (such as sodium) that are present or needed to bring the pH to the specified value.
  • monovalent cations such as sodium
  • the phrase “less than” relative to a specified concentration means that the specified component (e.g., buffering anions) is either not present in the composition at all or is present at a concentration less than the specified limit (e.g., 15 mM).
  • compositions of the present invention therefore preferably do not contain any multivalent buffering anions, other than borate-polyol complexes, which may be multivalent under certain conditions (e.g., pH and/or borate:polyol ratio), or are substantially free of such buffering anions.
  • the phrase “substantially free of multivalent buffering anions” means that the composition either does not contain any multivalent buffering anions or contains an amount of said anions that does not inhibit the ability of the composition to satisfy specified preservative efficacy standards (e.g., USP, EP or JP).
  • the amount of multivalent buffering anions in the compositions of the present invention is preferably less than 5 mM, with said concentration being determined in the same manner as specified in the preceding paragraph.
  • Zn 2 divalent zinc ions
  • Access to these transport proteins can be competitively inhibited by multivalent metal cations, particularly Mg 2+ , Ca 2+ , Mn 2+ , Ni 2+ , and Co 2+ .
  • multivalent metal cations particularly Mg 2+ , Ca 2+ , Mn 2+ , Ni 2+ , and Co 2+ .
  • the compositions of the present invention preferably do not contain such cations or are substantially free of said cations.
  • the phrase “substantially free of multivalent metal cations other than zinc” means that the composition either does not contain such cations or contains an amount of said cations that does not inhibit the ability of the composition to satisfy specified preservative efficacy standards (e.g., USP, EP or JP).
  • the amount of multivalent metal cations other than zinc in the compositions of the present invention is preferably less than 5 mM.
  • compositions of the present invention preferably do not contain ionized salts, or are substantially free of ionized salts.
  • substantially free of ionized salts means that the composition either does not contain any ionized salt or contains an amount of ionized salt that does not inhibit the ability of the composition to satisfy specified efficacy standards (e.g., USP, JP or EP).
  • the amount of ionized salt contained in the compositions of the present invention is preferably less than 50 mM.
  • borate includes boric acid, sodium borate and potassium borate.
  • divalent cations e.g., calcium borate
  • the self-preserved compositions of the present invention are preferably free of or substantially free of other sources of divalent cations, such as calcium chloride.
  • compositions of the present invention preferably contain one or more borates in an amount of from about 0.1 to about 2.0% w/v, more preferably 0.3 to 1.5% w/v, and most preferably 0.5 to 1.2% w/v.
  • polyol includes any compound having at least one hydroxyl group on each of two adjacent carbon atoms that are not in trans configuration relative to each other.
  • the polyols can be linear or cyclic, substituted or unsubstituted, or mixtures thereof, so long as the resultant complex is water soluble and pharmaceutically acceptable.
  • examples of such compounds include: sugars, sugar alcohols, sugar acids and uronic acids.
  • Preferred polyols are sugars, sugar alcohols and sugar acids, including, but not limited to: mannitol, glycerin, xylitol, sorbitol and propylene glycol.
  • propylene glycol is particularly preferred in order to limit the presence of anionic species.
  • Boric acid interacts with polyols, such as glycerol, propylene glycol, sorbitol and mannitol, to form borate polyol complexes.
  • polyols such as glycerol, propylene glycol, sorbitol and mannitol
  • the type and ratio of such complexes depends on the number of OH groups of a polyol on adjacent carbon atoms that are not in trans configuration relative to each other.
  • propylene glycol has only one OH group on each of two adjacent carbon atoms that are not in trans configuration. Consequently, one molecule of boric acid will interact and form a complex with one or two molecules of propylene glycol, resulting in a monovalent anion.
  • the compositions preferably also contain one or more polyols, at a total concentration of 0.25 to 2.5% w/v.
  • the polyol preferably is propylene glycol at a concentration of 0.25 to 1.80% w/v, preferably 0.25 to 1.25% w/v.
  • propylene glycol preferably is propylene glycol at a concentration of 0.25 to 1.80% w/v, preferably 0.25 to 1.25% w/v.
  • propylene glycol sorbitol and mannitol are also preferred polyols, and preferably are used at a concentration of 0.05 to 0.75% w/v, preferably 0.05 to 0.5% w/v.
  • compositions of the present invention preferably contain borate or a borate/polyol complex, most preferably a borate/polyol complex wherein the polyol portion of the complex is propylene glycol or a combination of propylene glycol and sorbitol.
  • the preference for propylene glycol is based on a discovery that sorbitol and other polyols have a greater tendency to form anionic species at pH values of 7.5 or less, and that such anionic species may interfere with the antimicrobial activity of zinc.
  • the graphs shown in FIGS. 1-3 demonstrate that sorbitol has a much higher tendency to form anionic species in the presence of boric acid, compared to propylene glycol.
  • FIGS. 1-3 The data shown in FIGS. 1-3 were compiled as follows: A 1 Kg solution containing the given concentrations of boric acid and propylene glycol or sorbitol or mannitol was prepared and the initial pH of the solution was determined. 1 N NaOH was then added to adjust the pH. The cumulative amount of sodium hydroxide used to adjust pH to different values was then recorded.
  • boric acid interacts and forms an ionic complex with species containing several hydroxyl groups, such as mannitol and sorbitol.
  • species containing several hydroxyl groups such as mannitol and sorbitol.
  • the interaction between boric acid and propylene glycol is more limited than with other polyols. This is represented by the amount of sodium hydroxide needed to adjust pH, as shown in FIG. 1 . Sorbitol and mannitol significantly shift the curve relative to the amount of NaOH required to lower pH, whereas propylene glycol only slightly shifts the curve. This is further evident in FIG. 2 .
  • the present invention is particularly directed to the provision of multi-dose, self-preserved ophthalmic compositions that have sufficient antimicrobial activity to allow the compositions to satisfy the USP preservative efficacy requirements, as well as other preservative efficacy standards for aqueous pharmaceutical compositions, without a conventional antimicrobial preservative.
  • PAT Preservative Efficacy Test
  • compositions of the present invention may optionally also include one or more low molecular weight amino alcohols as buffering agents.
  • the amino alcohols which may be utilized in the present invention are water-soluble and have a molecular weight in the range of from about 60 to about 200.
  • the following compounds are representative of the low molecular weight amino alcohols which may be utilized in the present invention: 2-amino-2-methyl-1-propanol (AMP), 2-dimethylamino-methyl-1-propanol (DMAMP), 2-amino-2-ethyl-1,3-propanediol (AEPD), 2-amino-2-methyl-1,3-propanediol (AMPD), 2-amino-1-butanol (AB).
  • AMP 2-amino-2-methyl-1-propanol
  • DMAMP 2-dimethylamino-methyl-1-propanol
  • AEPD 2-amino-2-ethyl-1,3-propanediol
  • AMPD 2-
  • AMP 95% pure AMP and 5% water
  • AMP 95% pure AMP and 5% water
  • the amount of amino alcohol used will depend on the molecular weight of the amino alcohol selected, and the presence (or absence) of other ingredients in the composition (e.g., chelating agents, buffering agents and/or tonicity agents).
  • the amino alcohol will generally be present in an amount necessary to enhance the antimicrobial activity of an aqueous self-preserved pharmaceutical composition of the type described herein.
  • the amount of amino alcohol required for a particular composition can be determined through comparative testing.
  • the above-described amino alcohols are also utilized in the compositions of the present invention to neutralize the pH of the borate or borate/polyol complex, or bring the composition to the desired pH level.
  • the amount of amino alcohol required for this purpose is a function of the particular borate or borate/polyol mixture selected and the concentration thereof.
  • the self-preserved compositions of the present invention may optionally contain one or more amino alcohols at a total concentration of from about 0.01 to about 2.0 percent by weight/volume (“% w/v”), and preferably from 0.1 to 1.0% w/v.
  • the zinc, zinc/borate, zinc/polyol and zinc/borate/polyol systems described herein may be included in various types of pharmaceutical compositions to enhance anti-microbial activity and self-preserve the compositions, such as ophthalmic, otic, nasal and dermatological compositions, but is particularly useful in ophthalmic compositions.
  • ophthalmic pharmaceutical compositions such as topical compositions used in the treatment of glaucoma, infections, allergies or inflammation
  • compositions for treating contact lenses such as cleaning products and products for enhancing the ocular comfort of patients wearing contact lenses
  • various other types of ophthalmic compositions such as ocular lubricating products, artificial tears, astringents, and so on.
  • the compositions may be aqueous or non-aqueous, but will generally be aqueous.
  • compositions of the present invention may contain various types of therapeutic agents. However, the invention is most useful relative to therapeutic agents that are nonionic, since nonionic agents do not interfere with the antimicrobial activity of zinc cations in solution. Cationic therapeutic agents may also be utilized in the compositions, particularly if the agent is included in the compositions in free base form or in the form of a salt with a monovalent anion, such as a hydrochloride salt. Cationic therapeutic agents that are included in the compositions in the form of a salt of a multivalent anion may interfere with the antimicrobial activity of the zinc preservative systems described herein, depending on the concentration of the anion. Such interference must be considered when selecting therapeutic agents that are suitable for use in the compositions of the present invention. Similarly, the use of therapeutic agents that are anionic may be considered; however, such agents may interfere with the activity of zinc ions, depending on the concentration of the agent and its dissociation constant.
  • therapeutic agents examples include prostaglandin analogs (e.g., latanoprost, travoprost and unoprostone), hypotensive lipids (e.g., bimatoprost), and glucocorticoids (e.g., prednisolone, dexamethasone and lotoporednol).
  • prostaglandin analogs e.g., latanoprost, travoprost and unoprostone
  • hypotensive lipids e.g., bimatoprost
  • glucocorticoids e.g., prednisolone, dexamethasone and lotoporednol
  • the present invention is particularly directed to the provision of self-preserved, multi-dose ophthalmic compositions in connection with the treatment of conditions wherein the cornea or adjacent ocular tissues are irritated, or conditions requiring frequent application of a composition, such as in the treatment of dry eye patients.
  • the self-preserved compositions of the present invention are therefore particularly useful in the field of artificial tears, ocular lubricants, and other compositions used to treat dry eye conditions, as well as other conditions involving ocular inflammation or discomfort.
  • compositions of the present invention will generally be formulated as sterile aqueous solutions.
  • the compositions of the present invention are also formulated so as to be compatible with the eye and/or other tissues to be treated with the compositions.
  • the ophthalmic compositions intended for direct application to the eye will be formulated so as to have a pH and tonicity that are compatible with the eye.
  • compositions will have a pH in the range of 4 to 9, preferably 5.5 to 8.5, and most preferably 5.5 to 8.0. It has been determined that a slightly alkaline pH increases the antimicrobial activity of the compositions of the present invention. The use of a pH in the range of 7.0 to 8.0 is therefore preferred.
  • compositions will have an osmolality of 200 to 350 milliosmoles per kilogram (mOsm/kg), more preferably 250 to 330 mOsm/kg.
  • mOsm/kg milliosmoles per kilogram
  • nonionic osmolality-adjusting agents is preferred, as ionic salts such as sodium chloride have been found to reduce the antimicrobial activity of the zinc-based preservative systems described herein.
  • the use of propylene glycol, glycerol, xylitol or combinations thereof as nonionic osmolality adjusting agents is particularly preferred.
  • Boric acid may also be utilized as an osmolality-adjusting agent in the compositions of the present invention. Boric acid, if utilized, will be present in the compositions as a mixture of ionic and nonionic species.
  • compositions of the present invention may contain various types of pharmaceutical excipients, such as surfactants, viscosity-modifying agents and so on, provided that such excipients are non-ionic.
  • excipients that are cationic or anionic is not preferred, since such ionic agents may interfere with the zinc-based preservation systems described herein. This is particularly true with respect to anionic excipients.
  • the compositions of the present invention are preferably free of or substantially free of anionic excipients.
  • the amount of excipient contained in the compositions must be limited to an amount that does not inhibit the ability of the composition to meet the applicable preservative efficacy requirements (e.g., USP, JP and/or EP) and adjustments to the formulation properties may be required.
  • the nonionic surfactant polyoxyl 40 hydrogenated castor oil can be used for solubilization or stabilization of drugs, such as travoprost.
  • 12-hydroxy stearic acid an anionic compound that has been determined to be present as an impurity and potential degradation product of the excipient polyoxyl 40 hydrogenated castor oil, interacts with zinc and forms particles.
  • the pH of the composition needs to be in the range 5.0 to 6.0, preferably in the range 5.5 to 5.9.
  • One or more conventional antimicrobial preservatives can be present in the compositions of the present invention, if desired, but the compositions preferably do not contain any conventional antimicrobial preservatives. If utilized, such preservatives can be present in conventional amounts, but in view of the self-preserving properties of the compositions of the present invention, such conventional antimicrobial preservatives can also be utilized in much lower concentrations than would be required to satisfy preservative efficacy requirements if only the conventional antimicrobial preservative were present.
  • the present compositions can be a self-preserved composition, if an anti-microbial preservative is present as an option, the amount can be an amount that would not be effective alone as an antimicrobial preservative agent. However, the overall composition would have sufficient antimicrobial activity to satisfy USP/FDA/ISO preservative efficacy requirements.
  • the conventional antimicrobial preservative if present, is not anionic and if anionic, it is preferred that the amount should be low enough to not substantially interfere with the antimicrobial activity of the preservative systems described herein.
  • Antimicrobial preservative effectiveness as set forth by the examples infra was determined using an organism challenge test according to the methods described in the United States Pharmacopeia 24 (USP) for category 1A products. Samples were inoculated with known levels of one or more of the following: gram-positive vegetative bacteria ( Staphylococcus aureus ATCC 6538), gram-negative vegetative bacteria ( Pseudomonas aeruginosa ATCC 9027 and Escherichia coli ATCC 8739), yeast ( Candida albicans ATCC 10231) and mold ( Aspergillus niger ATCC 16404).
  • the samples were then pulled at specified intervals to determine if the antimicrobial preservative system was capable of killing or inhibiting the propagation of organisms purposely introduced into the formulation.
  • the rate or level of antimicrobial activity determines compliance with the USP preservative efficacy standards for the cited categories of preparations.
  • the PET screen test was conducted for only 7 days, rather than 14 or 28 days, with additional time points of 6 and 24 hours being added to evaluate preservative efficacy relative to Ph. Eur. B. criteria. This modified PET screen test has been shown to be a reliable test for determining whether a composition will meet USP or Ph. Eur. B criteria.
  • the USP 24 Antimicrobial Effectiveness Test requires that compositions containing Category 1A products have sufficient anti-bacterial activity to reduce an initial inoculum of approximately 10 5 to 10 6 bacteria by one log (i.e., a 90% reduction in the microorganism population) over a period of seven (7) days and by three logs (i.e., a 99.9% reduction in the microorganism population) over a period of fourteen (14) days, and requires that there cannot be any increase in the microorganism population following the conclusion of the fourteen day period.
  • the USP standards require that the compositions maintain stasis (i.e., no growth) relative to the population of the initial inoculum over the entire 28 day test period.
  • a category 1A product is an injection, or other parenteral including emulsions, otic, sterile nasal products and ophthalmic products made with aqueous bases or vehicles.
  • the margin of error in calculating microorganism populations is generally accepted to be +/ ⁇ 0.5 logs. Accordingly, the term “stasis”, as utilized herein relative to the above-discussed USP standards, means that the initial population cannot increase by more than 0.5 log orders, relative to the initial population.
  • the formulations of Examples A-E were evaluated to determine the effect of buffering anions on preservative efficacy. As discussed in greater detail below, the formulations of Examples A and B do not contain buffering agents. Although these formulations satisfied the USP preservative efficacy requirements, the presence of a buffering system is highly desirable, so as to prevent pH drift over the life of a commercial product (i.e., a period of up to two years or more).
  • the formulation of Example C include a borate/polyol buffering system, but the system has minimal buffering capacity. As with the formulations of Examples A and B, the formulation of Example C satisfied the USP requirements.
  • the formulations of Examples D and E contain significantly greater concentrations of buffering agents and consequently a higher buffering capacity.
  • Examples A-E demonstrates the need to balance the requirements for an effective buffering system with the antimicrobial activity required to satisfy preservative efficacy requirements.
  • Example A does not have any buffering ingredient.
  • the amount of sodium hydroxide used in the formulation (0.2 mM) to adjust pH is minimal, which means that the buffering anion concentration is very low.
  • This formulation containing 0.18 mM zinc (0.0025% zinc chloride) meets USP preservation criteria, but is not desirable from a commercial perspective due to the lack of buffering capacity.
  • Example B contains boric acid, it does not have buffering capacity as the pKa of boric acid (alone) is much higher than 6.
  • the amount of sodium hydroxide used in the formulation (0.3 mM) to adjust pH is minimal.
  • This formulation containing 0.18 mM zinc (0.0025% zinc chloride) meets USP preservation criteria, but is not commercially desirable due to the lack of buffering capacity.
  • Example C includes two excipients, boric acid and propylene glycol, which together add significantly to the osmolality of the composition and provide minimal buffering capacity.
  • the amount of sodium hydroxide required in this formulation to adjust pH (0.5 mM) is somewhat higher than for the formulations of Examples A and B, but still very low compared to the limits specified herein (i.e., less than 15 mM, more preferably less than 5 mM).
  • This formulation, containing 0.18 mM Zinc (0.0025% zinc chloride) meets USP preservation criteria, but the buffering capacity is not ideal relative to commercial viability.
  • Example D does not meet USP preservation criteria for either S. aureus or E. coli at days 7 and 14.
  • Example E does not meet USP preservation criteria for S. aureus at day 14 or for E. coli at days 7 and 14.
  • examples G, I, and J contain 0.75% propylene glycol. All five examples have an anionic buffer concentration of about 19 mM.
  • compositions of Examples F and G contain 0.18 mM of zinc. These have much better anti-microbial activity against S. Aureus than the formulations of Examples D and E, above. Specifically, the compositions of Examples F and G meet USP preservation criteria for S. aureus . However, although the antimicrobial activity against E. coli at zinc concentrations of 0.18 mM (Examples F and G) and 0.36 mM (Example H and I) is improved, compared to examples D and E, it is not sufficient to consistently meet USP preservation criteria at day 14 . Increasing the zinc concentration to 1.8 mM (Example J) improved the antimicrobial activity of the solution, so as to allow it to meet USP criteria. However, as indicated above, such higher concentration of zinc are not preferred in ophthalmic products, as zinc may provide astringent activity at these concentrations.
  • the amount of sorbitol was reduced to 0.25%, while keeping the boric acid concentration at 1%, in order to reduce the concentration of buffering anionic species.
  • the compositions of Examples L-N contain 0.75% propylene glycol.
  • the formulations of Examples K and L have an anionic buffer concentration of about 4 mM, which is within the preferred range of less than 5 mM specified herein.
  • the antimicrobial activity of these compositions against E. coli at a zinc concentration of 0.18 mM (0.0025 w/v %) is significantly improved, relative to the activity of the formulations in Examples F-J, and the compositions meet USP preservation criteria.
  • examples M and N the pH was adjusted to 5.5 and 6.5, respectively, while maintaining the USP preservation efficacy.
  • the results obtained with the formulations of Examples K through N, which are representative of the compositions of the present invention, further demonstrate the importance of limiting the concentration of buffering anions, relative to satisfying preservative efficacy requirements.
  • Example K L M N FID 107046 107047 109032 109033 Lot Number 04-36523 37157-3 05-40452 05-40453 Ingredient Travoprost 0.004 0.004 0.004 0.004 Polyoxyl 40 0.5 0.5 0.5 0.5 0.5 Hydrogenated Castor Oil (HCO-40) Zinc Chloride 0.0025 0.0025 0.0025 0.0025 Boric Acid 1 1 1 1 Sorbitol 0.25 0.25 0.25 0.25 Propylene None 0.75 0.75 0.75 Glycol Sodium Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Adjust Hydroxide, pH to pH to pH to pH to and/or 6.0 6.0 5.5 6.5 Hydrochloric Acid Purified Water QS 100% QS 100% QS 100% QS 100% Osmolality 176 272 283 278 Monovalent 3.9 mM 4.1 mM 2 mM 7.5 mM cation (Na) conc.
  • HCO-40
  • Example O P FID 107519 107520 Lot Number 04-37442 04-37443 Ingredient Concentration (w/v %) Travoprost 0.004 0.004 Polyoxyl 40 Hydrogenated Castor Oil 0.5 0.5 (HCO-40) Zinc Chloride 0.0025 0.0025 Boric Acid 0.3 0.15 Sorbitol 0.25 0.125 Propylene Glycol 1.6 1.6 Sodium Hydroxide, and/or Adjust Adjust Hydrochloric Acid pH to 6.0 pH to 6.0 Purified Water QS 100% QS 100% Osmolality 281 247 Sodium Hydroxide conc. 2.2 mM 0.5 mM Monovalent cation (Na) conc.
  • Example R The preservation of formulations containing 0.18 mM zinc (0.0025% zinc chloride), with or without boric acid. was evaluated. The results show that antimicrobial activity was greater with the presence of boric acid/polyols. However, the formulation of Example R exhibited sufficient activity to satisfy USP preservative efficacy requirements, even though it did not contain boric acid. The ability of the formulation of Example R to meet preservative efficacy requirements is believed to be attributable in part to the fact that the formulation: (i) did not contain any multivalent anionic buffering agents and (ii) contained a non-ionic agent (i.e., propylene glycol) as the principal osmolality adjusting agent.
  • the formulations of Examples Q and R are representative of the compositions of the present invention.
  • a comparison of the formulations of Examples Q and S demonstrates that the preservation efficacy of formulations containing 0.18 mM zinc (0.0025% zinc chloride) is reduced in the presence of low levels of a multivalent metal cation, i.e., calcium.
  • a multivalent metal cation i.e., calcium.
  • the amount of multivalent metal cation in the formulation of Example S i.e., 2.3 mM
  • the upper limit specified herein i.e., less than 5 mM
  • the formulations of Examples Q and S are representative of the compositions of the present invention.
  • Example U The zinc concentration utilized in the formulation of Example U is outside the range specified herein (i.e., 0.04 to 0.9 mM). Consequently, the formulations of Examples Q and T are representative of the compositions of the present invention, while the formulation of Example U is comparative.
  • Example X which is representative of the compositions of the present invention, contained zinc at a concentration of 0.29 mM, had an alkaline pH and satisfied the USP and Ph. Eur. B. preservative efficacy requirements.
  • Example X FID 112736 Lot Number 07-48252 Concentration Ingredients (w/v %) Zinc Chloride 0.004 Propylene Glycol 1.7 Boric Acid 0.25 Tromethamine, and/or HCl Adjust pH to 8.0 Purified Water QS 100% Osmolality (mOsm/kg) 265 Tromethamine concentration mM 12.4 Monovalent Cation (Tromethamine) 8.2 Needed to adjust pH of buffering anions* Log Order Microorganism Reductions S. Aureus 6 Hours 1.9 24 Hours 3.9 7 Days 4.9 14 Days 4.9 28 Days 4.9 Pseudomonas A 6 Hours 2.2 24 Hours 3.0 7 Days 4.7 14 Days 4.7 28 Days. 4.7 E.
  • HSA 12-Hydroxystearic acid
  • HCO-40 hydrogenated castor oil
  • a threshold concentration of HSA zinc ions interact with HSA to form zinc di-12-hydroxystearate particles. This particulate matter formation is not acceptable for an ophthalmic solution.
  • Table Y-1 The potential for particulate formation was evaluated by adding varying amounts of HCO-40 to the composition. The results presented in Table Y-2 below show that as pH is decreased, a higher level of HSA is required to form particles.
  • a lower pH is preferred for a composition containing the surfactant HCO-40 and zinc ions, so that the composition remains free from particulate matter formation throughout its shelf-life.
  • the preferred pH range for such compositions is 5.0 to 6.0.
  • the most preferred pH range for such compositions is 5.5 to 5.9.
  • the formulation shown below represents a further example of a self-preserved pharmaceutical composition of the present invention.
  • Example Z Ingredients Conc. (w/v %) Olopatadine 0.111 Hydrochloride Propylene glycol 0.3 Boric Acid 1.0 Sodium Chloride 0.17 Zinc Chloride 0.0025 Sodium Hydroxide Adjust pH 7.0 Hydrochloric Acid Purified Water QS 100 II. Physical Parameters Osmolality (mOsm/kg) 267,268 Monovalent cation (Na) 6.9 mM concentration needed to adjust pH of buffering anions PET Results 6 h 24 h 7 d 14 d 28 d S. aureus 0.0 0.2 4.4 4.9 4.9 P. aeruginosa 0.4 1.3 3.7 4.9 4.9 E. coli 0.7 0.8 5.0 5.0 5.0 C. albicans 0.1 0.5 1.3 A. niger 1.5 1.8 1.3
  • the formulations in Examples AA and AB contain borate/polyol buffers, whereas the formulations in Example AC and AD contain citrate and phosphate buffers, respectively. All formulations contain 0.11 mM zinc (0.0015% zinc chloride).
  • the formulations in Examples AA and AB which are representative of the compositions of the present invention, satisfied USP preservative efficacy requirements for the microorganisms tested.
  • the formulations in Examples AC and AD failed to satisfy the USP preservative efficacy requirements, relative to all microorganisms tested.
  • the formulations in Examples AC and AD contained multivalent buffering anions (i.e., citrate and phosphate, respectively) at concentrations of greater than 5 mM.
  • Example AA AB AC AD FID 109997 110009 110002 110013 Lot Number 05-42424 05-42421 05-42428 05-42432
  • Ingredient Polyoxyl 40 Hydrogenated 0.5 0.5 0.5 0.5 0.5 Castor Oil (HCO-40) Zinc Chloride 0.0015 0.0015 0.0015 Boric Acid 1 1 None None Propylene Glycol 0.4 0.4 0.4 0.4 Sodium Chloride None 0.2 None None None None Sodium Citrate (Dihydrate) None None None 0.215 None Dibasic Sodium Phosphate None None None 0.156 (Anhydrous) Sodium Hydroxide, and/or Adjust pH to Adjust pH to Adjust pH to Hydrochloric Acid 7.0 7.0 7.0 7.0 Purified Water QS 100% QS 100% QS 100% QS 100% Osmolality 210 270 76 85 Monovalent cation (Na) conc.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Ophthalmology & Optometry (AREA)
  • Inorganic Chemistry (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medical Preparation Storing Or Oral Administration Devices (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The present invention is directed to the provision of multi-dose, self-preserved ophthalmic compositions. The compositions possess sufficient antimicrobial activity to satisfy USP preservative efficacy requirements, as well as similar preservative standards (e.g., EP and JP), without requiring the presence of conventional anti-microbial preservative agents, such as benzalkonium chloride. The compositions are effectively preserved by a balanced ionic buffer system containing zinc ions at a concentration of 0.04 to 0.9 mM, preferably 0.04 to 0.4 mM. One aspect of the balanced buffer system is limitation of the amount of buffering anions present to a concentration of 15 mM or less, preferably 5 mM or less. In a preferred embodiment, the compositions also contain borate or, most preferably, one or more borate/polyol complexes. The use of propylene glycol as the polyol in such complexes is strongly preferred. Limiting the amount of divalent metals other than zinc and the amount of ionized salts present has also been determined to be important to maximize the antimicrobial activity of the balanced buffer systems.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • The present application claims priority based on U.S. Provisional Patent Application Ser. Nos. 60/827,411 filed Sep. 28, 2006, and 60/826,529, filed Sep. 21, 2006.
  • BACKGROUND OF THE INVENTION
  • The present invention is directed to self-preserved pharmaceutical compositions. More specifically, the invention is directed to the provision of aqueous, multi-dose pharmaceutical compositions that have been formulated so as to have sufficient antimicrobial activity to satisfy the preservation efficacy requirements of the United States Pharmacopeia (“USP”) and analogous guidelines in other countries, without requiring a conventional antimicrobial preservative, such as benzalkonium chloride, polyquaternium-1, hydrogen peroxide (e.g., sodium perborate), or chorine-containing agents. The ability to achieve self-preservation is based on a unique combination of formulation components and criteria.
  • Many pharmaceutical compositions are required to be sterile (i.e., free of bacteria, fungi and other pathogenic microorganisms). Examples of such compositions include: solutions and suspensions that are injected into the bodies of humans or other mammals; creams, lotions, solutions or other preparations that are topically applied to wounds, abrasions, burns, rashes, surgical incisions, or other conditions where the skin is not intact; and various types of compositions that are applied either directly to the eye (e.g., artificial tears, irrigating solutions, and drug products), or are applied to devices that will come into contact with the eye (e.g., contact lenses).
  • The foregoing types of compositions can be manufactured under sterile conditions via procedures that are well known to those skilled in the art. However, once the packaging for a product is opened, such that the composition contained therein is exposed to the atmosphere and other sources of potential microbial contamination (e.g., the hands of a human patient), the sterility of the product may be compromised. Such products are typically utilized multiple times by the patient, and are therefore frequently referred to as being of a “multi-dose” nature.
  • Due to the frequent, repeated exposure of multi-dose products to the risk of microbial contamination, it is necessary to employ a means for preventing such contamination from occurring. The means employed may be: (i) a chemical agent that prevents the proliferation of microbes in a composition, which is referred to herein as an “antimicrobial preservative”; or (ii) a packaging system that prevents or reduces the risk of microbes reaching a pharmaceutical composition within a container.
  • Prior multi-dose ophthalmic compositions have generally contained one or more antimicrobial preservatives in order to prevent the proliferation of bacteria, fungi and other microbes. Such compositions may come into contact with the cornea either directly or indirectly. The cornea is particularly sensitive to exogenous chemical agents. Consequently, in order to minimize the potential for harmful effects on the cornea, it is preferable to use anti-microbial preservatives that are relatively non-toxic to the cornea, and to use such preservatives at the lowest possible concentrations (i.e., the minimum amounts required in order to perform their anti-microbial functions).
  • Balancing the anti-microbial efficacy and potential toxicological effects of anti-microbial preservatives is sometimes difficult to achieve. More specifically, the concentration of an antimicrobial agent necessary for the preservation of ophthalmic formulations from microbial contamination may create the potential for toxicological effects on the cornea and/or other ophthalmic tissues. Using lower concentrations of the anti-microbial agents generally helps to reduce the potential for such toxicological effects, but the lower concentrations may be insufficient to achieve the required level of biocidal efficacy (i.e., antimicrobial preservation).
  • The use of an inadequate level of antimicrobial preservation may create the potential for microbial contamination of the compositions and ophthalmic infections resulting from such contaminations. This is also a serious problem, since ophthalmic infections involving Pseudomonas aeruginosa or other virulent microorganisms can lead to loss of visual function or even loss of the eye.
  • Thus, there is a need for a means of enhancing the activity of anti-microbial agents so that very low concentrations of the agents can be utilized without increasing the potential for toxicological effects or subjecting patients to unacceptable risks of microbial contamination and resulting ophthalmic infections.
  • Ophthalmic compositions are generally formulated as isotonic, buffered solutions. One approach to enhancing the anti-microbial activity of such compositions is to include multi-functional components in the compositions. In addition to performing their primary functions, these multi-functional components also serve to enhance the overall anti-microbial activity of the compositions.
  • The following publications may be referred to for further background regarding the use of multi-functional components to enhance the antimicrobial activity of ophthalmic compositions:
    • 1. U.S. Pat. No. 5,817,277 (Mowrey-McKee, et al; tromethamine);
    • 2. U.S. Pat. No. 6,503,497 (Chowhan, et al.; borate/polyol complexes);
    • 3. U.S. Pat. No. 5,741,817 (Chowhan, et al.; low molecular weight amino acids such as glycine);
    • 4. U.S. Pat. No. 6,319,464 (Asgharian; low molecular weight amino alcohols);
    • 5. U.S. Patent Application Publication No. US 2002/0122831 A1 (Mowrey-McKee, et al.; bis-aminopolyols);
    • 6. U.S. Pat. No. 6,348,190 (Illes, et al.; zinc); and
    • 7. JP 2003-104870 (zinc).
  • The use of zinc to enhance the antimicrobial activity of pharmaceutical compositions, including ophthalmic solutions, is well known. See, for example, the following articles and patent publications, as well as U.S. Pat. No. 6,348,190 and JP 2003-104870, cited above:
    • McCarthy, “Metal Ions and Microbial Inhibitors”, Cosmetic & Toiletries, 100:69-72 (February 1985);
    • Zeelie, et al., “The Effects of Selected Metal Salts on the Microbial Activities of Agents used in the Pharmaceutical and Related Industries”, Metal Compounds in Environment and Life, 4:193-200 (1992);
    • Zeelie, et al., “Effects of Copper and Zinc Ions on the Germicidal Properties of Two Popular Pharmaceutical Antiseptic Agents, Cetylpyridinium Chloride and Povidone-iodine”, Analyst, 123:503-507 (March 1998);
    • McCarthy, et al., “The Effect of Zinc Ions on the Antimicrobial Activity of Selected Preservatives”, Journal of Pharmacy and Pharmacology, Vol. 41 (1989);
    • U.S. Pat. No. 6,482,799 (Tué, et al.);
    • U.S. Pat. No. 5,320,843 (Raheja, et al.);
    • U.S. Pat. No. 5,221,664 (Berkowitz, et al.);
    • U.S. Pat. No. 6,034,043 (Fujiwara, et al.);
    • U.S. Pat. No. 4,522,806 (Muhlemann, et al.);
    • U.S. Pat. No. 6,017,861 (Fujiwara, et al.); and
    • U.S. Pat. No. 6,121,315 (Nair, et al.).
      The present invention is directed to the provision of improved preservative systems containing zinc ions.
  • The compositions of the present invention are multi-dose products that do not require a conventional antimicrobial preservative (e.g., benzalkonium chloride), and yet are preserved from microbial contamination. Such compositions have been referred to in the art as being “preservative free” (see, e.g., U.S. Pat. No. 5,597,559 issued to Olejnik, et al.). Compositions that are preserved from microbial contamination as a result of the inherent antimicrobial activity of one or more components of the compositions are also referred to in the art as being “self-preserved” (see, e.g., U.S. Pat. No. 6,492,361 issued to Muller, et al.).
  • The following publication may be referred to for further background regarding pharmaceutical compositions that are “preservative-free” or “self-preserving”: Kabara, et al., Preservative-Free and Self-Preserving Cosmetics and Drugs—Principles and Practice, Chapter 1, pages 1-14, Marcel Dekker, Inc. (1997).
  • The multi-dose compositions of the present invention, which do not contain a conventional antimicrobial preservative, are referred to herein as being “self-preserved”.
  • SUMMARY OF THE INVENTION
  • The present invention is directed to the self-preservation of aqueous ophthalmic compositions via the use of very low concentration of zinc ions. The present invention is based in part on the finding that in order to utilize low concentrations of zinc ions to self-preserve multi-dose ophthalmic compositions having ophthalmically acceptable pH and osmolality values, certain formulation parameters must be maintained. Specifically, the concentration of buffering anions utilized to maintain the pH within an ophthalmically acceptable range must be limited to an amount of 15 millimolar (“mM”) or less in order to avoid interfering with the anti-microbial activity of the zinc ions.
  • In addition, it has been determined that the antimicrobial activity of the zinc-containing compositions of the present invention can be further enhanced by the use of zinc ions in combination with borate or a borate/polyol complex, and that if such a combination is utilized, the use of propylene glycol is strongly preferred, so as to avoid ionic interactions between anionic species generated by other polyols (e.g., sorbitol) and the zinc cations.
  • It has also been determined that the performance of the zinc-based preservative systems of the present invention is further enhanced by: (i) limiting the amount of multivalent metal cations other than zinc (e.g., calcium and magnesium) in the compositions of the present invention; and (ii) limiting the amount of ionized salts (e.g., sodium chloride and potassium chloride) in said compositions. As described in greater detail below, the compositions of the present invention are preferably free of or substantially free of both ionized salts and multivalent metal cations other than zinc.
  • The self-preserved, multi-dose compositions of the present invention have several advantages over existing ophthalmic formulations that are either: (i) packaged as a “single dose” or “unit of use” product, so as to avoid the inclusion of any antimicrobial preservative (e.g., BION®TEARS Lubricant Eye Drops, which is marketed by Alcon Laboratories, Inc.), or (ii) preserved by means of a so-called “disappearing” preservatives, such as the chlorite-based system described in U.S. Pat. Nos. 5,424,078; 5,736,165; 6,024,954; and 5,858,346 (e.g., the artificial tears product “REFRESH™ Tears”, which is marketed by Allergan), or the peroxide-containing system described in U.S. Pat. Nos. 5,607,698; 5,683,993; 5,725,887; and 5,858,996 (e.g., the artificial tear product “GenTeal™ Tears”, which is marketed by CIBA Vision).
  • Unlike these existing products, the multi-dose ophthalmic compositions of the present invention are able to satisfy the USP preservative efficacy requirements, as well as analogous requirements in other countries, including the Japanese Pharmacopoeia (“JP”) and European Pharmacopoeia (“EP”) preservative efficacy standards, without employing any conventional antimicrobial preservatives, such as chlorite or hydrogen peroxide.
  • The above-discussed findings regarding the zinc may be applied to enhance the antimicrobial activity of various types of pharmaceutical compositions. However, the present invention is particularly directed to the provision of aqueous ophthalmic solutions that are effective in preventing microbial contamination in the absence of conventional antimicrobial preservatives, such as benzalkonium chloride (“BAC”), polyquaternium-1, chlorite or hydrogen peroxide.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIGS. 1-3 are graphs showing the interaction of boric acid and various polyols.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The pharmaceutical compositions of the present invention contain zinc ions at a concentration of 0.04 to 0.9 millimoles/liter (“mM”), preferably 0.04 to 0.4 mM and most preferably 0.1 to 0.4 mM. The use of this very low concentration is particularly desirable in ophthalmic pharmaceutical compositions containing therapeutically active agents, such as prostaglandin analogues used to control intraocular pressure (e.g., travoprost), because at higher concentrations the zinc ions may produce an astringent effect when applied to the eye. The zinc ions are preferably provided in the form of zinc chloride, at a concentration of 0.0005 to 0.012 percent by weight/volume (“w/v %”), preferably 0.0005 to 0.005 w/v % and most preferably 0.001 to 0.005 w/v %.
  • The zinc may be provided in various forms, such as zinc chloride, zinc sulfate, zinc acetate or zinc carbonate. The use of zinc chloride is preferred.
  • As indicated above, the present invention is based on part on a finding that anionic agents utilized to buffer the compositions of the present invention may interfere with the ability of zinc to exert antimicrobial activity. Such interference can be very detrimental to the ability of the compositions to maintain sufficient antimicrobial activity to meet preservative efficacy standards, particularly in view of the very low concentrations of zinc utilized in the present invention. Accordingly, it has been determined that the total concentration of anionic species in the compositions of the present invention should be limited. Specifically, it is preferred that the total concentration of anionic species, particularly buffering anions, should be limited to an amount of less than 15 mM, more preferably less than 10 mM, and most preferably less than 5 mM. For simplicity and clarity, the concentration of buffering anionic species in this patent application will be represented by the concentration of monovalent cations (such as sodium) that are present or needed to bring the pH to the specified value.
  • As utilized herein, the phrase “less than” relative to a specified concentration (e.g., 15 mM) means that the specified component (e.g., buffering anions) is either not present in the composition at all or is present at a concentration less than the specified limit (e.g., 15 mM).
  • It has been determined that multivalent buffering anions, particularly citrate and phosphate, have a significant adverse effect on the antimicrobial activity of the zinc-based preservative systems described herein. The compositions of the present invention therefore preferably do not contain any multivalent buffering anions, other than borate-polyol complexes, which may be multivalent under certain conditions (e.g., pH and/or borate:polyol ratio), or are substantially free of such buffering anions. As utilized herein, the phrase “substantially free of multivalent buffering anions” means that the composition either does not contain any multivalent buffering anions or contains an amount of said anions that does not inhibit the ability of the composition to satisfy specified preservative efficacy standards (e.g., USP, EP or JP). The amount of multivalent buffering anions in the compositions of the present invention is preferably less than 5 mM, with said concentration being determined in the same manner as specified in the preceding paragraph.
  • As indicated above, it has been determined that the antimicrobial activity of the zinc-based preservative systems of the present invention is also adversely affected by other divalent cations, such as calcium and magnesium. The antimicrobial activity of divalent zinc ions (Zn2) is based upon the ability of the ions to competitively bind and inactivate macromolecular complexes that are critical to the central metabolic activity of the prokaryotic cell. In order for Zn2+ to kill, it must first gain access to the cytoplasm and its charge density prevents its diffusion across the membrane at a physiologically significant rate. Therefore, the ability of Zn2+ ions to enter the cell must be facilitated by membrane transport proteins. Access to these transport proteins can be competitively inhibited by multivalent metal cations, particularly Mg2+, Ca2+, Mn2+, Ni2+, and Co2+. Thus, increasing the extracellular concentration of these inhibitory cations diminishes the capacity of Zn2+ ions to gain access to the cytoplasm and subsequently reduces its cytotoxic activity to the microorganism.
  • In view of the potential interference of multivalent metal cations other than zinc, the compositions of the present invention preferably do not contain such cations or are substantially free of said cations. As utilized herein, the phrase “substantially free of multivalent metal cations other than zinc” means that the composition either does not contain such cations or contains an amount of said cations that does not inhibit the ability of the composition to satisfy specified preservative efficacy standards (e.g., USP, EP or JP). The amount of multivalent metal cations other than zinc in the compositions of the present invention is preferably less than 5 mM.
  • It has also been determined that ionized salts (e.g., sodium chloride and potassium chloride) adversely affect the antimicrobial activity of the preservative systems described herein. Accordingly, the compositions of the present invention preferably do not contain ionized salts, or are substantially free of ionized salts. As utilized herein, the phrase “substantially free of ionized salts” means that the composition either does not contain any ionized salt or contains an amount of ionized salt that does not inhibit the ability of the composition to satisfy specified efficacy standards (e.g., USP, JP or EP). The amount of ionized salt contained in the compositions of the present invention is preferably less than 50 mM.
  • As used herein, the term “borate” includes boric acid, sodium borate and potassium borate. The use of borates containing divalent cations (e.g., calcium borate) may adversely affect the antimicrobial action of zinc ions, by competing with zinc for binding sites on the cell walls of bacterial and other microbes, and is therefore should be avoided. For the same reason, the self-preserved compositions of the present invention are preferably free of or substantially free of other sources of divalent cations, such as calcium chloride.
  • The self-preserved compositions of the present invention preferably contain one or more borates in an amount of from about 0.1 to about 2.0% w/v, more preferably 0.3 to 1.5% w/v, and most preferably 0.5 to 1.2% w/v.
  • As used herein, the term “polyol” includes any compound having at least one hydroxyl group on each of two adjacent carbon atoms that are not in trans configuration relative to each other. The polyols can be linear or cyclic, substituted or unsubstituted, or mixtures thereof, so long as the resultant complex is water soluble and pharmaceutically acceptable. Examples of such compounds include: sugars, sugar alcohols, sugar acids and uronic acids. Preferred polyols are sugars, sugar alcohols and sugar acids, including, but not limited to: mannitol, glycerin, xylitol, sorbitol and propylene glycol.
  • As indicated above, the use of propylene glycol is particularly preferred in order to limit the presence of anionic species. Boric acid interacts with polyols, such as glycerol, propylene glycol, sorbitol and mannitol, to form borate polyol complexes. The type and ratio of such complexes depends on the number of OH groups of a polyol on adjacent carbon atoms that are not in trans configuration relative to each other. For example, propylene glycol has only one OH group on each of two adjacent carbon atoms that are not in trans configuration. Consequently, one molecule of boric acid will interact and form a complex with one or two molecules of propylene glycol, resulting in a monovalent anion. However, in the case of sorbitol, mannitol and other sugar-type polyols, this interaction is much more complex, because one molecule of such polyols can complex with two molecules of borate and then further complex with two additional molecules of the polyol, resulting in a multivalent anion.
  • When borate is present in the compositions of the present invention, the compositions preferably also contain one or more polyols, at a total concentration of 0.25 to 2.5% w/v. The polyol preferably is propylene glycol at a concentration of 0.25 to 1.80% w/v, preferably 0.25 to 1.25% w/v. Although less preferable than propylene glycol, sorbitol and mannitol are also preferred polyols, and preferably are used at a concentration of 0.05 to 0.75% w/v, preferably 0.05 to 0.5% w/v.
  • The compositions of the present invention preferably contain borate or a borate/polyol complex, most preferably a borate/polyol complex wherein the polyol portion of the complex is propylene glycol or a combination of propylene glycol and sorbitol. The preference for propylene glycol is based on a discovery that sorbitol and other polyols have a greater tendency to form anionic species at pH values of 7.5 or less, and that such anionic species may interfere with the antimicrobial activity of zinc. The graphs shown in FIGS. 1-3 demonstrate that sorbitol has a much higher tendency to form anionic species in the presence of boric acid, compared to propylene glycol.
  • The data shown in FIGS. 1-3 were compiled as follows: A 1 Kg solution containing the given concentrations of boric acid and propylene glycol or sorbitol or mannitol was prepared and the initial pH of the solution was determined. 1 N NaOH was then added to adjust the pH. The cumulative amount of sodium hydroxide used to adjust pH to different values was then recorded.
  • As explained above, boric acid interacts and forms an ionic complex with species containing several hydroxyl groups, such as mannitol and sorbitol. However, the interaction between boric acid and propylene glycol is more limited than with other polyols. This is represented by the amount of sodium hydroxide needed to adjust pH, as shown in FIG. 1. Sorbitol and mannitol significantly shift the curve relative to the amount of NaOH required to lower pH, whereas propylene glycol only slightly shifts the curve. This is further evident in FIG. 2.
  • The present invention is particularly directed to the provision of multi-dose, self-preserved ophthalmic compositions that have sufficient antimicrobial activity to allow the compositions to satisfy the USP preservative efficacy requirements, as well as other preservative efficacy standards for aqueous pharmaceutical compositions, without a conventional antimicrobial preservative.
  • The preservative efficacy standards for multi-dose ophthalmic solutions in the U.S. and other countries/regions are set forth in the following table:
  • Preservative Efficacy Test (“PET”) Criteria
    (Log Order Reduction of Microbial Inoculum Over Time
    Bacteria Fungi
    USP 27 A reduction of 1 log (90%), The compositions must demonstrate over
    by day 7; 3 logs (99.9%) by the entire test period, which means no
    day 14; and no increase after increases of 0.5 logs or greater, relative
    day 14 to the initial inoculum.
    Japan 3 logs by 14 days; and no No increase from initial count at 14 and
    increase from day 14 28 days
    through day 28.
    Ph. Eur. A1 A reduction of 2 logs (99%) A reduction of 2 logs (99%) by 7 days,
    by 6 hours; 3 logs by 24 and no increase thereafter
    hours; and no recovery after
    28 days
    Ph. Eur. B A reduction of 1 log at 24 A reduction of 1 log (90%) by day 14,
    hours; 3 logs by day 7; and and no increase thereafter
    no increase thereafter
    FDA/ISO A reduction of 3 logs from No increase higher than the initial value
    14730 initial challenge at day 14; at day 14, and no increase higher than the
    and a reduction of 3 logs day 14 rechallenge count through day 28.
    from rechallenge
    1There are two preservative efficacy standards in the European Pharmacopoeia ‘“A” and “B”.
  • The standards identified above for the USP 27 are substantially identical to the requirements set forth in prior editions of the USP, particularly USP 24, USP 25 and USP 26.
  • The compositions of the present invention may optionally also include one or more low molecular weight amino alcohols as buffering agents. The amino alcohols which may be utilized in the present invention are water-soluble and have a molecular weight in the range of from about 60 to about 200. The following compounds are representative of the low molecular weight amino alcohols which may be utilized in the present invention: 2-amino-2-methyl-1-propanol (AMP), 2-dimethylamino-methyl-1-propanol (DMAMP), 2-amino-2-ethyl-1,3-propanediol (AEPD), 2-amino-2-methyl-1,3-propanediol (AMPD), 2-amino-1-butanol (AB). “AMP (95%)”, which refers to 95% pure AMP and 5% water, is the most preferred low molecular weight amino alcohol of the present invention. These amino alcohols are available commercially from Angus Chemical Company (Buffalo Grove, Ill.). Tromethamine may also be utilized in the compositions of the present invention.
  • The amount of amino alcohol used will depend on the molecular weight of the amino alcohol selected, and the presence (or absence) of other ingredients in the composition (e.g., chelating agents, buffering agents and/or tonicity agents). The amino alcohol will generally be present in an amount necessary to enhance the antimicrobial activity of an aqueous self-preserved pharmaceutical composition of the type described herein. The amount of amino alcohol required for a particular composition can be determined through comparative testing. The above-described amino alcohols are also utilized in the compositions of the present invention to neutralize the pH of the borate or borate/polyol complex, or bring the composition to the desired pH level. The amount of amino alcohol required for this purpose is a function of the particular borate or borate/polyol mixture selected and the concentration thereof. In general, the self-preserved compositions of the present invention may optionally contain one or more amino alcohols at a total concentration of from about 0.01 to about 2.0 percent by weight/volume (“% w/v”), and preferably from 0.1 to 1.0% w/v.
  • The zinc, zinc/borate, zinc/polyol and zinc/borate/polyol systems described herein may be included in various types of pharmaceutical compositions to enhance anti-microbial activity and self-preserve the compositions, such as ophthalmic, otic, nasal and dermatological compositions, but is particularly useful in ophthalmic compositions. Examples of such compositions include: ophthalmic pharmaceutical compositions, such as topical compositions used in the treatment of glaucoma, infections, allergies or inflammation; compositions for treating contact lenses, such as cleaning products and products for enhancing the ocular comfort of patients wearing contact lenses; and various other types of ophthalmic compositions, such as ocular lubricating products, artificial tears, astringents, and so on. The compositions may be aqueous or non-aqueous, but will generally be aqueous.
  • The compositions of the present invention may contain various types of therapeutic agents. However, the invention is most useful relative to therapeutic agents that are nonionic, since nonionic agents do not interfere with the antimicrobial activity of zinc cations in solution. Cationic therapeutic agents may also be utilized in the compositions, particularly if the agent is included in the compositions in free base form or in the form of a salt with a monovalent anion, such as a hydrochloride salt. Cationic therapeutic agents that are included in the compositions in the form of a salt of a multivalent anion may interfere with the antimicrobial activity of the zinc preservative systems described herein, depending on the concentration of the anion. Such interference must be considered when selecting therapeutic agents that are suitable for use in the compositions of the present invention. Similarly, the use of therapeutic agents that are anionic may be considered; however, such agents may interfere with the activity of zinc ions, depending on the concentration of the agent and its dissociation constant.
  • Examples of therapeutic agents that may be contained in the ophthalmic compositions of the present invention include prostaglandin analogs (e.g., latanoprost, travoprost and unoprostone), hypotensive lipids (e.g., bimatoprost), and glucocorticoids (e.g., prednisolone, dexamethasone and lotoporednol).
  • The present invention is particularly directed to the provision of self-preserved, multi-dose ophthalmic compositions in connection with the treatment of conditions wherein the cornea or adjacent ocular tissues are irritated, or conditions requiring frequent application of a composition, such as in the treatment of dry eye patients. The self-preserved compositions of the present invention are therefore particularly useful in the field of artificial tears, ocular lubricants, and other compositions used to treat dry eye conditions, as well as other conditions involving ocular inflammation or discomfort.
  • The compositions of the present invention will generally be formulated as sterile aqueous solutions. The compositions of the present invention are also formulated so as to be compatible with the eye and/or other tissues to be treated with the compositions. The ophthalmic compositions intended for direct application to the eye will be formulated so as to have a pH and tonicity that are compatible with the eye.
  • The compositions will have a pH in the range of 4 to 9, preferably 5.5 to 8.5, and most preferably 5.5 to 8.0. It has been determined that a slightly alkaline pH increases the antimicrobial activity of the compositions of the present invention. The use of a pH in the range of 7.0 to 8.0 is therefore preferred.
  • The compositions will have an osmolality of 200 to 350 milliosmoles per kilogram (mOsm/kg), more preferably 250 to 330 mOsm/kg. As indicated above, the use of nonionic osmolality-adjusting agents is preferred, as ionic salts such as sodium chloride have been found to reduce the antimicrobial activity of the zinc-based preservative systems described herein. The use of propylene glycol, glycerol, xylitol or combinations thereof as nonionic osmolality adjusting agents is particularly preferred. Boric acid may also be utilized as an osmolality-adjusting agent in the compositions of the present invention. Boric acid, if utilized, will be present in the compositions as a mixture of ionic and nonionic species.
  • The compositions of the present invention may contain various types of pharmaceutical excipients, such as surfactants, viscosity-modifying agents and so on, provided that such excipients are non-ionic. The use of excipients that are cationic or anionic is not preferred, since such ionic agents may interfere with the zinc-based preservation systems described herein. This is particularly true with respect to anionic excipients. Accordingly, the compositions of the present invention are preferably free of or substantially free of anionic excipients.
  • In the event cationic or anionic excipients are utilized, the amount of excipient contained in the compositions must be limited to an amount that does not inhibit the ability of the composition to meet the applicable preservative efficacy requirements (e.g., USP, JP and/or EP) and adjustments to the formulation properties may be required. For example, the nonionic surfactant polyoxyl 40 hydrogenated castor oil can be used for solubilization or stabilization of drugs, such as travoprost. However, it has been determined that 12-hydroxy stearic acid, an anionic compound that has been determined to be present as an impurity and potential degradation product of the excipient polyoxyl 40 hydrogenated castor oil, interacts with zinc and forms particles. In order to avoid particle formation throughout the commercial shelf-life of a composition containing these components, the pH of the composition needs to be in the range 5.0 to 6.0, preferably in the range 5.5 to 5.9. These finding are further illustrated in Example Y, below.
  • One or more conventional antimicrobial preservatives (e.g., benzalkonium chloride and polyquaternium-1) can be present in the compositions of the present invention, if desired, but the compositions preferably do not contain any conventional antimicrobial preservatives. If utilized, such preservatives can be present in conventional amounts, but in view of the self-preserving properties of the compositions of the present invention, such conventional antimicrobial preservatives can also be utilized in much lower concentrations than would be required to satisfy preservative efficacy requirements if only the conventional antimicrobial preservative were present. Since the present compositions can be a self-preserved composition, if an anti-microbial preservative is present as an option, the amount can be an amount that would not be effective alone as an antimicrobial preservative agent. However, the overall composition would have sufficient antimicrobial activity to satisfy USP/FDA/ISO preservative efficacy requirements.
  • Preferably the conventional antimicrobial preservative, if present, is not anionic and if anionic, it is preferred that the amount should be low enough to not substantially interfere with the antimicrobial activity of the preservative systems described herein.
  • Applicants specifically incorporate the entire contents of all cited references in this disclosure. Further, when an amount, concentration, or other value or parameter is given as either a range, preferred range, or a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range. It is not intended that the scope of the invention be limited to the specific values recited when defining a range.
  • Other embodiments of the present invention will be apparent to those skilled in the art from consideration of the present specification and practice of the present invention disclosed herein. It is intended that the present specification and examples be considered as exemplary only with a true scope and spirit of the invention being indicated by the following claims and equivalents thereof.
  • The following examples are presented to further illustrate selected embodiments of the present invention. The formulations shown in the examples were prepared using procedures that are well-known to persons of ordinary skill in the field of ophthalmic pharmaceutical compositions.
  • Antimicrobial preservative effectiveness as set forth by the examples infra was determined using an organism challenge test according to the methods described in the United States Pharmacopeia 24 (USP) for category 1A products. Samples were inoculated with known levels of one or more of the following: gram-positive vegetative bacteria (Staphylococcus aureus ATCC 6538), gram-negative vegetative bacteria (Pseudomonas aeruginosa ATCC 9027 and Escherichia coli ATCC 8739), yeast (Candida albicans ATCC 10231) and mold (Aspergillus niger ATCC 16404). The samples were then pulled at specified intervals to determine if the antimicrobial preservative system was capable of killing or inhibiting the propagation of organisms purposely introduced into the formulation. The rate or level of antimicrobial activity determines compliance with the USP preservative efficacy standards for the cited categories of preparations. In some instances, the PET screen test was conducted for only 7 days, rather than 14 or 28 days, with additional time points of 6 and 24 hours being added to evaluate preservative efficacy relative to Ph. Eur. B. criteria. This modified PET screen test has been shown to be a reliable test for determining whether a composition will meet USP or Ph. Eur. B criteria.
  • TABLE 1
    Preservative Standards for U.S. Category 1A Products presented
    as Log Reduction of Organism Population
    Time Pulls
    24 Hours 7 days 14 days 28 days
    For Bacteria (S. aureus, P. aeruginosa, and E. coli)
    Ph. Eur. B 1.0 3.0 NI NI
    USP NA 1.0 3.0 NI
    For Fungi (C. albicans and A. niger)
    Ph. Eur. B NA NA 1.0 NI
    USP NA NI NI NI
    NI = No increase at this or any following time pulls
    NA = Time point not required for applicable standard (e.g., USP or Ph. Eur. B)
  • As shown in Table 1, the USP 24 Antimicrobial Effectiveness Test requires that compositions containing Category 1A products have sufficient anti-bacterial activity to reduce an initial inoculum of approximately 105 to 106 bacteria by one log (i.e., a 90% reduction in the microorganism population) over a period of seven (7) days and by three logs (i.e., a 99.9% reduction in the microorganism population) over a period of fourteen (14) days, and requires that there cannot be any increase in the microorganism population following the conclusion of the fourteen day period. Relative to fungi, the USP standards require that the compositions maintain stasis (i.e., no growth) relative to the population of the initial inoculum over the entire 28 day test period. A category 1A product is an injection, or other parenteral including emulsions, otic, sterile nasal products and ophthalmic products made with aqueous bases or vehicles.
  • The margin of error in calculating microorganism populations is generally accepted to be +/−0.5 logs. Accordingly, the term “stasis”, as utilized herein relative to the above-discussed USP standards, means that the initial population cannot increase by more than 0.5 log orders, relative to the initial population.
  • Examples A-E
  • The formulations of Examples A-E were evaluated to determine the effect of buffering anions on preservative efficacy. As discussed in greater detail below, the formulations of Examples A and B do not contain buffering agents. Although these formulations satisfied the USP preservative efficacy requirements, the presence of a buffering system is highly desirable, so as to prevent pH drift over the life of a commercial product (i.e., a period of up to two years or more). The formulation of Example C include a borate/polyol buffering system, but the system has minimal buffering capacity. As with the formulations of Examples A and B, the formulation of Example C satisfied the USP requirements. The formulations of Examples D and E contain significantly greater concentrations of buffering agents and consequently a higher buffering capacity. However, the relatively large amount of buffering anions present resulted in a failure of the formulations to satisfy preservative efficacy requirements. Thus, a comparison of Examples A-E demonstrates the need to balance the requirements for an effective buffering system with the antimicrobial activity required to satisfy preservative efficacy requirements.
  • The formulation of Example A does not have any buffering ingredient. The amount of sodium hydroxide used in the formulation (0.2 mM) to adjust pH is minimal, which means that the buffering anion concentration is very low. This formulation containing 0.18 mM zinc (0.0025% zinc chloride) meets USP preservation criteria, but is not desirable from a commercial perspective due to the lack of buffering capacity.
  • Though the formulation of Example B contains boric acid, it does not have buffering capacity as the pKa of boric acid (alone) is much higher than 6. The amount of sodium hydroxide used in the formulation (0.3 mM) to adjust pH is minimal. This formulation containing 0.18 mM zinc (0.0025% zinc chloride) meets USP preservation criteria, but is not commercially desirable due to the lack of buffering capacity.
  • The formulation of Example C includes two excipients, boric acid and propylene glycol, which together add significantly to the osmolality of the composition and provide minimal buffering capacity. The amount of sodium hydroxide required in this formulation to adjust pH (0.5 mM) is somewhat higher than for the formulations of Examples A and B, but still very low compared to the limits specified herein (i.e., less than 15 mM, more preferably less than 5 mM). This formulation, containing 0.18 mM Zinc (0.0025% zinc chloride), meets USP preservation criteria, but the buffering capacity is not ideal relative to commercial viability.
  • Adding boric acid and sorbitol in the amounts indicated for the formulations of Examples D and E provides significant buffering capacity, but results in very high buffering anion concentrations (i.e., 77 and 49 mM, respectively). Example D does not meet USP preservation criteria for either S. aureus or E. coli at days 7 and 14. Example E does not meet USP preservation criteria for S. aureus at day 14 or for E. coli at days 7 and 14. These results demonstrate that the addition of significant amounts of buffering anions disrupted the preservation activity of the compositions. Thus, although the buffering systems of the formulations in Examples D and E are commercially viable, the preservative systems do not satisfy USP requirements and consequently would not be acceptable for a commercial product subject to the USP requirements or similar requirements in countries other than the U.S.
  • Example
    A B C D E
    FID 107339 107340 107431 106737 106757
    Lot Number 04-37152 04-37160-1 04-37290 04-36171 04-36176
    Ingredient Concentration (w/v %)
    Travoprost 0.004 0.004 0.004 0.004 0.004
    Polyoxyl 40 0.5 0.5 0.5 0.5 0.5
    Hydrogenated Castor Oil
    (HCO-40)
    Zinc Chloride 0.0025 0.0025 0.0025 0.0025 0.0025
    Boric Acid None 1 1 1 0.5
    Sorbitol 0.25 None None 3.8 3.2
    Propylene Glycol 0.75 None 0.75 None None
    Sodium Hydroxide, Adjust pH Adjust pH Adjust pH Adjust pH Adjust pH
    and/or Hydrochloric to 6.0 to 6.0 to 6.0 to 6.0 to 6.0
    Acid
    Purified Water QS 100% QS 100% QS 100% QS 100% QS 100%
    Osmolality 113 Not tested 274 291 208
    Monovalent cation (Na) 0.2 mM 0.3 mM 0.5 mM 77 mM 49 mM
    conc. needed to adjust
    pH of buffering anions
    Microorganism Log Order Reductions
    S. aureus
     7 D 5.0 5.0 4.7 0.9 1.1
    14 D 5.0 5.0 4.7 1.8 2.3
    28 D 5.0 5.0 4.7 4.4 4.7
    P. aeruginosa
     7 D 5.0 5.0 4.9 2.1 4.0
    14 D 5.0 5.0 4.9 4.3 4.9
    28 D 5.0 5.0 4.9 5.1 4.9
    E. coli
     7 D 5.0 5.0 4.5 0.9 0.9
    14 D 5.0 5.0 5.1 1.4 2.1
    28 D 5.0 5.0 5.1 5.2 4.9
    C. albican
     7 D 1.4 0.0 0.0 0.3 0.1
    14 D 3.3 0.6 0.2 0.4 0.6
    28 D 3.4 4.9 0.9 0.7 1.5
    A. niger
     7 D 0.0 1.4 0.7 3.4 2.7
    14 D 0.7 2.2 0.2 3.7 3.7
    28 D 0.6 2.3 0.5 4.9 4.3
  • Examples F through J
  • In these examples, the amount of sorbitol was reduced to 1%, while keeping the boric acid concentration at 1%, in order to reduce the concentration of buffering anionic species. In addition, examples G, I, and J contain 0.75% propylene glycol. All five examples have an anionic buffer concentration of about 19 mM.
  • The compositions of Examples F and G contain 0.18 mM of zinc. These have much better anti-microbial activity against S. Aureus than the formulations of Examples D and E, above. Specifically, the compositions of Examples F and G meet USP preservation criteria for S. aureus. However, although the antimicrobial activity against E. coli at zinc concentrations of 0.18 mM (Examples F and G) and 0.36 mM (Example H and I) is improved, compared to examples D and E, it is not sufficient to consistently meet USP preservation criteria at day 14. Increasing the zinc concentration to 1.8 mM (Example J) improved the antimicrobial activity of the solution, so as to allow it to meet USP criteria. However, as indicated above, such higher concentration of zinc are not preferred in ophthalmic products, as zinc may provide astringent activity at these concentrations.
  • All of the formulations of Examples F-J contained anionic buffer concentrations of 19 mM, which is greater than the preferred limit of 15 mM specified herein. The fact that these compositions were not able to consistently meet or exceed the USP preservative efficacy requirements, even at relatively high zinc concentrations, further demonstrates the importance of limiting the concentration of buffering anions.
  • Example
    F G H I J
    FID 106039 106755 107038 107039 107099
    Lot Number 04-36405 04-36173 04-36479 04-36476 04-36632
    Ingredient Concentration (w/v %)
    Travoprost 0.004 0.004 0.004 0.004 0.004
    Polyoxyl 40 0.5 0.5 0.5 0.5 0.5
    Hydrogenated Castor Oil
    (HCO-40)
    Zinc Chloride 0.0025 0.0025 0.005 0.005 0.025
    Boric Acid 1 1 1 1 1
    Sorbitol 1 1 1 1 1
    Propylene Glycol None 0.6 None 0.6 0.6
    Sodium Hydroxide, Adjust Adjust Adjust Adjust Adjust pH
    and/or pH to pH to pH to pH to to 6.0
    Hydrochloric Acid 6.0 6.0 6.0 6.0
    Purified Water QS 100% QS 100% QS 100% QS 100% QS 100%
    Osmolality 279 204 288 291
    Monovalent cation (Na) 19 mM 19 mM 19 mM 19 mM 19 mM
    conc. needed to adjust
    pH of buffering anions
    Microorganism Log Order Reductions
    S. aureus
     7 D 2.1 2.2 1.7 3.4 4.4
    14 D 3.7 4.4 4.0 3.7 5.1
    28 D 5.0 5.2 5.0 5.0 5.1
    P. aeruginosa
     7 D 2.6 3.2 3.0 3.4 4.9
    14 D 4.6 5.1 4.7 4.6 4.9
    28 D 5.0 5.1 5.0 5.0 4.9
    E. coli
     7 D 1.7 1.7 1.4 1.5 3.4
    14 D 2.3 2.8 3.0 2.3 4.9
    28 D 5.1 5.2 5.1 5.1 4.9
    C. albican
     7 D 0.2 0.3 0.2 0.2 0.7
    14 D 0.1 0.4 0.2 0.9 1.0
    28 D 0.4 0.7 0.6 1.3 1.2
    A. niger
     7 D 3.0 2.7 3.0 3.0 3.4
    14 D 3.1 3.6 3.7 3.0 3.6
    28 D 3.7 4.3 3.8 3.8 3.6
  • Examples K through N
  • In these examples, the amount of sorbitol was reduced to 0.25%, while keeping the boric acid concentration at 1%, in order to reduce the concentration of buffering anionic species. In addition, the compositions of Examples L-N contain 0.75% propylene glycol. The formulations of Examples K and L have an anionic buffer concentration of about 4 mM, which is within the preferred range of less than 5 mM specified herein. The antimicrobial activity of these compositions against E. coli at a zinc concentration of 0.18 mM (0.0025 w/v %) is significantly improved, relative to the activity of the formulations in Examples F-J, and the compositions meet USP preservation criteria. In examples M and N, the pH was adjusted to 5.5 and 6.5, respectively, while maintaining the USP preservation efficacy. The results obtained with the formulations of Examples K through N, which are representative of the compositions of the present invention, further demonstrate the importance of limiting the concentration of buffering anions, relative to satisfying preservative efficacy requirements.
  • Example
    K L M N
    FID 107046 107047 109032 109033
    Lot Number 04-36523 37157-3 05-40452 05-40453
    Ingredient
    Travoprost 0.004 0.004 0.004 0.004
    Polyoxyl 40 0.5 0.5 0.5 0.5
    Hydrogenated
    Castor Oil
    (HCO-40)
    Zinc Chloride 0.0025 0.0025 0.0025 0.0025
    Boric Acid 1 1 1 1
    Sorbitol 0.25 0.25 0.25 0.25
    Propylene None 0.75 0.75 0.75
    Glycol
    Sodium Adjust Adjust Adjust Adjust
    Hydroxide, pH to pH to pH to pH to
    and/or 6.0 6.0 5.5 6.5
    Hydrochloric
    Acid
    Purified Water QS 100% QS 100% QS 100% QS 100%
    Osmolality 176 272 283 278
    Monovalent 3.9 mM 4.1 mM 2 mM 7.5 mM
    cation (Na)
    conc. needed
    to adjust
    pH of buffering
    anions
    Microorganism Log Order Reductions
    S. aureus
     7 D 2.6 4.1 3.2 3.4
    14 D 4.7 5.0 4.8 4.8
    28 D 5.0 5.0 4.8 4.8
    P. aeruginosa
     7 D 4.6 4.5 4.9 4.9
    14 D 5.0 5.0 4.9 4.9
    28 D 5.0 5.0 4.9 4.9
    E. coli
     7 D 2.7 1.9 3.4 3.4
    14 D 5.1 5.0 4.9 4.9
    28 D 5.1 5.0 4.9 4.9
    C. albican
     7 D 0.1 0.2 0.1 0.2
    14 D 0.1 0.6 0.3 0.4
    28 D 0.4 1.0 0.9 1.3
    A. niger
     7 D 2.2 2.3 2.7 2.6
    14 D 2.3 3.8 3.1 2.6
    28 D 3.0 3.5 3.8 2.8
  • Examples O and P
  • In these examples, the amount of boric acid was reduced. The formulations meet USP preservation criteria and are representative of the compositions of the present invention.
  • Example
    O P
    FID 107519 107520
    Lot Number 04-37442 04-37443
    Ingredient Concentration (w/v %)
    Travoprost 0.004 0.004
    Polyoxyl 40 Hydrogenated Castor Oil 0.5 0.5
    (HCO-40)
    Zinc Chloride 0.0025 0.0025
    Boric Acid 0.3 0.15
    Sorbitol 0.25 0.125
    Propylene Glycol 1.6 1.6
    Sodium Hydroxide, and/or Adjust Adjust
    Hydrochloric Acid pH to 6.0 pH to 6.0
    Purified Water QS 100% QS 100%
    Osmolality 281 247
    Sodium Hydroxide conc. 2.2 mM 0.5 mM
    Monovalent cation (Na) conc. needed 2.2 mM 0.5 mM
    to adjust pH of buffering anions
    Microorganism Log Order Reductions
    S. aureus
     7 D 4.9 5.0
    14 D 4.9 5.0
    28 D 4.9 5.0
    P. aeruginosa
     7 D 5.0 5.0
    14 D 5.0 5.0
    28 D 5.0 5.0
    E. col
     7 D 5.1 5.1
    14 D 5.1 5.1
    28 D 5.1 5.1
    C. albican
     7 D 0.3 0.2
    14 D 0.9 1.0
    28 D 1.5 2.0
    A. niger
     7 D 2.6 2.6
    14 D 3.0 2.3
    28 D 3.7 2.6
  • Examples Q and R
  • The preservation of formulations containing 0.18 mM zinc (0.0025% zinc chloride), with or without boric acid. was evaluated. The results show that antimicrobial activity was greater with the presence of boric acid/polyols. However, the formulation of Example R exhibited sufficient activity to satisfy USP preservative efficacy requirements, even though it did not contain boric acid. The ability of the formulation of Example R to meet preservative efficacy requirements is believed to be attributable in part to the fact that the formulation: (i) did not contain any multivalent anionic buffering agents and (ii) contained a non-ionic agent (i.e., propylene glycol) as the principal osmolality adjusting agent. The formulations of Examples Q and R are representative of the compositions of the present invention.
  • Examples
    Q R
    FID 112306 112308
    Lot Number 07-47316 07-47318
    Ingredients Concentration (w/v %)
    Zinc Chloride 0.0025 0.0025
    Tromethamine None 0.13
    Propylene Glycol 1.6 1.6
    Boric Acid 0.25 None
    Mannitol 0.1 None
    Sodium Hydroxide, and/or Adjust pH to 7.5 Adjust pH to 7.5
    Hydrochloric Acid
    Purified Water QS 100% QS 100%
    Osmolality (mOsm/kg) 261 232
    Sodium Hydroxide concentration 4.4 mM NaOH None
    Monovalent Cation (sodium) 4.4 mM NaOH *
    needed to adjust pH of buffering
    anions
    Microorganism Log Order Reductions
    S. Aureus
     6 Hours 0.5 1.4
    24 Hours 2.6 3.5
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days NT NT
    Pseudomonas A  6 Hours 1.4 2.8
    24 Hours 4.0 3.8
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days. NT NT
    E. Coli
     6 Hours 0.8 0.7
    24 Hours 1.5 1.7
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days. NT NT
    Candida A.  7 Days 0.9 0.3
    14 Days NT NT
    28 Days. NT NT
    A. Niger
     7 Days 1.7 0.4
    14 Days NT NT
    28 Days. NT NT
    * This formulation does not contain any buffering anion. However, it contains a buffering cation, tromethamine. pH is adjusted using 8.8 mM HCl.
    NT = Not Tested
  • Examples Q and S
  • A comparison of the formulations of Examples Q and S demonstrates that the preservation efficacy of formulations containing 0.18 mM zinc (0.0025% zinc chloride) is reduced in the presence of low levels of a multivalent metal cation, i.e., calcium. However, the amount of multivalent metal cation in the formulation of Example S (i.e., 2.3 mM), which is less than the upper limit specified herein (i.e., less than 5 mM), was not great enough to significantly inhibit the preservative efficacy of the formulation. The formulations of Examples Q and S are representative of the compositions of the present invention.
  • Examples
    Q S
    FID 112306 112307
    Lot Number 07-47316 07-47317
    Ingredients Concentration (w/v %)
    Zinc Chloride 0.0025 0.0025
    Calcium Chloride None 0.025
    Propylene Glycol 1.6 1.6
    Boric Acid 0.25 0.25
    Mannitol 0.1 0.1
    Sodium Hydroxide, and/or Adjust pH to 7.5 Adjust pH to 7.5
    Hydrochloric Acid
    Purified Water QS 100% QS 100%
    Osmolality (mOsm/kg) 261 264
    Sodium Hydroxide Conc. 4.4 mM 4.5 mM
    Monovalent Cation (Sodium) 4.4 mM 4.5 mM
    needed to adjust pH of buffering
    anions
    Microorganism Log Order Reductions
    S. Aureus
     6 Hours 0.5 0.2
    24 Hours 2.6 1.2
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days NT NT
    Pseudomonas A  6 Hours 1.4 0.6
    24 Hours 4.0 0.8
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days. NT NT
    E. Coli
     6 Hours 0.8 0.6
    24 Hours 1.5 0.7
     7 Days 5.1 5.1
    14 Days NT NT
    28 Days. NT NT
    Candida A.  7 Days 0.9 0.6
    14 Days NT NT
    28 Days. NT NT
    A. Niger
     7 Days 1.7 1.4
    14 Days NT NT
    28 Days. NT NT
    NT = Not Tested
  • Examples O, T and U
  • A comparison of the results obtained with the formulations of Examples Q, T and U demonstrates that preservation efficacy improves as the zinc chloride concentration is increased from 0.18 mM zinc (0.0025% zinc chloride) to 1.8 mM zinc (0.025% zinc chloride). All three formulations satisfied USP preservative efficacy requirements. However, the formulation of Example Q (0.18 mM zinc) did not clearly satisfy the Ph. Eur. B. requirements. The formulations of Examples T and U (0.88 and 1.8 mM of zinc, respectively) did clearly satisfy the Ph. Eur. B requirements; however, the use of higher concentrations of zinc (i.e., 1.8 mM in Example U) is not desirable, as such concentrations may product an astringent affect when applied to the eye. The zinc concentration utilized in the formulation of Example U is outside the range specified herein (i.e., 0.04 to 0.9 mM). Consequently, the formulations of Examples Q and T are representative of the compositions of the present invention, while the formulation of Example U is comparative.
  • Examples
    Q T U
    FID 112306 112294 112148
    Lot Number 07-47316 07-47278 07-46931
    Ingredients Concentration (w/v %)
    Zinc Chloride 0.0025 0.012 0.025
    Propylene Glycol 1.6 1.6 1.6
    Boric Acid 0.25 0.25 0.25
    Mannitol 0.1 0.1 0.1
    Sodium Hydroxide, and/or Adjust Adjust Adjust
    Hydrochloric Acid pH to 7.5 pH to 7.5 pH to 7.5
    Purified Water QS 100% QS 100% QS 100%
    Osmolality (mOsm/kg) 261 261 265
    Sodium Hydroxide Conc. 4.4 mM 4.4 mM 4.6 mM
    Monovalent Cation (Sodium) 4.4 mM 4.4 mM 4.6 mM
    needed to adjust pH of
    buffering anions
    Microorganism Log Order Reductions
    S. Aureus
     6 Hours 0.5 1.2 2.6
    24 Hours 2.6 3.5 4.3
     7 Days 5.1 5.0 5.0
    14 Days NT NT NT
    28 Days NT NT NT
    Pseudomonas A  6 Hours 1.4 1.3 2.7
    24 Hours 4.0 3.3 4.5
     7 Days 5.1 4.9 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    E. Coli
     6 Hours 0.8 0.8 1.0
    24 Hours 1.5 1.6 1.8
     7 Days 5.1 5.0 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    Candida A.  7 Days 0.9 2.8 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    A. Niger
     7 Days 1.7 1.3 1.6
    14 Days NT NT NT
    28 Days. NT NT NT
    NT = Not Tested
  • Examples U, V and W
  • A comparison of the results obtained with the formulations of Examples U, V and W demonstrates the effect of pH on the antimicrobial activity of the zinc-based preservative systems of the present invention. Specifically, even at a high zinc concentration (i.e., 1.8 mM), the formulation of Example V (pH 5.5) did not satisfy the Ph. Eur. B. preservative efficacy requirements, but the same formulation did satisfy those requirements when the pH was increased to 6.5 (Example W) or 7.5 (Example U). These results demonstrate the preference for use of a slightly alkaline pH in the compositions of the present invention, as specified above. This preference is of even greater importance when concentrations of zinc lower than 1.8 mM are utilized, as in the compositions of the present invention.
  • Examples
    V W U
    FID 112286 112287 112148
    Lot Number 07-47249 07-47632 07-46931
    Ingredients Concentration (w/v %)
    Zinc Chloride 0.025 0.025 0.025
    Propylene Glycol 1.6 1.6 1.6
    Boric Acid 0.25 0.25 0.25
    Mannitol 0.1 0.1 0.1
    Sodium Hydroxide, and/or Adjust Adjust Adjust
    Hydrochloric Acid pH to 5.5 pH to 6.5 pH to 7.5
    Purified Water QS 100% QS 100% QS 100%
    Osmolality (mOsm/kg) 263 265 265
    Sodium Hydroxide Conc. 0.1 mM 1.0 mM 4.6 mM
    Monovalent Cation (Sodium) 0.1 mM 1.0 mM 4.6 mM
    needed to adjust pH of
    buffering anions
    Microorganism Log Order Reductions
    S. Aureus
     6 Hours 0.1 0.2 2.6
    24 Hours 0.2 2.3 4.3
     7 Days 4.2 5.0 5.0
    14 Days NT NT NT
    28 Days NT NT NT
    Pseudomonas A  6 Hours 1.2 1.4 2.7
    24 Hours 2.1 3.2 4.5
     7 Days 4.9 4.9 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    E. Coli
     6 Hours 0.4 0.5 1.0
    24 Hours 0.9 1.3 1.8
     7 Days 2.2 5.0 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    Candida A.  7 Days 1.0 2.0 5.0
    14 Days NT NT NT
    28 Days. NT NT NT
    A. Niger
     7 Days 2.3 2.0 1.6
    14 Days NT NT NT
    28 Days. NT NT NT
    NT = Not Tested
  • Example X
  • The formulation of Example X, which is representative of the compositions of the present invention, contained zinc at a concentration of 0.29 mM, had an alkaline pH and satisfied the USP and Ph. Eur. B. preservative efficacy requirements. These results further demonstrate the basis for the above-specified preference for the use of a slightly alkaline pH in the compositions of the present invention.
  • Example
    X
    FID 112736
    Lot Number 07-48252
    Concentration
    Ingredients (w/v %)
    Zinc Chloride 0.004
    Propylene Glycol 1.7
    Boric Acid 0.25
    Tromethamine, and/or HCl Adjust pH to 8.0
    Purified Water QS 100%
    Osmolality (mOsm/kg) 265
    Tromethamine concentration mM 12.4
    Monovalent Cation (Tromethamine) 8.2
    Needed to adjust pH of buffering
    anions*
    Log Order
    Microorganism Reductions
    S. Aureus
     6 Hours 1.9
    24 Hours 3.9
     7 Days 4.9
    14 Days 4.9
    28 Days 4.9
    Pseudomonas A  6 Hours 2.2
    24 Hours 3.0
     7 Days 4.7
    14 Days 4.7
    28 Days. 4.7
    E. Coli  6 Hours 0.8
    24 Hours 1.5
     7 Days 3.9
    14 Days 5.0
    28 Days. 5.0
    Candida A.  7 Days 2.1
    14 Days 2.9
    28 Days. 4.1
    A. Niger  7 Days 0.9
    14 Days 1.9
    28 Days. 1.8
    *Calculated using pKa of 8.3
  • Example Y
  • 12-Hydroxystearic acid (HSA) is an impurity and potential degradation product of the excipient polyoxyl 40 hydrogenated castor oil (“HCO-40”). Above a threshold concentration of HSA, zinc ions interact with HSA to form zinc di-12-hydroxystearate particles. This particulate matter formation is not acceptable for an ophthalmic solution. A study was conducted to assess the effect of pH on particulate matter formation in freshly prepared samples of the composition shown in Table Y-1 below. The potential for particulate formation was evaluated by adding varying amounts of HCO-40 to the composition. The results presented in Table Y-2 below show that as pH is decreased, a higher level of HSA is required to form particles. Thus, a lower pH is preferred for a composition containing the surfactant HCO-40 and zinc ions, so that the composition remains free from particulate matter formation throughout its shelf-life. The preferred pH range for such compositions is 5.0 to 6.0. The most preferred pH range for such compositions is 5.5 to 5.9.
  • TABLE Y-1
    Composition of used for the study effect of pH on zinc
    di-12-hydroxystearate particulate matter formationa
    Concentration
    Component W/V %
    Travoprost 0.004% 
    Polyoxyl 40 Hydrogenated  0.5%
    Castor Oil (HCO-40)
    Boric Acid  1.0%
    Zinc Chloride 0.0025% 
    Sorbitol 0.25%
    Propylene Glycol 0.75%
    Sodium Hydroxide/ Adjust pH.b
    Hydrochloric Acid
    Purified Water q.s. 100%
    aThese samples were spiked with HSA.
    bpH was adjusted to pre-determined values between 5.5 to 6.5
  • TABLE Y-2
    Relationship Between pH and Particulate Matter Formation
    (by Microscopic Observation) in Freshly Prepared Samples
    of Composition Containing HSA at Room Temperature
    Total Concentration pH at which Particulate pH at which Particulate
    of HSA Mattera was not formed Mattera was formed
    5 ppm 6.00 6.10b
    6.5 ppm   5.75 5.90
    8 ppm 5.58 5.75
    aBased on microscopic observation of white crystalline particles.
    bParticles observed visually; hence were not checked microscopically.
  • Example Z
  • The formulation shown below represents a further example of a self-preserved pharmaceutical composition of the present invention.
  • Example
    Z
    Ingredients Conc. (w/v %)
    Olopatadine 0.111
    Hydrochloride
    Propylene glycol 0.3
    Boric Acid 1.0
    Sodium Chloride 0.17
    Zinc Chloride 0.0025
    Sodium Hydroxide Adjust pH 7.0
    Hydrochloric Acid
    Purified Water QS 100
    II. Physical Parameters
    Osmolality (mOsm/kg) 267,268
    Monovalent cation (Na) 6.9 mM
    concentration needed to adjust pH
    of buffering anions
    PET Results 6 h 24 h 7 d 14 d 28 d
    S. aureus 0.0 0.2 4.4 4.9 4.9
    P. aeruginosa 0.4 1.3 3.7 4.9 4.9
    E. coli 0.7 0.8 5.0 5.0 5.0
    C. albicans 0.1 0.5 1.3
    A. niger 1.5 1.8 1.3
  • Examples AA through AD
  • The formulations in Examples AA and AB contain borate/polyol buffers, whereas the formulations in Example AC and AD contain citrate and phosphate buffers, respectively. All formulations contain 0.11 mM zinc (0.0015% zinc chloride). The formulations in Examples AA and AB, which are representative of the compositions of the present invention, satisfied USP preservative efficacy requirements for the microorganisms tested. The formulations in Examples AC and AD failed to satisfy the USP preservative efficacy requirements, relative to all microorganisms tested. The formulations in Examples AC and AD contained multivalent buffering anions (i.e., citrate and phosphate, respectively) at concentrations of greater than 5 mM. These results demonstrate the importance of limiting the concentration of multivalent buffering anions in the compositions of the present invention.
  • Example
    AA AB AC AD
    FID 109997 110009 110002 110013
    Lot Number 05-42424 05-42421 05-42428 05-42432
    Ingredient
    Polyoxyl 40 Hydrogenated 0.5 0.5 0.5 0.5
    Castor Oil (HCO-40)
    Zinc Chloride 0.0015 0.0015 0.0015 0.0015
    Boric Acid 1 1 None None
    Propylene Glycol 0.4 0.4 0.4 0.4
    Sodium Chloride None 0.2 None None
    Sodium Citrate (Dihydrate) None None 0.215 None
    Dibasic Sodium Phosphate None None None 0.156
    (Anhydrous)
    Sodium Hydroxide, and/or Adjust pH to Adjust pH to Adjust pH to Adjust pH to
    Hydrochloric Acid 7.0 7.0 7.0 7.0
    Purified Water QS 100% QS 100% QS 100% QS 100%
    Osmolality 210 270 76 85
    Monovalent cation (Na) conc. 4.4 mM 4.7 mM 20.4 mM* 15.8 mM*
    needed to adjust pH of
    buffering anions
    Microorganism Log Order Reductions
    S. aureus  7 D 4.8 4.8 0.9 0.9
    14 D 4.8 4.8 4.8 3.5
    28 D 4.8 4.8 4.8 4.3
    P. aeruginosa  7 D 4.9 4.9 0.4 −0.3
    14 D 4.9 4.9 0.5 −0.4
    28 D 4.9 4.9 0.3 −0.2
    E. col  7 D 4.4 4.4 −0.6 −0.9
    14 D 4.4 4.4 −0.4 −0.8
    28 D 4.4 4.4 −0.3 −0.5
    C. albican  7 D NT NT NT NT
    14 D NT NT NT NT
    28 D NT NT NT NT
    A. niger  7 D NT NT NT NT
    14 D NT NT NT NT
    28 D NT NT NT NT
    *Calculated based on Pka and concentration of buffer used.

Claims (25)

1-18. (canceled)
19. A multi-dose, self-preserved ophthalmic composition, comprising:
a therapeutically effective amount of an ophthalmic therapeutic agent selected from the group consisting of bimatoprost, latanoprost and travoprost;
water; and
a zinc/borate/polyol system consisting essentially of:
i. zinc ions at a concentration of 0.04 to 0.4 mM;
ii. borate; and
iii. polyol comprising sorbitol and propylene glycol;
wherein the composition has a concentration of anionic species less than 15 mM.
20. A composition according to claim 19 wherein the composition satisfies USP 27 preservative efficacy requirements.
21. A composition according to claim 19 wherein the sorbitol is in the composition at a concentration of 0.05 to 0.75% w/v.
22. A composition according to claim 19 wherein the sorbitol is in the composition at a concentration of 0.25 to 0.75% w/v.
23. A composition according to claim 19 wherein the propylene glycol is in the composition at a concentration of 0.25 to 2.5% w/v.
24. A composition according to claim 19 wherein the borate is in the composition at a concentration of 0.3 to 1.5% w/v.
25. A composition according to claim 19 wherein the zinc ions are provided by zinc chloride, the zinc chloride being present in the composition at a concentration of 0.001 to 0.005 w/v %.
26. A composition according to claim 19 wherein the ophthalmic therapeutic agent is travoprost.
27. A composition according to claim 19 wherein the composition has a concentration of multivalent buffering anions that is less than 5 mM.
28. A composition according to claim 19 wherein: (i) the composition has a concentration of multivalent buffering anions that is less than 5 mM; and (ii) the composition has a concentration of multivalent metal cations other than zinc that is less than 5 mM.
29. A composition according to claim 19 further comprising polyoxyl 40 hydrogenated castor oil wherein the composition has a pH from 5.5 to 5.9 and wherein the zinc ions are provided by zinc chloride, the zinc chloride being present in the composition at a concentration of 0.001 to 0.005 w/v %.
30. A composition according to claim 19 wherein the propylene glycol is present in the composition at a concentration of 0.75 w/v %, the borate is boric acid and is present in the composition at a concentration of 1.0 w/v % and the zinc ions are provided by zinc chloride, the zinc chloride being present in the composition at a concentration of 0.0025 w/v %.
31. A composition according to claim 19 wherein the composition has a pH from 5.5 to 5.9.
32. A composition according to claim 31 further comprising polyoxyl 40 hydrogenated castor oil.
33. A composition according to claim 19 wherein the zinc ions are in the composition at a concentration of 0.1 to 0.4 mM.
34. A multi-dose, self-preserved ophthalmic composition, comprising:
a therapeutically effective amount of an ophthalmic therapeutic agent selected from the group consisting of bimatoprost, latanoprost and travoprost;
water; and
a zinc/borate/polyol system consisting essentially of:
i. zinc ions at a concentration of 0.04 to 0.4 mM;
ii. borate at a concentration of 0.3 to 1.5% w/v; and
iii. polyol comprising sorbitol at a concentration of 0.05 to 0.75% w/v and propylene glycol at a concentration of 0.25 to 2.5% w/v;
wherein the composition has a concentration of anionic species less than 15 mM.
35. A composition according to claim 34 wherein the sorbitol is in the composition at a concentration of 0.25 to 0.75% w/v.
36. A composition according to claim 35 wherein the zinc ions are provided by zinc chloride, the zinc chloride being present in the composition at a concentration of 0.001 to 0.005 w/v %.
37. A composition according to claim 36 wherein the therapeutic agent is travoprost.
38. A composition according to claim 37 wherein: (i) the composition has a concentration of multivalent buffering anions that is less than 5 mM; and (ii) the composition has a concentration of multivalent metal cations other than zinc that is less than 5 mM.
39. A composition according to claim 38 wherein the composition has a pH from 5.5 to 5.9.
40. A composition according to claim 39 wherein the zinc ions are in the composition at a concentration of 0.1 to 0.4 mM.
41. A composition according to claim 40 wherein the propylene glycol is present in the composition at a concentration of 0.75 w/v %, the borate is boric acid and is present in the composition at a concentration of 1.0 w/v % and the zinc ions are provided by zinc chloride at a concentration of 0.0025 w/v %.
42. A composition according to claim 41 further comprising polyoxyl 40 hydrogenated castor oil.
US13/664,049 2006-09-21 2012-10-30 Self-Preserved Aqueous Pharmaceutical Compositions Abandoned US20130053440A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US13/664,049 US20130053440A1 (en) 2006-09-21 2012-10-30 Self-Preserved Aqueous Pharmaceutical Compositions

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US82652906P 2006-09-21 2006-09-21
US82741106P 2006-09-28 2006-09-28
US11/858,781 US8268299B2 (en) 2006-09-21 2007-09-20 Self preserved aqueous pharmaceutical compositions
US13/086,950 US8323630B2 (en) 2006-09-21 2011-04-14 Self-preserved aqueous pharmaceutical compositions
US13/664,049 US20130053440A1 (en) 2006-09-21 2012-10-30 Self-Preserved Aqueous Pharmaceutical Compositions

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US13/086,950 Continuation US8323630B2 (en) 2006-09-21 2011-04-14 Self-preserved aqueous pharmaceutical compositions

Publications (1)

Publication Number Publication Date
US20130053440A1 true US20130053440A1 (en) 2013-02-28

Family

ID=39156274

Family Applications (3)

Application Number Title Priority Date Filing Date
US11/858,781 Active 2029-10-13 US8268299B2 (en) 2006-09-21 2007-09-20 Self preserved aqueous pharmaceutical compositions
US13/086,950 Active US8323630B2 (en) 2006-09-21 2011-04-14 Self-preserved aqueous pharmaceutical compositions
US13/664,049 Abandoned US20130053440A1 (en) 2006-09-21 2012-10-30 Self-Preserved Aqueous Pharmaceutical Compositions

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US11/858,781 Active 2029-10-13 US8268299B2 (en) 2006-09-21 2007-09-20 Self preserved aqueous pharmaceutical compositions
US13/086,950 Active US8323630B2 (en) 2006-09-21 2011-04-14 Self-preserved aqueous pharmaceutical compositions

Country Status (22)

Country Link
US (3) US8268299B2 (en)
EP (1) EP2068822B2 (en)
JP (2) JP4785970B2 (en)
KR (1) KR101021933B1 (en)
AR (1) AR062929A1 (en)
AT (1) ATE531358T1 (en)
AU (1) AU2007299727B2 (en)
BR (1) BRPI0717067A2 (en)
CA (1) CA2606370C (en)
CL (1) CL2007002705A1 (en)
CY (1) CY1112138T1 (en)
DK (1) DK2068822T4 (en)
ES (1) ES2374444T5 (en)
HK (1) HK1126667A1 (en)
MX (1) MX2009002221A (en)
PL (1) PL2068822T5 (en)
PT (1) PT2068822E (en)
RU (1) RU2436568C2 (en)
SI (1) SI2068822T2 (en)
TW (1) TWI394564B (en)
UY (1) UY30605A1 (en)
WO (1) WO2008036847A2 (en)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7767217B2 (en) 2006-03-14 2010-08-03 Foresight Biotherapeutics Ophthalmic compositions comprising povidone-iodine
TWI394564B (en) 2006-09-21 2013-05-01 Alcon Res Ltd Self-preserved aqueous pharmaceutical compositions
BRPI0717093A2 (en) 2006-09-28 2013-11-26 Alcon Res Ltd SELF-PRESERVED WATER PHARMACEUTICAL COMPOSITIONS
TW200904485A (en) * 2007-05-18 2009-02-01 Alcon Res Ltd Phospholipid compositions for contact lens care and preservation of pharmaceutical compositions
EP2420223B1 (en) 2008-03-17 2017-07-19 Novartis Ag Aqueous pharmaceutical compositions containing borate-polyol complexes
JP2009256281A (en) * 2008-04-21 2009-11-05 Teika Seiyaku Kk Isopropyl unoprostone containing ophthalmic preparation formulation
TW201010727A (en) * 2008-09-03 2010-03-16 Alcon Res Ltd Pharmaceutical composition having relatively low ionic strength
MX2011005586A (en) * 2008-12-22 2011-06-20 Alcon Res Ltd Compositions of topical ocular solutions to deliver effective concentrations of active agent to the posterior segment of the eye.
EP2228058A1 (en) 2009-03-04 2010-09-15 Novagali Pharma S.A. Anionic oil-in-water emulsion containing prostaglandins and uses thereof
TWI489997B (en) * 2009-06-19 2015-07-01 Alcon Res Ltd Aqueous pharmaceutical compositions containing borate-polyol complexes
EP2389939A1 (en) 2010-05-28 2011-11-30 Novagali Pharma S.A. Use of prostaglandins F2alpha and analogues for the healing of corneal and conjunctival lesions
KR20190049931A (en) * 2009-12-15 2019-05-09 포어사이트 바이오쎄라퓨틱스, 인코퍼레이티드 Non-Irritating Ophthalmic Povidone-Iodine Compositions
TW201127423A (en) * 2009-12-17 2011-08-16 Alcon Res Ltd Ophthalmic solutions with improved disinfection profiles
LT2680832T (en) 2011-03-04 2019-10-25 Gruenenthal Gmbh Aqueous pharmaceutical formulation of tapentadol for oral administration
CA2828635C (en) * 2011-03-04 2020-01-14 Grunenthal Gmbh Parenteral administration of tapentadol
JP6150510B2 (en) * 2011-12-12 2017-06-21 ロート製薬株式会社 Ophthalmic aqueous composition
EP2630952A1 (en) 2012-02-23 2013-08-28 Novagali Pharma S.A. Self-preserved oil dispersions comprising boric acid
TW201417814A (en) * 2012-09-28 2014-05-16 Otsuka Pharma Co Ltd Pharmaceutical composition comprising rebamipide
US20150374820A1 (en) * 2013-02-15 2015-12-31 Senju Pharmaceutical Co., Ltd. Difluprednate emulsion composition containing zinc
RU2015142245A (en) 2013-03-13 2017-04-18 Кур Фармасьютикалз Дивелопмент Компани IMMUNOMODIFICATION PARTICLES FOR THE TREATMENT OF INFLAMMATION
EP3037094A1 (en) 2014-12-23 2016-06-29 Poifa Warszawa SA Ophthalmic pharmaceutical composition
BR112017018569A2 (en) 2015-03-27 2018-04-24 Gruenenthal Gmbh stable formulation for parenteral administration of tapentadol
US11458041B2 (en) 2015-10-08 2022-10-04 Ocular Therapeutix, Inc. Punctal plug and bioadhesives
US10632202B2 (en) 2016-03-04 2020-04-28 Johnson & Johnson Consumer Inc. Preservative containing compositions
JP7160799B2 (en) 2016-09-23 2022-10-25 グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング Stable formulation of tapentadol for parenteral administration
WO2019123266A1 (en) 2017-12-20 2019-06-27 Novartis Ag Ophthalmic composition having a prostaglandin and a beta-blocker
PT3861985T (en) 2020-02-06 2023-08-03 Ocular Therapeutix Inc Compositions and methods for treating ocular diseases
US20220031739A1 (en) * 2020-07-31 2022-02-03 Eye Therapies Llc Anti-viral compositions and methods of use thereof
WO2023054669A1 (en) 2021-09-30 2023-04-06 ロート製薬株式会社 Ophthalmological composition
WO2024003078A1 (en) * 2022-06-27 2024-01-04 Warszawskie Zaklady Farmaceutyczne Polfa Sa Preservative-free ophthalmic composition comprising a prostaglandin analogue
EP4309644A1 (en) * 2022-07-22 2024-01-24 Warszawskie Zaklady Farmaceutyczne Polfa S.A. Preservative-free ophthalmic composition comprising an antiglaucoma agent

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2084870B (en) * 1980-10-10 1985-05-09 Muhlemann R Hans Oral compositions containing pyrimidine amine compounds and zinc salts
US5607698A (en) * 1988-08-04 1997-03-04 Ciba-Geigy Corporation Method of preserving ophthalmic solution and compositions therefor
CA2003198C (en) * 1988-11-29 1995-03-21 Anthony J. Dziabo, Jr. Aqueous ophthalmic solutions and method for preserving same
US5130298A (en) * 1989-05-16 1992-07-14 Ethicon, Inc. Stabilized compositions containing epidermal growth factor
US5221664A (en) * 1990-04-23 1993-06-22 Magainin Pharmaaceuticals Inc. Composition and treatment with biologically active peptides and toxic cations
CA2098299C (en) * 1990-12-27 1997-05-20 Mary Mowrey-Mckee Method and composition for disinfecting contact lenses
US5460834A (en) * 1991-12-13 1995-10-24 Alcon Laboratories, Inc. Combinations of polymers for use in physiological tear compositions
US5505953A (en) * 1992-05-06 1996-04-09 Alcon Laboratories, Inc. Use of borate-polyol complexes in ophthalmic compositions
DE69333850T3 (en) * 1992-05-06 2011-03-17 Alcon Laboratories, Inc., Fort Worth APPLICATION OF BORAL-POLYOL COMPLEXES FOR OPHTHALMIC DRUG COMPOSITIONS
US5352708A (en) * 1992-09-21 1994-10-04 Allergan, Inc. Non-acidic cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents
US5320843A (en) * 1992-12-10 1994-06-14 Polymer Technology Corporation Method for improving antibacterial properties of ophthalmic solutions
NZ247516A (en) * 1993-04-28 1995-02-24 Bernard Charles Sherman Water dispersible pharmaceutical compositions comprising drug dissolved in solvent system comprising at least one alcohol and at least one surfactant
US5736165A (en) * 1993-05-25 1998-04-07 Allergan In-the-eye use of chlorine dioxide-containing compositions
TW274516B (en) 1993-11-12 1996-04-21 Ciba Geigy Ag
AU3070395A (en) * 1994-07-22 1996-02-22 Alcon Laboratories, Inc. Use of low molecular weight amino acids in ophthalmic compositions
US6024954A (en) * 1994-12-12 2000-02-15 Allergan Compositions and methods for disinfecting contact lenses and preserving contact lens care products
EP0817607A1 (en) * 1995-03-20 1998-01-14 Unilever Plc Liquid cleansing formulations
US5683993A (en) * 1995-06-22 1997-11-04 Ciba Vision Corporation Compositions and methods for stabilizing polymers
HU225329B1 (en) 1996-09-12 2006-09-28 Richter Gedeon Vegyeszet Use of zinc or cobalt hyaluronate associate for the manufacture of pharmaceutical compositions of antimicrobial activity
WO1998011867A1 (en) * 1996-09-20 1998-03-26 Warner-Lambert Company Oral compositions containing a zinc compound
US5820822A (en) * 1996-10-25 1998-10-13 Kross; Robert D. Antimicrobial composition and method of use
CN1157227C (en) * 1996-12-13 2004-07-14 阿尔康实验室公司 Use of low molecular weight amino alcohols in ophthalmic compositions
US5858346A (en) * 1997-05-09 1999-01-12 Allergan Compositions and methods for enhancing contact lens wearability
DE69818675T2 (en) * 1997-07-29 2004-07-29 Alcon Laboratories, Inc., Fort Worth GALACTOMANAN POLYMERS AND BORATE CONTAINING EYE MEDICINAL PRODUCTS
US6034043A (en) * 1999-04-20 2000-03-07 Lever Brothers Company, Division Of Conopco, Inc. Mild antimicrobial liquid cleansing formulations comprising polyvalent cation or cations for improving an antimicrobial effectiveness
US6482799B1 (en) * 1999-05-25 2002-11-19 The Regents Of The University Of California Self-preserving multipurpose ophthalmic solutions incorporating a polypeptide antimicrobial
US6166012A (en) * 1999-07-30 2000-12-26 Allergan Sales, Inc. Antibiotic compositions and method for using same
CN1477929A (en) * 2000-11-29 2004-02-25 ��˹��ŵ�� Aqueous disinfecting systems
AR035509A1 (en) * 2000-12-21 2004-06-02 Alcon Inc SOLUTION OF IMPROVED ARTIFICIAL TEARS CONTAINING A COMBINATION OF THREE EMOLIENTS AND THE USE OF SUCH SOLUTION FOR THE MANUFACTURE OF A MEDICINAL PRODUCT
JP4863589B2 (en) 2001-09-28 2012-01-25 ロート製薬株式会社 Aqueous composition
US7074827B2 (en) * 2002-10-24 2006-07-11 Sucampo Ag (Usa) Inc. Method for treating ocular hypertension and glaucoma
JP2004339104A (en) * 2003-05-14 2004-12-02 Rohto Pharmaceut Co Ltd Method for solution stabilization
ES2323132T3 (en) * 2003-12-09 2009-07-07 Alcon, Inc. USE OF BIS-AMINAS TO INCREASE ANTIMICROBIAL ACTIVITY OF WATER COMPOSITIONS.
US7968122B2 (en) * 2003-12-10 2011-06-28 Adventrx Pharmaceuticals, Inc. Anti-viral pharmaceutical compositions
JP2007513952A (en) * 2003-12-11 2007-05-31 アルコン、インコーポレイテッド Ophthalmic composition comprising a polysaccharide / borate gelling system
US20050214382A1 (en) * 2004-03-29 2005-09-29 Erning Xia Zinc preservative composition and method of use
GB0501192D0 (en) * 2005-01-20 2005-03-02 Resolution Chemicals Ltd Stable prostaglandin-containing compositions
US20070212420A1 (en) * 2006-03-10 2007-09-13 Bausch & Lomb Incorporated Pharmaceutical formulations comprising polyanionic materials and zinc-based preservatives
US20070297990A1 (en) 2006-06-27 2007-12-27 Shah Mandar V Self-preserving composition
TWI394564B (en) 2006-09-21 2013-05-01 Alcon Res Ltd Self-preserved aqueous pharmaceutical compositions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Gadd et al. Microbiol Ecology 1978 4:303-317. *
typically [online] retrieved on 3/17/14 from: http://www.collinsdictionary.com/dictionary/english/typically; 3 pages. *
typically [online] retrieved on 3/18/14 from: http://www.merriam-webster.com/dictionary/typically; 4 pages. *

Also Published As

Publication number Publication date
DK2068822T4 (en) 2022-10-31
EP2068822B2 (en) 2022-07-27
HK1126667A1 (en) 2009-09-11
CA2606370C (en) 2012-03-27
ES2374444T3 (en) 2012-02-16
DK2068822T3 (en) 2012-01-23
KR20090058567A (en) 2009-06-09
US8268299B2 (en) 2012-09-18
JP2010504358A (en) 2010-02-12
ATE531358T1 (en) 2011-11-15
PL2068822T3 (en) 2012-03-30
SI2068822T2 (en) 2022-10-28
CA2606370A1 (en) 2008-03-21
JP4785970B2 (en) 2011-10-05
BRPI0717067A2 (en) 2013-09-24
KR101021933B1 (en) 2011-03-16
PT2068822E (en) 2012-01-10
EP2068822A2 (en) 2009-06-17
UY30605A1 (en) 2008-03-31
US8323630B2 (en) 2012-12-04
AU2007299727B2 (en) 2011-10-06
TW200820962A (en) 2008-05-16
CL2007002705A1 (en) 2008-05-16
SI2068822T1 (en) 2012-02-29
US20080075790A1 (en) 2008-03-27
AR062929A1 (en) 2008-12-17
MX2009002221A (en) 2009-03-13
EP2068822B1 (en) 2011-11-02
AU2007299727A8 (en) 2009-04-09
JP5411897B2 (en) 2014-02-12
ES2374444T5 (en) 2022-11-21
TWI394564B (en) 2013-05-01
US20110195132A1 (en) 2011-08-11
RU2436568C2 (en) 2011-12-20
WO2008036847A3 (en) 2008-05-29
CY1112138T1 (en) 2015-11-04
RU2009114849A (en) 2010-10-27
PL2068822T5 (en) 2022-11-14
WO2008036847A2 (en) 2008-03-27
JP2011246476A (en) 2011-12-08
AU2007299727A1 (en) 2008-03-27

Similar Documents

Publication Publication Date Title
US8268299B2 (en) Self preserved aqueous pharmaceutical compositions
US8388941B2 (en) Self preserved aqueous pharmaceutical compositions
US9044484B2 (en) Aqueous pharmaceutical compositions containing borate-polyol complexes
EP2420223B1 (en) Aqueous pharmaceutical compositions containing borate-polyol complexes
CN101516332B (en) Self preserved aqueous pharmaceutical compositions
US20100021561A1 (en) Self-preserved aqueous pharmaceutical compositions

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: EXPRESSLY ABANDONED -- DURING PUBLICATION PROCESS