JP2003221323A - Capsule - Google Patents
CapsuleInfo
- Publication number
- JP2003221323A JP2003221323A JP2002016909A JP2002016909A JP2003221323A JP 2003221323 A JP2003221323 A JP 2003221323A JP 2002016909 A JP2002016909 A JP 2002016909A JP 2002016909 A JP2002016909 A JP 2002016909A JP 2003221323 A JP2003221323 A JP 2003221323A
- Authority
- JP
- Japan
- Prior art keywords
- starch
- gelatin
- hydroxypropylated
- strength
- capsules
- 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.)
- Granted
Links
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- Medicinal Preparation (AREA)
Abstract
Description
【発明の詳細な説明】
【0001】
【産業上の利用分野】本発明はカプセル剤に関する。よ
り詳細には、カプセル剤の皮膜に関する。
【0002】
【従来の技術】従来、カプセル剤の皮膜は、一般にゼラ
チンとグリセリンやソルビトール等の可塑剤と防腐剤や
甘味剤から製造されている。特開平5−5065号に
は,ヒドロキシプロピル化澱粉等の誘導体澱粉が皮膜の
組成物に使用できることが記載されている。特開200
0−35534号には、ゼラチン状の性質を有するよう
に変性された澱粉として、予めゼラチン化された酸化小
麦澱粉の使用が提案されている。WO01/03677A
1には、イオターカラギーナンとヒドロキシプロピル化
タピオカ澱粉、ヒドロキシプロピル化コーンスターチ、
酸処理ヒドロキシプロピル化コーンスターチ等のグルー
プから選ばれた少なくとも一つの澱粉かなるカプセル剤
の皮膜のの組成物が提案されている。
【0003】
【発明が解決しようとする課題】ゼラチンは、動物性の
物質であるため、菜食主義者の人から嫌われている。ま
た、狂牛病のような病気の感染という観点から、使用す
ることは好ましくない。これに替えて誘導体澱粉も提案
されているが、柔軟性に欠ける。また、ヒートシールで
きないという問題がある。
【0004】
【問題を解決するための方法】本発明者等は、検討を重
ねた結果、25%水溶液の粘度が、30℃で、BM粘度
計30rpmで測定し10〜300cps、好ましくは
10〜200cpsであり、かつヒドロキシプロポキシ
ル基が3〜10%、好ましくは4〜8%であるヒドロシ
キプロピル化澱粉の酵素分解物を使用することにより、
ゼラチンを含有しなくても、柔軟性、ヒートシール性に
優れた皮膜を得られることを見出し、鋭意研究の結果、
本発明を完成した。
【0005】
【発明の実施の形態】本発明に使用できるヒドロキシプ
ロピル化澱粉の酵素分解物は、コーンスターチ、ハイア
ミロースコーンスターチ、ワキシコーンスターチ、馬鈴
薯澱粉、タピオカ澱粉、小麦澱粉、米澱粉等の天然澱粉
やそれらのアセチル化、コハク酸化、オクテニルコハク
酸化、リン酸化、カルボキシメチル化、リン酸架橋化等
の誘導体澱粉を通常の方法によりヒドロキシプロピル化
し、酵素分解すれば得られる。
【0006】例えば、澱粉の水懸濁液にプロピレンオキ
サイドを加え、触媒として苛性ソーダを入れ、撹拌反応
させ、中和後、濾過、乾燥させる。ヒドロキシプロポキ
シル基は3〜10%、好ましくは4〜8%のものが使用
できる。これ以下では、澱粉分解物が老化して、白濁
し、皮膜の柔軟性がなく脆くなる。また、これ以上でも
皮膜の柔軟性は、さらに良くはならず、ヒドロキシプロ
ピル化澱粉の製造コストが高くなる。
【0007】皮膜の柔軟性向上のためとヒートシール性
の向上のため、このヒドロキシプロピル化澱粉を、水中
で加熱糊化し、αーアミラーゼ等の酵素により分解し、
酵素を失活、脱色、精製、乾燥する。この際、25%水
溶液の粘度が、30℃で、BM型粘度計で30rpmで
測定し10〜300cps、好ましくは10〜200c
psのものが使用できる。300cps以上では、ヒー
トシール性が悪くなる。また、粘度が高いと、水溶液の
濃度を高くすると、流動性が悪くなるため、シート作成
時に濃度を高くできず、乾燥コストが高くなる。10c
ps以下では、皮膜の形成性が悪くなる。澱粉の酵素分
解物は、酸分解物に比較して、同じ粘度であれば、分子
量分布が広くなるため、比較的高分子のものと低分子の
ものが混在し、皮膜の形成性と柔軟性と共にヒートシー
ル性が良くなると考えられる。
【0008】上記ヒドロキシプロピル化澱粉分解物にさ
らに柔軟性を付与するため、可塑剤としてグリセリン、
プロピレングリコール、ソルビトール、マルチトール、
キシリトール等の多価アルコールや、グルコース、フラ
クトース、砂糖、還元水飴等の糖類を皮膜の成分の5〜
50%混合することが好ましい。また、天然澱粉、ヒド
ロキシプロピル化やアセチル化等の誘導体澱粉、カラギ
ーナン、寒天、ローカストビーンガム、グアーガム、グ
ルコマンナン、アラビアガム、大豆多糖類、ペクチン、
アルギン酸ナトリウム等の多糖類を皮膜の強度を上げる
ために混合しても良い。
【0009】本発明におけるカプセルの皮膜の調製方法
は、従来行われている皮膜の調製方法と同じように行え
る。例えば、ロータリー式、平板式等の製造方法を使用
して製造できる。
【0010】以下、実施例を挙げて、本発明を詳細に説
明するが、本発明は、これらの実施例に限定されない。
【0011】<実施例1〜4、比較例1、2>ヒドロキ
シプロポキシル基の量が異なるヒドロキシプロピル化馬
鈴薯澱粉と馬鈴薯澱粉を常法により酵素分解し、25%
水溶液の粘度が、30℃で、BM型粘度計30rpmで
測定し、150cpsの澱粉酵素分解物を製造した。こ
の澱粉酵素分解物100gとグリセリン30gとイオン
交換水120gを混合し、加熱溶解し、減圧下に脱泡し
た後、ポリエチレンテレフタレートフィルム上に流延
し、熱風乾燥し、水分12%、厚み0.6mmのシート
を得た。1cm×3cmの試験片を作成し、テンシロン
モデルUTM−III−100((株)東洋ボールドウ
イン製、万能引張試験機)にて、引張速度20mm/m
inで、強度と伸度を測定した。なお、澱粉分解物に替
えてゼラチンを用い、同様の操作により作成したシート
の強度は、220gf/mm2、伸度は、420%であ
った。また、この試験片を2枚重ねてSEALER30
6(日光(株)製、シーラー)で目盛り5でヒートシー
ルした後、2枚を手で引き剥がしてヒートシール性能を
試験した。結果を表1に示した。なお表中のHP基は、
ヒドロキシプロポキシル基を表し、ヒートシール性は、
ゼラチンに比較しての評価である。また、比較例2の馬
鈴薯澱粉のHP基は、0%である。
【0012】
【表1】
【0013】なお、比較例2のシートは、作成1日後に
は白濁した。本発明のシートは強度、伸度ともカプセル
剤の皮膜として使用できることが明らかであり、ヒート
シール性能も、良好であった。
【0014】<実施例5、6、比較例4、5>ヒドロキ
シプロポキシル基7%のヒドロキシプロピル馬鈴薯澱粉
を常法により、αーアミラーゼにて、所定の粘度になる
ように分解した。この澱粉酵素分解物を実施例1と同様
の操作を行い、水分12%、厚み0.6mmのシートを
得た。このシートの強度、伸度、ヒートシール性を実施
例1と同様の方法にて測定した。結果を表2に示した。
なお、表中の粘度は、濃度25%、30℃、BM型粘度
計30rpmの粘度である。
【0015】
【表2】
【0016】本発明のシートは強度、伸度ともカプセル
剤の皮膜として使用できることが明らかであり、ヒート
シール性能も、良好であった。
【0017】<実施例7>実施例2のヒドロキシプロピ
ル化澱粉分解物60gとソルビトール40gとイオン交
換水90gを混合し加熱溶解し、実施例1と同様の操作
を行い、水分12%、厚み0.5mmのシートを得た。
このシートの強度は、190gf/mm2、伸度は、2
40%であった。強度、伸度ともカプセル剤の皮膜とし
て使用できることが明らかであり、ヒートシール性能も
良好であった。
【0018】<実施例8>実施例2のヒドロキシプロピ
ル化澱粉分解物30gとヒドロキシプロピル基7%のヒ
ドロキシプロピル化馬鈴薯澱粉30gとソルビトール4
0gとイオン交換水90gを混合し加熱溶解し、実施例
1と同様の操作を行い、水分12%、厚み0.6mmの
シートを得た。このシートの強度は200gf/mm
2、伸度は340%であった。強度、伸度ともカプセル
剤の皮膜として使用できることが明らかである。ヒート
シール性能も、良好であった。
【0019】<実施例9>実施例2のヒドロキシプロピ
ル化澱粉分解物60gとNEWGELIN KC−20
0S(中央化成(株)製、カラギーナン)4gとソルビ
トール40gとイオン交換水90gを混合し加熱溶解
し、実施例1と同様の操作を行い、水分13%、厚み
0.6mmのシートを得た。このシートの強度は240
gf/mm2、2、伸度は200%であった。強度、伸
度ともカプセル剤の皮膜として使用できることが明らか
である。ヒートシール性能も、良好であった。
【0020】<比較例6>実施例2のヒドロキシプロピ
ル化澱粉の酵素分解物に替えてヒドロキシプロポキシル
基7%で、25%水溶液の粘度が、30℃で、BM型粘
度計30rpmで測定し、200cpsのヒドロキシプ
ロピル化馬鈴薯澱粉の酸分解物を用いて、実施例1と同
様の操作を行ない水分12%、厚み0.6mmのシート
を得た。このシートの強度、伸度、ヒートシート性を実
施例1同様の方法で測定した。強度は440gf/mm
2、伸度は150%であり、皮膜の形成性は良いが、柔
軟性に欠け、カプセル剤として使用できない。またヒー
トシール性も悪く、シート同士は接着しなかった。
【0021】
【発明の効果】本発明は、以上のように構成されている
ので、ゼラチンを含有しない、強度、柔軟性、ヒートシ
ール性に優れたカプセル剤の皮膜を製造することができ
る。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a capsule. More particularly, it relates to a capsule coating. 2. Description of the Related Art Conventionally, capsule films are generally produced from gelatin, a plasticizer such as glycerin or sorbitol, a preservative and a sweetener. JP-A-5-5065 discloses that derivative starch such as hydroxypropylated starch can be used in the composition of the film. JP 200
No. 0-35534 proposes the use of pregelatinized oxidized wheat starch as a starch modified to have gelatinous properties. WO01 / 03677A
1, iota carrageenan and hydroxypropylated tapioca starch, hydroxypropylated corn starch,
Compositions of capsule coatings comprising at least one starch selected from the group of acid-treated hydroxypropylated corn starch and the like have been proposed. [0003] Gelatin is hated by vegetarians because it is an animal substance. Further, it is not preferable to use it from the viewpoint of infection of diseases such as mad cow disease. A derivative starch has been proposed instead, but lacks flexibility. In addition, there is a problem that heat sealing cannot be performed. As a result of repeated studies, the present inventors have determined that the viscosity of a 25% aqueous solution is 10 to 300 cps, preferably 10 to 300 cps, measured at 30 ° C. with a BM viscometer at 30 rpm. By using an enzymatically decomposed product of hydroxypropylated starch which is 200 cps and has 3 to 10%, preferably 4 to 8% of hydroxypropoxyl groups,
Even without gelatin, it was found that a film excellent in flexibility and heat sealability could be obtained.
The present invention has been completed. DETAILED DESCRIPTION OF THE INVENTION Enzymatic degradation products of hydroxypropylated starch which can be used in the present invention include natural starch such as corn starch, high amylose corn starch, waxy corn starch, potato starch, tapioca starch, wheat starch, rice starch and the like. And derivatives thereof, such as acetylation, succination, octenyl succination, phosphorylation, carboxymethylation, and phosphoric acid cross-linking, can be obtained by subjecting them to hydroxypropylation by a conventional method and subjecting them to enzymatic decomposition. For example, propylene oxide is added to an aqueous suspension of starch, caustic soda is added as a catalyst, the mixture is stirred and reacted, neutralized, filtered and dried. A hydroxypropoxyl group having 3 to 10%, preferably 4 to 8% can be used. Below this, the starch degradation product ages, becomes cloudy, and becomes inflexible and brittle. Even above this, the flexibility of the film is not further improved, and the production cost of the hydroxypropylated starch increases. In order to improve the flexibility of the film and the heat sealing property, the hydroxypropylated starch is gelatinized by heating in water and decomposed by an enzyme such as α-amylase.
Inactivate, decolorize, purify and dry the enzyme. At this time, the viscosity of the 25% aqueous solution is measured at 30 ° C. with a BM viscometer at 30 rpm, and is 10 to 300 cps, preferably 10 to 200 cps.
ps can be used. If it is 300 cps or more, the heat sealing property deteriorates. In addition, when the viscosity is high, when the concentration of the aqueous solution is increased, the fluidity is deteriorated. 10c
Below ps, the film formability is poor. Enzyme decomposed products of starch have a broader molecular weight distribution if they have the same viscosity as compared with acid decomposed products. It is considered that the heat sealing property is improved. In order to further impart flexibility to the hydrolyzate of hydroxypropylated starch, glycerin as a plasticizer,
Propylene glycol, sorbitol, maltitol,
Polyhydric alcohols such as xylitol and saccharides such as glucose, fructose, sugar, reduced starch syrup, etc.
It is preferable to mix by 50%. Also, natural starch, derivative starch such as hydroxypropylated or acetylated, carrageenan, agar, locust bean gum, guar gum, glucomannan, gum arabic, soy polysaccharide, pectin,
Polysaccharides such as sodium alginate may be mixed to increase the strength of the film. The method for preparing a capsule film in the present invention can be carried out in the same manner as a conventional method for preparing a film. For example, it can be manufactured using a manufacturing method such as a rotary type or a flat plate type. Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples. <Examples 1 to 4, Comparative Examples 1 and 2> Hydroxypropylated potato starch and potato starch having different amounts of hydroxypropoxyl groups were enzymatically decomposed by a conventional method to obtain 25%
The viscosity of the aqueous solution was measured at 30 ° C. with a BM type viscometer at 30 rpm to produce a 150 cps starch enzyme degradation product. 100 g of the enzyme digest of starch, 30 g of glycerin and 120 g of ion-exchanged water were mixed, dissolved by heating, defoamed under reduced pressure, cast on a polyethylene terephthalate film, dried with hot air, and dried with hot water at a moisture content of 12%. A 6 mm sheet was obtained. A test piece of 1 cm × 3 cm was prepared, and the tensile speed was 20 mm / m using Tensilon Model UTM-III-100 (a universal tensile tester manufactured by Toyo Baldwin Co., Ltd.).
In, the strength and elongation were measured. The sheet prepared by the same operation using gelatin instead of the starch hydrolyzate had a strength of 220 gf / mm 2 and an elongation of 420%. In addition, two of these test pieces were stacked and SEALER 30
6 (Nikko Co., Ltd., sealer), heat-sealed at a scale of 5, and then peeled off by hand to test the heat-sealing performance. The results are shown in Table 1. The HP group in the table is
Represents a hydroxypropoxyl group, and the heat sealability is
It is an evaluation in comparison with gelatin. The potato starch of Comparative Example 2 has 0% of the HP group. [Table 1] The sheet of Comparative Example 2 became cloudy one day after the preparation. It is clear that the sheet of the present invention can be used as a capsule film in both strength and elongation, and the heat sealing performance was also good. <Examples 5 and 6, Comparative Examples 4 and 5> Hydroxypropyl potato starch having a hydroxypropoxyl group content of 7% was decomposed by an α-amylase to a predetermined viscosity by a conventional method. This starch enzyme hydrolyzate was subjected to the same operation as in Example 1 to obtain a sheet having a moisture content of 12% and a thickness of 0.6 mm. The strength, elongation, and heat sealability of this sheet were measured in the same manner as in Example 1. The results are shown in Table 2.
In addition, the viscosity in a table | surface is a density | concentration of 25%, 30 degreeC, and a BM type viscometer 30 rpm viscosity. [Table 2] It is clear that the sheet of the present invention can be used as a capsule film in both strength and elongation, and the heat sealing performance was also good. Example 7 60 g of the hydroxypropylated starch hydrolyzate of Example 2, 40 g of sorbitol and 90 g of ion-exchanged water were mixed and dissolved by heating. The same operation as in Example 1 was carried out to obtain a water content of 12% and a thickness of 0 g. A sheet of 0.5 mm was obtained.
The strength of this sheet is 190 gf / mm 2 and the elongation is 2
It was 40%. It was clear that both the strength and the elongation could be used as a capsule film, and the heat sealing performance was also good. Example 8 30 g of the hydroxypropylated starch hydrolyzate of Example 2, 30 g of hydroxypropylated potato starch having 7% hydroxypropyl group and sorbitol 4
0 g and 90 g of ion-exchanged water were mixed and dissolved by heating, and the same operation as in Example 1 was performed to obtain a sheet having a water content of 12% and a thickness of 0.6 mm. The strength of this sheet is 200gf / mm
2. The elongation was 340%. It is clear that both strength and elongation can be used as a capsule film. The heat sealing performance was also good. Example 9 60 g of the hydroxypropylated starch hydrolyzate of Example 2 and NEWGELIN KC-20
4 g of OSS (carrageenan, manufactured by Chuo Kasei Co., Ltd.), 40 g of sorbitol, and 90 g of ion-exchanged water were mixed and dissolved by heating. . The strength of this sheet is 240
gf / mm 2 , elongation was 200%. It is clear that both strength and elongation can be used as a capsule film. The heat sealing performance was also good. Comparative Example 6 The viscosity of a 25% aqueous solution containing 7% of hydroxypropoxyl group was measured at 30 ° C. using a BM type viscometer at 30 rpm instead of the enzymatically decomposed product of the hydroxypropylated starch in Example 2. The same operation as in Example 1 was carried out using an acid hydrolyzate of hydroxypropylated potato starch of 200 cps to obtain a sheet having a water content of 12% and a thickness of 0.6 mm. The strength, elongation, and heat sheet properties of this sheet were measured in the same manner as in Example 1. Strength is 440gf / mm
2. The elongation is 150% and the film formability is good, but lacks flexibility and cannot be used as a capsule. The heat sealability was poor, and the sheets did not adhere to each other. According to the present invention, as described above, it is possible to produce a capsule film which does not contain gelatin and which is excellent in strength, flexibility and heat sealability.
フロントページの続き (72)発明者 大野 秀美 大阪府大阪市淀川区三津屋北3丁目3番29 号 (72)発明者 田中 信正 大阪府大阪市淀川区三津屋北3丁目3番29 号 Fターム(参考) 4C076 AA53 AA58 EE38 FF70 Continuation of front page (72) Inventor Hidemi Ohno 3-29 Mitsuya Kita 3-chome, Yodogawa-ku, Osaka-shi, Osaka issue (72) Inventor Nobumasa Tanaka 3-29 Mitsuya Kita 3-chome, Yodogawa-ku, Osaka-shi, Osaka issue F term (reference) 4C076 AA53 AA58 EE38 FF70
Claims (1)
粘度計30rpmで測定し10〜300cpsであり、
かつヒドロキシプロポキシル基が3〜10%であるヒド
ロシキプロピル化澱粉の酵素分解物を含有することを特
徴とするカプセル剤の皮膜。Claims: 1. The viscosity of a 25% aqueous solution is BM at 30 ° C.
It is 10 to 300 cps measured by a viscometer at 30 rpm,
A capsule film comprising an enzymatically decomposed product of hydroxypropylated starch having a hydroxypropoxyl group content of 3 to 10%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002016909A JP4220159B2 (en) | 2002-01-25 | 2002-01-25 | Capsule |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002016909A JP4220159B2 (en) | 2002-01-25 | 2002-01-25 | Capsule |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2003221323A true JP2003221323A (en) | 2003-08-05 |
JP4220159B2 JP4220159B2 (en) | 2009-02-04 |
Family
ID=27742789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2002016909A Expired - Fee Related JP4220159B2 (en) | 2002-01-25 | 2002-01-25 | Capsule |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4220159B2 (en) |
Cited By (7)
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---|---|---|---|---|
WO2006132398A1 (en) * | 2005-06-06 | 2006-12-14 | Ajinomoto Co., Inc. | Capsule coating composition |
JP2007176908A (en) * | 2005-12-28 | 2007-07-12 | Towa Chem Ind Co Ltd | Hard coating layer, hard coated product and method for producing the same |
JP2007254299A (en) * | 2006-03-20 | 2007-10-04 | Towa Chem Ind Co Ltd | Film coating layer, film coated product and method for producing the same |
JP2008088111A (en) * | 2006-10-02 | 2008-04-17 | Nakanihon Capsule Co Ltd | Composition for film |
JP2009513612A (en) * | 2005-10-28 | 2009-04-02 | パリス,ロウレンス | Coating agent |
JP4790629B2 (en) * | 2003-12-17 | 2011-10-12 | アール.ピー. シェーラー テクノロジーズ エルエルシー | Chewable soft capsules containing non-gelatinized starch |
JP2015040186A (en) * | 2013-08-21 | 2015-03-02 | アピ株式会社 | Capsule coating composition |
-
2002
- 2002-01-25 JP JP2002016909A patent/JP4220159B2/en not_active Expired - Fee Related
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4790629B2 (en) * | 2003-12-17 | 2011-10-12 | アール.ピー. シェーラー テクノロジーズ エルエルシー | Chewable soft capsules containing non-gelatinized starch |
US9241902B2 (en) | 2003-12-17 | 2016-01-26 | R.P. Scherer Technologies, Llc | Chewable soft capsules containing ungelatinized starch |
WO2006132398A1 (en) * | 2005-06-06 | 2006-12-14 | Ajinomoto Co., Inc. | Capsule coating composition |
JP5061897B2 (en) * | 2005-06-06 | 2012-10-31 | 味の素株式会社 | Composition for capsule film |
JP2009513612A (en) * | 2005-10-28 | 2009-04-02 | パリス,ロウレンス | Coating agent |
JP2007176908A (en) * | 2005-12-28 | 2007-07-12 | Towa Chem Ind Co Ltd | Hard coating layer, hard coated product and method for producing the same |
JP2007254299A (en) * | 2006-03-20 | 2007-10-04 | Towa Chem Ind Co Ltd | Film coating layer, film coated product and method for producing the same |
JP2008088111A (en) * | 2006-10-02 | 2008-04-17 | Nakanihon Capsule Co Ltd | Composition for film |
JP2015040186A (en) * | 2013-08-21 | 2015-03-02 | アピ株式会社 | Capsule coating composition |
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