JPS63264519A - Gelatin film coating for soft capsule - Google Patents
Gelatin film coating for soft capsuleInfo
- Publication number
- JPS63264519A JPS63264519A JP9478187A JP9478187A JPS63264519A JP S63264519 A JPS63264519 A JP S63264519A JP 9478187 A JP9478187 A JP 9478187A JP 9478187 A JP9478187 A JP 9478187A JP S63264519 A JPS63264519 A JP S63264519A
- Authority
- JP
- Japan
- Prior art keywords
- gelatin
- acid
- gelatin film
- moisture absorption
- film
- 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.)
- Pending
Links
- 108010025899 gelatin film Proteins 0.000 title claims abstract description 19
- 239000007901 soft capsule Substances 0.000 title claims description 23
- 239000007888 film coating Substances 0.000 title 1
- 238000009501 film coating Methods 0.000 title 1
- 108010010803 Gelatin Proteins 0.000 claims abstract description 28
- 239000008273 gelatin Substances 0.000 claims abstract description 28
- 229920000159 gelatin Polymers 0.000 claims abstract description 28
- 235000019322 gelatine Nutrition 0.000 claims abstract description 28
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 28
- 229920000388 Polyphosphate Polymers 0.000 claims abstract description 7
- 239000001205 polyphosphate Substances 0.000 claims abstract description 7
- 235000011176 polyphosphates Nutrition 0.000 claims abstract description 7
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract description 10
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract description 10
- 238000010521 absorption reaction Methods 0.000 abstract description 9
- 239000000600 sorbitol Substances 0.000 abstract description 9
- 235000010356 sorbitol Nutrition 0.000 abstract description 9
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 abstract description 8
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 abstract description 8
- 235000010447 xylitol Nutrition 0.000 abstract description 8
- 239000000811 xylitol Substances 0.000 abstract description 8
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 abstract description 8
- 229960002675 xylitol Drugs 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 6
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 3
- 235000015110 jellies Nutrition 0.000 abstract description 3
- 239000008274 jelly Substances 0.000 abstract description 3
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 3
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 abstract description 2
- 238000004806 packaging method and process Methods 0.000 abstract description 2
- 229940005657 pyrophosphoric acid Drugs 0.000 abstract description 2
- 150000003839 salts Chemical class 0.000 abstract description 2
- 159000000000 sodium salts Chemical class 0.000 abstract description 2
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002932 luster Substances 0.000 abstract 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 235000019830 sodium polyphosphate Nutrition 0.000 description 11
- 229960002920 sorbitol Drugs 0.000 description 9
- 239000002775 capsule Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 238000010586 diagram Methods 0.000 description 5
- 239000007902 hard capsule Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 description 1
- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 description 1
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000576 food coloring agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 229960001855 mannitol Drugs 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は軟カプセル剤用ゼラチン皮膜に関し、詳しくは
軟カプセル剤の外殻として用いられる低吸湿性のゼラチ
ン皮膜に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a gelatin film for soft capsules, and more particularly to a gelatin film with low hygroscopicity used as an outer shell of soft capsules.
ここで言う軟カプセル剤とは、通常ゼラチンにグリセリ
ンやソルビトール等の可塑剤を配合して得られる軟化ゼ
ラチンから形成されるカプセル剤であり、例えば2枚の
軟化ゼラチンシートの間に充填物をはさみ込み、適当な
形に成形する方法、あるいは袋状の軟化ゼラチンシート
中に充填物を流し込んで適当な形に成形する方法によっ
て得られるものである。The soft capsules mentioned here are capsules formed from softened gelatin, which is usually obtained by blending gelatin with a plasticizer such as glycerin or sorbitol. It can be obtained by pouring the filling into a bag-like softened gelatin sheet and molding it into an appropriate shape.
従来の軟カプセル剤の外殻として利用されているゼラチ
ン皮膜はゼラチンを基剤とし、グリセリン、D−ソルビ
トール、ポリエチレングリコール等の可塑剤を添加して
構成されている。特にグリセリンを添加することによっ
て調製されるゼラチン皮膜はゼリー強度、接着力、粘性
等において非常にすぐれた特性を有するため、従来から
実用化されている軟カプセル外殻を構成しているゼラチ
ン皮膜の殆どすべてがグリセリンを含有している。The gelatin film used as the outer shell of conventional soft capsules is composed of gelatin as a base and a plasticizer such as glycerin, D-sorbitol, or polyethylene glycol added thereto. In particular, gelatin films prepared by adding glycerin have very excellent properties such as jelly strength, adhesive strength, and viscosity. Almost all contain glycerin.
近年、調剤作業の効率化を目的として各種の自動調剤機
が開発され、利用されつつある。又、特に老人への薬剤
投与の簡便性からUnit−dose−packagi
ngが利用されている。しかしながら通常の軟カプセル
剤をこれらの利用に供する場合、自動調剤機に対しては
すべり易さが、更にUnit−dose−packag
ingに対しては、付着性がそれぞれ使用性の障害とな
っている。In recent years, various automatic dispensing machines have been developed and are being used to improve the efficiency of dispensing operations. In addition, unit-dose-packages are used because of the ease of drug administration, especially to the elderly.
ng is used. However, when ordinary soft capsules are used for these purposes, they tend to be slippery for automatic dispensing machines, and the unit-dose-pack
For ing, adhesion is an obstacle to usability.
第1図には硬カプセル剤外殻と軟カプセル剤外殻につい
ての吸湿平衡図を示した。第1図から明らかな如く軟カ
プセル剤外殻は硬カプセル剤外殻に比較して、吸湿性が
明らかに高く、前述の各種障害は本性質に起因するもの
と考えられる。FIG. 1 shows moisture absorption equilibrium diagrams for hard capsule shells and soft capsule shells. As is clear from FIG. 1, the soft capsule shell has clearly higher hygroscopicity than the hard capsule shell, and the various problems described above are thought to be due to this property.
しかしながら、従来の軟カプセル剤外殻に関する特許は
、外殻溶解性に関するものが多く、吸湿防止に関するも
のはわずかであり、いまだ十分な効果が得られていない
。However, most of the conventional patents related to the outer shell of soft capsules are related to the solubility of the outer shell, and only a few are related to prevention of moisture absorption, so that sufficient effects have not yet been obtained.
上記の如く軟カプセル外殻は硬カプセル外殻に比べて吸
湿性が大きく、そのために自動調剤機やUnit−do
se−packagingへの適応に対して、すべりや
、癒着、付着の障害が発生し、これらの用途に軟カプセ
ル剤を利用するのが困難な状況に至っている。As mentioned above, the soft capsule shell has greater hygroscopicity than the hard capsule shell, and for this reason, it is difficult to use in automatic dispensing machines or unit-do
When applied to se-packaging, problems such as slippage, adhesion, and adhesion occur, making it difficult to use soft capsules for these applications.
〔問題点を解決するための手段〕
本発明者らは上記の如き軟カプセル剤外殻の問題点を解
決すべく鋭意研究の結果、本発明を完成するに到った。[Means for Solving the Problems] The present inventors have completed the present invention as a result of intensive research to solve the above-mentioned problems with the soft capsule shell.
即ち、本発明はポリリン酸塩を含有することを特徴とす
る軟カプセル剤用ゼラチン皮膜を提供するものである。That is, the present invention provides a gelatin film for soft capsules, which is characterized by containing a polyphosphate.
本発明に用いられるポリリン酸塩としては、ピロリン酸
、トリポリリン酸、テトラポリリン酸、ペンタポリリン
酸、ヘキサポリリン酸等の塩の単独又は混合物が挙げら
れ、ナトリウム塩が好ましい。ポリリン酸塩の含有量は
ゼラチンに対して0.2〜40重量%が好ましく、5〜
40重量%が更に好ましい。Examples of the polyphosphate used in the present invention include salts such as pyrophosphoric acid, tripolyphosphoric acid, tetrapolyphosphoric acid, pentapolyphosphoric acid, hexapolyphosphoric acid, etc. alone or in mixtures, and sodium salts are preferred. The content of polyphosphate is preferably 0.2 to 40% by weight, and 5 to 40% by weight based on gelatin.
40% by weight is more preferred.
本発明のゼラチン皮膜には、ゼラチン、ポリリン酸塩の
他に、キシリトール、ソルビトール、マンニトール、ポ
リエチレングリコール等ヲ配合することができる。これ
らの配合量はゼラチンに対して10〜50重量%が好ま
しい。In addition to gelatin and polyphosphate, xylitol, sorbitol, mannitol, polyethylene glycol, etc. can be added to the gelatin film of the present invention. The blending amount of these ingredients is preferably 10 to 50% by weight based on gelatin.
本発明の軟カプセル剤用ゼラチン皮膜は、低吸湿性で、
更に、ゼリー強度、接着力、粘性、光沢等の通常の軟カ
プセル剤外殻の具備している優れた性質を損なうことの
ない有用なゼラチン皮膜である。The gelatin film for soft capsules of the present invention has low hygroscopicity,
Furthermore, it is a useful gelatin film that does not impair the excellent properties of a normal soft capsule shell, such as jelly strength, adhesive strength, viscosity, and gloss.
以下に実施例をもって、本発明を更に詳細に説明するが
、本発明はこれらの実施例に限定されるものではない。The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to these Examples.
実施例1
あらかじめ40mZの水を入れたビーカー中にゼラチン
20gを入れ、吸水膨潤させた。ゼラチンが十分に吸水
膨潤した後、60℃に加温し、攪拌してゼラチンを均一
に溶解させた。更にあらかじめ市販のポリリン酸ナトリ
ウム1gに水4−を加えて溶解させたポリリン酸ナトリ
ウム水溶液を上記ゼラチン溶液中に加えて攪拌して均一
にした。このように調製したゼラチン組成物をガラス板
上に均一に流し込み、室温中で48時間乾燥させてゼラ
チン皮膜を得た。Example 1 20 g of gelatin was placed in a beaker containing 40 mZ water in advance and allowed to absorb water and swell. After the gelatin had sufficiently absorbed water and swelled, it was heated to 60° C. and stirred to uniformly dissolve the gelatin. Furthermore, an aqueous solution of sodium polyphosphate prepared by adding 4-4ml of water to 1 g of commercially available sodium polyphosphate was added to the gelatin solution and stirred to make it homogeneous. The gelatin composition thus prepared was uniformly poured onto a glass plate and dried at room temperature for 48 hours to obtain a gelatin film.
実施例2
1gのポリリン酸ナトリウムの代わりに1gのポリリン
酸ナトリウムと4gのソルビトールを用いた以外は実施
例1に準じてゼラチン皮膜を得た。Example 2 A gelatin film was obtained according to Example 1 except that 1 g of sodium polyphosphate and 4 g of sorbitol were used instead of 1 g of sodium polyphosphate.
実施例3
1gのポリリン酸ナトリウムの代わりにIgのポリリン
酸ナトリウムと4gのキシリトールを用いた以外は実施
例1に準じてゼラチン皮膜を得た。Example 3 A gelatin film was obtained according to Example 1, except that Ig sodium polyphosphate and 4 g xylitol were used instead of 1 g sodium polyphosphate.
実施例4
1gのポリリン酸ナトリウムの代わりに1gのポリリン
酸ナトリウムと2gのソルビトールと2gのキシリトー
ルを用いた以外は実施例1に準じてゼラチン卒膜を得た
。Example 4 A gelatin membrane was obtained according to Example 1 except that 1 g of sodium polyphosphate, 2 g of sorbitol, and 2 g of xylitol were used instead of 1 g of sodium polyphosphate.
実施例5
あらかじめ40m7の1%塩化ナトリウム溶液を入れた
ビーカーの中にゼラチン20gを入れ、吸水膨潤させた
。その後ソルビトール4g、市販のポリリン酸ナトリウ
ム1gを加え温浴(60℃)にて溶解させ、ガラス板上
に均一に流し込み、その後室温中で48時間乾燥させて
ゼラチン皮膜を得た。Example 5 20 g of gelatin was placed in a beaker containing 40 m7 of 1% sodium chloride solution in advance and allowed to absorb water and swell. Thereafter, 4 g of sorbitol and 1 g of commercially available sodium polyphosphate were added and dissolved in a hot bath (60° C.), poured uniformly onto a glass plate, and then dried at room temperature for 48 hours to obtain a gelatin film.
対照例1
あらかじめ40IIIlの水を入れたビーカー中にゼラ
チン20gを入れ、吸水膨潤させた。ゼラチンが十分に
吸水膨潤した後60℃に加温し、攪拌して、ゼラチン溶
液を均一に溶解させた。次に4gのグリセリン及び2g
のソルビトールを入れ透明になるまで十分に攪拌溶解し
た。その後ゼラチン組成液をガラス板上に均一に流し込
み、室温中で48時間乾燥させてゼラチン皮膜を得た。Control Example 1 20g of gelatin was placed in a beaker containing 40IIIl of water in advance and allowed to absorb water and swell. After the gelatin had sufficiently absorbed water and swelled, it was heated to 60° C. and stirred to uniformly dissolve the gelatin solution. Then 4g glycerin and 2g
Add sorbitol and stir thoroughly until it becomes transparent. Thereafter, the gelatin composition solution was uniformly poured onto a glass plate and dried at room temperature for 48 hours to obtain a gelatin film.
対照例2
あらかじめ20mZの水を入れたビーカーの中にゼラチ
ン20gを入れ、吸水膨潤させた。その後温浴(60℃
)にて溶解させ、ガラス板上に均一に流し込み、室温中
で48時間乾燥させてゼラチン皮膜を得た。Comparative Example 2 20 g of gelatin was placed in a beaker containing 20 mZ water in advance and allowed to absorb water and swell. Afterwards, take a warm bath (60℃)
), poured uniformly onto a glass plate, and dried at room temperature for 48 hours to obtain a gelatin film.
実験例1 (吸湿平衡)
実施例1〜4及び対照例1で得られたゼラチン皮膜の切
片を37℃各相対湿度下に2週間保存し、水分量の脱着
を調べた。Experimental Example 1 (Moisture Absorption Equilibrium) Sections of the gelatin films obtained in Examples 1 to 4 and Control Example 1 were stored at 37° C. under various relative humidity conditions for two weeks, and the desorption of water content was investigated.
その結果を第2図に示す。The results are shown in FIG.
実施例1〜4で得られた本発明品は対照例1で得られた
対照品に比べ相対湿度70%以上でも吸湿は軽度であり
、また切片同士の付着は対照品では相対湿度59%以上
で起こるが本発明品はいずれも相対湿度82%以上でし
か起こらず、優位に付着性が改善されている。Compared to the control product obtained in Control Example 1, the products of the present invention obtained in Examples 1 to 4 exhibit slight moisture absorption even at a relative humidity of 70% or higher, and the adhesion of sections to each other is less severe in the control product at a relative humidity of 59% or higher. However, this phenomenon occurs only at relative humidity of 82% or higher in all of the products of the present invention, and the adhesion properties are significantly improved.
実験例2(皮膜引張試験)
実施例1〜5及び対照例1〜2で得られたゼラチン皮膜
を巾1.5cmX長さ5 cmに裁断し、Mg(NO,
Ih・6H20飽和水溶液上(25℃xR,8,53%
)で調湿し有効試料長1cI11にて引張試験を行った
。Experimental Example 2 (Film Tensile Test) The gelatin films obtained in Examples 1 to 5 and Control Examples 1 to 2 were cut into pieces with a width of 1.5 cm and a length of 5 cm.
Ih 6H20 saturated aqueous solution (25℃ x R, 8,53%
), and a tensile test was conducted with an effective sample length of 1cI11.
その結果を第3図に示す。The results are shown in FIG.
第3図から明らかな如く、対照例2の皮膜ではヤング率
は高いが伸びが小さく、ひび割れを生じる可能性がある
。対照例1の皮膜はヤング率は低いが伸びが大きいため
ひび割れは生じないが変形しやすい。実施例1〜5で得
られた皮膜は皮膜として要求される硬くて粘り強く、大
きな伸びを示している。特に実施例3〜5の皮膜は良好
である。As is clear from FIG. 3, although the film of Comparative Example 2 has a high Young's modulus, its elongation is low and there is a possibility that cracks may occur. The film of Comparative Example 1 has a low Young's modulus but a high elongation, so it does not crack but is easily deformed. The films obtained in Examples 1 to 5 were hard and tenacious as required for films, and exhibited great elongation. In particular, the films of Examples 3 to 5 are good.
実験例3
実施例1〜5及び対照例1〜2で得られたゼラチン皮膜
を巾1.5CIIX長さ5(Jに裁断した切片を塩化ナ
トリウム飽和水溶液上(25℃XR,11゜75%)で
調湿し、有効試料長1cn+にて引張試験を行った。そ
の結果を第4図に示す。Experimental Example 3 Gelatin films obtained in Examples 1 to 5 and Control Examples 1 to 2 were cut into pieces with a width of 1.5 CIIX and a length of 5 (J) on a saturated sodium chloride aqueous solution (25°C XR, 11° 75%). A tensile test was conducted using an effective sample length of 1 cn+.The results are shown in FIG.
第4図から明らかな如く、対照例1の皮膜は降伏応力が
小さく変形しやすい。実施例1〜5の皮膜はいずれも対
照例1の皮膜より降伏応力が大きく変形しにくい。As is clear from FIG. 4, the film of Comparative Example 1 has a small yield stress and is easily deformed. The coatings of Examples 1 to 5 all have a larger yield stress than the coating of Control Example 1 and are less likely to deform.
実験例4
実施例2〜5及び対照例1〜2で得られたゼラチン皮膜
を巾1.5cmX長さ2.5 cmに裁断し、Mg (
NOり z・611□0飽和水溶液上(25℃XR,H
,53%)で調湿した。その後切片をステンレス板上に
置き、切片の上に種々の分銅を乗せて水平に引っばり、
動かすのに必要な引張応力を求めた。結果を第5図に示
す。Experimental Example 4 The gelatin films obtained in Examples 2 to 5 and Control Examples 1 to 2 were cut into 1.5 cm width x 2.5 cm length, and Mg (
NOri z・611□0 on saturated aqueous solution (25℃XR, H
, 53%). After that, the section was placed on a stainless steel plate, various weights were placed on top of the section, and the section was pulled horizontally.
The tensile stress required for movement was determined. The results are shown in Figure 5.
第5図のグラフの傾きからすべりの程度を求めると、実
施例2〜5は対照例1の従来の軟カプセルよりすべり性
が良く、対照例2の硬カプセルと同程度のすべり性を有
している。When the degree of slippage is determined from the slope of the graph in FIG. 5, Examples 2 to 5 have better slipperiness than the conventional soft capsule of Comparative Example 1, and have the same slipperiness as the hard capsule of Comparative Example 2. ing.
く軟カプセル製剤の試作例〉
試作例1
エチルパラベン60g、メチルパラベン20g1キシリ
トール4kg、ポリリン酸ナトリウム1 kgに水40
kgを加えて溶解させた後、ゼラチン20kgを加えて
膨潤させ60℃で溶解させた。その後酸化チタン200
g、食用色素6gを加えて分散させ、皮膜液調製を行
った。内容液にはゴマ油を用い、ロータリ一式自動機に
より軟カプセル剤を得た。Prototype example of soft capsule formulation> Prototype example 1 60g of ethylparaben, 20g of methylparaben, 4kg of xylitol, 1kg of sodium polyphosphate, 40g of water
After adding 20 kg of gelatin and dissolving it, 20 kg of gelatin was added to swell and dissolve at 60°C. Then titanium oxide 200
g, and 6 g of food coloring were added and dispersed to prepare a coating liquid. Sesame oil was used as the content liquid, and soft capsules were obtained using a rotary automatic machine.
試作例2
キシリトール4 kgのかわりにキシリトール2kgと
ソルビトール液(70%)2kgを用いた以外は試作例
1に準じて軟カプセル剤を得た。Prototype Example 2 Soft capsules were obtained according to Prototype Example 1, except that 2 kg of xylitol and 2 kg of sorbitol liquid (70%) were used instead of 4 kg of xylitol.
試作対照例1
キシリトール4 kg、ポリリン酸ナトリウム1−の代
わりにグリセリン4kg、ソルビトール液(70%)2
kgを用いた以外は試作例1に準じて軟カプセル剤を得
た。Prototype control example 1 xylitol 4 kg, glycerin 4 kg instead of sodium polyphosphate 1-, sorbitol solution (70%) 2
Soft capsules were obtained according to Prototype Example 1, except that 1 kg was used.
試作例1.2で得られたカプセルは接着力もよく、外観
(つや)も良好であった。吸湿平衡をみると試作例1.
2のカプセルは試作対照例1のカプセルよりも低吸湿性
であった(第6図参照)。又、相対湿度75%(温度4
0℃)条件下で1力月間保存したところ試作対照例1の
カプセルはブロッキングを起こしたが試作例1.2のカ
プセルはプロ7キングを起こさず良好であり皮膜試験で
も何ら問題はなかった。The capsules obtained in Prototype Example 1.2 had good adhesive strength and good appearance (gloss). Looking at moisture absorption equilibrium, prototype example 1.
Capsules No. 2 had lower hygroscopicity than the capsules of Prototype Control Example 1 (see Figure 6). Also, relative humidity 75% (temperature 4
When stored for one month under conditions (0°C), the capsules of Prototype Control Example 1 suffered from blocking, but the capsules of Prototype Example 1.2 did not cause Pro7 King and showed no problems in the film test.
第1図は硬カプセル剤外殻と軟カプセル剤外殻について
の吸湿平衡図、第2図は実験例1の結果を示す図、第3
図は実験例2の結果を示す図、第4図は実験例3の結果
を示す図、第5図は実験例4の結果を示す図、第6図は
試作例1〜2及び試作対照例1で得られた軟カプセル剤
の吸湿平衡図である。Figure 1 is a moisture absorption equilibrium diagram for hard capsule shells and soft capsule shells, Figure 2 is a diagram showing the results of Experimental Example 1, and Figure 3 is a diagram showing the results of Experimental Example 1.
The figure shows the results of Experimental Example 2, Fig. 4 shows the results of Experimental Example 3, Fig. 5 shows the results of Experimental Example 4, and Fig. 6 shows the results of Experimental Examples 1 and 2 and the prototype control example. 1 is a moisture absorption balance diagram of the soft capsule obtained in 1.
Claims (1)
ル剤用ゼラチン皮膜。 2、ポリリン酸塩の含有量がゼラチンに対して0.2〜
40重量%である特許請求の範囲第1項記載のゼラチン
皮膜。[Scope of Claims] 1. A gelatin film for soft capsules, characterized by containing a polyphosphate. 2. The content of polyphosphate is 0.2 to gelatin
The gelatin film according to claim 1, which has a content of 40% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9478187A JPS63264519A (en) | 1987-04-17 | 1987-04-17 | Gelatin film coating for soft capsule |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9478187A JPS63264519A (en) | 1987-04-17 | 1987-04-17 | Gelatin film coating for soft capsule |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63264519A true JPS63264519A (en) | 1988-11-01 |
Family
ID=14119630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9478187A Pending JPS63264519A (en) | 1987-04-17 | 1987-04-17 | Gelatin film coating for soft capsule |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63264519A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1254935A3 (en) * | 2001-05-02 | 2002-12-04 | Degussa Health & Nutrition Holding France SAS | Gelatins with good slipping properties, processes for their preparation and their uses |
JP2004331510A (en) * | 2003-04-30 | 2004-11-25 | Sansho Pharmaceutical Co Ltd | Capsule |
-
1987
- 1987-04-17 JP JP9478187A patent/JPS63264519A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1254935A3 (en) * | 2001-05-02 | 2002-12-04 | Degussa Health & Nutrition Holding France SAS | Gelatins with good slipping properties, processes for their preparation and their uses |
JP2004331510A (en) * | 2003-04-30 | 2004-11-25 | Sansho Pharmaceutical Co Ltd | Capsule |
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