JP4279361B2 - Hydrogel base for skin application - Google Patents
Hydrogel base for skin application Download PDFInfo
- Publication number
- JP4279361B2 JP4279361B2 JP09663595A JP9663595A JP4279361B2 JP 4279361 B2 JP4279361 B2 JP 4279361B2 JP 09663595 A JP09663595 A JP 09663595A JP 9663595 A JP9663595 A JP 9663595A JP 4279361 B2 JP4279361 B2 JP 4279361B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- glucomannan
- base
- hydrogel
- locust bean
- 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.)
- Expired - Lifetime
Links
Description
【0001】
【産業上の利用分野】
この発明は、含水ゲル基剤に関するものである。
【0002】
【従来の技術】
従来より寒天ゲル、カラギーナン、アルギン酸ナトリウム、ゼラチンなどの天然物ゲルが知られているが、その高い含水性に着目し、対象物の保湿・保冷(例えば湿布の用途など)に用いようと試みた。しかし、これらの天然物ゲルは非常に脆いものであり、保型性に乏しいという問題があった。
【0003】
一方、同様に天然物ゲルであるグルコマンナンは、強アルカリ性領域に維持した場合は、型崩れが生じにくく安定で保型性を有する。しかし、人の肌は弱酸性領域にある方が好ましいので、湿布としての用途などには不具合であるという問題があった。
【0004】
【発明が解決しようとする課題】
そこで、この発明は、弱酸性領域においても型崩れが生じにくく安定な含水ゲル基剤を提供しようとするものである。
【0005】
【課題を解決するための手段】
前記課題を解決すべく鋭意検討した結果、グルコマンナンに、ローカストビーンガムやカラギーナンなどの高分子を添加して含水ゲル基剤を構成することにより、弱酸性領域においても型崩れが生じにくく安定となることを見出しこの発明を完成するに到った。
【0006】
請求項1記載の発明の含水ゲル基剤はグルコマンナンとローカストビーンガムとを有効成分として含有するが、ローカストビーンガムは離水防止剤として機能するとともに、弱酸性領域においてもグルコマンナンの型崩れが生じにくく安定に維持させることができる。なお、ローカストビーンガムの含有量が、約0.1重量%未満とすると保型性を維持でき難いという不具合が生ずる場合があり、約5.0重量%を越えると硬すぎてゲル状になり難いという不具合が生ずる場合がある。
【0007】
また、グルコマンナンの含有量が、約0.1重量%未満とすると保型性不足という不具合が生ずる場合があり、約5.0重量%を越えると透明性や弾力性に乏しいという不具合が生ずる場合がある。
【0008】
【発明の効果】
この発明は上述のような構成であり、次の効果を有する。
【0009】
弱酸性領域においても型崩れが生じにくく安定な含水ゲル基剤を提供することができる。
【0010】
【実施例】
以下、この発明の構成を実施例により説明する。
【0011】
この実施例の含水ゲル基剤は、グルコマンナン並びにローカストビーンガムを有効成分として含有する。前記グルコマンナンはグルコースとマンノースとが約7:3から成る中性複合多糖であり、こんにゃくの元の物質である。
【0012】
各実施例に於ける配合量の割合を、表1及び表2に示す。表中示されるように、グルコマンナンは約0.1〜5.0重量%、ローカストビーンガムは約0.1〜5.0重量%配合しており、この程度の配合量の範囲内が含水ゲル基剤が安定化し易く好ましい。また、グルコマンナンを用いていない比較例の配合量の割合を、表5に示す。
【0013】
なお、保水性物質として濃グリセリン、カルボキシメチルセルロース(CMC)、ゼラチン、アルギン酸カルシウムなどを約5〜20重量%配合することができる。これは離水防止のための保湿剤として機能し、ゲル強度を出すことができる。
【0014】
また、防腐剤としてパラベンなどを少量例えば約0.1重量%以下程度配合することができる。粘着性付与剤としてPEG,PVAなどを例えば約5.0重量%以下程度配合することができる。香料としてl−メントールを例えば約5.0重量%以下程度配合することができる。その他、清涼剤としてカンフルを少量例えば約5.0重量%以下程度配合することができる。そして、残量の殆どは水である。
【0015】
次に、この含水ゲル基剤の製造方法を説明する。先ず濃グリセリンを約60℃に加温しながら、グルコマンナンとローカストビーンガム及びカラギーナンの全量を徐々に加えていく。次に、蒸留水をダマ(ゲル状の塊)ができない程度に、その全体の配合量の約50%位まで徐々に加える。そして、配合する他の成分を順次加えていき、最後に蒸留水を所定の配合量に至るまで加える。なお、これらの手順中は常に攪拌する。ダマがないことを確認してから、これを速やかに型に流し込み徐冷して固化させた後、型から外すと完成した含水ゲル基剤が得られる。
【0016】
グルコマンナンは保型剤として機能し、この含水ゲル基剤は保型性、柔軟性、弾力性、付着性、保水性、放湿性、透明性等に優れるという利点がある。また、弱酸性領域でもそのゲル強度が経時的に安定している。
【0017】
この含水ゲル基剤を皮膚に貼付した場合、そのpHは弱酸性領域にあるので皮膚に対する刺激が少なく好ましい。また、皮膚への付着性もよく快適な状態で長時間冷却することができた。
【0018】
この実施例の含水ゲル基剤を官能試験により評価した。評価は次の項目・方法によった。
【0019】
保型性は含水ゲル基剤の製造の際、脱型時にその形状が保持されているかどうかにより、柔軟性は含水ゲル基剤が硬くなく皮膚にフィットし得るかどうかにより、弾力性は含水ゲル基剤を押すと復元してくるかどうかにより、付着性は皮膚や物体に付着し易いかどうかにより、保水性は含水ゲル基剤が24時間保水されており離水しないかどうかにより、透明性は濁りがないかどうかにより判断評価した。各実施例の結果を表3及び表4に、各比較例の結果を表5に示す。
【0020】
これらの各評価項目に対し、表中◎は「良好」、○は「良」、△は「悪い」、×は「非常に悪い」という評価結果を示している。
【0021】
表に示される通り、各実施例のものは各比較例のものと比べて保型性に優れており、型崩れが生じにくく安定である。
【0022】
【表1】
【0023】
【表2】
【0024】
【表3】
【0025】
【表4】
【0026】
【表5】
[0001]
[Industrial application fields]
The present invention relates to a hydrogel base.
[0002]
[Prior art]
Conventionally, natural gels such as agar gel, carrageenan, sodium alginate, and gelatin are known. However, focusing on their high water content, we tried to use it for the purpose of keeping the object moist and cold (for example, in the application of a compress). . However, these natural product gels are very brittle and have a problem of poor shape retention.
[0003]
On the other hand, similarly, glucomannan, which is a natural product gel, is stable and retains its shape when it is maintained in a strong alkaline region. However, since it is preferable that the human skin is in a weakly acidic region, there is a problem in that it is defective for use as a poultice.
[0004]
[Problems to be solved by the invention]
Accordingly, the present invention is intended to provide a stable water-containing gel base shapeless also hardly occurs in the weakly acidic region.
[0005]
[Means for Solving the Problems]
As a result of diligent investigation to solve the above problems, by adding a polymer such as locust bean gum or carrageenan to glucomannan, and forming a hydrous gel base, it is stable and hardly loses its shape even in weakly acidic regions. As a result, the present invention has been completed.
[0006]
Hydrogel base of the invention of claim 1, wherein the containing as an active ingredient and glucomannan and locust bean gum, but with locust bean gum functions as inhibitor syneresis, the shapeless glucomannan even in the weakly acidic region It is hard to occur and can be maintained stably. In addition, when the content of locust bean gum is less than about 0.1% by weight, it may be difficult to maintain the shape retention, and when it exceeds about 5.0% by weight, it becomes too hard and becomes a gel. There may be a problem that it is difficult.
[0007]
Further, if the content of glucomannan is less than about 0.1% by weight, there may be a problem that the shape retention is insufficient, and if it exceeds about 5.0% by weight, there is a problem that the transparency and elasticity are poor. There is a case.
[0008]
【The invention's effect】
The present invention is configured as described above and has the following effects.
[0009]
It is possible to provide a stable water-containing gel base that does not easily lose its shape even in a weakly acidic region.
[0010]
【Example】
The configuration of the present invention will be described below with reference to examples.
[0011]
Hydrogel base in this example, contains glucomannan and locust bean gum as an active ingredient. The glucomannan is a neutral complex polysaccharide composed of about 7: 3 glucose and mannose, and is the original substance of konjac.
[0012]
Tables 1 and 2 show the proportions of the blending amounts in each Example. As shown in Table, Glucomannan about 0.1 to 5.0 wt%, locust bean gum are blended about 0.1 to 5.0 wt%, the range of the amount of the extent water A gel base is preferable because it is easy to stabilize. In addition, Table 5 shows the ratio of the amount of the comparative example that does not use glucomannan.
[0013]
Concentrated glycerin, carboxymethylcellulose (CMC), gelatin, calcium alginate and the like can be blended in an amount of about 5 to 20% by weight as a water retention substance. This functions as a moisturizing agent for preventing water separation and can provide gel strength.
[0014]
Further, a small amount of paraben or the like, for example, about 0.1% by weight or less can be blended as a preservative. As a tackifier, PEG, PVA, etc. can be blended, for example, at about 5.0% by weight or less. For example, about 5.0% by weight or less of l-menthol can be blended as a fragrance. In addition, a small amount of camphor, for example, about 5.0% by weight or less can be blended as a refreshing agent. And most of the remaining amount is water.
[0015]
Next, the manufacturing method of this hydrogel base is demonstrated . First, the whole amount of glucomannan, locust bean gum and carrageenan is gradually added while heating concentrated glycerin to about 60 ° C. Next, distilled water is gradually added to the extent that about 50% of the total amount is added to such an extent that no lumps (gel-like lumps) are formed. Then, other components to be blended are added sequentially, and finally distilled water is added until a predetermined blending amount is reached. During these procedures, always stir. Make sure there are no lumps, after which the solidified promptly cooled slowly poured into a mold, the water-containing gel base was completed and removed from the mold is obtained.
[0016]
Glucomannan functions as a shape-retaining agent, and this water-containing gel base has the advantage of being excellent in shape retention, flexibility, elasticity, adhesion, water retention, moisture release, transparency and the like. Moreover, the gel strength is stable over time even in a weakly acidic region.
[0017]
When this hydrogel base is affixed to the skin, its pH is in a weakly acidic region, so that there is less irritation to the skin, which is preferable. Moreover, it was able to cool for a long time in a comfortable state with good adhesion to the skin.
[0018]
The water-containing gel base of this example was evaluated by a sensory test. Evaluation was based on the following items and methods.
[0019]
The production of shape retention hydrous gel base, depending on whether its shape during demolding is held, flexibility depending on whether hydrogel bases may fit to the skin without stiff, resilient hydrogel depending on whether coming restored by pressing base, depending on whether adhesion is liable to adhere to the skin and body, water retention by whether hydrogel base is not syneresis are 24 hours water retention, transparency Judgment was made based on whether there was turbidity. The results of each example are shown in Tables 3 and 4, and the results of each comparative example are shown in Table 5.
[0020]
For each of these evaluation items, “◎” in the table indicates evaluation results of “good”, “◯” indicates “good”, Δ indicates “bad”, and × indicates “very bad”.
[0021]
As shown in the table, each of the examples is superior in shape retention as compared with each of the comparative examples, and is not easily deformed and is stable.
[0022]
[Table 1]
[0023]
[Table 2]
[0024]
[Table 3]
[0025]
[Table 4]
[0026]
[Table 5]
Claims (3)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP09663595A JP4279361B2 (en) | 1995-04-21 | 1995-04-21 | Hydrogel base for skin application |
JP2006154075A JP4955310B2 (en) | 1995-04-21 | 2006-06-01 | Skin patch |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP09663595A JP4279361B2 (en) | 1995-04-21 | 1995-04-21 | Hydrogel base for skin application |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006154075A Division JP4955310B2 (en) | 1995-04-21 | 2006-06-01 | Skin patch |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH08290051A JPH08290051A (en) | 1996-11-05 |
JP4279361B2 true JP4279361B2 (en) | 2009-06-17 |
Family
ID=14170300
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP09663595A Expired - Lifetime JP4279361B2 (en) | 1995-04-21 | 1995-04-21 | Hydrogel base for skin application |
Country Status (1)
Country | Link |
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JP (1) | JP4279361B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004231516A (en) * | 2001-12-13 | 2004-08-19 | Daiya Seiyaku Kk | External gel-like composition, pad material and pad material to be filled in blister container |
KR100506543B1 (en) | 2003-08-14 | 2005-08-05 | 주식회사 제닉 | Temperature Sensitive State-Changing Hydrogel Composition and Method for their Preparation |
KR100864541B1 (en) * | 2007-06-15 | 2008-10-21 | 주식회사 제닉 | Phase-change hydrogel composition and method for use of the same |
WO2012133409A1 (en) | 2011-03-28 | 2012-10-04 | 株式会社 資生堂 | Externally used drug kit |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55148064A (en) * | 1979-04-11 | 1980-11-18 | Mars Ltd | Edible substance |
JPS62129052A (en) * | 1985-11-29 | 1987-06-11 | ユニコロイド株式会社 | Wound covering material |
JPS6379572A (en) * | 1986-09-22 | 1988-04-09 | Nitto Shokuhin Seizo Kk | Preparation of frozen 'konjak' |
JPH0576519A (en) * | 1991-09-20 | 1993-03-30 | Arakawa Chem Ind Co Ltd | Auxiliary sheet for nmr diagnosis |
JPH05163384A (en) * | 1991-12-12 | 1993-06-29 | Asahi Chem Ind Co Ltd | Material for contact lens |
WO1994002029A1 (en) * | 1992-07-23 | 1994-02-03 | Fmc Corporation | Glucomannan spongeous matrices |
-
1995
- 1995-04-21 JP JP09663595A patent/JP4279361B2/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55148064A (en) * | 1979-04-11 | 1980-11-18 | Mars Ltd | Edible substance |
JPS62129052A (en) * | 1985-11-29 | 1987-06-11 | ユニコロイド株式会社 | Wound covering material |
JPS6379572A (en) * | 1986-09-22 | 1988-04-09 | Nitto Shokuhin Seizo Kk | Preparation of frozen 'konjak' |
JPH0576519A (en) * | 1991-09-20 | 1993-03-30 | Arakawa Chem Ind Co Ltd | Auxiliary sheet for nmr diagnosis |
JPH05163384A (en) * | 1991-12-12 | 1993-06-29 | Asahi Chem Ind Co Ltd | Material for contact lens |
WO1994002029A1 (en) * | 1992-07-23 | 1994-02-03 | Fmc Corporation | Glucomannan spongeous matrices |
Also Published As
Publication number | Publication date |
---|---|
JPH08290051A (en) | 1996-11-05 |
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