JP2599415B2 - Chitosan gel composition and method for producing the same - Google Patents
Chitosan gel composition and method for producing the sameInfo
- Publication number
- JP2599415B2 JP2599415B2 JP63043068A JP4306888A JP2599415B2 JP 2599415 B2 JP2599415 B2 JP 2599415B2 JP 63043068 A JP63043068 A JP 63043068A JP 4306888 A JP4306888 A JP 4306888A JP 2599415 B2 JP2599415 B2 JP 2599415B2
- Authority
- JP
- Japan
- Prior art keywords
- chitosan
- gel composition
- wood vinegar
- chitosan gel
- producing
- 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
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- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- General Preparation And Processing Of Foods (AREA)
- Jellies, Jams, And Syrups (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、キトサンゲル組成物に関し、特にキトサン
と木酢液とから成るキトサンゲル組成物及びその製造方
法に関する。Description: TECHNICAL FIELD The present invention relates to a chitosan gel composition, and more particularly to a chitosan gel composition comprising chitosan and wood vinegar and a method for producing the same.
(従来の技術) キチン(β−1,4−ポリ−N−アセチルグルコサミ
ン)は、カニ、エビなどの甲殻類、昆虫、きのこ及び微
生物の細胞壁に存在しており、年間1000億トン(推定)
も生物生産され、セルロースについで多く自然界に存在
する天然高分子である。(Prior Art) Chitin (β-1,4-poly-N-acetylglucosamine) is present in the cell walls of crustaceans such as crabs and shrimps, insects, mushrooms and microorganisms, and has an estimated 100 billion tons per year.
Is a natural macromolecule that is also produced biologically and exists in nature next to cellulose.
キトサン(chitosan)は、このキチンを濃アルカリで
処理することによって得られるキチンの脱アセチル化物
であり、グルコサミン(2−アミノ−D−グルコース)
からなる下記の一般式からなる塩基性多糖類である。Chitosan is a deacetylated product of chitin obtained by treating this chitin with a concentrated alkali, and glucosamine (2-amino-D-glucose).
Which is a basic polysaccharide having the following general formula:
近年、未利用資源の有効利用についての研究が盛んに
なるにつれ、キチン、キトサンについても研究がなさ
れ、多くの報告がなされている。例えば、キトサンが植
物病原性のカビの生育に対して影響を及ぼすこと〔スト
エッセル等、フィットパソロギッシュ ツアイトシュリ
フト(Stoessel et al.,“Phytopathologische Zeitsch
rift")、第111巻、第82〜89頁(1984年)〕、キトサン
が細菌の生育の及び増殖に効果のあること(特開昭62−
83877号)などの報告がある。 In recent years, as research on the effective use of unused resources has become active, studies have been made on chitin and chitosan, and many reports have been made. For example, the effect of chitosan on the growth of phytopathogenic fungi [Stoessel et al., Stoessel et al., “Phytopathologische Zeitsch
rift "), Vol. 111, pp. 82-89 (1984)], that chitosan is effective for the growth and growth of bacteria (Japanese Patent Application Laid-Open No. Sho 62-62).
No. 83877).
また、キトサンのゲル化に関しても幾つかの報告がさ
れており、この中でキトサンゲルの利用法として、平
野、「別冊フードケミカル」,1,1(1987年)には、機能
性低食品素材、栄養素、酵素、有効微生物などの固定化
担体、或いは食品形成材として有用であることが報告さ
れている。Some reports have also been made on the gelation of chitosan. Among them, the use of chitosan gel is described in Hirano, "Supplied Food Chemicals", 1, 1 (1987), as a functional low-food material. It is reported to be useful as an immobilized carrier for nutrients, enzymes, effective microorganisms and the like, or as a food-forming material.
さらに、キトサンゲルの製法については、キチンゲル
とする方法〔平野等、「バイオポリマー(Biopolyme
r)」、第15巻、第1685頁(1976年)〕、及びその方法
に従ってN−プロピオニル、N−ヘキサノイル、N−オ
クタノイル、N−デカノイル、N−ラウロイル、N−ベ
ンゾイルキトサンゲルを調製する方法が開示されている
〔平野等、“Carbohyd.Res.",47,315(1976);平野
等、“Agric.Biol.Chem.",39,1335(1975);平野等、
“Agric.Biol.Chem.",41,1547(1977);平野等、“8th
International Symposium on Carbohydrate Chemistr
y",Kyoto,August 16−20(1976)Abst.p.766〕。Further, regarding the method for producing chitosan gel, a method for preparing chitin gel [Hirano et al., “Biopolymer (Biopolyme
r), Vol. 15, p. 1685 (1976)], and a method for preparing N-propionyl, N-hexanoyl, N-octanoyl, N-decanoyl, N-lauroyl, N-benzoyl chitosan gel according to the method. [Hirano et al., "Carbohyd. Res.", 47,315 (1976); Hirano et al., "Agric. Biol. Chem.", 39, 1335 (1975); Hirano et al.
"Agric. Biol. Chem.", 41, 1547 (1977); Hirano et al., "8th.
International Symposium on Carbohydrate Chemistr
y ", Kyoto, August 16-20 (1976) Abst. p. 766].
また、キトサンを酢酸に溶解した後ホルマリンを加え
て放置することでゲル化させる方法〔平野等、“Agric.
Biol.Chem.",41,1547(1977)〕、或いは同様の方法で
グルタルアルデヒドゲルを製造する方法が開示されてい
る。(発明が解決しようとする問題点) 上記したように、キトサンは天然に多量に存在するキ
チンを脱アセチル化して得られる塩基性多糖類であるの
で、そのゲル化したキトサンゲルが、食品、化粧品、或
いは薬品素材として利用できれば、製造コストなどの面
から有利である。Also, a method of gelling by dissolving chitosan in acetic acid, adding formalin and allowing to stand (Hirano et al., “Agric.
Biol. Chem. ", 41, 1547 (1977)] or a method for producing a glutaraldehyde gel by a similar method. (Problems to be Solved by the Invention) As described above, chitosan is a natural product. Since it is a basic polysaccharide obtained by deacetylating chitin that is present in a large amount in water, if the gelled chitosan gel can be used as a food, cosmetic, or drug material, it is advantageous in terms of production costs and the like.
しかしながら、上記した従来の方法のキトサンゲル調
製方法によれば、その製造工程において、食品、化粧
品、或いは薬品素材として好ましくない、例えばホルマ
リンなどを使用するため、上記した食品、化粧品、或い
は薬品素材として利用するには、安全性の点で問題があ
った。However, according to the chitosan gel preparation method of the conventional method described above, in the manufacturing process, food, cosmetics, or undesired as a drug material, for example, because formalin is used, the above-mentioned food, cosmetics, or drug material as There was a problem in terms of security when using it.
従って、食品添加物として認可されているもの、化粧
品として認可されているもの、或いは薬品素材として認
可されているもので、キトサンをゲル化できれば好都合
である。Therefore, it is convenient to be able to gel chitosan, which is approved as a food additive, approved as cosmetics, or approved as a drug material.
(問題点を解決するための手段) 本発明は上述の問題点に鑑がみ発明がなされたもので
あり、本発明者等は、キトサンを木酢液、特に食品添加
物、化粧品、或いは薬品素材として認可されている木酢
液に溶解させることにより、容易にキトサンがゲル化す
ることを見出し本発明を完成したものである。(Means for Solving the Problems) The present invention has been made in view of the above-mentioned problems, and the present inventors have made chitosan a wood vinegar solution, particularly a food additive, a cosmetic, or a chemical material. It has been found that chitosan can be easily gelled by dissolving it in a wood vinegar solution that has been approved as the present invention, thereby completing the present invention.
すなわち、本発明のキトサンゲル組成物は、キトサン
を木酢液中に加え溶解した後、所定の時間、所定温度で
放置することにより、溶解物をゲル化させて得られる、
キトサンと木酢液とから成るキトサンゲル組成物であ
る。That is, the chitosan gel composition of the present invention is obtained by dissolving chitosan in a wood vinegar solution, leaving it at a predetermined temperature for a predetermined time, and gelling the dissolved substance,
It is a chitosan gel composition comprising chitosan and wood vinegar.
本発明に使用するキトサンとしては、好ましくはその
脱アセチル化度が、60%以上のものを使用するが、脱ア
サチル化度が60%未満のものを使用し木酢液に溶解した
場合には、不溶物を生じてしまうので好ましくないから
である。The chitosan used in the present invention preferably has a degree of deacetylation of 60% or more, and when the degree of deacetylation is less than 60% and is dissolved in wood vinegar, This is because it is not preferable because insolubles are generated.
また、使用する木酢液としてはいずれも使用可能であ
るが、好ましくは、食品添加物、化粧品、或いは薬品素
材として認可されているもの(好ましくは有機酸を、酢
酸として定量した場合に約3〜10%含み、pHが約1.0〜
3.0であるもの)を用い、好ましくは20〜100%木酢液を
含む水溶液として用いるのが有利である(下記参考例参
照)。Any of the wood vinegar liquids used can be used, but preferably, those approved as food additives, cosmetics, or drug materials (preferably, about 3 to about 3 to about 3% when organic acids are quantified as acetic acid). Contains 10%, pH is about 1.0 ~
3.0), and is advantageously used as an aqueous solution containing 20 to 100% wood vinegar (see Reference Example below).
上記のように調製したキトサンを木酢液に加えて、室
温にて、好ましくは2時間以上攪拌溶解を行い、その
後、室温にて、所定時間静置すれば、褐色のキトサンゲ
ル組成物が得られる。The chitosan prepared as described above is added to the wood vinegar solution, and the mixture is stirred and dissolved at room temperature, preferably for 2 hours or longer, and then left at room temperature for a predetermined time to obtain a brown chitosan gel composition. .
参考例(キトサンゲル化に及ぼすキトサンと木酢液との
割合) 0.5g、1g、2g、3g、4g、5g、6gのキトサン(脱アセチ
ル化度90%)をそれぞれ、木酢液(「香味煙SF 2」;東
海化成株式会社製)99.5g、99g、98g、97g、96g、95g、
94g(原液〜10倍希釈)に加えて、室温にて、約2時間
攪拌溶解を行い、その後、室温にて、22時間静置してキ
トサンのゲル化実験を行った。その結果を下記の表に示
した。ただし、ゲル化の判断は目視にて行った。Reference Example (Ratio of chitosan and wood vinegar effect on chitosan gelation) 0.5 g, 1 g, 2 g, 3 g, 4 g, 5 g, and 6 g of chitosan (degree of deacetylation 90%) were each added to wood vinegar solution ("Flavour Smoke SF 2 "; manufactured by Tokai Chemical Co., Ltd.) 99.5 g, 99 g, 98 g, 97 g, 96 g, 95 g,
In addition to 94 g (stock solution to 10-fold dilution), the mixture was stirred and dissolved at room temperature for about 2 hours, and then allowed to stand at room temperature for 22 hours to conduct a gelation experiment of chitosan. The results are shown in the table below. However, gelation was judged visually.
実施例1 キトサン(ヤエガキ醗酵技研株式会社製;脱アセチル
化度90%)3gを、200ml容のビーカーに入れた木酢液
(「香味煙SF 2」、東海化成株式会社製)の原液97gに
加えた後、室温にて攪拌溶解させ、その後室温にて5時
間静置すると、褐色のキトサンゲル98.2gが得られた。 Example 1 3 g of chitosan (manufactured by Yaegaki Fermentation Giken Co., Ltd .; degree of deacetylation: 90%) was added to 97 g of a stock solution of wood vinegar ("Flavored Smoke SF2", manufactured by Tokai Kasei Co., Ltd.) in a 200 ml beaker. Thereafter, the mixture was stirred and dissolved at room temperature, and then allowed to stand at room temperature for 5 hours to obtain 98.2 g of a brown chitosan gel.
実施例2 キトサン(ヤエガキ醗酵技研株式会社製;脱アセチル化
度70%)2gを、200ml容のビーカーに入れた木酢液
(「香味煙SF 2」、東海化成株式会社製)の2倍希釈液
98gに加えた後、室温にて攪拌溶解させ、その後室温に
て20時間静置すると、褐色のキトサンゲル98.4gが得ら
れた。Example 2 A 2-fold dilution of wood vinegar ("Flavour Smoke SF2", manufactured by Tokai Kasei Co., Ltd.) in which 2 g of chitosan (manufactured by Yaegaki Fermentation Giken Co., Ltd .; deacetylation degree: 70%) was placed in a 200 ml beaker.
After addition to 98 g, the mixture was stirred and dissolved at room temperature, and then allowed to stand at room temperature for 20 hours to obtain 98.4 g of brown chitosan gel.
(効果) 本発明によるキトサンゲル組成物は、キトサンと、木
酢液、特に食品添加物、化粧品、或いは薬品素材として
認可されえいる木酢液とから成り、且つキトサンは天然
に多量に存在する物質であるキチンより得られるもので
あるので、食品、化粧品、或いは薬品素材として鑑がみ
れば、安全性及び製造コストなどの面からもきわめて優
れたものである。(Effect) The chitosan gel composition according to the present invention comprises chitosan and wood vinegar, especially wood vinegar which has been approved as a food additive, cosmetic or chemical material, and chitosan is a naturally occurring substance present in a large amount. Since it is obtained from a certain chitin, it is extremely excellent in terms of safety, production cost, and the like when considered as a food, cosmetic, or drug material.
さらに、本発明のキトサンゲル組成物は、上記食品、
化粧品、或いは薬品素材としてだけでなく、例えば微生
物などの培養培地などとしても利用が考えられるなど利
用分野の広い優れた組成物である。Further, the chitosan gel composition of the present invention, the food,
It is an excellent composition with a wide range of applications, such as being considered not only as a cosmetic or pharmaceutical material, but also as a culture medium for microorganisms, for example.
また、本発明のキトサンゲル組成物の製造方法によれ
ば、天然に多量に存在する物質であるキチンより得られ
るキトサンを木酢液、特に食品添加物、化粧品、或いは
薬品素材として認可されている木酢液に溶解し放置する
だけで、キトサンと木酢酸とから成るキトサンゲル組成
物が得られるので、簡単で且つ製造コストも低く工業的
生産に供し得る優れた製造方法である。In addition, according to the method for producing a chitosan gel composition of the present invention, chitosan obtained from chitin, which is a naturally occurring substance, is a wood vinegar solution, particularly a food additive, cosmetics, or wood vinegar that has been approved as a drug material. Since a chitosan gel composition composed of chitosan and wood acetic acid can be obtained simply by dissolving in a liquid and allowing it to stand, this is an excellent production method that is simple, has low production cost, and can be used for industrial production.
Claims (2)
組成物。1. A chitosan gel composition comprising chitosan and wood vinegar.
定の時間、所定温度で放置することにより、溶解物をゲ
ル化させて、キトサンと木酢液とから成るキトサンゲル
組成物を得ることを特徴とするキトサンゲル組成物の製
造方法。2. A chitosan gel composition comprising chitosan and wood vinegar is obtained by adding chitosan to a wood vinegar solution and dissolving it, and then leaving the mixture to stand for a predetermined time at a predetermined temperature to gel the dissolved substance. A method for producing a chitosan gel composition, comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63043068A JP2599415B2 (en) | 1988-02-24 | 1988-02-24 | Chitosan gel composition and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63043068A JP2599415B2 (en) | 1988-02-24 | 1988-02-24 | Chitosan gel composition and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01215836A JPH01215836A (en) | 1989-08-29 |
JP2599415B2 true JP2599415B2 (en) | 1997-04-09 |
Family
ID=12653538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63043068A Expired - Lifetime JP2599415B2 (en) | 1988-02-24 | 1988-02-24 | Chitosan gel composition and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2599415B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5599916A (en) * | 1994-12-22 | 1997-02-04 | Kimberly-Clark Corporation | Chitosan salts having improved absorbent properties and process for the preparation thereof |
KR19990039747A (en) * | 1997-11-14 | 1999-06-05 | 한형수 | Manufacturing method of complex functional plant growth promoter |
ES2166724B2 (en) * | 2000-07-27 | 2003-04-01 | Idebio S L | DIETETIC SAUCES BASED ON QUITOSANE. |
JP5207015B2 (en) * | 2004-08-03 | 2013-06-12 | 地方独立行政法人鳥取県産業技術センター | Method for producing chitosan gel |
-
1988
- 1988-02-24 JP JP63043068A patent/JP2599415B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH01215836A (en) | 1989-08-29 |
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