JPH06192443A - Production of re-formed egg shell membrane - Google Patents

Production of re-formed egg shell membrane

Info

Publication number
JPH06192443A
JPH06192443A JP3314341A JP31434191A JPH06192443A JP H06192443 A JPH06192443 A JP H06192443A JP 3314341 A JP3314341 A JP 3314341A JP 31434191 A JP31434191 A JP 31434191A JP H06192443 A JPH06192443 A JP H06192443A
Authority
JP
Japan
Prior art keywords
membrane
thiopropionic acid
eggshell membrane
solution
drying
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.)
Withdrawn
Application number
JP3314341A
Other languages
Japanese (ja)
Inventor
Kozo Arai
幸三 新井
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.)
QP Corp
Original Assignee
QP Corp
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
Application filed by QP Corp filed Critical QP Corp
Priority to JP3314341A priority Critical patent/JPH06192443A/en
Publication of JPH06192443A publication Critical patent/JPH06192443A/en
Withdrawn legal-status Critical Current

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  • Materials For Medical Uses (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

PURPOSE:To obtain a water-insoluble membrane useful for treating a wound, etc., without the necessity for the addition of components other than those of the egg shell membrane, such as glycerol, by solubilizing the membrane with thiopropionic acid, forming the solution into a thin layer, and drying this layer. CONSTITUTION:A membrane attached to the inside of an avian egg is mixed with thiopropionic acid and heated to desirably 40-90 deg.C to solubilize the membrane. Although thiopropionic acid exists in two isomeric forms alpha and beta, beta-thiopropionic acid is desirably used. The solution of the solubilized egg shell membrane is applied, cast or sprayed in any desired form to form a thin membrane, and this membrane is dried by heating, in a vacuum or by other means to obtain a re-formed egg shell membrane. The thiopropionic acid slightly remaining in the membrane can be removed by immersing it in an alcoholic solution after drying, withdrawing it from the solution, and drying it.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、再形成卵殻膜の製造方
法に関する。
TECHNICAL FIELD The present invention relates to a method for producing a reshaped eggshell membrane.

【0002】[0002]

【従来の技術】卵殻膜は、創傷治療に利用できることが
知られているが、湾曲しており広い平面を覆うには適し
ていない。このため、広い平面を覆う場合には、例えば
特開平2−26560号公報に見られるように、水中で
卵殻膜を塩とpH調整により親水性に改質して乾燥した
後、これをフッ素系アルコール、酢酸、グリセリンなど
と混合してキャスティング用の紙やフィルムに塗布し、
さらに乾燥して広いシート状の膜に再形成する方法等が
用いられている。
BACKGROUND OF THE INVENTION Eggshell membranes are known to be useful for wound healing, but they are curved and not suitable for covering a wide flat surface. Therefore, in the case of covering a wide flat surface, as shown in, for example, Japanese Patent Application Laid-Open No. 26560/1990, the eggshell membrane is modified to be hydrophilic by salt and pH adjustment in water and dried, and then the fluorine-based coating is used. Mix with alcohol, acetic acid, glycerin, etc. and apply it to casting paper or film,
Further, a method of drying and reforming into a wide sheet-shaped film is used.

【0003】[0003]

【発明が解決しようとする課題】ところが、上記の方法
により製造した膜は、卵殻膜を親水性に改質したものを
用いるため、そのままでは水性媒体に不溶性の膜になら
ず、不容性とするためには製造に際してグリセリンなど
の原料を必ず必要とするものであった。
However, since the membrane produced by the above-mentioned method uses the eggshell membrane modified to be hydrophilic, it does not become an insoluble membrane in an aqueous medium as it is and is made insoluble. In order to do so, a raw material such as glycerin was indispensable for the production.

【0004】本発明は、グリセリンなどの卵殻膜成分以
外の成分を含ませなくても水不溶性の膜にすることがで
きる再形成卵殻膜の製造方法を提供することを目的とす
る。
It is an object of the present invention to provide a method for producing a reshaped eggshell membrane which can be made into a water-insoluble membrane without containing components other than eggshell membrane components such as glycerin.

【0005】[0005]

【課題を解決するための手段】前記目的を達成する本発
明に係る再形成卵殻膜の製造方法は、卵殻膜をチオプロ
ピオン酸により可溶化した後、これを薄層にして乾燥す
ることを特徴とする。
The method for producing a reshaped eggshell membrane according to the present invention which achieves the above object is characterized in that the eggshell membrane is solubilized with thiopropionic acid and then dried to form a thin layer. And

【0006】以下、本発明の内容を詳細に説明する。The details of the present invention will be described below.

【0007】本発明で再形成卵殻膜とは、卵殻膜を可溶
化した後、任意に膜状に形成したものをいう。また、本
発明で卵殻膜とは、鳥類の卵の卵殻内面に付着する膜を
いい、代表的なものとしては、鶏卵の卵殻膜を挙げるこ
とができる。
In the present invention, the reshaped eggshell membrane refers to the eggshell membrane which is solubilized and then formed into an arbitrary membrane. In the present invention, the eggshell membrane refers to a membrane attached to the inner surface of the eggshell of an avian egg, and a representative example thereof is the eggshell membrane of chicken eggs.

【0008】本発明でチオプロピオン酸とは、プロピオ
ン酸にメルカプト基がついたものをいい、異性体として
はα型およびβ型のものが存在する。本発明では、いず
れの異性体のものを用いてもよいが、β型のチオプロピ
オン酸(β−チオプロピオン酸)を用いるのが特に好適
である。
In the present invention, thiopropionic acid means propionic acid having a mercapto group, and isomers include α-type and β-type. In the present invention, any isomer may be used, but it is particularly preferable to use β-type thiopropionic acid (β-thiopropionic acid).

【0009】上記チオプロピオン酸は、無水のものを用
いてもよいが、水溶液としたものを用いてもよい。ここ
で水溶液とした場合には、1モル/リットル(Mと表示
する)以上、より好ましくは5M以上の濃度のものを用
いるのが望ましい。チオプロピオン酸は、無水状態に近
い程、得られる再形成卵殻膜の力学的物性が強いという
傾向にあるが、水が存在している場合の方が、無水に近
い状態のものより、低温でかつ短時間で卵殻膜が可溶化
する傾向にある。このため、チオプロピオン酸の水溶液
の場合の濃度は、その目的に応じて適宜調整するように
すればよい。
The above-mentioned thiopropionic acid may be anhydrous or may be an aqueous solution. When the aqueous solution is used here, it is desirable to use one having a concentration of 1 mol / liter (denoted as M) or more, more preferably 5 M or more. Thiopropionic acid tends to have stronger mechanical properties in the re-formed eggshell membrane as it approaches the anhydrous state, but in the presence of water, it is lower at a lower temperature than that in the nearly anhydrous state. Moreover, the eggshell membranes tend to be solubilized in a short time. Therefore, the concentration of thiopropionic acid in the case of an aqueous solution may be appropriately adjusted according to the purpose.

【0010】本発明で卵殻膜をプロピオン酸により可溶
化するとは、卵殻膜をプロピオン酸の溶液中で溶液状に
存在させることをいう。ここで可溶化させるための割合
としては、卵殻膜(乾燥物重量換算)を無水チオプロピ
オン酸の重量に対して1〜20%、好ましくは3〜10
%程度の割合で混合すればよい。また可溶化する際の温
度は常温でもよいが、適宜加温した方が速く可溶化する
傾向にあるので、チオプロピオン酸の溶液温度は一般に
40〜90℃とするのが望ましい。また可溶化の時間
は、加温の程度によって左右されるが一般に2〜50時
間程度とするのが望ましい。
In the present invention, solubilizing the eggshell membrane with propionic acid means allowing the eggshell membrane to exist in a solution state in a solution of propionic acid. The proportion for solubilization here is 1 to 20%, preferably 3 to 10% of the eggshell membrane (dry matter weight conversion) based on the weight of thiopropionic anhydride.
It may be mixed at a ratio of about%. The temperature for solubilization may be room temperature, but the temperature of the solution of thiopropionic acid is generally preferably 40 to 90 ° C., since it tends to solubilize faster when appropriately heated. The solubilization time depends on the degree of heating, but it is generally desirable to set the time to about 2 to 50 hours.

【0011】本発明で薄層にするとは、薄い膜状にする
ことをいい、具体的には、卵殻膜の可溶化液を、得よう
とする形状の型に塗布、展開または噴霧して薄い膜とす
る。尚、膜の厚みは必ずしも均一である必要はなく、用
途に応じて部分的に厚みを変えるようにしてもよく、ま
た、膜は用途に応じて曲面や凹凸部などを付与するよう
にしてもよい。尚、膜の厚みは、余り厚いと乾燥工程に
時間がかかりすぎるので、一般的には1mm以下とすれ
ばよい。
The thin layer in the present invention means to form a thin film. Specifically, the eggshell membrane solubilizing solution is applied, spread or sprayed on a mold having a shape to be obtained, to form a thin layer. The film. Incidentally, the thickness of the film does not necessarily have to be uniform, and the thickness may be partially changed according to the use, and the film may be provided with a curved surface or an uneven portion according to the use. Good. If the thickness of the film is too thick, the drying step will take too much time, so it is generally 1 mm or less.

【0012】本発明で乾燥するとは、卵殻膜の可溶化液
中の溶媒成分のほとんどを蒸発させることをいい、乾燥
は具体的には加熱、減圧などの手段を用いて行えばよ
い。尚、加熱によって乾燥を行う場合は余り高温で行う
と卵殻膜が変質してしまうので、約60〜80℃程度で
行うのが望ましい。以上のようにして、再形成卵殻膜が
製造される。
Drying in the present invention means evaporating most of the solvent components in the solubilized liquid of eggshell membranes, and drying may be carried out specifically by means of heating, decompression or the like. When the drying is performed by heating, the eggshell membrane is deteriorated if it is performed at an excessively high temperature, so it is desirable to perform the drying at about 60 to 80 ° C. The reshaped eggshell membrane is manufactured as described above.

【0013】以下、再形成卵殻膜の製造方法の一例を説
明する。例えば、鶏卵の卵殻膜を、チオプロピオン酸中
で攪拌しながら例えば80℃で48時間保持し、卵殻膜
を可溶化する。次いで可溶化液中の非溶解物を除去した
後ガラス板にキャストし、乾燥によりチオプロピオン酸
を除去して、再形成卵殻膜を得る。
An example of the method for producing the reformed eggshell membrane will be described below. For example, the eggshell membranes of chicken eggs are kept in thiopropionic acid with stirring at, for example, 80 ° C. for 48 hours to solubilize the eggshell membranes. Then, after removing the non-dissolved material in the solubilized solution, it is cast on a glass plate and thiopropionic acid is removed by drying to obtain a reshaped eggshell membrane.

【0014】尚、上記の加熱または減圧による乾燥法の
みでは再形成卵殻膜中にチオプロピオン酸が若干残留す
ることが多いが、この残留の度合を実質的にゼロに近く
する必要がある場合には、次の又はの方法を経れば
よい。 アルコールを用いる場合 乾燥工程終了後にアルコール液(濃度が高い方が後で蒸
発させやすい)に5〜30時間浸漬し、取り出して乾燥
させる。 蛋白質成分だけを取り出す場合 チオプロピオン酸を用いて卵殻膜の可溶化液を製造した
とき、例えばアセトンなどの有機溶媒を加えて卵殻膜の
蛋白質成分を沈澱させる。そしてこの沈澱物を分取し
て、これを必要により有機溶媒で洗浄した後、水に溶解
させ、この溶解液を型に塗布、展開および噴霧して乾燥
させる。尚、卵殻膜の可溶化した液は、卵殻膜をチオプ
ロピオン酸により可溶化したままの液の他、卵殻膜成分
を分取し、別の溶媒に溶解した液などを含むものであ
る。
Although only a small amount of thiopropionic acid remains in the re-formed eggshell membrane only by the above-mentioned drying method by heating or reduced pressure, when the degree of this residual needs to be substantially close to zero, The following or method may be used. In the case of using alcohol After the drying step is completed, it is immersed in an alcohol solution (the higher the concentration, the easier it is to evaporate later) for 5 to 30 hours, taken out and dried. When only the protein component is taken out When a solubilized solution of the eggshell membrane is produced using thiopropionic acid, an organic solvent such as acetone is added to precipitate the protein component of the eggshell membrane. Then, the precipitate is separated, washed with an organic solvent if necessary, dissolved in water, and the solution is applied to a mold, spread and sprayed to dry. The solubilized liquid of the eggshell membrane includes a liquid in which the eggshell membrane is solubilized with thiopropionic acid, and a liquid in which the components of the eggshell membrane are fractionated and dissolved in another solvent.

【0015】[0015]

【作用】本発明の方法により製された再形成卵殻膜が、
いかなる理由により水性媒体に不溶性の膜となるのかは
明らかではないが、本発明の方法により製造された再形
成卵殻膜は、チオプロピオン酸により可溶化された卵殻
膜が、水性媒体の蒸散に伴い、再び三次元的に強固に結
合するからではないかと推察される。
The reshaped eggshell membrane produced by the method of the present invention
Although it is not clear for any reason why it becomes an insoluble membrane in an aqueous medium, the reshaped eggshell membrane produced by the method of the present invention shows that the eggshell membrane solubilized by thiopropionic acid is accompanied by evaporation of the aqueous medium. , It is presumed that it is strongly connected three-dimensionally again.

【0016】[0016]

【実施例】卵殻の卵殻膜(よく洗浄して乾燥したもの)
1gに5Mのβ−チオプロピオン酸水溶液を20ml加
え、攪拌しながら80℃で48時間保持して卵殻膜を可
溶化した。得られた卵殻膜の可溶化液をフィルターによ
り濾過して非溶解物を除去した。この濾液1.5ml
を、表面をよく洗浄して乾燥させたガラス板(20cm
×50cm)に均一に塗布し、80℃の恒温室に減圧下
で24時間放置して乾燥させた。次に、恒温室からガラ
ス板を取り出してメタノール中に24時間浸漬して、蒸
発しきれなかったβ−チオプロピオン酸をほとんど完全
に除去した。そして、メタノール中からガラス板を取り
出して膜をガラス板より剥離し、この膜を室温に放置し
てメタノールを蒸発させ、チオプロピオン酸の残留が実
質的にゼロに近い再形成卵殻膜を得た。この膜は大きさ
が20cm×50cmで、厚さが15μmであり、水に
不溶のものであった。
[Example] Eggshell membrane of eggshell (those that have been thoroughly washed and dried)
20 ml of 5M β-thiopropionic acid aqueous solution was added to 1 g, and the mixture was kept at 80 ° C. for 48 hours with stirring to solubilize the eggshell membrane. The resulting solubilized liquid of eggshell membranes was filtered with a filter to remove non-dissolved substances. 1.5 ml of this filtrate
The glass plate (20 cm
X 50 cm), and the mixture was allowed to stand in a thermostatic chamber at 80 ° C for 24 hours under reduced pressure to dry. Next, the glass plate was taken out from the thermostatic chamber and immersed in methanol for 24 hours to almost completely remove the β-thiopropionic acid that could not be evaporated. Then, the glass plate was taken out from the methanol, the film was peeled from the glass plate, and the film was left at room temperature to evaporate the methanol to obtain a reshaped egg shell film in which the residual thiopropionic acid was substantially zero. . This film had a size of 20 cm × 50 cm, a thickness of 15 μm, and was insoluble in water.

【0017】[0017]

【発明の効果】以上実施例と共に述べたように、本発明
によれば、卵殻膜の再形成をするに際し、従来のように
例えばグリセリンなどを含有することなく、水性媒体に
不溶性でかつ実質的に卵殻膜成分だけからなる再形成卵
殻膜を製造することができる。
INDUSTRIAL APPLICABILITY As described above in connection with the examples, according to the present invention, when the eggshell membrane is reformed, it is insoluble in an aqueous medium and substantially free from the conventional inclusion of glycerin or the like. It is possible to produce a reshaped eggshell membrane consisting only of eggshell membrane components.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 卵殻膜をチオプロピオン酸により可溶化
した後、これを薄層にして乾燥することを特徴とする再
形成卵殻膜の製造方法。
1. A method for producing a reshaped eggshell membrane, which comprises solubilizing the eggshell membrane with thiopropionic acid, forming a thin layer of the eggshell membrane, and drying.
JP3314341A 1991-11-28 1991-11-28 Production of re-formed egg shell membrane Withdrawn JPH06192443A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3314341A JPH06192443A (en) 1991-11-28 1991-11-28 Production of re-formed egg shell membrane

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3314341A JPH06192443A (en) 1991-11-28 1991-11-28 Production of re-formed egg shell membrane

Publications (1)

Publication Number Publication Date
JPH06192443A true JPH06192443A (en) 1994-07-12

Family

ID=18052166

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3314341A Withdrawn JPH06192443A (en) 1991-11-28 1991-11-28 Production of re-formed egg shell membrane

Country Status (1)

Country Link
JP (1) JPH06192443A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2020455A2 (en) 2007-07-30 2009-02-04 Idemitsu Technofine Co. Ltd Fiber, fiber assembly, and fiber producing method
JP2009089859A (en) * 2007-10-05 2009-04-30 Idemitsu Technofine Co Ltd Wound covering material
WO2012036645A3 (en) * 2010-09-15 2012-08-16 Ercan Durmus Oral care gel containing eggshell powder
JP2018100469A (en) * 2016-12-21 2018-06-28 国立大学法人信州大学 Nanofiber, production method of nanofiber, and face mask
KR102191912B1 (en) 2020-03-31 2020-12-16 강경수 Method for Egg Shell Membrane
US10932952B2 (en) 2015-11-11 2021-03-02 Biovotec As Dry biocompatible disintegratable films for delivering particulate egg shell membrane to a wound
US11992508B2 (en) 2014-10-28 2024-05-28 Biovotec As Micronized eggshell membrane particles and the use thereof to promote the healing of wounds

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2020455A2 (en) 2007-07-30 2009-02-04 Idemitsu Technofine Co. Ltd Fiber, fiber assembly, and fiber producing method
US7767297B2 (en) 2007-07-30 2010-08-03 Idemitsu Technofine Co., Ltd. Fiber, fiber assembly, and fiber producing method
JP2009089859A (en) * 2007-10-05 2009-04-30 Idemitsu Technofine Co Ltd Wound covering material
WO2012036645A3 (en) * 2010-09-15 2012-08-16 Ercan Durmus Oral care gel containing eggshell powder
US11992508B2 (en) 2014-10-28 2024-05-28 Biovotec As Micronized eggshell membrane particles and the use thereof to promote the healing of wounds
US10932952B2 (en) 2015-11-11 2021-03-02 Biovotec As Dry biocompatible disintegratable films for delivering particulate egg shell membrane to a wound
JP2018100469A (en) * 2016-12-21 2018-06-28 国立大学法人信州大学 Nanofiber, production method of nanofiber, and face mask
KR102191912B1 (en) 2020-03-31 2020-12-16 강경수 Method for Egg Shell Membrane

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