High-strength biological scaffold material and preparation method thereof

US2016184069A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016184069-A1
Application numberUS-201615064925-A
CountryUS
Kind codeA1
Filing dateMar 9, 2016
Priority dateJan 27, 2011
Publication dateJun 30, 2016
Grant date

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  5. First independent claim

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Abstract

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A high-strength biological scaffold and preparation method thereof. The biological scaffold is comprised of a framework of boiled-off silk woven material, the form of the framework is determined by actual needs; the framework surface is coated with a layer of silk protein scaffold material, fibroin protein/gelatin biological scaffold material or fibroin protein/collagen biological scaffold material having a thickness of 100 micrometers to 5 centimeters. The high-strength biological scaffold material has high tear resistance strength and mechanical strength and good biocompatibility, has a porous structure suitable for tissue regeneration, and can be used for preparing anal fistula repair plugs.

First claim

Opening claim text (preview).

1 . A method for preparing a high-strength biological scaffold material, characterized in that, the method comprises the following steps: boiled-off silk obtained by degumming silk is woven into a woven material by a textile machine to form a framework according to the desired shape, and then the framework is placed into a mold; a solution containing silk fibroin is injected into the mold having the framework placed therein, and subjected to freezing and vacuum treatment; thereby a coating layer having a thickness of 100 microns to 5 cm is formed on the surface of the framework, and the high-strength biological scaffold material is prepared, wherein said solution containing silk fibroin is one selected from the group consisting of: an aqueous silk fibroin solution, a mixed solution of silk fibroin and gelatin, and a mixed solution of silk fibroin and collagen; the weave density of the woven material is such that the distance between adjacent boiled-off silks is between 0.5 mm and 3 mm, and the material of the coating layer is selected from the group consisting of: silk protein scaffold material, silk fibroin/gelatin biological scaffold material or silk fibroin/collagen biological scaffold material. 2 . The method for preparing a high-strength biological scaffold material according to claim 1 , characterized in that, the step of coating the surface of the framework with a coating layer comprises the specific steps of: 1) preparing a solution containing silk fibroin, the solution containing silk fibroin being one selected from the group consisting of: an aqueous silk fibroin solution, a mixed solution of silk fibroin and gelatin, and a mixed solution of silk fibroin and collagen; injecting the solution containing silk fibroin into the mold having the framework placed therein, and subjecting it to freezing under a low temperature of −10 to −80° C. for 1 to 24 hours to obtain frozen crystals; freeze-drying the frozen crystals to obtain a composite material, the composite material having boiled-off silk woven material as a framework and a layer of soluble silk fibroin layer/silk fibroin and gelatin composite layer/silk fibroin and collagen composite layer coated on the framework; 2) placing the composite material obtained in step 1) into a vacuum dryer and performing a vacuum treatment for 20 minutes to 24 hours to obtain a water-insoluble composite high-strength biological scaffold material, the composite high-strength biological scaffold material having boiled-off silk woven material as a framework and a coating layer provided on the framework, the material of the coating layer being selected from the group consisting of: silk protein scaffold material, silk fibroin/gelatin biological scaffold material or silk fibroin/collagen biological scaffold material; and the vacuum dryer containing water, aqueous methanol or aqueous ethanol at the bottom thereof; wherein in step 1), the aqueous silk fibroin solution is prepared by: subjecting silk to degumming, dissolution, and dialysis to obtain a silk fibroin solution, the aqueous silk fibroin solution having a mass concentration of 0.1 to 20%; leaving the aqueous silk fibroin solution at 0 to 80° C. for 1 to 48 hours; the mixed solution of silk fibroin and gelatin is prepared by: preparing an aqueous gelatin solution by adding medical gelatin into distilled water, heating to obtain an aqueous gelatin solution, and leaving the solution at 0 to 10° C. for 30 minutes to 2 hours, the aqueous gelatin solution having a mass concentration of 0.01 to 20%; then mixing an aqueous silk fibroin solution with the aqueous gelatin solution at a mass ratio of silk fibroin to gelatin of 100:2 to 20, to obtain the mixed solution of silk fibroin and gelatin; the mixed solution of silk fibroin and collagen is prepared by: preparing an aqueous silk fibroin solution by subjecting silk to degumming, dissolution, and dialysis to obtain a silk fibroin solution, the aqueous silk fibroin solution having a mass concentration of 0.1 to 20%; leaving the aqueous silk fibroin solution at 0 to 80° C. for 1 to 48 hours; preparing a solution of collagen in acetic acid at a concentration of 0.01% to 2%, and leaving the solution at 0 to 10° C. for 30 minutes to 2 hours; then mixing the aqueous silk fibroin solution with the solution of collagen in acetic acid at a mass ratio of silk fibroin to collagen of 100:2 to 20, to obtain the mixed solution of silk fibroin and collagen. 3 . A method for preparing a high-strength anal fistula repair plug, characterized in that, the method comprises the following steps: 1) preparing a solution containing silk fibroin, the solution containing silk fibroin being one selected from the group consisting of: an aqueous silk fibroin solution, a mixed solution of silk fibroin and gelatin, and a mixed solution of silk fibroin and collagen; 2) weaving degummed boiled-off silk into a tubular material to provide a framework and placing the tubular material into a mold for preparing anal fistula repair plug, the weave density of the tubular material being such that the distance between adjacent boiled-off silks is between 0.5 mm and 3 mm; 3) injecting the solution containing silk fibroin into the mold having the tubular material placed therein, and subjecting it to freezing under a low temperature of −10 to −30° C. for 20 to 24 hours to obtain a frozen body; freeze-drying the frozen body to obtain a soluble composite anal fistula repair plug, the soluble composite anal fistula repair plug having the tubular material woven from boiled-off silk as a framework and a layer of soluble silk fibroin layer/silk fibroin and gelatin composite layer/silk fibroin and collagen composite layer coated on the framework; 4) placing the soluble composite anal fistula repair plug into a vacuum dryer and performing a vacuum treatment for 4 hours or more to obtain a water-insoluble composite anal fistula repair plug, the water-insoluble composite anal fistula repair plug having the tubular material woven from boiled-off silk as a framework and a biological scaffold material as a coating layer, the biological scaffold material being selected from the group consisting of: silk protein biological scaffold material, silk fibroin/gelatin biological scaffold material or silk fibroin/collagen biological scaffold material, the framework being embedded inside the coating layer; and the vacuum dryer containing water, aqueous methanol or aqueous ethanol at the bottom thereof; wherein in step 1), the aqueous silk fibroin solution is prepared by: preparing an aqueous silk fibroin solution having a mass concentration of 0. 5 % to 5% by a conventional method, and leaving the aqueous silk fibroin solution at 0 to 10° C. for 30 minutes or more; the mixed solution of silk fibroin and gelatin is prepared by: preparing an aqueous gelatin solution having a mass concentration of 0.05% to 1%, and leaving the solution at 0 to 10° C. for 30 minutes to 2 hours; mixing an aqueous silk fibroin solution with the aqueous gelatin solution uniformly such that the mass concentration of silk fibroin is 0.2% to 3% and the mass concentration of gelatin is 0.02% to 0.2% upon mixing; and leaving the mixture stand for 4 to 10 hours to obtain the mixed solution of silk fibroin and gelatin; the mixed solution of silk fibroin and collagen is prepared by: preparing a solution of collagen in acetic acid at a concentration of 0.05% to 1%, and leaving the solution at 0 to 10° C. for 30 minutes to 2 hours; mixing an aqueous silk fibroin solution with the solution of collagen in acetic acid uniformly at 0 to 10° C. such that the mass concentration of silk fibroin is 0.2% to 3% and the mass concentration of collagen is 0.02% to 0.2% upon mixing; and leaving the mixture stand for 4 to 10 hours to obtain the mixed solution of silk fibroin and collagen. 4 . The method for preparing a high

Assignees

Inventors

Classifications

  • A61L27/227Primary

    Other specific proteins or polypeptides not covered by A61L27/222, A61L27/225 or A61L27/24 · CPC title

  • A61F2/0009Primary

    placed in or outside the body opening close to the surface of the body (plugging an opening in the wall of a hollow or tubular organ A61B17/0057) · CPC title

  • complete occlusion · CPC title

  • Macromolecular materials · CPC title

  • Porous materials, {e.g. foams or sponges} · CPC title

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What does patent US2016184069A1 cover?
A high-strength biological scaffold and preparation method thereof. The biological scaffold is comprised of a framework of boiled-off silk woven material, the form of the framework is determined by actual needs; the framework surface is coated with a layer of silk protein scaffold material, fibroin protein/gelatin biological scaffold material or fibroin protein/collagen biological scaffold mate…
Who is the assignee on this patent?
Univ Soochow, Silk Plug Beijing Biomedicine Technology Company Ltd
What technology area does this patent fall under?
Primary CPC classification A61L27/227. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Jun 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).