Collagen fibre extracting method and manufacture of tissue filling material therefrom
A collagen fiber and extraction method technology, applied in the field of collagen fiber extraction, can solve the problems of limited clinical application, high product viscosity, low extraction rate, etc.
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Embodiment 1
[0023] Example 1 The newly slaughtered cattle were washed and peeled, and 500 grams of tendons were taken, soaked in 2N hydrochloric acid for 48 hours at room temperature; The temperature was 20° C., and the cells were placed in 0.1% pepsin solution for 12 hours; the tissue to be used was taken out and washed with water to obtain an acellular collagen framework. Cut the acellular collagen framework into tissue blocks with a size of 0.05cm---0.5cm; repeat the above acid leaching and enzymolysis steps once; grind the tissue blocks to a diameter of 10μm---50μm and a length of 300μm under the monitoring of a polarizing microscope ---500μm collagen fiber filaments. A total of 2000 g of product was obtained.
[0024] Take a certain volume of collagen filament product and dry it at a constant temperature between 50°C and 90°C, weigh it, and calculate the content to be 400 mg / ml.
[0025] The following component identification experiments were performed using the collagen fibers obt...
Embodiment 2
[0030] Example 2 Newly slaughtered pigs were washed and dehaired, and 500 grams of full-thickness skin without fat on the back was taken, soaked in 10N acetic acid for 68 hours at room temperature; the tissues to be used were taken out, washed with distilled water, neutralized with 0.5N alkali, and then It was soaked in 0.2% pepsin solution at a temperature of 4°C for 24 hours; the tissue to be used was taken out and washed with water to obtain an acellular collagen framework. Cut the acellular collagen framework into tissue blocks with a size of 0.05cm---0.5cm; repeat the above acid leaching and enzymolysis steps once; 300μm---500μm collagen fibers, a total of 2000 grams of products were obtained.
Embodiment 3
[0031] Example 3 According to the method described in Example 1, wherein the acid leaching was immersed in 3N hydrochloric acid for 72 hours, and the enzymatic hydrolysis was immersed in 1.5% pepsin solution for 18 hours.
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Abstract
Description
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