A kind of preparation method of edible collagen film
A collagen film and collagen technology, applied in the field of preparation of edible collagen film, can solve the problems of high mechanical properties of materials, low cross-linking degree, limited contribution to the tensile strength of collagen film, etc. The effect of uniformity and excellent performance
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Embodiment 1
[0027] Stir pigskin collagen with 0.1mol / L acetic acid solution at 0°C until it is completely dissolved, and prepare a 2.5mg / mL collagen solution, then add 1% citric acid-N-hydroxysuccinyl based on the weight of animal collagen Imino ester, stirred and reacted at 0°C for 6 hours, casted to form a film after removing air bubbles, and dried to obtain a white transparent collagen film; firstly, tyrosinase was prepared into a solution with a concentration of 1% by weight, and then the dried collagen The membrane was soaked in the above solution, and reacted at 20°C for 4 hours. After the reaction, the collagen membrane was taken out, the surface was washed with water, and dried to obtain the modified collagen membrane.
[0028] The tensile strength of the obtained collagen film was 22.401 MPa, the elongation at break was 6.57%, and the water absorption rate was 151.37%.
Embodiment 2
[0030] Stir pigskin collagen with 0.2mol / L acetic acid solution at 2°C until completely dissolved, and prepare a 5mg / mL collagen solution, then add 2% malic acid-N-hydroxysuccinyl based on the weight of animal collagen Urethane, stirred and reacted at 2°C for 5 hours, casted to form a film after removing air bubbles, and dried to obtain a white transparent collagen film; firstly, tyrosinase was prepared into a solution with a concentration of 3% by weight, and then the dried collagen film was Soak in the above solution, react at 25°C for 3 hours, take out the collagen film after the reaction, rinse the surface with water, and dry to obtain the modified collagen film.
[0031] The tensile strength of the obtained collagen film was 25.652 MPa, the elongation at break was 6.12%, and the water absorption rate was 144.57%.
Embodiment 3
[0033] Stir fish skin collagen with 0.5mol / L acetic acid solution at 5°C until completely dissolved, and prepare a 7.5mg / mL collagen solution, then add 3% tartaric acid-N-hydroxysuccinyl based on the weight of animal collagen Urethane, stirred and reacted at 5°C for 4.5h, casted to form a film after removing air bubbles, and dried to obtain a white transparent collagen film; firstly, laccase was prepared into a solution with a concentration of 5% by weight, and then the dried collagen film was soaked In the above solution, react at 30° C. for 2 hours, take out the collagen membrane after the reaction, rinse the surface with water, and dry to obtain the modified collagen membrane.
[0034] The tensile strength of the obtained collagen film was 24.02 MPa, the elongation at break was 5.71%, and the water absorption rate was 138.22%.
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