Preparation method of protein-polyphenol-polysaccharide covalent complex and application of protein-polyphenol-polysaccharide covalent complex
A compound and protein technology, applied in applications, food science, food ingredients as emulsifiers, etc., can solve the problems of many by-products, difficult to achieve product purification, etc., to achieve simple method, good antioxidant capacity and thermal stability, The effect of improving emulsification
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Embodiment 1
[0028] The preparation method of β-lactoglobulin-ferulic acid-chitosan covalent complex, the steps are as follows:
[0029] (1) Disperse 0.50 g of chitosan in 70 mL of deionized water, adjust the chitosan solution to pH 6.0, and swell overnight to fully dissolve it. Add 1.20g of ferulic acid, 2.38g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.43g of N-hydroxysuccinimide into 30mL of absolute ethanol, 4 ° C and stirred for 1 h to obtain a mixed solution. The chitosan solution was added to the above mixed solution, stirred at 4° C. for 1 h, and then the temperature was raised to 25° C. and the stirring reaction was continued for 24 h. The reaction product was placed in a 12kDa dialysis bag and dialyzed with deionized water for 24 hours; then the mixed solution in the dialysis bag was centrifuged at 4500 rpm for 1 hour, and the supernatant was placed in a 12kDa dialysis bag and dialyzed with deionized water for 48 hours. Then freeze-dry to obtain the cov...
Embodiment 2
[0036] The preparation method of lactoferrin-chlorogenic acid-chitosan covalent complex, the steps are as follows:
[0037](1) Disperse 0.50 g of chitosan in 70 mL of deionized water, adjust the chitosan solution to pH 6.0, and swell overnight to fully dissolve it. Add 14.19g of chlorogenic acid, 2.38g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.43g of N-hydroxysuccinimide into 30mL of absolute ethanol at 4°C Stir for 1 h to obtain a mixed solution. The chitosan solution was added to the above mixed solution, and stirred at 4 °C for 1 h. Subsequently, the temperature was raised to 25° C. and the stirring reaction was continued for 24 h. The reaction product was placed in a 12kDa dialysis bag and dialyzed with deionized water for 24 hours; then the mixed solution in the dialysis bag was centrifuged at 4500 rpm for 1 hour, and the supernatant was placed in a 12kDa dialysis bag and dialyzed with deionized water for 48 hours. Then freeze-dry to obtain a...
Embodiment 3
[0040] The preparation method of α-lactalbumin-chlorogenic acid-sodium alginate covalent compound, the steps are as follows:
[0041] (1) Disperse 0.50 g of sodium alginate in 70 mL of deionized water, adjust the pH of the sodium alginate solution to 6.0, and swell overnight to fully dissolve it. Add 0.88g chlorogenic acid, 0.96g 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 0.58g N-hydroxysuccinimide to 30mL absolute ethanol, 4 ° C and stirred for 1 h to obtain a mixed solution. Sodium alginate solution was added to the above mixed solution, and stirred at 4 °C for 1 h. Subsequently, the temperature was raised to 25° C., and the stirring reaction was continued for 24 h. The reaction product was placed in a 12kDa dialysis bag and dialyzed with deionized water for 24 hours; then the mixed solution in the dialysis bag was centrifuged at 4500 rpm for 1 hour, and the supernatant was placed in a 12kDa dialysis bag and dialyzed with deionized water for 48 hours. ...
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