Preparation method of anticoagulant material with function of inducing and catalyzing release of endogenous NO
An induced catalysis, endogenous technology, applied in the field of biomedical engineering functional materials, can solve the problems of limited anticoagulation aging, limited application, fast release rate, etc., and achieve excellent scavenging of oxygen free radicals, excellent antioxidant properties, The effect of high application value
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Embodiment 1
[0027] A method for preparing a novel anticoagulant material capable of inducing and catalyzing the release of endogenous NO, obtained by the following steps:
[0028] A. Polish, clean and dry the pure iron material that needs to be modified;
[0029] B. Place the sample obtained in step A in a buffer system with pH=5, then add a dopamine compound with a concentration of 0.01 mg / ml and cystamine with a concentration of 0.01 mg / ml to the system, and react at 10° C. for 1 h;
[0030] C. For the sample obtained in step B, immerse it in deionized water, clean it ultrasonically for 3 times, each time for 5min, and then wash it in N 2 The target material can be obtained by drying under the conditions.
Embodiment 2
[0032] A method for preparing a novel anticoagulant material capable of inducing and catalyzing the release of endogenous NO, obtained by the following steps:
[0033] A. Polish, clean and dry the magnesium-based material that needs to be modified;
[0034] B. Place the sample obtained in step A in a buffer system of pH=12, then add epigallocatechin gallate (EGCG) with a concentration of 10 mg / ml and selenocystamine with a concentration of 10 mg / ml to the system, At 30°C, react for 24h;
[0035] C. For the sample obtained in step B, immerse it in deionized water, clean it ultrasonically for 3 times, each time for 5min, and then wash it in N 2 The target material can be obtained by drying under the conditions.
Embodiment 3
[0037] A method for preparing a novel anticoagulant material capable of inducing and catalyzing the release of endogenous NO, obtained by the following steps:
[0038] A. Polish, clean and dry the medical 316L stainless steel that needs to be modified;
[0039] B. Place the sample obtained in step A in a buffer system of pH=7, then add epicatechin gallate (ECG) with a concentration of 2mg / ml and selenocystine with a concentration of 3mg / ml to the system, At 15°C, react for 4h;
[0040] C. For the sample obtained in step B, immerse it in deionized water, clean it ultrasonically for 3 times, each time for 5min, and then wash it in N 2 The target material can be obtained by drying under the conditions.
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