Injection for treating cerebral thrombus and preparation thereof
A cerebral thrombosis and injection technology, applied in the field of thrombolytic injection for the treatment of cerebral thrombosis and its preparation, can solve the problems of poor treatment effect, high price, insignificant effect, etc., and achieve the purpose of promoting nerve cell recovery, dilating blood vessels, and resisting platelets. The effect of adhesion aggregation
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Embodiment 1
[0056] The first step: G75 chromatography column chromatography, after treatment with 0.2M NaOH, pack the column, use 0.2M disodium hydrogen phosphate buffer to balance the pH6.8, take Agkistrodon venom and dissolve it in 10ml of 0.2M disodium hydrogen phosphate buffer, The sample was loaded by centrifugation, loaded on the column, eluted with 0.02M disodium hydrogen phosphate buffer, collected with a fractional collector, and the collected enzyme activity peak was concentrated and freeze-dried. Agkistrodon venom is freeze-dried powder of Jiangsu-Zhejiang Agkistrodon venom.
[0057] The second step: Sephadex-A25 chromatography column chromatography, with 0.01M Tris-HCl buffer solution, PH7.0 soaks gel, in Tris (trishydroxymethylaminomethane)-HCl buffer solution (trishydroxymethylaminomethane The concentration in the buffer solution is 0.01M-0.05M, the pH value is 7.5), Sephadex (cross-linked dextran). It was then loaded into a column and equilibrated with 0.01 M Tris-HCl buff...
Embodiment 2
[0061] The first step: G75 column chromatography, after treatment with 0.15M NaOH, install the column, use 0.15M sodium dihydrogen phosphate buffer to balance pH 6.8, take Agkistrodon venom and dissolve it in 10ml of the above buffer, centrifuge and load the sample, put on the column, and use The 0.01M sodium dihydrogen phosphate buffer was eluted, collected with a fractional collector, and the collected enzyme activity peaks were concentrated and freeze-dried.
[0062] The second step: Sephadex-A25 chromatography column chromatography, soak the gel with 0.01M Tris-HCl buffer solution, pH7.0, then load it into the column, and equilibrate it with 0.01M Tris-HCl buffer solution. Dissolve the sample from the first step of chromatography in 0.01M Tris-HCl buffer and put it on the column, equilibrate the buffer, wash away impurity proteins with 0.01M NaCl buffer, change to 0.45M NaCl buffer for elution, and collect enzyme activity peak, concentrated and lyophilized. Step 3: Same a...
Embodiment 3
[0065] The first step: G75 column chromatography, after treatment with 0.3M NaOH, install the column, use 0.3M disodium hydrogen phosphate buffer to balance the pH6.8, take Agkistrodon venom and dissolve it in 10ml of the above buffer, centrifuge and load the sample, and put it on the column. It was eluted with 0.03M disodium hydrogen phosphate buffer, collected with fractional collector, and the collected enzyme activity peak was concentrated and freeze-dried.
[0066] The second step: Sephadex-A25 chromatography column chromatography, soak the gel with 0.01M Tris-HCl buffer solution, pH7.0, then load it into the column, and equilibrate it with 0.01M Tris-HCl buffer solution. Dissolve the sample from the first step of chromatography in 0.01 M Tris-HCl buffer and put it on the column, equilibrate the buffer, wash with 0.01M NaCl buffer to remove impurities, change to 0.8M NaCl buffer for elution, and collect enzyme activity peak, concentrated and lyophilized. Step 3: Same as ...
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Abstract
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