Application of aromatase inhibitor in preparation of anti-cirrhosis or anti-liver fibrosis drugs
A technology of anti-liver fibrosis and aromatase, applied in the application field of medicine
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Embodiment 2
[0029] Example 2: Acquisition of Serum and Liver Specimens
[0030] a) Serum preparation: After 8 weeks, the rats were sacrificed. The blood was placed in a refrigerator at 4°C overnight, and the next day, the supernatant was drawn and centrifuged at 3000rpm for 20 minutes, and the supernatant was carefully drawn and stored at -20°C.
[0031] b) Treatment of the liver: cut the left liver lobe and wash it twice in PBS, then put it into a 50ml centrifuge tube and fix it by soaking in paraformaldehyde solution for paraffin sectioning.
Embodiment 3
[0032] Embodiment 3: detection of serum ALT and AST
[0033] Alanine aminotransferase (ALT) kit and aspartate aminotransferase (AST) kit were purchased from Shanghai Shensuo Youfu Medical Diagnostic Products Co., Ltd.
[0034] a) Take a 96-well plate, add 7.5 μl of rat serum respectively, and make three replicate wells for each sample. Then add 150 μl of the R-1 solution in the kit to the sample well, mix well and react for 5 minutes;
[0035] b) Add 50 μl of the R-2 solution in the kit and mix;
[0036] c) Measure the absorbance A1 at 340nm wavelength after 1 minute;
[0037] d) Measure the absorbance A2 at 340nm wavelength again after 4 minutes;
[0038] e) Calculation of rat serum ALT value:
[0039] ALT(U / L)=(A1-A2) / 4 minutes×207.5μl×1000 / (6.22×7.5μl×1cm)
[0040] AST(U / L)=(A1-A2) / 4 minutes×207.5μl×1000 / (6.22×7.5μl×1cm)
[0041] Carbon tetrachloride (CCl 4 ) induced rat liver fibrosis model is currently the most commonly used animal model for studying liver fibrosis...
Embodiment 4
[0042] Embodiment 4: making of paraffin section and section H&E staining and Sirius red staining
[0043] Hematoxylin, eosin and Sirius red were purchased from Sinopharm Chemical Reagent Co., Ltd., and saturated picric acid buffer was purchased from Yuanye Biotechnology Co., Ltd.
[0044] After paraformaldehyde-fixed rat liver tissue pieces were dehydrated, transparent, and soaked in wax, they were embedded in paraffin with an embedding machine, and the wax pieces were solidified and stored in a refrigerator at 4°C. Subsequently, the tissue wax blocks were made into paraffin sections for H&E staining and Sirius red staining.
[0045] (1) H&E staining
[0046] a) Dewaxing: dewaxing by xylene I and II for 10 minutes each;
[0047] b) Hydration: Put the slices in 100%, 95%, 85%, 75% alcohol solutions of various levels for 10 minutes each, rinse with tap water for 5 minutes, 1×PBS for 5 minutes, and incubate in 0.3% H2O2 at 37°C for 30 minutes. Minutes later, wash again with 1×...
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