Pharmaceutical composition for treating ovarian cancer and related preparation thereof
A composition and chemotherapeutic drug technology, which is applied in the direction of drug combination, medical preparations containing active ingredients, antineoplastic drugs, etc., can solve the problem of poor curative effect, no reports of thymoquinone combined with dihydromyricetin in treating cancer, drug resistance Sexual problems are difficult to overcome and other problems, to achieve the effect of improving drug efficacy, protecting the liver, and reducing ROS levels
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Embodiment 1
[0023] Example 1 Effects of Pharmaceutical Compositions and Monomers Thereon on the Proliferation of Ovarian Cancer Cell Lines
[0024] 1. In vitro culture of ovarian cancer cell lines
[0025] 1) Cell source
[0026] Human ovarian cancer cell lines SKOV3 and HO-8910 cells were purchased from the Shanghai Cell Bank of the Chinese Academy of Sciences.
[0027] 2) Cell culture and passage
[0028] SKOV3 and HO-8910 cells used 1640 medium (Gibico). 10% fetal bovine serum (fetalbovineserum, FBS, Gibco) was added during cell culture. The above cell lines were all cultured in a 37°C, 5% CO2 incubator. When the cells grew to 80-90% of the bottom of the culture dish, they were digested and passaged with 0.25% trypsin+EDTA.
[0029] 2. Test method
[0030] Main experimental materials: Thymoquinone (Thymoquinone, TQ, Sigma) dissolved in methanol, prepared as a 10mM concentrated solution, at -20°C, diluted to 10, 20, 40, 80 and 100μM when used, ready to use. Dihydromyrictin (DHM, S...
Embodiment 2
[0051] Example 2 Induction Effect of Pharmaceutical Composition and Its Monomer on Ovarian Cancer Cell Apoptosis
[0052] Human ovarian cancer cell lines were purchased from Shanghai Institute of Cells, Chinese Academy of Sciences, and SKOV3 and HO-8910 cells used 1640 medium (Gibico). 10% fetal bovine serum (fetalbovineserum, FBS, Gibco) was added during cell culture. The above cell lines were all stored at 37°C, 5% CO 2 Culture in an incubator. When the cells grow to 80-90% of the bottom of the culture dish, they are digested with 0.25% trypsin+EDTA and passaged.
[0053] Test method: After the cells are digested into a cell suspension, they are spread in a 60mm culture dish at a suitable density, at 37°C, 5% CO 2 Incubate in the incubator for about 24 hours. When the cells grow to about 50% of the bottom of the culture dish, remove the original culture medium and add freshly prepared culture medium containing 20 μM TQ, 20 μM DHM and / or 5 mg / L cisplatin to continue the cul...
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