Drug composition for treating diseases caused by fat deposition and application of drug composition
A fat accumulation and composition technology, applied in the medical field, can solve problems such as discomfort
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Embodiment 1
[0035] Example 1 Effects of Compounds 1-12 on the Survival Rate of 3T3-L1 Preadipocytes
[0036] The effect of 12 monomeric compounds on the survival rate of 3T3-L1 cells was detected by MTS method, specifically:
[0037] (1) In a 96-well plate, add 100 μL of culture medium containing 3T3-L1 preadipocytes to each well. The cells were grown in the 96-well plate and covered the bottom of the plate, the original culture medium was discarded, and 200 μL of drugs diluted with DMEM medium (respectively compounds 1-12) were added to each well, and the final concentrations of the drugs were 10, 20, and 40 , 80 μmol / L. Place the treated cells at 37°C, 5% CO 2 Continue to grow under the conditions. After 96 hours, the original culture medium was discarded, 15 μL of MTS solution was added to each well, and the wells were placed in the dark at 37°C for 1 hour. The absorbance A value was measured at a wavelength of 490 nm in a microplate reader (infinite M200PRO, TECAN, Switzerland). ...
Embodiment 2
[0040] Example 2 Effects of Compounds 1-12 on the Differentiation of 3T3-L1 Preadipocytes
[0041] (1) Induction and differentiation of 3T3-L1 preadipocytes
[0042]3T3-L1 preadipocytes were subcultured into 6-well plates and cultured with high-glucose DMEM medium containing 10% FCS. When the cells adhered to the wall and grew to cover the 6-well plate (defined as day 0), they were induced to differentiate. Set up a group of normal group (Con group, add 10% FCS medium); 5% FBS+high sugar DMEM); Set up a group of fat differentiation positive control group (PIO group, add inducing differentiation agent I+10 μ mol / L pioglitazone); Each sample experimental group adds inducing differentiation agent I, and preparation final concentration is respectively: 1, Compounds 4 and 9 were all 10 μmol / L, and compounds 2, 3, 5, 6, 7, 8, 10, 11, and 12 were all 20 μmol / L, and cultured for 4 days. On day 4, the culture medium was replaced. The Con group was replaced with fresh 10% FCS cultur...
Embodiment 3
[0051] Example 3 Effects of Compounds 1-12 on Triglyceride Content in HepG2 Cells
[0052] (1) MTS cytotoxicity test
[0053] Through the MTS experiment, the non-toxic concentration of 12 monomeric compounds to HepG2 cells was determined. The results showed that compound 5 was 0-5 μmol / L, compound 12 was 0-10 μmol / L, compound 7 was 0-20 μmol / L, , 2, 3, 6, and 8 in the range of 0-40 μmol / L, and compounds 4, 9, 10, and 11 in the concentration range of 0-80 μmol / L, the cell survival rate reached more than 95%, that is, there was no obvious effect on cell proliferation, that is No toxic effect on cells. Therefore, the cells were treated with corresponding concentrations of drugs, respectively.
[0054] (2) Determination of triglyceride content
[0055] HepG2 cells were seeded in 6-well plates (1×10 6 cells / well) were cultured in DMEM medium containing 10% FBS. When the cells adhere to the wall and grow to cover the 6-well plate, add compounds 1 to 12 at a certain concentratio...
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