Application of adenosine triphosphate in preparation of slimming product for external use
A technology of adenosine triphosphate and adenosine phosphate, which is applied in the field of medicine, can solve the problems that adenosine triphosphate has not been reported, and achieve the effect of reducing fat mass
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Embodiment 1
[0029] 1. Preparation of adenosine triphosphate
[0030] When the temperature of the reaction pot is 20°C, put magnesium chloride solution, benzalkonium bromide solution, and adenosine solution in sequence, continue to heat the reaction solution to 36-39°C, keep it warm, and start sampling to measure the conversion rate of adenosine triphosphate when the reaction reaches End the reaction when the adenosine triphosphate band appears, then add NaOH solution in proportion to continue the reaction, and obtain the pure product of adenosine triphosphate disodium salt through removal of impurities, elution, crystallization and drying.
[0031] 2. Preparation of quince extract, centella asiatica extract and kelp extract
[0032] Preparation of Vitex quinquefolium extract
[0033] Weigh the dry plant powder of Vitex japonicus, add 5 times the amount of ethanol to the dry powder, extract twice at room temperature, each time for 3 days, concentrate under reduced pressure, and filter to ...
Embodiment 2
[0039] 1. Test method
[0040] 3T3-L1 preadipocytes were induced to differentiate into adipocytes. Rat fibroblast cell line 3T3-L1 was used at 5×10 4 The cells were inoculated into 12-well culture plates at a density of 1 / ml, and cultured in high-glucose DMEM medium (GIBCO, Life technology) containing 10% fetal bovine serum (FBS, GIBCO, Life technology). When the cells reached 70% confluence, the culture medium was replaced with a medium containing 1 μg / ml insulin, 0.25 μmol / L dexamethasone and 0.5 mmol / L 3-isobutyl-1-methyl yellow Purine (IBMX) in new DMEM medium (containing 10% FBS) to induce differentiation; 2 days later, the medium was changed to 1 μg / ml insulin in new DMEM medium (containing 10% FBS); 2 days later, the medium was changed to into normal DMEM medium (containing 10% FBS) and observed until adipocytes were formed.
[0041] Experimental method 1: Detect the accumulation of fat by Oil Red O staining method and microplate reader. Use Oil Red O purchased from...
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