Application of cyclic adenosine monophosphate in preparation of fat reducing and weight losing product for external use
A technology of cyclic adenosine monophosphate and adenosine phosphate, which is applied in the field of medicine, can solve the problem that cyclic adenosine monophosphate has not been reported, and achieves the effect of reducing fat mass
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Embodiment 1
[0029] 1. Preparation of cyclic adenosine monophosphate
[0030] Adenosine is used as raw material, phosphorus oxychloride is used as phosphating reagent, and triethyl phosphate is used as solvent to generate 5' dichlorophosphate of adenosine at low temperature. The intermediate is separated from the reaction system and dissolved in an appropriate slowly added to KOH in water and acetonitrile solution under stirring, strong base cyclization to obtain 3',5'-cyclic adenosine monophosphate. Weigh cyclic adenosine monophosphate and sodium bicarbonate in a weight ratio of 1:0.25, dissolve the prescribed amount of sodium bicarbonate in water for injection of 60% of the liquid dosage, and then add the prescribed amount of cyclic adenosine monophosphate while stirring to make It is completely dissolved; add 0.01% g / mL of medicinal activated carbon, stir and adsorb for 30 minutes, filter through a 0.45 μm microporous membrane to remove carbon, add water for injection to the filtrate 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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