Application of annona squamosa seed total lactones to preparation of medicines for controlling diabetes
A technology of custard lactone and total lactone, applied in the application field of medicine, can solve problems such as adverse reactions, rebound, and pollute the environment, and achieve the effect of broadening clinical activity
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Embodiment 1
[0044] A kind of preparation method of anemone lactone for treating diabetic nephropathy, it comprises the following steps:
[0045] Take the custard apple seeds, crush them through a 80-mesh sieve, add ethanol in an amount 10 times the weight of the custard apple seeds, extract twice by reflux, each time for 2 hours, filter, combine the filtrates, concentrate to obtain a concentrate, and put it on the large hole D101 Hole resin column, first eluted with 10% ethanol for 6 times column volume, then 50% ethanol for 6 times column volume, and then chloroform for 10 times column volume, collected chloroform eluted parts, concentrated to obtain custard apple seeds Total lactones of custard apple.
Embodiment 2
[0047] A kind of preparation method of anemone lactone for treating diabetic nephropathy, it comprises the following steps:
[0048] Take the custard apple seeds, crush them through an 80-mesh sieve, and use supercritical CO 2 Extraction of anemone lactones from custard apple seeds; supercritical CO 2 The extraction process is a pressure of 25Mpa, an extraction temperature of 35°C, and an extraction time of 3 hours. The entraining agent is ethanol, and the amount of ethanol is 20% of the amount of medicinal materials.
Embodiment 3
[0049] Example 3 Lowering Blood Sugar, Lowering Blood Fat and Protecting Kidney Damage Experiments
[0050] 1. Test drug:
[0051] The total annona lactones prepared in Example 1, the compounds bullatacin, squamostatin and amurisolin;
[0052] 2. Experimental method:
[0053] (1), get SD rats, body weight (220 ± 20) g, male barrier environment rats (SPF grade), adaptive feeding 5 days, during the experiment, 10 rats in the blank group were fed with conventional feeds, and the rest of the rats were fed with Feed high-sugar, high-fat and 0.5% glucose water. After 3 weeks, inject STZ intraperitoneally at 30 mg / kg for 3 consecutive days. After feeding with high-sugar, high-fat and glucose water for 4 days, the rats were fasted and could not hold water. Blood was taken to measure fasting blood glucose, and the modeling was successful when the blood glucose value was higher than 13mmol / L. The diabetic rats successfully modeled were randomly divided into a normal group, a model gr...
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