A kind of curcumin nano-micelle preparation and preparation method thereof
A technology of nano micelles and curcumin, applied in the field of medical applications, can solve the problems of poor oral absorption, low solubility, limited application, etc., and achieve the effects of increasing stability, good safety, and prolonging circulation time.
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Embodiment 1
[0033] Weigh 8.0 mg of curcumin, 80.0 mg of amphiphilic block copolymer methoxypolyethylene glycol-polylactic acid, stir and dissolve with an appropriate amount of dichloromethane, remove the organic solvent by rotary evaporation in a water bath at 30 ° C, and place in a vacuum oven After drying overnight, a dry and transparent drug film skeleton was obtained. Add 2.0ml of deionized water, ultrasonically disperse at room temperature for 15 minutes, combine with constant temperature oscillation at 37°C, and centrifuge at 10,000rpm for 20 minutes (to remove unencapsulated crystalline drug). Qing is a transparent curcumin micellar preparation.
[0034] In the micellar preparation, the encapsulation rate of curcumin was 87.5%, the drug loading capacity was 8.05%, and it was stored at 4° C. for 24 hours without precipitation of the drug. Take the micellar preparation and dilute it in an appropriate amount, drop it on the copper grid, carry out negative staining with 2% phosphotungs...
Embodiment 2
[0036] Weigh 4.8mg of curcumin, 80.0mg of amphiphilic block copolymer methoxypolyethylene glycol-polylactic acid, stir and dissolve with an appropriate amount of methanol, remove the organic solvent by rotary evaporation in a water bath at 40°C, and dry in a vacuum oven overnight Finally, to obtain a dry and transparent drug film skeleton, add 13.95ml of deionized water, ultrasonically disperse at room temperature for 20 minutes, and combine with constant temperature oscillation at 37°C, centrifuge at 10000rpm for 20 minutes (to remove unencapsulated crystalline drug), the supernatant is ready It is a transparent curcumin micellar preparation. The encapsulation rate of curcumin in the micellar preparation was 82.4%, and the drug loading capacity was 6.82%. It was stored at 4°C for 24 hours, and no drug precipitated out.
Embodiment 3
[0038] Weigh 1.6mg of curcumin, 80.0mg of amphiphilic block copolymer methoxypolyethylene glycol-polylactic acid, stir and dissolve with an appropriate amount of acetone, remove the organic solvent by rotary evaporation in a water bath at 60°C, and dry in a vacuum oven overnight Finally, to obtain a dry and transparent drug film skeleton, add 9ml of deionized water, ultrasonically disperse at room temperature for 15 minutes, and combine with constant temperature oscillation at 37°C, centrifuge at 10000rpm for 25 minutes (to remove unencapsulated crystalline drug), the supernatant is Clear curcumin micellar formulation.
[0039] Add 4% (w / v) mannitol and freeze-dry to prepare a freeze-dried preparation. Take an appropriate amount of freeze-dried agent and redissolve it with physiological saline, take an appropriate amount of the solution, drop it on the copper grid, use 2% (w / v) phosphotungstic acid solution for negative staining, and observe it under the transmission electron ...
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