Preparation method of nano ginsenoside CK
A ginsenoside and nanotechnology, applied in the field of preparation of nanometer ginsenoside CK, can solve the problems of limited efficacy, poor oral absorption, low solubility of ginsenoside CK, etc., and achieve the effects of improving water solubility and enhancing drug efficacy.
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Embodiment 1
[0029] Embodiment 1: the preparation of nanometer ginsenoside CK
[0030] Prepare each polymer micelle by film hydration method, weigh 100mg each of PEG-PLA2k / 2k, PEG-PLA5k / 5k, 1-10mg of ginsenoside CK, add 1-50mL of methanol to dissolve, and rotate at 25-60℃ under reduced pressure Evaporate to form a uniform transparent film, add 1-20mL deionized water to shake, and filter through a 0.22 μm microporous membrane to obtain PEG-PLA nanomicelles with different drug loadings loaded with ginsenoside CK. Freeze-dried for later use. The preparation method of nano ginsenoside containing azone (NT) is as follows: mixing ginsenoside with 0.1% NT, and preparing nano micelles by film-forming method. For the stability of nano-ginsenosides, see figure 1 .
Embodiment 2
[0031] Example 2: Capability of Nano Ginsenosides to Free Radicals
[0032] To culture human melanocytes, add 0, 10, 50, 100, 250, 500, 1000 μg / mL free CK and 4 kinds of nano-CKs to the culture plate, culture at 37°C for 48 hours, and detect the ability of different nano-ginsenosides to capture free radicals, see figure 2 .
Embodiment 3
[0033] Embodiment 3: melanin content
[0034] Human melanocytes were treated with different concentrations of CK and four nano-CKs (0, 10, 100, 1000 μg / mL) for 72 hours. Collect the cells, dissolve them in 200 μL of a solution containing 1NNaOH and 10% DMSO, treat them at 100°C for 30 minutes, centrifuge at 13,000 rpm for 10 minutes, and use a microplate reader to analyze the melanin content at 415nm, see image 3 .
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