Microneedle patch capable of programmatically releasing psoriasis treatment medicine and preparation method thereof
A treatment drug and psoriasis technology, applied in the field of microneedle patch and its preparation, can solve the problems of not meeting the long-term treatment needs of moderate to severe patients, reduction, uneven drug distribution, etc., to achieve rapid and long-lasting psoriasis disease treatment, improve uniformity, and meet the effect of rapid onset of action
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Embodiment 1
[0032] Include the following steps:
[0033] 1. Use a laser engraving machine to etch out a 10*10 polydimethylsiloxane (PDMS) negative template with a bottom diameter of 200 μm, a height of 850 μm, and a distance between adjacent microneedles of 600 μm;
[0034] 2. Prepare a mixed solution of 10 mg / mL methotrexate and 5 mg / mL poly(lactide-co-glycolide) in chloroform, then pass through the membrane with a 0.45 μm filter membrane to obtain a coated Nanoparticles of methotrexate (in these nanoparticles, the poly(lactide-co-glycolide) component is outside and the methotrexate component is encapsulated); the size of the nanoparticles is directly affected by the pore size of the filter membrane , the pore size of the filter membrane can be adjusted according to the actual needs of the particle size; the methotrexate used in this step corresponds to the psoriasis drug that can be slowly released in subsequent applications, and the methotrexate used The specific concentration and vol...
Embodiment 6
[0040] The microneedles prepared in the above-mentioned Example 1 were used on severe psoriasis model mice, and a microneedle patch of a 10*10 array was used every 3 days, and the therapeutic effect was observed after 3 weeks for liver toxicity (alanine aminotransferase , aspartate aminotransferase levels). image 3 The results (Ki67) of middle tissue section (H&E staining) and skin lesion thickening expression factor show that the present invention has obvious curative effect to the ear skin lesion of treatment psoriasis mouse; Figure 4 The levels of the two enzymes (alanine aminotransferase ALT, aspartate aminotransferase AST) in the liver of the mice did not change significantly compared with those of normal mice without disease, indicating that the present invention has no obvious liver toxicity.
[0041] The "poorly soluble", "soluble" and "easy soluble" in the present invention meet the conventional definitions.
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