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Modulation of Drug Release in Poly( ε-caprolactone) Blend Microfibers -

机译:聚(ε-己内酯)共混微纤维中药物释放的调节 -

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Electrospun poly(ε-caprolactone), PCL based microfibers were obtained by electrospinning of 15 % polymer solutions at 20 kV. Timolol maleate and acetazolamide (both anti-glaucoma drugs) were loaded in the fibers at different concentrations. Sustained release was observed during 1 month for PCL samples, while burst was shown by blends. Drug loading and drug solubility in the polymers affect the drug state in the fibers and drug release. Desorption and degradation models equations were fitted to the release data to understand the phenomena involved in the release process.
机译:电纺聚(ε-己内酯),通过在20kV的20kV下静电纺丝得到15%聚合物溶液获得的PCL基微纤维。 Matolol Maleate和乙酰唑胺(抗青光眼药物)以不同浓度的纤维装载在纤维中。对于PCL样品,1个月期间观察到持续释放,而共混物显示突发。聚合物中的药物负载和药物溶解度会影响纤维和药物释放中的药物状态。解吸和降解模型方程被安装到释放数据中以了解释放过程中涉及的现象。

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