首页> 美国卫生研究院文献>ISRN Pharmaceutics >Biodegradable In Situ Gel-Forming Controlled Drug Delivery System Based on Thermosensitive Poly(ε-caprolactone)-Poly(ethylene glycol)-Poly(ε-caprolactone) Hydrogel
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Biodegradable In Situ Gel-Forming Controlled Drug Delivery System Based on Thermosensitive Poly(ε-caprolactone)-Poly(ethylene glycol)-Poly(ε-caprolactone) Hydrogel

机译:基于热敏聚(ε-己内酯)-聚(乙二醇)-聚(ε-己内酯)水凝胶的可生物降解的原位形成凝胶的药物控制系统

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摘要

Traditional drug delivery systems which are based on multiple dosing regimens usually pose many disadvantages such as poor compliance of patients and drug plasma level variation. To overcome the obstacles of traditional drug formulations, novel drug delivery system PCL-PEG-PCL hydrogels have been purposed in this study. Copolymers were synthesized by rapid microwave-assisted and conventional synthesis methods. Polymer characterizations were done using gel permeation chromatography and 1H-NMR. Phase transition behavior was evaluated by inverting tube method and in vitro drug release profile was determined using naltrexone hydrochloride and vitamin B12 as drug models. The results indicated that loaded drug structure and copolymer concentration play critical roles in release profile of drugs from these hydrogels. This study also confirmed that synthesis of copolymer using microwave is the most effective method for synthesis of this kind of copolymer.
机译:基于多种给药方案的传统药物递送系统通常具有许多缺点,例如患者依从性差和药物血浆水平变化。为了克服传统药物制剂的障碍,本研究旨在使用新型药物递送系统PCL-PEG-PCL水凝胶。通过快速微波辅助和常规合成方法合成共聚物。使用凝胶渗透色谱法和 1 H-NMR对聚合物进行表征。通过倒相管法评估相变行为,并使用盐酸纳曲酮和维生素B12作为药物模型确定体外药物释放曲线。结果表明,加载的药物结构和共聚物浓度在这些水凝胶的药物释放过程中起关键作用。该研究还证实,使用微波合成共聚物是合成这种共聚物的最有效方法。

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