Biodegradable In Situ Gel-Forming Controlled Drug Delivery System Based on Thermosensitive Poly(ε-caprolactone)-Poly(ethylene glycol)-Poly(ε-caprolactone) Hydrogel.

Elham Khodaverdi, Ali Golmohammadian, Seyed Ahmad Mohajeri, Gholamhossein Zohuri, Farnaz Sadat Mirzazadeh Tekie, Farzin Hadizadeh
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引用次数: 17

Abstract

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 (1)H-NMR. Phase transition behavior was evaluated by inverting tube method and in vitro drug release profile was determined using naltrexone hydrochloride and vitamin B(12) 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.

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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原位凝胶控制给药系统。
基于多种给药方案的传统给药系统存在患者依从性差、血浆药物水平变化等缺点。为了克服传统药物配方的障碍,本研究旨在研究新型给药系统PCL-PEG-PCL水凝胶。采用微波辅助快速合成法和常规合成法合成共聚物。聚合物的表征采用凝胶渗透色谱和(1)H-NMR。以盐酸纳曲酮和维生素B(12)为药物模型,采用倒置管法评价其相变行为,测定其体外释放谱。结果表明,载药结构和共聚物浓度对这些水凝胶的药物释放特性起关键作用。本研究也证实了微波合成共聚物是合成该类共聚物最有效的方法。
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