Khodaverdi Elham, Golmohammadian Ali, Mohajeri Seyed Ahmad, Zohuri Gholamhossein, Mirzazadeh Tekie Farnaz Sadat, Hadizadeh Farzin
Department of Pharmaceutics, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran ; Targeted Drug Delivery Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
ISRN Pharm. 2012;2012:976879. doi: 10.5402/2012/976879. Epub 2012 Nov 27.
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.
基于多剂量给药方案的传统药物递送系统通常存在许多缺点,例如患者依从性差和药物血浆水平波动。为了克服传统药物制剂的障碍,本研究提出了新型药物递送系统聚己内酯-聚乙二醇-聚己内酯水凝胶。共聚物通过快速微波辅助和传统合成方法合成。使用凝胶渗透色谱法和(1)H-NMR进行聚合物表征。通过倒置管法评估相变行为,并使用盐酸纳曲酮和维生素B12作为药物模型测定体外药物释放曲线。结果表明,载药结构和共聚物浓度对这些水凝胶中药物的释放曲线起着关键作用。本研究还证实,使用微波合成共聚物是合成这类共聚物的最有效方法。