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Synthesis and Characterization of PEG-PBS Copolymersto Obtain Microspheres With Different NaproxenRelease Profiles

机译:PEG-PBS Copolymersto的合成与表征利用不同的萘普生酶促型材获得微球

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Researching for new biomaterials intended for drug delivery systems hasconsiderably intensified in recent years. There is an increasing interest inPBS (poly[butylene succinate]) and its copolymers as biomaterials due to thepossibility of synthesis of the PBS from a renewable source. Among thesecopolymers, PBS-PEG (poly[butylene succinate-co-polyethylene glycol]) isstudied for materials that have shape memory and are biodegradable.However, to date, no research into the use of PBS-PEG to preparemicrospheres for drugs release has been reported. Herein, PBS-PEGs withthree PEG with different chain0s length were synthesized by polycondensationreaction and characterized by means of SEC, FTIR, DSC, TGA, and DRX.Naproxen loaded microspheres were prepared by an oil-in-water (o/w) singleemulsion technique. The drug release was followed by UV-Vis. The presenceof PEG had a marked effect on the in vitro release profiles. The mathematicalmodels employed show that the fundamental mechanism of release isdiffusion when PEG is present in the polymer matrix of the particle.
机译:研究一种针对近年来愈演愈烈hasconsiderably药物传递系统的新生物材料。有越来越多的兴趣PBS中(聚[丁二酸丁二醇酯])和它用作生物材料由于来自可再生来源的PBS的合成thepossibility共聚物。间thesecopolymers,isstudied用于具有形状记忆和是biodegradable.However,迄今为止,没有研究使用PBS-PEG与preparemicrospheres药物释放一直材料PBS-PEG(聚[丁二酸丁二醇酯 - 共 - 聚乙二醇])报道。这里,PBS-PEG的PEG withthree具有不同长度chain0s通过polycondensationreaction合成并表征了通过SEC,FTIR,DSC,TGA的装置,以及装载DRX.Naproxen由油包水型(O / W)singleemulsion技术制备的微球。药物释放其次紫外可见。该presenceof PEG对体外释放曲线有显着影响。所述mathematicalmodels雇表明释放isdiffusion的基本机构,当PEG是存在于颗粒的聚合物基质。

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