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The Release characteristics of Different Model Drugs from Medicated PLGA Microspheres

机译:来自药物PLGA微球的不同模型药物的释放特征

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In this study, four model drugs, i.e., Meloxicam (MEL), Risperidone (RIS), Eprinomectin (EPR), and Bull Serum Albumin (BSA), were encapsulated in PLGA microspheres via solvent evaporation methods. The encapsulation efficiency and in vitro release profiles of different drugs with various water solubilities from medicated PLGA microspheres were investigated. The surface morphologies of microspheres were detected by scanning electron microscope (SEM). The release characteristics of the model drugs from the medicated microspheres were carried out in the phosphate buffer solution (PBS), pH7.4, at 37°C. Studies found that the water solubility of model drugs had significant influences on their in vitro release profiles and the release rates of four model drugs were in the orders of BSA>MEL>RIS>EPR.
机译:在该研究中,通过溶剂蒸发方法将四种模型药物,即美洛昔康(MEL),Rispericone(MEL),丙酮酮(RIS),乙烯酮(EPR),ePRINMENCER(EPR)和牛血清白蛋白(BSA)包封在PLGA微球中。研究了不同药物具有来自药物PLGA微球的各种水溶性的不同药物的封装效率和体外释放曲线。通过扫描电子显微镜(SEM)检测微球的表面形态。在37℃下,在磷酸盐缓冲溶液(PBS),pH7.4中进行来自含药微球的模型药物的释放特性。研究发现,模型药物的水溶性对其体外释放曲线的影响显着,四种模型药物的释放速率在BSA> Mel> Ris> EPR的顺序中。

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