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Synthesis and Physicochemical Characterization of Biodegradable PLGA-based Magnetic Nanoparticles Containing Amoxicilin

机译:可生物降解的含阿莫西林的PLGA基磁性纳米粒子的合成和理化性质

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摘要

The purposes of this research were to synthesize amoxicillin-carrying magnetic nanoparticles. Magnetic nanoparticles were prepared by a chemical precipitation of ferric and ferrous chloride salts in the presence of a strong basic solution. PLGA and PLGA-PEG copolymers were prepared by ring opening polymerization of lactide (LA) and glycolide (GA) (mole ratio of LA: GA 3:1) with or without polyethylene glycol (PEG). Amoxicillin loaded magnetic PLGA and PLGA-PEG nanoparticles were prepared by an emulsion-evaporation process (o/w). Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) photomicrographs showed that the magnetic nanoparticles have the mean diameter within the range of 65-260 ran also they were almost spherical in shape. Magnetic nanoparticles prepared with PLGA showed more efficient entrapment (90%) as compared with PLGA-PEG (48-52%) nanoparticles. In-vitro release of amoxicillin from magnetic PLGA nanoparticles showed that 78% of drug was released over 24 hours. The amount of amoxicillin released from PLGA-PEG s was higher than PLGA.
机译:这项研究的目的是合成载有阿莫西林的磁性纳米粒子。通过在强碱性溶液中化学沉淀三氯化铁和氯化亚铁盐来制备磁性纳米颗粒。 PLGA和PLGA-PEG共聚物是通过在有或没有聚乙二醇(PEG)的情况下,丙交酯(LA)和乙交酯(GA)(LA:GA 3:1的摩尔比)的开环聚合反应制得的。载有阿莫西林的磁性PLGA和PLGA-PEG纳米粒子是通过乳液蒸发工艺(o / w)制备的。透射电子显微镜(TEM)和扫描电子显微镜(SEM)的显微照片显示,磁性纳米颗粒的平均直径在65-260nm范围内,并且它们的形状几乎为球形。与PLGA-PEG(48-52%)纳米粒子相比,使用PLGA制备的磁性纳米粒子表现出更有效的包封(90%)。阿莫西林从磁性PLGA纳米粒子中的体外释放表明78%的药物在24小时内释放。从PLGA-PEG释放的阿莫西林的量高于PLGA。

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