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首页> 外文期刊>Journal of Applied Polymer Science >Synthesis and Characterization of Polyelectrolyte Complex Microparticles for Drug Release
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Synthesis and Characterization of Polyelectrolyte Complex Microparticles for Drug Release

机译:药物释放用聚电解质复合物微粒的合成与表征

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摘要

Free radical copolymerization of acryloxyethyl-trimethylammonium chloride with 2-hydroxyethyl methacrylate using sodium persulfate as initiator was carried out at 60℃ and of its electrostatic interaction with sodium alginate (NaAlg) allowed obtaining polymeric microparticles by complex coacervation. The solute transport in this swellable matrix was investigated to check the effect of cross-linking and simulated physiological condition over release process. Cefazolin Sodium loaded microparticles were prepared by incorporation of drug directly in the reaction mixture and their ability of releasing resulted in more extensive in enzyme-free simulated intestinal medium. The polymeric microparticles prepared in this study were characterized by scanning electron microscopy showing irregular spherical form and rough structure. Particles showed unimodal distribution and the size distribution ranged from 1.1 to 1.8 mm (n =100).
机译:以过硫酸钠为引发剂,将丙烯酰氯乙基三甲基氯化铵与甲基丙烯酸2-羟乙酯进行自由基共聚反应,于60℃进行了自由基共聚,并与藻酸钠(NaAlg)发生了静电相互作用,通过络合凝聚获得了聚合物微粒。研究了该溶胀基质中的溶质运移,以检查交联和模拟生理条件对释放过程的影响。通过将药物直接掺入反应混合物中来制备头孢唑啉钠负载的微粒,其释放能力导致在无酶的模拟肠道培养基中具有更广泛的作用。在本研究中制备的聚合物微粒通过扫描电子显微镜表征,显示不规则球形和粗糙结构。颗粒表现出单峰分布,尺寸分布范围为1.1至1.8毫米(n = 100)。

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