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用于呋喃唑酮结肠给药的刀豆球蛋白A偶联粘膜粘附微球。

Con-A conjugated mucoadhesive microspheres for the colonic delivery of diloxanide furoate.

作者信息

Anande Nalini M, Jain Sunil K, Jain Narendra K

机构信息

SLT Institute of Pharmaceutical Sciences, Guru Ghasidas University, Bilaspur (C.G.) 495009, India.

出版信息

Int J Pharm. 2008 Jul 9;359(1-2):182-9. doi: 10.1016/j.ijpharm.2008.04.009. Epub 2008 Apr 12.

Abstract

The aim of the research work was to develop cyst-targeted novel concanavalin-A (Con-A) conjugated mucoadhesive microspheres of diloxanide furoate (DF) for the effective treatment of amoebiasis. Eudragit microspheres of DF were prepared using emulsification-solvent evaporation method. Formulations were characterized for particle size and size distribution, % drug entrapment, surface morphology and in vitro drug release in simulated gastrointestinal (GI) fluids. Eudragit microspheres of DF were conjugated with Con-A. IR spectroscopy and DSC were used to confirm successful conjugation of Con-A to Eudragit microspheres while Con-A conjugated microspheres were further characterized using the parameters of zeta potential, mucoadhesiveness to colonic mucosa and Con-A conjugation efficiency with microspheres. IR studies confirmed the attachment of Con-A with Eudragit microspheres. All the microsphere formulations showed good % drug entrapment (78+/-5%). Zeta potential of Eudragit microspheres and Con-A conjugated Eudragit microspheres were found to be 3.12+/-0.7mV and 16.12+/-0.5mV, respectively. Attachment of lectin to the Eudragit microspheres significantly increases the mucoadhesiveness and also controls the release of DF in simulated GI fluids. Gamma scintigraphy study suggested that Eudragit S100 coated gelatin capsule retarded the release of Con-A conjugated microspheres at low pH and released microspheres slowly at pH 7.4 in the colon.

摘要

该研究工作的目的是开发以囊肿为靶点的新型呋喃妥因(DF)与伴刀豆球蛋白A(Con-A)偶联的黏膜黏附微球,用于有效治疗阿米巴病。采用乳化溶剂蒸发法制备了DF的Eudragit微球。对制剂的粒径及粒径分布、药物包封率、表面形态以及在模拟胃肠道(GI)液中的体外药物释放进行了表征。将DF的Eudragit微球与Con-A偶联。采用红外光谱和差示扫描量热法确认Con-A成功偶联到Eudragit微球上,同时利用zeta电位、对结肠黏膜的黏膜黏附性以及Con-A与微球的偶联效率等参数对Con-A偶联微球进行了进一步表征。红外研究证实了Con-A与Eudragit微球的结合。所有微球制剂均显示出良好的药物包封率(78±5%)。发现Eudragit微球和Con-A偶联的Eudragit微球的zeta电位分别为3.12±0.7mV和16.12±0.5mV。凝集素与Eudragit微球的结合显著增加了黏膜黏附性,同时也控制了DF在模拟GI液中的释放。γ闪烁显像研究表明,Eudragit S100包衣的明胶胶囊在低pH值下延迟了Con-A偶联微球的释放,并在结肠中pH值为7.4时缓慢释放微球。

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