首页|庆大霉素/壳聚糖局部注射微球给药系统的特性及细胞毒性研究

庆大霉素/壳聚糖局部注射微球给药系统的特性及细胞毒性研究

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目的 构建用于局部注射的庆大霉素/壳聚糖微球给药系统,评价其理化特性及细胞毒性.方法 以庆大霉素为模型药物,壳聚糖为载体,磷脂、羟丙基-β-环糊精为辅料,采用喷雾干燥法制备庆大霉素/壳聚糖/磷脂/羟丙基-β-环糊精局部注射微球,以紫外分光光度法(UV)、扫描电子显微镜(SEM)、X线衍射分析(XRD)、动态膜透析法和四甲基偶氮唑盐法(MTT)等考察微球理化特性及体外细胞毒性.结果 喷雾干燥法成功制备不同药物/载体比例的A、B、C、D、E5种壳聚糖微球,其产率、载药量、包封率分别为34.38%~46.94%、10.20%~18.67%、61.20%~74.72%,电镜结果显示微球A、B、C成球性差,微球间粘连严重,微球D、E成球形,表面有褶皱,粒径较均匀,粒径在0.5~3μm之间,无粘连;X射线衍射分析结果表明药物已包封在微球中;体外释放结果显示微球D缓释效果较好,24 h累计释放量为83.32%.细胞毒性实验结果表明庆大霉素浓度达到400μg/mL时,微球D的细胞相对增值率仍高于80%,细胞毒性分级为1级,即无细胞毒性.结论 微球D具有良好的理化性质及缓释作用,生物相容性好,有望成为前列腺局部给药的良好载体.
Studies on the characteristics and cytotoxicity of gentamicin/chitosan microspheres for local injection
Objective To construct the drug delivery system of gentamicin/chitosan microspheres for local injection, and evaluate its physicochemical properties and cell cytotoxicity.Methods Gentamicinwas used as model drug, chitosan as carrier, lecithinand hydroxypropyl-β-cyclodextrin as accessories, and the microspheres of gentamicin/chitosan/lecithin/hydroxypropyl-β-cyclodextrinwas prepared by spray drying method.The physicochemical properties and cell cytotoxicity of themicrospheres were investigated by UV spectrophotometry , scanning electron microscopy, X-ray diffraction, dynamic membrane dialysis and MTT assay.Results Five kinds of chitosan microspheres ( A, B, C, D and E) with different drug/carrier ratios were successfully prepared by spray drying method.The yield, drug loading and entrapment efficiency of the drug-loaded microspheres were 34.38%~46.94%, 10.20% ~18.67%, 61.20% ~74.72%, respectively.SEM results showed that compared with microspheres A, B and C, microspheres D and E own the spherical shape with wrinkled surface and uniform particle size, particle size between 0.5 ~3 μm, no adhesion.X-ray diffraction analysis showed that the drug was encapsulated in the microspheres.The results of in vitro release indicated that microspheres D had a good sustained release effect in the four drug-loaded microspheres.The results of cytotoxicity test showed that when the concentration of gentamicin reached 400 μg/mL, the relative growth rate of microspheres D was still higher than 80% with the cytotoxicity grade was one, ie, no cytotoxicity.Conclusion The microspheres D with good physicochemical properties, sustained-release effect and biocompatibility, is expected to be a good carrier of prostate local drug delivery.

chronicbacterial prostatitislocal treatmentgentamicinchitosan microspheresspray drying method

庞昌伟、于洪丽、王永红、秦梦、高佃军、张维芬

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潍坊医学院,山东潍坊261053

潍坊医学院药学院,山东潍坊261053

慢性细菌性前列腺炎 局部治疗 庆大霉素 壳聚糖微球 喷雾干燥法

国家自然科学基金国家科技部科技计划项目山东省自然科学基金山东省医药卫生科技发展计划项目山东省潍坊市科技计划项目

815737172013GA740103ZR2012CM0252015WS00572014WS045

2017

中国生化药物杂志
南京生物化学制药研究所,全国生化制药情报中心站,中国生化制药工业协会,中国药品生物制品检定所

中国生化药物杂志

ISSN:1005-1678
年,卷(期):2017.37(3)
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