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雷公藤甲素壳聚糖纳米粒的制备与初步评价

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目的:制备包载雷公藤甲素的壳聚糖纳米粒系统(triptolide-chitosan nanoparticles,TP-CS NPs),并考察其理化性质及体外释药性能.方法:采用非溶剂辅助络合-化学交联法制备壳聚糖纳米粒.利用透射电镜、粒度仪、HPLC法等对制备的纳米粒性质进行表征.结果:制得的纳米粒呈球形,平均粒径为(151.2±5.4)nm,Zeta电位(20.1±1.2)mV,纳米粒收率(78.0±3.3)%,包封率(77.0±1.2)%,载药量(2.0±0.4)%,体外模拟释药结果表明载药纳米粒药物释放速率在24h内持续稳定.结论:非溶剂辅助络合-化学交联法制备的雷公藤甲素壳聚糖纳米粒简便可靠,体外释药具有明显的缓释作用.
Preparation and Evaluation of Triptolide-Loaded Chitosan Nanoparticles
Objective:To prepare the triptolide-loaded chitosan nanoparticles (TP-CS NPs) and to investigate their physicochemical properties and in vitro release characteristics.Methods:TP-CS NPs were prepared by non-solvent-aided complexation-chemical cross-linking method.Their properties were determined by transmission electron microscopy,particle size analyzer,HPLC and so on.Results:The prepared nanoparticles were spherical with an average size at (151.2 ± 5.4)nm,a Zeta potential at (20.1 ± 1.2) mV,a yield of (78.0 ± 3.3) %,encapsulation efficiency of (77.0 ± 1.2) % and drug loading content of (2.0 ± 0.4) %.In vitro,the drug release rate was continuously stable in 24 h.Conclusion:TP-CS NPs prepared by non solvent assisted complexation-chemical crosslinking method is convient and reliable,showing a sustained release behavior in vitro.

triptolidechitosan nanoparticlesnonsolvent-aided complexationdrug controlled release

陈瑞、赵群、邵江娟、王耀帅

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南京中医药大学药学院,江苏南京210023

南京中医药大学第二临床医学院,江苏南京210023

雷公藤甲素 壳聚糖纳米粒 非溶剂辅助络合法 药物缓释

江苏高校优势学科建设工程资助项目南京中医药大学青年自然科学基金

13XZR22

2016

辽宁中医杂志
辽宁中医药大学,辽宁省中医药学会

辽宁中医杂志

CSTPCD北大核心
影响因子:0.815
ISSN:1000-1719
年,卷(期):2016.43(4)
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