LIN Xiao-jie, ZHANG Hua, JIN Shao-gang, et al. Preparation and Release of Sinomenine Hydrochloride-loaded Chitosan Nanoparticles[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(4): 22-25.
LIN Xiao-jie, ZHANG Hua, JIN Shao-gang, et al. Preparation and Release of Sinomenine Hydrochloride-loaded Chitosan Nanoparticles[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(4): 22-25.DOI:
盐酸青藤碱壳聚糖纳米粒的制备及体外释放性能的研究
摘要
目的 :制备盐酸青藤碱壳聚糖纳米粒
并考察其性质和体外释药特性。 方法: 通过微乳液-离子交联法制备盐酸青藤碱壳聚糖纳米粒
考察纳米粒的形态、 粒径和zeta电位
紫外分光光度法测定其载药量和包封率
透析法研究其体外释药特性。 结果: 制得的纳米粒呈球形或类球形
平均粒径为98.3 nm
包封率为67.2%
体外模拟释药结果表明载药纳米粒药物释放速率在24 h 内持续稳定。 结论: 微乳液-离子交联法制备盐酸青藤碱壳聚糖纳米粒简便可靠
体外释药具有明显的缓释作用。
Abstract
Objective: To prepare sinomenine hydrochloride-loaded chitosan nanoparticles and investigate their characteristics and in vitro drug release ability. Method: The nanoparticles were prepared by microemulsion-ionic crosslinking method with Na5P3O10 used as crosslinkers.The morphology of nanoparticles was evaluated by the transmission electron microscopy (TEM).The mean size and zeta potential of nanoparticles were determined by dynamic light scattering (DLS).The in vitro release of the drug-loaded chitosan nanoparticles was evaluated using a dialysis method. Result: The nanoparticles were successfully prepared with the spherical or para-spherical shape.Their mean diameter was 98.3 nm.The encapsulation efficiency was 67.2%.The release experiment of drug in vitro showed that the release rate of drug-loaded nanoparticles was stable and sustained for 24 hours. Conclusion: The preparation method is reliable and simple.The nanoparticles possessed good physical performance and sustained release character in vitro .