摘要
采用乳化溶剂挥发的方法制备MeOCPT纳米粒子,结果表明:MeOCPT纳米粒子具有明显的圆形结构,且表面光滑,大小均匀,粒度分布在100~300nm之间。MeOCPT的栽药量和包封率分别为(3.10±1.19)%和(83.57±3.45)%,在体外可以持续缓慢释放,累积释放率接近60%,达到了预期的药物缓慢释放及降低毒性的结果。
The nanoparticles contained MeOCPT prepared with the method emulsion and solvent evaporation.The MeOCPT nanoparticles had a circular structure,with a smooth surface ,uniform size, and its particle size distributed between 100 nm and 300 nm.The drug-loading rate and entrapment efficiency of MeOCPT nanoparticles were (3.10± 1.19 )% and (83.57±3.45)%.MeOCPT nanoparticles released slowly and lastingly in vitro whose cumulative release rate was nearly 60%,which could release the drugs slowly and reduce the toxicity of drugs.
出处
《现代农业科技》
2015年第8期173-173,179,共2页
Modern Agricultural Science and Technology
关键词
甲氧基喜树碱
聚乳酸
纳米粒子
体外释放
Methoxycamptothecin
polylactic acid
nanoparticles
in vitro drug release