摘要
应用改进的悬浮交联技术制备磁性壳聚糖(chitosan,CS)纳米微球。结果显示:该药物微球基本呈球形,其粒径在200-800 nm之间,并且显示了好的磁响应性。阿霉素(doxorubicin,DOX)为试验药物,DOX和CS以化学键(-N=C-)结合在一起,药物含量在1%-15%(w/w)。pH值的大小对其药物体外释放试验的影响很大,当pH为1、2和4时,7 d内药物的释放从22.0%、13.4%降至4.1%。该微球为pH敏感的磁靶向药物微球。
Magnetic chitosan(CS) nano-spheres were prepared by the modified suspension cross-linking technique.The results demonstrated that the magnetic drug nano-spheres are mainly spherical in form with a size of 200 to 800 nm,and show good magnetic responsivity.Here,Doxorubicin was used as exam drug.Glutaraldehyde connects Doxorubicin to CS by the chemical bond(-N=C-), and the drug content is in range of 1% to 15%(w/w).The chemical bond is broken depending on pH,so pH is the important factor for the release of doxorubicin.The doxorubicin release was 22.0%,13.4%,and 4.1% in the space of 7d,when pH was 1,2,4.So the nano-spheres are pH-sensitive magnetic targeting drug micro-spheres.
出处
《生物医学工程学杂志》
EI
CAS
CSCD
北大核心
2010年第1期86-90,共5页
Journal of Biomedical Engineering
基金
广东省自然科学基金资助项目(04006966)
广东省卫生科研基金资助项目(A2003697)
关键词
纳米粒子
乳液
磁性药物靶向
药物载体
Nano-particle
Emulsion
Magnetic drug targeting
Drug carrier