Zhou Xianfeng, Liu Bin, Yu Xianghui, Zha Xiao, Zhang Xizhen, Wang Xueyun, Jin Yinghua, Wu Yongge, Chen Yue, Shan Yaming, Chen Yan, Liu Junqiu, Kong Wei, Shen Jiacong
College of Life Science, Jilin University, Changchun, PR China.
Eur J Pharm Biopharm. 2008 Mar;68(3):589-95. doi: 10.1016/j.ejpb.2007.09.006. Epub 2007 Sep 21.
A novel approach involving the preparation of biodegradable PLGA microspheres containing entrapping complexes of DNA and polyethylenimine was developed to improve the delivery of DNA into antigen-presenting cells after intramuscular injection. Compared to the traditional biodegradable microspheres which release naked DNA, these microspheres released intact and penetrative PEI/DNA complexes over a period of 2 weeks in vitro. In addition, the DNA was not degraded during encapsulation in the PLGA microspheres, owing to the protection of polyethylenimine. After i.m. immunization, the microspheres induced significantly enhanced serum antibody responses 2-3 orders of magnitude greater than naked DNA. Additionally, in contrast to naked DNA, the microspheres induced potent CTL responses at a low dose.
开发了一种新方法,该方法涉及制备含有DNA与聚乙烯亚胺包封复合物的可生物降解聚乳酸-羟基乙酸共聚物(PLGA)微球,以改善肌内注射后DNA向抗原呈递细胞的递送。与释放裸DNA的传统可生物降解微球相比,这些微球在体外2周的时间内释放完整且具有穿透性的聚乙烯亚胺/DNA复合物。此外,由于聚乙烯亚胺的保护作用,DNA在包封于PLGA微球的过程中未发生降解。肌内免疫后,微球诱导的血清抗体反应显著增强,比裸DNA大2至3个数量级。此外,与裸DNA相比,微球在低剂量时就能诱导出有效的细胞毒性T淋巴细胞(CTL)反应。