Pharmacokinetic analysis of site-directed and light-sensitive liposome

点击翻译按钮获取中文摘要

The site-directed and light-sensitive liposome (SDLSL) was prepared using a light-sensitive substance verteporfin in this study. SDLSL could be effectively destroyed by laser irradiation of 532nm and 698nm. We also encapsulated the cisplatin (CDDP), an anticancer agent, into SDLSL in order to investigate further to check the release of CDDP by laser irradiation. As a result, we observed the release of anticancer agent. We validated tumor-suppressive efficacy of the CDDP encapsulating SDLSL in vitro and in vivo. Using colon 26 cell line and CDDP encapsulating SDLSL, strong cancer cell growth inhibitory effect was obtained with light irradiation group in vitro and in vivo, respectively. From these results, SDLSL can be a highly efficacious site-directed drug delivery system in vitro and in vivo. Using SDLSL as a vehicle for drug delivery, substantial pharmacologic effects with minimum side effects into site-directed tissues should be achieved.