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乳铁蛋白修饰的多柔比星载前体脂质体用于治疗神经胶质瘤。

Lactoferrin modified doxorubicin-loaded procationic liposomes for the treatment of gliomas.

机构信息

Key Laboratory of Drug Targeting, Ministry of Education, Sichuan University, Chengdu, PR China.

出版信息

Eur J Pharm Sci. 2011 Sep 18;44(1-2):164-73. doi: 10.1016/j.ejps.2011.07.007. Epub 2011 Jul 18.

DOI:10.1016/j.ejps.2011.07.007
PMID:21782939
Abstract

In this study, a brain-targeted chemotherapeutical delivery system, doxorubicin-loaded lactoferrin-modified procationic liposome (DOX-Lf-PCL) was developed, and its therapeutic effect for glioma was evaluated. The uptake profile of various DOX formulations in vitro by primary brain capillary endothelial cells (BCECs) and glioma cell C6 were studied by laser scanning confocal microscope and flow cytometry. An intracranial tumor model of rats was employed to evaluate the therapeutic effect of DOX-Lf-PCLs for glioma. Five groups of glioma-bearing rats (total n=50) were subjected to three cycles of 2.5mg/kg body weight of doxorubicin in different formulations or normal saline (N.S.) and analyzed for survival (median survival time, Kaplan-Meier). The results indicated that compared with the DOX solution or DOX-loaded conventional liposomes (DOX-Lips), DOX-PCLs and DOX-Lf-PCLs showed an improved performance in the uptake efficiency in BCECs and C6 cells. The DOX-Lf-PCLs can inhibit the growth of C6 more efficiently in vitro than other DOX formulations. The endocytosis involved in the DOX-Lf-PCLs uptake of C6 was mediated by both receptor- and absorption-mediated transcytosis. DOX-Lf-PCLs could significantly extend the survival time compared with the N.S. control and other DOX formulations. This study showed that the therapy with DOX-Lf-PCLs offers an effective therapeutic potential for gliomas.

摘要

在这项研究中,开发了一种脑靶向化疗药物传递系统,即载多柔比星的乳铁蛋白修饰的前质子化脂质体(DOX-Lf-PCL),并评估了其治疗脑胶质瘤的效果。通过激光共聚焦显微镜和流式细胞术研究了各种 DOX 制剂在原代脑毛细血管内皮细胞(BCECs)和脑胶质瘤细胞 C6 中的体外摄取情况。采用大鼠颅内肿瘤模型评价 DOX-Lf-PCLs 对脑胶质瘤的治疗效果。将 5 组荷脑胶质瘤大鼠(共 50 只)分别用不同制剂的 2.5mg/kg 体重的多柔比星或生理盐水(N.S.)进行三个周期治疗,并分析其生存情况(中位生存时间,Kaplan-Meier)。结果表明,与 DOX 溶液或载 DOX 的普通脂质体(DOX-Lips)相比,DOX-PCLs 和 DOX-Lf-PCLs 提高了在 BCECs 和 C6 细胞中的摄取效率。DOX-Lf-PCLs 在体外对 C6 的抑制生长作用优于其他 DOX 制剂。C6 对 DOX-Lf-PCLs 的内吞作用涉及受体介导和吸收介导的转胞吞作用。与 N.S. 对照组和其他 DOX 制剂相比,DOX-Lf-PCLs 可显著延长生存时间。这项研究表明,DOX-Lf-PCLs 治疗可为脑胶质瘤提供有效的治疗潜力。

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