Université Paris-Sud XI, UMR CNRS 8612, 5 rue J.B. Clément, 92290, Châtenay-Malabry, France.
Nanoscale. 2010 Aug;2(8):1521-6. doi: 10.1039/c0nr00132e. Epub 2010 Jul 5.
A new prodrug of gemcitabine, based on the covalent coupling of squalene to gemcitabine (GemSQ), has been designed to enhance the anticancer activity of gemcitabine, a nucleoside analogue active against a wide variety of tumors. In the present study, the feasibility of encapsulating GemSQ into liposomes either PEGylated or non-PEGylated has been investigated. The in vivo anticancer activity of these formulations has been tested on subcutaneous grafted L1210wt leukemia model and compared to that of free gemcitabine. The liposomal GemSQ appears to be a potential delivery system for the effective treatment of tumors.
一种新型的吉西他滨前药,基于将角鲨烯与吉西他滨(GemSQ)共价偶联,旨在增强吉西他滨的抗癌活性,吉西他滨是一种针对多种肿瘤有效的核苷类似物。在本研究中,研究了将 GemSQ 包封到 PEG 化或非 PEG 化脂质体中的可行性。这些制剂的体内抗癌活性已在皮下移植的 L1210wt 白血病模型中进行了测试,并与游离吉西他滨进行了比较。脂质体 GemSQ 似乎是一种有效的肿瘤治疗的潜在递药系统。