Huxford Rachel C, Dekrafft Kathryn E, Boyle William S, Liu Demin, Lin Wenbin
Department of Chemistry, CB#3290, University of North Carolina, Chapel Hill, NC 27599, USA ; Tel: 1-919-962-6320.
Chem Sci. 2012;3(1). doi: 10.1039/C1SC00499A.
Nanoscale coordination polymers (NCPs) have been demonstrated as an interesting platform for drug delivery, as they possess many advantages over small-molecule chemotherapeutics, such as high payloads, lower systemic toxicity, tunability, and enhanced tumor uptake. Existing formulations for the delivery of methotrexate (MTX), an antifolate cancer drug, have very low drug loadings. Herein, we report the incorporation of MTX as a building block in an NCP formulation with exceptionally high drug loadings (up to 79.1 wt%) and the selective delivery of the NCP to cancer cells. Encapsulation of the NCP in a functionalized lipid bilayer allows for targeted delivery and controlled release to cancer cells. A phosphor can be doped into the NCPs for monitoring particle uptake by optical imaging. The lipid-coated and anisamide-targeted NCPs have superior efficacy against acute lymphoblastic leukemia cells when compared to free drug.
纳米级配位聚合物(NCPs)已被证明是一个有趣的药物递送平台,因为它们相对于小分子化疗药物具有许多优势,如高载药量、较低的全身毒性、可调节性以及增强的肿瘤摄取。用于递送抗叶酸癌症药物甲氨蝶呤(MTX)的现有制剂的药物载量非常低。在此,我们报告了将MTX作为一个构建单元纳入具有极高药物载量(高达79.1 wt%)的NCP制剂中,并将该NCP选择性递送至癌细胞。将NCP封装在功能化脂质双层中可实现对癌细胞的靶向递送和控释。可以将一种磷光体掺杂到NCPs中,用于通过光学成像监测颗粒摄取。与游离药物相比,脂质包被且靶向茴香酰胺的NCPs对急性淋巴细胞白血病细胞具有更强的疗效。