Cyclo(RGD)-Decorated Reduction-Responsive Nanogels Mediate Targeted Chemotherapy of Integrin Overexpressing Human Glioblastoma In Vivo

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• 作者：Wei Chen ; Yan Zou ; Zhiyuan Zhong and Rainer Haag
• 刊名：Small
• 出版年：2017
• 出版时间：February 10, 2017
• 年：2017
• 卷：13
• 期：6
• 全文大小：2026K
• ISSN：1613-6829

文摘

Cyclo(Arg-Gly-Asp) peptide (cRGD) decorated disulfide (SS) containing poly(vinyl alcohol) nanogels (cRGD-SS-NGs) with an average diameter of 142 nm prepared by inverse nanoprecipitation, “click” reaction, and cRGD conjugation are developed for targeted treatment of integrin overexpressing human glioblastoma in vivo. Doxorubicin (DOX) release from cRGD-SS-NGs is highly inhibited under physiological conditions, while accelerated at endosomal pH and in response to cytoplasmic concentration of glutathione. Confocal microscopy shows that cRGD-SS-NGs facilitate the cellular uptake and intracellular DOX release in α_vβ₃ integrin overexpressing human glioblastoma U87-MG cells. DOX-loaded cRGD-SS-NGs present much better killing activity toward U87-MG cells than that for nontargeted nanogels determined by MTT assay. The in vivo imaging and biodistribution studies reveal that DOX-loaded cRGD-SS-NGs have a much better tumor targetability toward human U87-MG glioblastoma xenograft in nude mice. Also the tumor growth is effectively inhibited by treatment with DOX-loaded cRGD-SS-NGs, while continuous tumor growth is observed for mice treated with nondecorated nanogels as well as free DOX. Furthermore, the treatment with DOX-loaded cRGD-SS-NGs has much fewer side effects, rendering these nanogels as a new platform for cancer chemotherapy in vivo.