Center for Research at Bio/Nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, UF Health Cancer Center, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, FL, 32611-7200, USA.
George & Josephine Butler Polymer Research Laboratory, Center for Macromolecular Science & Engineering, Department of Chemistry, University of Florida, Gainesville, FL, 32611-7200, USA.
Angew Chem Int Ed Engl. 2018 Dec 21;57(52):17048-17052. doi: 10.1002/anie.201809753. Epub 2018 Nov 26.
Photoresponsive materials are emerging as ideal carriers for precisely controlled drug delivery owing to their high spatiotemporal selectivity. However, drawbacks such as slow release kinetics, inherent toxicity, and lack of targeting ability hinder their translation into clinical use. We constructed a new DNA aptamer-grafted photoresponsive hyperbranched polymer, which can self-assemble into nanoparticles, thereby achieving biocompatibility and target specificity, as well as light-controllable release behavior. Upon UV-irradiation, rapid release induced by disassembly was observed for Nile Red-loaded nanoparticles. Further in vitro cell studies confirmed this delivery system's specific binding and internalization performance arising from the DNA aptamer corona. The DOX-loaded nanoassembly exhibited selective phototriggered cytotoxicity towards cancer cells, indicating its promising therapeutic effect as a smart drug delivery system.
光响应材料由于具有高时空选择性,正成为精确控制药物传递的理想载体。然而,其释放动力学缓慢、固有毒性和缺乏靶向能力等缺点限制了它们在临床应用中的转化。我们构建了一种新的 DNA 适体接枝光响应超支化聚合物,它可以自组装成纳米颗粒,从而实现生物相容性和靶向特异性以及光控释放行为。在 UV 照射下,负载尼罗红的纳米颗粒观察到快速解组装诱导的释放。进一步的体外细胞研究证实,这种递药系统的特异性结合和内化性能源于 DNA 适体冠。负载 DOX 的纳米组装体对癌细胞表现出选择性的光触发细胞毒性,表明其作为智能药物递送系统具有有前景的治疗效果。