Song Xiao-Rong, Li Shi-Hua, Guo Hanhan, You Wenwu, Tu Datao, Li Juan, Lu Chun-Hua, Yang Huang-Hao, Chen Xueyuan
CAS Key Laboratory of Design and Assembly of Functional Nanostructures Fujian Key Laboratory of Nanomaterials Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou Fujian 350002 China.
MOE Key Laboratory for Analytical Science of Food Safety and Biology State Key Laboratory of Photocatalysis on Energy and Environment College of Chemistry Fuzhou University Fuzhou Fujian 350116 China.
Adv Sci (Weinh). 2018 Oct 26;5(12):1801201. doi: 10.1002/advs.201801201. eCollection 2018 Dec.
The exploitation of smart nanoagents based drug delivery systems (DDSs) has proven to be a promising strategy for fighting cancers. Hitherto, such nanoagents still face challenges associated with their complicated synthesis, insufficient drug release in tumors, and low cancer cell chemosensitivity. Here, the engineering of an adenosine triphosphate (ATP)-activatable nanoagent is demonstrated based on self-assembled quantum dots-phenolic nanoclusters to circumvent such challenges. The smart nanoagent constructed through a one-step assembly not only has high drug loading and low cytotoxicity to normal cells, but also enables ATP-activated disassembly and controlled drug delivery in cancer cells. Particularly, the nanoagent can induce cell ATP depletion and increase cell chemosensitivity for significantly enhanced cancer chemotherapy. Systematic in vitro and in vivo studies further reveal the capabilities of the nanoagent for intracellular ATP imaging, high tumor accumulation, and eventual body clearance. As a result, the presented multifunctional smart nanoagent shows enhanced antitumor efficacy by simultaneous ATP-responsive chemodrug release and cancer cell sensitization. These findings offer new insights toward the design of smart nanoagents for improved cancer therapeutics.
基于智能纳米载体的药物递送系统(DDSs)的开发已被证明是对抗癌症的一种有前景的策略。迄今为止,此类纳米载体仍面临着与复杂合成、肿瘤中药物释放不足以及癌细胞化疗敏感性低相关的挑战。在此,展示了基于自组装量子点-酚类纳米簇构建三磷酸腺苷(ATP)激活的纳米载体,以克服这些挑战。通过一步组装构建的智能纳米载体不仅具有高载药量和对正常细胞的低细胞毒性,还能在癌细胞中实现ATP激活的解离和可控的药物递送。特别地,该纳米载体可诱导细胞ATP耗竭并提高细胞化疗敏感性,从而显著增强癌症化疗效果。系统的体外和体内研究进一步揭示了该纳米载体用于细胞内ATP成像、高肿瘤蓄积以及最终从体内清除的能力。因此,所展示的多功能智能纳米载体通过同时实现ATP响应的化学药物释放和癌细胞致敏,显示出增强的抗肿瘤功效。这些发现为设计用于改善癌症治疗的智能纳米载体提供了新的见解。