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近红外调控高效 siRNA 递药与治疗的光致撕裂胶带包裹上转换纳米胶囊

Photo-tearable tape close-wrapped upconversion nanocapsules for near-infrared modulated efficient siRNA delivery and therapy.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, PR China.

Jiangsu Collaborative Innovation Centre of Biomedical Functional Materials and Jiangsu Key Laboratory of Biofunctional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, PR China.

出版信息

Biomaterials. 2018 May;163:55-66. doi: 10.1016/j.biomaterials.2018.02.019. Epub 2018 Feb 9.

Abstract

RNA interference (RNAi) has become an appealing therapeutic approach for cancer and other diseases. One key challenge is the effective protection of these small fragile biomolecules against complicated physiological environments as well as efficient on-demand release. Here we design a photo-tearable polymer tape close-wrapped nanocapsule for efficient NIR modulated siRNA delivery. The photo-tearable nanocapsules comprise core-shell upconversion nanoparticles (UCNPs) coated with mesoporous silica layer for loading of photosensitizer hypocrellin A (HA) and small interfering RNA (siRNA) against polo-like kinase 1 (PLK1), and covalently bound thin membranes of polyethylene glycol (PEG) via a synthesized photocleavable linker (PhL). Upon irradiation at 980 nm, the UCNPs produce UV emissions to break PhL and tear out PEG membrane for siRNA release, and blue emissions to activate HA for generating reactive oxygen species (ROS). The close PEG membrane wrapping not only guarantees the efficient intracellular photocleavage, but also extends the circulation time and protects the loaded cargos from leakage and degradation. The ROS assists endosomal escape of the loaded cargos, therefore effectively improves the gene silencing efficiency and the suppressions of cell proliferation in vitro and tumor growth in vivo. The proposed photo-tearable tape-wrapped nanocapsules have promising potential application in precision medicine.

摘要

RNA 干扰 (RNAi) 已成为癌症和其他疾病有吸引力的治疗方法。一个关键的挑战是有效地保护这些小而脆弱的生物分子免受复杂的生理环境的影响,以及高效的按需释放。在这里,我们设计了一种光可撕裂的聚合物带紧密包裹的纳米胶囊,用于高效的近红外调制 siRNA 递药。光可撕裂的纳米胶囊由核壳上转换纳米粒子 (UCNPs) 组成,表面包覆有介孔硅层,用于负载光增敏剂竹红菌素 A (HA) 和针对 Polo 样激酶 1 (PLK1) 的小干扰 RNA (siRNA),并通过合成的光裂解连接子 (PhL) 共价结合薄的聚乙二醇 (PEG) 膜。在 980nm 照射下,UCNPs 产生紫外发射以断裂 PhL 并撕开 PEG 膜以释放 siRNA,并产生蓝移发射以激活 HA 产生活性氧物种 (ROS)。紧密的 PEG 膜包裹不仅保证了高效的细胞内光裂解,还延长了循环时间,并保护负载的货物免受泄漏和降解。ROS 有助于负载货物的内体逃逸,因此有效提高了体外基因沉默效率和细胞增殖抑制作用,并在体内抑制肿瘤生长。所提出的光可撕裂的带缠绕纳米胶囊在精准医学中有很好的应用前景。

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