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受隐生现象启发构建“与”逻辑门平台用于潜在的肿瘤特异性药物递送

Cryptobiosis-inspired assembly of "AND" logic gate platform for potential tumor-specific drug delivery.

作者信息

Zhou Hu, He Gang, Sun Yanbin, Wang Jingguo, Wu Haitao, Jin Ping, Zha Zhengbao

机构信息

Shenzhen Maternity and Child Healthcare Hospital, Shandong University, Shenzhen 518028, China.

School of Food and Biological Engineering, School of Instrument Science and Opto-Electronics Engineering, Hefei University of Technology, Hefei 230009, China.

出版信息

Acta Pharm Sin B. 2021 Feb;11(2):534-543. doi: 10.1016/j.apsb.2020.08.007. Epub 2020 Aug 25.

Abstract

Developing tumor-specific drug delivery systems with minimized off-target cargo leakage remains an enduring challenge. In this study, inspired from the natural cryptobiosis explored by certain organisms and stimuli-responsive polyphenol‒metal coordination chemistry, doxorubicin (DOX)-conjugated gelatin nanoparticles with protective shells formed by complex of tannic acid and Fe (DG@TA-Fe NPs) were successfully developed as an "AND" logic gate platform for tumor-targeted DOX delivery. Moreover, benefiting from the well-reported photothermal conversion ability of TA-Fe complex, a synergistic tumor inhibition effect was confirmed by treating 4T1 tumor-bearing mice with DG@TA-Fe NPs and localized near-infrared (NIR) laser irradiation. As a proof of concept study, this work present a simple strategy for developing "AND" logic gate platforms by coating enzyme-degradable drug conjugates with detachable polyphenol‒metal shells.

摘要

开发具有最小脱靶药物泄漏的肿瘤特异性药物递送系统仍然是一项持久的挑战。在本研究中,受某些生物体探索的自然隐生现象和刺激响应性多酚-金属配位化学的启发,成功开发了由鞣酸和铁络合物形成保护壳的阿霉素(DOX)共轭明胶纳米颗粒(DG@TA-Fe NPs),作为用于肿瘤靶向DOX递送的“与”逻辑门平台。此外,受益于已充分报道的TA-Fe络合物的光热转换能力,通过用DG@TA-Fe NPs和局部近红外(NIR)激光照射治疗4T1荷瘤小鼠,证实了协同肿瘤抑制作用。作为概念验证研究,这项工作提出了一种通过用可分离的多酚-金属壳包裹酶可降解药物共轭物来开发“与”逻辑门平台的简单策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d837/7893123/c15cbd474838/fx1.jpg

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