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集成“与”逻辑计算和无酶扩增的智能下转换/上转换纳米机器用于近红外二区荧光辅助精确增强光动力治疗。

Smart down/upconversion nanomachines integrated with "AND" logic computation and enzyme-free amplification for NIR-II fluorescence-assisted precise and enhanced photodynamic therapy.

作者信息

Pang Lifang, Tang Xiaolan, Yao Lijia, Zhou Liuyan, Hu Shengqiang, Zhao Shulin, Zhang Liangliang

机构信息

State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University Guilin 541004 P. R. China

出版信息

Chem Sci. 2023 Feb 21;14(11):3070-3075. doi: 10.1039/d2sc06601g. eCollection 2023 Mar 15.

Abstract

Upconversion nanoparticles enable indirect activation of photodynamic therapy (PDT) using near-infrared (NIR) light, providing an excellent alternative for treating deep tumors. However, conventional NIR light-triggered PDT systems suffered from low spatiotemporal accuracy and restricted therapeutic efficiency . In this work, DNA logic circuits were functionally modified on down/upconversion nanoparticles (D/UCNPs) to construct smart down/upconversion nanomachines (D/UCNMs) for NIR light-triggered PDT toward target tumors. Upon dual inputs of tumor-associated GSH and TK1 mRNA, DNA logic circuits perform "AND" logic computation and initiate the toehold-mediated strand displacement reaction. Meanwhile, the quenched upconversion fluorescence was recovered and then the approaching photosensitizers were activated, leading to output of singlet oxygen (O) for precise and enhanced PDT. Importantly, the biodistribution of the D/UCNMs could be visualized by second near-infrared (NIR-II) fluorescence imaging the downconversion luminance of D/UCNPs, which further contributed to performing precise PDT. This work provides new insights into the development of precise and highly efficient PDT systems.

摘要

上转换纳米粒子能够利用近红外(NIR)光间接激活光动力疗法(PDT),为深部肿瘤的治疗提供了一种极佳的替代方案。然而,传统的近红外光触发的光动力疗法系统存在时空精度低和治疗效率受限的问题。在这项工作中,在向下/向上转换纳米粒子(D/UCNPs)上对DNA逻辑电路进行功能修饰,以构建用于近红外光触发的针对靶肿瘤的光动力疗法的智能向下/向上转换纳米机器(D/UCNMs)。在肿瘤相关的谷胱甘肽(GSH)和胸苷激酶1(TK1)mRNA的双重输入下,DNA逻辑电路执行“与”逻辑计算并启动引发链介导的链置换反应。同时,淬灭的上转换荧光得以恢复,随后接近的光敏剂被激活,从而产生单线态氧(O)输出以实现精确且增强的光动力疗法。重要的是,D/UCNMs的生物分布可以通过第二近红外(NIR-II)荧光成像(D/UCNPs的向下转换发光)来可视化,这进一步有助于实现精确的光动力疗法。这项工作为精确高效的光动力疗法系统的开发提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f40d/10016622/b8ebfae41088/d2sc06601g-f1.jpg

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