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A sequence-activated AND logic dual-channel fluorescent probe for tracking programmable drug release

机译:用于跟踪可编程药物释放的序列激活的AND逻辑双通道荧光探针

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摘要

The translation of biomarker sensing into programmable diagnostics or therapeutic applications in vivo is greatly challenging, especially for eliminating the ‘false positive’ signals from OR logic gates. Herein we present a sense-of-logic dual-channel nanoprobe, operating through a sequence-activated AND logic gate by responding ultra-sensitively to pH changes and being subsequently triggered with biothiol for the controllable release of anti-cancer drugs. Specifically, programmable drug release is conducted in a multistage tumor microenvironment (acidic endocytic organelles followed by abnormal glutathione-overexpressing cell cytosol), which is synchronous with dual-channel near-infrared (NIR) fluorescence output. This approach represents the merging of sensing and release, including logically enabled molecular design, biomarker sensing, and controllable drug release. Impressively, the sequential AND logic feature within an unprecedented framework provides feedback on the diversity and complexity of biological milieu, along with remarkably enhancing the tumor therapeutic efficiency via its precise targeting ability and programmable drug release.
机译:将生物标志物传感转换为体内的可编程诊断或治疗应用具有极大的挑战性,尤其是对于消除O​​R逻辑门的“假阳性”信号而言。在本文中,我们介绍了一种逻辑双通道纳米探针,它通过对pH值的变化做出超灵敏的响应,并通过序列激活的AND逻辑门操作,随后被生物硫醇触发,从而可控地释放抗癌药物。具体而言,在多阶段肿瘤微环境(酸性内吞细胞器,随后异常表达谷胱甘肽过表达的细胞胞质溶胶)中进行可编程药物释放,这与双通道近红外(NIR)荧光输出同步。这种方法代表了传感和释放的结合,包括逻辑上可行的分子设计,生物标志物传感和可控药物释放。令人印象深刻的是,前所未有的框架内的顺序AND逻辑功能可提供有关生物环境多样性和复杂性的反馈,并通过其精确的靶向能力和可编程的药物释放显着提高肿瘤治疗效率。

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