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首页> 外文期刊>Angewandte Chemie >Amplified Self-Immolative Release of Small Molecules by Spatial Isolation of Reactive Groups on DNA-Minimal Architectures
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Amplified Self-Immolative Release of Small Molecules by Spatial Isolation of Reactive Groups on DNA-Minimal Architectures

机译:通过在DNA-最小架构上的反应基团的空间分离扩增自我侵略性的小分子释放

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摘要

Triggering the release of small molecules in response to unique biomarkers is important for applications in drug delivery and biodetection. Due to low quantities of biomarker, amplifying release is necessary to gain appreciable responses. Nucleic acids have been used for both their biomarker-recognition properties and as stimuli, notably in amplified small-molecule release by nucleic-acid-templated catalysis (NATC). The multiple components and reversibility of NATC, however, make it difficult to apply in vivo. Herein, we report the use of the hybridization chain reaction (HCR) for the amplified, conditional release of small molecules from standalone nanodevices. We couple HCR with a DNA-templated reaction resulting in the amplified, immolative release of small molecules. We integrate the HCR components into single nanodevices as DNA tracks and spherical nucleic acids, spatially isolating reactive groups until triggering. This could be applied to biosensing, imaging, and drug delivery.
机译:响应独特的生物标志物触发小分子的释放对于药物递送和生物渗透的应用对于应用很重要。 由于少量的生物标志物,扩增释放是获得可观的反应所必需的。 核酸已被用于其生物标志物识别性质和刺激,特别是通过核酸模板催化(NATC)扩增的小分子释放。 然而,NATC的多个组件和可逆性使得难以在体内申请。 在此,我们报告使用杂交链反应(HCR)用于从独立纳米型纳米石的放大的,条件释放的小分子。 我们将HCR耦合通过DNA模板化反应,导致小分子的扩增的,侵略性的释放。 我们将HCR组分集成到单个纳米型中作为DNA轨道和球形核酸,在空间分离的反应性基团直至触发。 这可以应用于生物传感,成像和药物递送。

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