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首页> 外文期刊>Particle & Particle Systems Characterization: Measurement and Description of Particle Properties and Behavior in Powders and Other Disperse Systems >NIR-Triggered Release of Nitric Oxide with Upconversion Nanoparticles Inhibits Platelet Aggregation in Blood Samples
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NIR-Triggered Release of Nitric Oxide with Upconversion Nanoparticles Inhibits Platelet Aggregation in Blood Samples

机译:用上转换纳米颗粒触发一氧化氮的释放释放血液样品中的血小板聚集

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摘要

There is a great challenge to overcome the limitation of tissue penetration depth, while maximizing the benefit of light-triggered biochemical cascades in a well-defined mode simultaneously. Here, a new method of near-infrared (NIR) light-triggered release of nitric oxide (NO) by developing upconversion nanoparticles (UCNPs)-based conjugate chemistry is reported. As the key nanotransducer in the design, core-shell-structured UCNPs are encapsulated with a layer of SiO2 and then covalently linked with a potent NO-releasing donor (S-nitroso-N-acetyl-dl-penicillamine, SNAP). It is featured with highly localized breakage of chemical bonds of SNAP molecules by NIR-UV upconversion, enabling simultaneous NO release in a light dosage-dependent manner. The biological effects of NO releasing are demonstrated by cellular imaging and inhibition of platelet aggregation from blood samples. This work provides a flexible and robust platform to generate cell-signaling gas molecules trigged by NIR laser with deep tissue penetration.
机译:克服组织穿透深度的限制存在巨大挑战,同时同时最大化光触发的生物化学级联的益处。这里,通过显影上转化纳米颗粒(UCNPS)基于缀合物化学,据报道,通过显影基于缀合物化学的近红外(NIR)近红外(NIR)光触发的一氧化物(NO)的新方法。作为设计中的关键纳米转铜剂,核 - 壳结构的UCNP用一层SiO 2封装,然后与有效的无释放供体共价连接(S-Nitroso-N-乙酰基-D1-青霉胺,捕获量。通过NIR-UV上转化具有高度本地化的卡扣分子化学键的高度局部破损,使得依赖于光剂量依赖性的方式同时释放。通过细胞成像和抑制来自血液样品的血小板聚集的生物学效应。这项工作提供了一种灵活且强大的平台,可以产生具有深层组织渗透的NIR激光器突出的细胞信号气体分子。

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