用于心肌梗塞早期干预的尖端技术:基于指尖的便携式免疫生物传感器

Zhichao Yu, Di Wu, Yuan Gao, Yunsen Wang, Yongyi Zeng, Dianping Tang, Xiaolong Liu
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引用次数: 0

摘要

对急性心肌梗死进行早期干预可以最大限度地减少心肌损伤,提高患者存活率。本文报告了一种用于灵活监测急性心肌梗死的低成本无设备便携式免疫生物传感平台。通过液相极性介导合成法合成了光热转换效率高(≈26.41%)的 CuS-Pt 纳米碎片(CuS-Pt NFs)。利用溶解热还原策略将 CuS NFs 原位负载到铂(Pt)纳米反应器中,以提高气体生产效率。生成的 CuS-Pt 纳米催化剂被封装在脂质体中,用于信号级联放大。具体来说,血清中的目标生物标记物心肌肌钙蛋白 I(cTn I)被捕获到预修饰的微孔板上,并形成经典的夹心模型。热化学动力学增强型 CuS-Pt 反应器经一步化学处理后释放,并转移到一个封闭的气体发生器中。在近红外激光发射器的激发下,气体发生器装置中的内压随着时间的推移而增加,并推动碳量子点溶液在连接的软管中移动。移动距离与目标浓度相关。这项工作为开发低成本、高效率的压力免疫传感器提供了一种新的实现方法,而不需要读出装置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cutting-Edge Technology for Early Intervention in Myocardial Infarction: Portable Fingertips-Based Immunobiosensor

Cutting-Edge Technology for Early Intervention in Myocardial Infarction: Portable Fingertips-Based Immunobiosensor

Early intervention in acute myocardial infarction can minimize myocardial damage and improve patient survival. Herein, a low-cost device-free portable immunobiosensing platform for flexible monitoring of immediate myocardial infarction is reported. CuS-Pt nanofragments (CuS-Pt NFs) with high photothermal conversion efficiency (≈26.41%) are synthesized by liquid-phase polarity-mediated synthesis. The CuS NFs are loaded in situ with platinum (Pt) nanoreactors using a solvothermal reduction strategy, which is employed to enhance the efficiency of gas production. The resulting CuS-Pt nanocatalysts are encapsulated within liposomes for signal cascade amplification. Specifically, cardiac troponin I (cTn I), a target biomarker in serum, is captured on pre-modified microtiter plates and formed into a classical sandwich model. The thermo-chemically kinetically enhanced CuS-Pt reactor is released through a one-step chemical treatment and transferred to a closed gas generator. Under the excitation of a near-infrared laser emitter, the internal pressure in the gas generator device increases with time and drives the carbon quantum dot solution in the connected hose. The moving distance shows a correlation with the target concentration. This work provides a new implementation for the development of low-cost, efficient pressure immunosensors without the requirement of a readout device.

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