利用可穿戴传感器对甲基苯丙胺和可卡因进行床旁检测

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Ying Wang , Ke Li , Weijian Shen , Xingxu Huang , Lina Wu
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引用次数: 0

摘要

为预防药物滥用,必须对甲基苯丙胺和可卡因进行床旁检测,这就需要创新的解决方案。为了满足这一需求,我们推出了一种利用 CRISPR/Cas12a 系统的多通道可穿戴传感器。我们设计了一个基于 CRISPR/Cas12a 的系统,其中集成了针对甲基苯丙胺和可卡因的适配体。这些适配体作为信号媒介,将甲基苯丙胺和可卡因转化为核酸信号,随后生成单链 DNA 激活 Cas12 蛋白。此外,我们还在 CRISPR 系统中集成了微流体系统和磁分离技术,从而能够快速、精确地检测可卡因和甲基苯丙胺。拟议的传感平台表现出了极高的灵敏度,检测限低至 0.1 纳克/毫升。这种传感器有望在未来用于现场毒品检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Point-of-care testing of methamphetamine and cocaine utilizing wearable sensors

Point-of-care testing of methamphetamine and cocaine utilizing wearable sensors

The imperative for the point-of-care testing of methamphetamine and cocaine in drug abuse prevention necessitates innovative solutions. To address this need, we have introduced a multi-channel wearable sensor harnessing CRISPR/Cas12a system. A CRISPR/Cas12a based system, integrated with aptamers specific to methamphetamine and cocaine, has been engineered. These aptamers function as signal-mediated intermediaries, converting methamphetamine and cocaine into nucleic acid signals, subsequently generating single-stranded DNA to activate the Cas12 protein. Additionally, we have integrated a microfluidic system and magnetic separation technology into the CRISPR system, enabling rapid and precise detection of cocaine and methamphetamine. The proposed sensing platform demonstrated exceptional sensitivity, achieving a detection limit as low as 0.1 ng/mL. This sensor is expected to be used for on-site drug detection in the future.

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来源期刊
Analytical biochemistry
Analytical biochemistry 生物-分析化学
CiteScore
5.70
自引率
0.00%
发文量
283
审稿时长
44 days
期刊介绍: The journal''s title Analytical Biochemistry: Methods in the Biological Sciences declares its broad scope: methods for the basic biological sciences that include biochemistry, molecular genetics, cell biology, proteomics, immunology, bioinformatics and wherever the frontiers of research take the field. The emphasis is on methods from the strictly analytical to the more preparative that would include novel approaches to protein purification as well as improvements in cell and organ culture. The actual techniques are equally inclusive ranging from aptamers to zymology. The journal has been particularly active in: -Analytical techniques for biological molecules- Aptamer selection and utilization- Biosensors- Chromatography- Cloning, sequencing and mutagenesis- Electrochemical methods- Electrophoresis- Enzyme characterization methods- Immunological approaches- Mass spectrometry of proteins and nucleic acids- Metabolomics- Nano level techniques- Optical spectroscopy in all its forms. The journal is reluctant to include most drug and strictly clinical studies as there are more suitable publication platforms for these types of papers.
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