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基于酶促等温扩增策略的氧化型烟酰胺腺嘌呤二核苷酸检测方法

张攀松 贺芳芳 白泽辉 谭一诺 常新 任晨霞

分析化学2026,Vol.54Issue(3):381-388,8.
分析化学2026,Vol.54Issue(3):381-388,8.DOI:10.19756/j.issn.0253-3820.251313

基于酶促等温扩增策略的氧化型烟酰胺腺嘌呤二核苷酸检测方法

A Method for Detection of Nicotinamide Adenine Dinucleotide Based on Enzymatic Isothermal Amplification Strategy

张攀松 1贺芳芳 1白泽辉 2谭一诺 3常新 1任晨霞4

作者信息

  • 1. 长治医学院 老年健康研究中心,长治 046000
  • 2. 长治医学院 基础医学部,长治 046000
  • 3. 长治医学院 第一临床学院,长治 046000
  • 4. 长治医学院 中心实验室,长治 046000
  • 折叠

摘要

Abstract

Nicotinamide adenine dinucleotide(NAD+)is a key indicator reflecting the body's physiological state,and its accurate detection is of great significance for scientific research and clinical diagnosis.However,traditional detection methods have limitations of long detection cycles and high operation cost,which make it difficult to meet the needs of wide application.Based on the cofactor dependence of ligase and DNA isothermal amplification technology,a novel NAD+detection system was developed in this study.The detection process of the system included three steps:Taq DNA ligase catalyzed the ligation of oligonucleotides in the presence of NAD+;Nt.BstNBI endonuclease and Bst polymerase worked synergistically to achieve isothermal amplification,generating a large number of single-stranded DNA;the fluorescent signal was triggered by molecular beacons to complete the qualitative and quantitative analysis of NAD+.Experimental results showed that this detection method could complete the detection within 1‒2 h,with a detection limit of 3.16 pmol/L,significantly improving the detection speed and sensitivity.This method effectively broke through the limitations of traditional technologies in many aspects,provided efficient and economical technical support for medical diagnosis,environmental monitoring,food safety and other fields,and had broad industrialization prospects.

关键词

烟酰胺腺嘌呤二核苷酸//等温扩增/检测

Key words

Nicotinamide adenine dinucleotide/Enzymatic/Isothermal amplification/Detection

引用本文复制引用

张攀松,贺芳芳,白泽辉,谭一诺,常新,任晨霞..基于酶促等温扩增策略的氧化型烟酰胺腺嘌呤二核苷酸检测方法[J].分析化学,2026,54(3):381-388,8.

基金项目

国家自然科学基金项目(No.22507013)和山西省基础研究计划项目(No.202403021212062)资助. Supported by the National Natural Science Foundation of China(No.22507013)and the Fundamental Research Program of Shanxi Province(No.202403021212062). (No.22507013)

分析化学

0253-3820

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