Multiplexed aptasensor for detection of acute myocardial infraction (AMI) biomarkers†

IF 3.5 Q2 CHEMISTRY, ANALYTICAL
Duygu Beduk, Tutku Beduk, Abdellatif Ait Lahcen, Veerappan Mani, Emine Guler Celik, Gamze Iskenderoglu, Ferhat Demirci, Soysal Turhan, Oner Ozdogan, Su Ozgur, Tuncay Goksel, Kutsal Turhan, Khaled Nabil Salama and Suna Timur
{"title":"Multiplexed aptasensor for detection of acute myocardial infraction (AMI) biomarkers†","authors":"Duygu Beduk, Tutku Beduk, Abdellatif Ait Lahcen, Veerappan Mani, Emine Guler Celik, Gamze Iskenderoglu, Ferhat Demirci, Soysal Turhan, Oner Ozdogan, Su Ozgur, Tuncay Goksel, Kutsal Turhan, Khaled Nabil Salama and Suna Timur","doi":"10.1039/D4SD00010B","DOIUrl":null,"url":null,"abstract":"<p >Acute myocardial infarction (AMI) is a leading global cause of death. Diagnosis is challenging as cardiac biomarkers are only detectable for a few hours after AMI onset, and current methods are time-consuming and lack selectivity. Therefore, multiple immunological test systems have great importance for rapid and accurate diagnosis. In this context, we developed a rapid immunodiagnostic sensor platform for simultaneous electrochemical detection of cardiac troponin T (cTnT), troponin I (cTnI), and C-reactive protein (CRP) using nanostructured gold-modified laser-scribed graphene (LSG). Aptamer sensors were integrated into the LSG platform for selective AMI biomarkers sensing. Clinical validation was performed on biomarkers from blood samples of 51 AMI patients and 9 healthy controls. Limits of detection were 1.65 ng mL<small><sup>−1</sup></small> cTnT, 2.58 ng mL<small><sup>−1</sup></small> cTnI, and 1.84 ng mL<small><sup>−1</sup></small> CRP. The analytical results determined by the developed platform were compared with the routine standard values of the same patients to prove the accuracy of aptasensors. Sensor results agreed well with standard laboratory assays, highlighting the accuracy of the test platform. The cTnT, cTnI and CRP multiplexed sensor platform demonstrates excellent performance for rapid and sensitive AMI screening.</p>","PeriodicalId":74786,"journal":{"name":"Sensors & diagnostics","volume":" 6","pages":" 1020-1027"},"PeriodicalIF":3.5000,"publicationDate":"2024-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/sd/d4sd00010b?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sensors & diagnostics","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/sd/d4sd00010b","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Acute myocardial infarction (AMI) is a leading global cause of death. Diagnosis is challenging as cardiac biomarkers are only detectable for a few hours after AMI onset, and current methods are time-consuming and lack selectivity. Therefore, multiple immunological test systems have great importance for rapid and accurate diagnosis. In this context, we developed a rapid immunodiagnostic sensor platform for simultaneous electrochemical detection of cardiac troponin T (cTnT), troponin I (cTnI), and C-reactive protein (CRP) using nanostructured gold-modified laser-scribed graphene (LSG). Aptamer sensors were integrated into the LSG platform for selective AMI biomarkers sensing. Clinical validation was performed on biomarkers from blood samples of 51 AMI patients and 9 healthy controls. Limits of detection were 1.65 ng mL−1 cTnT, 2.58 ng mL−1 cTnI, and 1.84 ng mL−1 CRP. The analytical results determined by the developed platform were compared with the routine standard values of the same patients to prove the accuracy of aptasensors. Sensor results agreed well with standard laboratory assays, highlighting the accuracy of the test platform. The cTnT, cTnI and CRP multiplexed sensor platform demonstrates excellent performance for rapid and sensitive AMI screening.

Abstract Image

用于检测急性心肌梗死 (AMI) 生物标记物的多重 Aptasensor
急性心肌梗死(AMI)是导致全球死亡的主要原因。由于心脏生物标志物只能在急性心肌梗死发病后数小时内检测到,而目前的方法耗时且缺乏选择性,因此诊断具有挑战性。因此,多种免疫学检测系统对快速准确诊断具有重要意义。在此背景下,我们开发了一种快速免疫诊断传感器平台,利用纳米结构金修饰的激光刻蚀石墨烯(LSG)同时电化学检测心肌肌钙蛋白 T(cTnT)、肌钙蛋白 I(cTnI)和 C 反应蛋白(CRP)。在 LSG 平台上集成了选择性急性心肌梗死生物标记物传感的色素传感器。对 51 名急性心肌梗塞患者和 9 名健康对照者血液样本中的生物标记物进行了临床验证。检测限分别为 1.65 纳克/毫升 cTnT、2.58 纳克/毫升 cTnI 和 1.84 纳克/毫升 CRP。将所开发平台测定的分析结果与同一患者的常规标准值进行了比较,以证明灵敏传感器的准确性。传感器的结果与实验室标准测定结果吻合得很好,凸显了测试平台的准确性。cTnT、cTnI 和 CRP 多路复用传感器平台在快速灵敏地筛查急性心肌梗死方面表现出卓越的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.30
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信