{"title":"用于快速无创检测心肌纤维化的多重离心微流控系统。","authors":"Luhai Wang, Jiaze Sun, Siwei Dai, Pengfei Zhang, Yefei Zhu and Yu Zhang","doi":"10.1039/D4AY01703J","DOIUrl":null,"url":null,"abstract":"<p >Myocardial fibrosis is a pathological condition characterized by the excessive accumulation of extracellular matrix proteins, primarily collagen, within the myocardium. Early symptoms of myocardial fibrosis are often subtle, leading to late detection. As the disease progresses, it is often associated with life-threatening complications. Therefore, myocardial fibrosis urgently demands a diagnostic system that is rapid, effective, and preferably non-invasive. In this study, we developed a highly sensitive microfluidic light-initiated chemiluminescent assay (LICA) for the simultaneous detection of cTnI, NT-proBNP, HA, LN, PICP, and PIIINP, the key biomarkers involved in the occurrence and development of myocardial fibrosis. The system is highly integrated and compact, incorporating reagent lyophilization and whole blood separation technologies, and is suitable for point-of-care testing. By combining advantages of centrifugal microfluidics and LICA, the system effectively shortens the detection time for key biomarkers associated with MACEs. Moreover, the system provides optimal analytical performance, with LoDs of 0.0018 ng mL<small><sup>−1</sup></small>, 0.0127 ng mL<small><sup>−1</sup></small>, 3.52 ng mL<small><sup>−1</sup></small>, 6.88 ng mL<small><sup>−1</sup></small>, 4.68 ng mL<small><sup>−1</sup></small>, and 0.072 ng mL<small><sup>−1</sup></small> for cTnI, NT-proBNP, HA, LN, PIIINP and PICP, respectively. Ultimately, the system can achieve an AUC of 0.548, 0.670, 0.772, 0.752, 0.833 and 0.713 for cTnI, NT-proBNP, HA, LN, PIIINP, and PICP, respectively, and an overall combined ROC of 0.946 for the detection of myocardial fibrosis, indicating its excellent efficacy and potential for widespread clinical applications.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" 3","pages":" 601-610"},"PeriodicalIF":2.7000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiplexed centrifugal microfluidic system for rapid and non-invasive detection of myocardial fibrosis†\",\"authors\":\"Luhai Wang, Jiaze Sun, Siwei Dai, Pengfei Zhang, Yefei Zhu and Yu Zhang\",\"doi\":\"10.1039/D4AY01703J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Myocardial fibrosis is a pathological condition characterized by the excessive accumulation of extracellular matrix proteins, primarily collagen, within the myocardium. Early symptoms of myocardial fibrosis are often subtle, leading to late detection. As the disease progresses, it is often associated with life-threatening complications. Therefore, myocardial fibrosis urgently demands a diagnostic system that is rapid, effective, and preferably non-invasive. In this study, we developed a highly sensitive microfluidic light-initiated chemiluminescent assay (LICA) for the simultaneous detection of cTnI, NT-proBNP, HA, LN, PICP, and PIIINP, the key biomarkers involved in the occurrence and development of myocardial fibrosis. The system is highly integrated and compact, incorporating reagent lyophilization and whole blood separation technologies, and is suitable for point-of-care testing. By combining advantages of centrifugal microfluidics and LICA, the system effectively shortens the detection time for key biomarkers associated with MACEs. Moreover, the system provides optimal analytical performance, with LoDs of 0.0018 ng mL<small><sup>−1</sup></small>, 0.0127 ng mL<small><sup>−1</sup></small>, 3.52 ng mL<small><sup>−1</sup></small>, 6.88 ng mL<small><sup>−1</sup></small>, 4.68 ng mL<small><sup>−1</sup></small>, and 0.072 ng mL<small><sup>−1</sup></small> for cTnI, NT-proBNP, HA, LN, PIIINP and PICP, respectively. 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引用次数: 0
摘要
心肌纤维化是以细胞外基质蛋白(主要是胶原蛋白)在心肌内过度堆积为特征的一种病理状态。心肌纤维化的早期症状往往不明显,因此发现较晚。随着病情的发展,往往会出现危及生命的并发症。因此,心肌纤维化迫切需要一种快速、有效且最好是非侵入性的诊断系统。在这项研究中,我们开发了一种高灵敏度的微流控光引发化学发光测定(LICA),用于同时检测 cTnI、NT-proBNP、HA、LN、PICP 和 PIIINP,它们是心肌纤维化发生和发展过程中的关键生物标志物。该系统高度集成,结构紧凑,融合了试剂冻干和全血分离技术,适用于床边检测。通过结合离心微流控技术和 LICA 的优势,该系统有效缩短了与 MACEs 相关的关键生物标记物的检测时间。此外,该系统还具有最佳的分析性能,对 cTnI、NT-proBNP、HA、LN、PIIINP 和 PICP 的 LoD 分别为 0.0018 ng mL-1、0.0127 ng mL-1、3.52 ng mL-1、6.88 ng mL-1、4.68 ng mL-1 和 0.072 ng mL-1。最终,该系统检测 cTnI、NT-proBNP、HA、LN、PIIINP 和 PICP 的 AUC 分别为 0.548、0.670、0.772、0.752、0.833 和 0.713,检测心肌纤维化的综合 ROC 为 0.946,这表明该系统具有卓越的功效和广泛的临床应用潜力。
Multiplexed centrifugal microfluidic system for rapid and non-invasive detection of myocardial fibrosis†
Myocardial fibrosis is a pathological condition characterized by the excessive accumulation of extracellular matrix proteins, primarily collagen, within the myocardium. Early symptoms of myocardial fibrosis are often subtle, leading to late detection. As the disease progresses, it is often associated with life-threatening complications. Therefore, myocardial fibrosis urgently demands a diagnostic system that is rapid, effective, and preferably non-invasive. In this study, we developed a highly sensitive microfluidic light-initiated chemiluminescent assay (LICA) for the simultaneous detection of cTnI, NT-proBNP, HA, LN, PICP, and PIIINP, the key biomarkers involved in the occurrence and development of myocardial fibrosis. The system is highly integrated and compact, incorporating reagent lyophilization and whole blood separation technologies, and is suitable for point-of-care testing. By combining advantages of centrifugal microfluidics and LICA, the system effectively shortens the detection time for key biomarkers associated with MACEs. Moreover, the system provides optimal analytical performance, with LoDs of 0.0018 ng mL−1, 0.0127 ng mL−1, 3.52 ng mL−1, 6.88 ng mL−1, 4.68 ng mL−1, and 0.072 ng mL−1 for cTnI, NT-proBNP, HA, LN, PIIINP and PICP, respectively. Ultimately, the system can achieve an AUC of 0.548, 0.670, 0.772, 0.752, 0.833 and 0.713 for cTnI, NT-proBNP, HA, LN, PIIINP, and PICP, respectively, and an overall combined ROC of 0.946 for the detection of myocardial fibrosis, indicating its excellent efficacy and potential for widespread clinical applications.