TY - JOUR
T1 - A Locked Aptamer-Magnetic Nanoparticle Assay for Cardiac Troponin I Classification to Support Myocardial Infarction Diagnosis in Resource-Limited Environments
AU - Tripathy, Sayantan
AU - Wai, Ng Ka
AU - Sharma, Sahil
AU - Vu, Ngoc Nhu
AU - Jaitpal, Siddhant
AU - Zare, Fatemah
AU - Singh, Muskaan
AU - McDaid, LJ
AU - Bhattacharyya, Saugat
AU - Coté, Gerard L.
AU - Mabbott, Samuel B.
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/5/15
Y1 - 2025/5/15
N2 - Clinical classification of cardiac troponin I (cTnI) levels is essential for accurately diagnosing acute myocardial infarction. This study introduces an innovative point-of-care test that combines an engineered locked aptamer, magnetic nanoparticle and isothermal, non-enzymatic hybridization chain reaction with surface-enhanced resonance Raman scattering for the sensitive and specific detection of cTnI at clinically significant concentrations. This high sensitivity cTnI assay enabled accurate quantification of cTnI in 25 μL of cTnl doped serum, with a detection limit of 0.403 ng/L and a quantification limit of 1.22 ng/L with a dynamic range spanning from 0.5 ng/L to 50,000 ng/L. Further, optimized to classify cTnI levels beyond the established clinical threshold of 40 ng/L, the assay demonstrates its efficacy by accurately distinguishing between healthy and unhealthy individual clinical samples, achieving over 83 % accuracy and 86 % precision. This approach represents a significant advancement in the point-of-care diagnosis of myocardial infarction, offering a rapid, reliable, and accessible diagnostic tool for cardiac troponin testing.
AB - Clinical classification of cardiac troponin I (cTnI) levels is essential for accurately diagnosing acute myocardial infarction. This study introduces an innovative point-of-care test that combines an engineered locked aptamer, magnetic nanoparticle and isothermal, non-enzymatic hybridization chain reaction with surface-enhanced resonance Raman scattering for the sensitive and specific detection of cTnI at clinically significant concentrations. This high sensitivity cTnI assay enabled accurate quantification of cTnI in 25 μL of cTnl doped serum, with a detection limit of 0.403 ng/L and a quantification limit of 1.22 ng/L with a dynamic range spanning from 0.5 ng/L to 50,000 ng/L. Further, optimized to classify cTnI levels beyond the established clinical threshold of 40 ng/L, the assay demonstrates its efficacy by accurately distinguishing between healthy and unhealthy individual clinical samples, achieving over 83 % accuracy and 86 % precision. This approach represents a significant advancement in the point-of-care diagnosis of myocardial infarction, offering a rapid, reliable, and accessible diagnostic tool for cardiac troponin testing.
UR - http://www.scopus.com/inward/record.url?scp=105005576967&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2025.117590
DO - 10.1016/j.bios.2025.117590
M3 - Article
SN - 0956-5663
VL - 286
SP - 1
EP - 12
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
M1 - 117590
ER -