TY - JOUR
T1 - Troponin I biomarker sensing from clinical patient samples using molecularly imprinted polymer nanoparticles for advancing healthcare approaches in cardiovascular disease
AU - Saczek, Joshua
AU - Jamieson, Oliver
AU - McClements, Jake
AU - Dann, Amy
AU - Johnson, Rhiannon E.
AU - Stokes, Alexander D.
AU - Crapnell, Robert D.
AU - Banks, Craig E.
AU - Canfarotta, Francesco
AU - Spyridopoulos, Ioakim
AU - Thomson, Alan
AU - Zaman, Azfar
AU - Novakovic, Katarina
AU - Peeters, Marloes
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/8/15
Y1 - 2025/8/15
N2 - Cardiac troponin I (cTnI) is a critical protein biomarker for heart attack diagnosis. This study presents a thorough analysis of a novel biosensing device utilizing molecularly imprinted polymer nanoparticles (nanoMIPs) for detecting cTnI in clinical patient serum samples post myocardial infarction. The methodology, based on the heat-transfer method approach, offers faster measurements times than the current gold standard and sample volumes equivalent to a single blood drop. Biomarker binding shows performance comparable to a high-sensitivity ELISA, accurately identifying patients with elevated cTnI levels (R2 = 0.893). The cTnI peak concentration time variations are attributed to heterogeneous serum complexes, with different troponin complex sizes potentially generating differing thermal insulation levels. Comparison with an established patient database demonstrates robust correlations between our cTnI concentrations and clinical parameters (R2 = 0.855). This underscores the potential of nanoMIP sensors for sensitive cTnI detection, providing insights into post-heart attack biomarker levels. Furthermore, our methodology presents the additional benefits of being low cost and portable enabling measurements at time and place of patients. Consequently, it holds the potential to become a vital part of the diagnostic pathway for heart attack treatment, ultimately reducing healthcare costs and improving patient outcomes.
AB - Cardiac troponin I (cTnI) is a critical protein biomarker for heart attack diagnosis. This study presents a thorough analysis of a novel biosensing device utilizing molecularly imprinted polymer nanoparticles (nanoMIPs) for detecting cTnI in clinical patient serum samples post myocardial infarction. The methodology, based on the heat-transfer method approach, offers faster measurements times than the current gold standard and sample volumes equivalent to a single blood drop. Biomarker binding shows performance comparable to a high-sensitivity ELISA, accurately identifying patients with elevated cTnI levels (R2 = 0.893). The cTnI peak concentration time variations are attributed to heterogeneous serum complexes, with different troponin complex sizes potentially generating differing thermal insulation levels. Comparison with an established patient database demonstrates robust correlations between our cTnI concentrations and clinical parameters (R2 = 0.855). This underscores the potential of nanoMIP sensors for sensitive cTnI detection, providing insights into post-heart attack biomarker levels. Furthermore, our methodology presents the additional benefits of being low cost and portable enabling measurements at time and place of patients. Consequently, it holds the potential to become a vital part of the diagnostic pathway for heart attack treatment, ultimately reducing healthcare costs and improving patient outcomes.
KW - Biosensors
KW - Cardiovascular disease
KW - Molecularly imprinted polymer nanoparticles (NanoMIPs)
KW - Myocardial infarction
KW - Troponin I (cTnI)
UR - http://www.scopus.com/inward/record.url?scp=105003015001&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2025.117467
DO - 10.1016/j.bios.2025.117467
M3 - Article
AN - SCOPUS:105003015001
SN - 0956-5663
VL - 282
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
M1 - 117467
ER -