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Using Extraordinary Optical Transmission to Quantify Cardiac Biomarkers in Human Serum
Published on: December 13, 2017
Unlocking interstitial fluid for acute coronary syndrome diagnosis: ultrasensitive troponin I detection using
Joshua Saczek1,2, Amy Dann1,2, Robert D Crapnell3
1Newcastle University, School of Engineering, Merz Court, Claremont Road, NE1 7RU Newcastle Upon Tyne, UK. jake.mcclements@newcastle.ac.uk.
Insights
Researchers developed a novel method to detect cardiac troponin I (cTnI) in interstitial fluid (ISF) for rapid acute coronary syndrome (ACS) diagnosis. This non-invasive biosensor offers high sensitivity and speed for point-of-care testing.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Clinical Diagnostics
Background:
- Acute coronary syndrome (ACS) diagnosis relies on cardiac biomarkers like cardiac troponin I (cTnI).
- Current detection methods often require invasive blood draws and can be time-consuming.
- Interstitial fluid (ISF) offers a potential alternative biofluid for non-invasive biomarker monitoring.
Purpose of the Study:
- To develop and validate a novel biosensor for the rapid and sensitive detection of cTnI in human interstitial fluid (ISF).
- To assess the feasibility of using ISF collected via electroporation for point-of-care ACS diagnosis.
- To compare the performance of the developed sensor with conventional methods using plasma and serum samples.
Main Methods:
- Detection of cTnI in ISF using molecularly imprinted polymer nanoparticles as recognition elements.
- Utilized a heat-transfer method within a microfluidic system for rapid measurements (15-20 min).
- ISF was collected non-invasively using electroporation, followed by cTnI quantification.
Main Results:
- Achieved a highly sensitive detection limit of 1.85 ± 0.32 pg mL⁻¹ for cTnI in spiked ISF.
- Demonstrated reliable quantification across a wide concentration range (0.1–1000 pg mL⁻¹).
- Similar low detection limits were observed in spiked plasma and serum samples, validating the sensor's performance.
Conclusions:
- The developed sensor provides a rapid, highly sensitive, and non-invasive method for cTnI detection in ISF.
- This platform is suitable for point-of-care ACS diagnosis, potentially improving patient outcomes.
- The approach offers a cost-effective alternative to conventional diagnostic methods, reducing healthcare burdens.
Abstract:
This study presents the first detection of cardiac troponin I (cTnI), a vital biomarker for acute coronary syndrome diagnosis (ACS), in human interstitial fluid (ISF) collected via electroporation. Measurements were performed using molecularly imprinted polymer nanoparticles as synthetic recognition elements and a heat-transfer method within a microfluidic system, yielding results within 15-20 min. This approach demonstrated reliable cTnI quantification across a wide, physiologically relevant concentration range of 0.1 to 1000 pg mL-1 in spiked ISF, achieving an excellent detection limit of 1.85 ± 0.32 pg mL-1. Comparisons with conventional patient sample fluids were conducted by repeating experiments with cTnI-spiked plasma and serum, which exhibited similar detection limits of 1.78 ± 0.28 and 1.80 ± 0.22 pg mL-1, respectively. The developed sensor offers a rapid, highly sensitive, non-invasive, and cost-effective platform for point-of-care ACS diagnosis in ISF, potentially improving patient outcomes and easing healthcare burdens.
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