MIP-Chip: Integrated Microfluidic Plasma Separation and Redox-Enhanced Molecularly Imprinted Polymer Succinate Sensor for Whole Blood Metabolite Analysis

The precise quantification of metabolites in bodily fluids is essential for advancing digital health monitoring and clinical diagnostics. Among these fluids, whole blood stands out as a valuable source of predictive metabolite biomarkers, providing critical insights into disease diagnosis and progression. However, traditional blood testing methods often require expensive instrumentation and specialized training, primarily due to the need for plasma extraction to remove interfering blood cells. This study addresses these limitations by introducing a novel, sensitive, rapid, reagent-free, and cost-effective capillary microfluidic-integrated molecularly imprinted polymer (MIP) sensor (MIP-Chip) designed for metabolite detection in whole blood. The MIP-Chip integrates two key components: (1) a highly efficient plasma separation module capable of extracting plasma from whole blood (∼95% efficiency) without requiring sample pretreatment or external active forces and (2) an electrochemical MIP sensor employing an ultrasensitive electrode with on-electrode Prussian Blue nanoparticles (PB NPs) as embedded redox probes for sensitive and specific metabolite detection in the extracted plasma. Using this platform, we successfully quantified succinate, a critical metabolite, across a wide linear concentration range (50 nM-250 μM) with a limit of detection of 5 nM. The device processed 120 μL of whole blood, delivering 8 μL of plasma, and completed the entire workflow-from sample introduction to biomarker detection within 25 min. The MIP-Chip demonstrated exceptional performance, including self-powered assay automation, high specificity for succinate quantification in whole blood, excellent reproducibility, and long-term stability of the MIP-based sensor. These features establish the MIP-Chip as a powerful analytical platform for point-of-care diagnostics, offering a significant step forward in clinical metabolite detection and digital health monitoring.

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Publication Details

Journal
ACS Sensors
Published
2025-03-27
DOI
https://doi.org/10.1021/acssensors.5c00355
Citations
5
Primary Topic
Microfluidic and Capillary Electrophoresis Applications
Type
article
Field-Weighted Citation Impact
3.37

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article

MIP-Chip: Integrated Microfluidic Plasma Separation and Redox-Enhanced Molecularly Imprinted Polymer Succinate Sensor for Whole Blood Metabolite Analysis

Bahareh Babamiri, Mehdi Mohammadi, Amir Sanati‐Nezhad, Mohammadreza Farrokhnia
5 citations
ACS Sensors
Microfluidic and Capillary Electrophoresis Applications
3.37
article

MIP-Chip: Integrated Microfluidic Plasma Separation and Redox-Enhanced Molecularly Imprinted Polymer Succinate Sensor for Whole Blood Metabolite Analysis

Bahareh Babamiri, Mehdi Mohammadi, Amir Sanati‐Nezhad, Mohammadreza Farrokhnia
article en
5 citations

Abstract

The precise quantification of metabolites in bodily fluids is essential for advancing digital health monitoring and clinical diagnostics. Among these fluids, whole blood stands out as a valuable source of predictive metabolite biomarkers, providing critical insights into disease diagnosis and progression. However, traditional blood testing methods often require expensive instrumentation and specialized training, primarily due to the need for plasma extraction to remove interfering blood cells. This study addresses these limitations by introducing a novel, sensitive, rapid, reagent-free, and cost-effective capillary microfluidic-integrated molecularly imprinted polymer (MIP) sensor (MIP-Chip) designed for metabolite detection in whole blood. The MIP-Chip integrates two key components: (1) a highly efficient plasma separation module capable of extracting plasma from whole blood (∼95% efficiency) without requiring sample pretreatment or external active forces and (2) an electrochemical MIP sensor employing an ultrasensitive electrode with on-electrode Prussian Blue nanoparticles (PB NPs) as embedded redox probes for sensitive and specific metabolite detection in the extracted plasma. Using this platform, we successfully quantified succinate, a critical metabolite, across a wide linear concentration range (50 nM-250 μM) with a limit of detection of 5 nM. The device processed 120 μL of whole blood, delivering 8 μL of plasma, and completed the entire workflow-from sample introduction to biomarker detection within 25 min. The MIP-Chip demonstrated exceptional performance, including self-powered assay automation, high specificity for succinate quantification in whole blood, excellent reproducibility, and long-term stability of the MIP-based sensor. These features establish the MIP-Chip as a powerful analytical platform for point-of-care diagnostics, offering a significant step forward in clinical metabolite detection and digital health monitoring.

ACS SensorsVol. 10(4)
University of Calgary (CA), Université Bourgogne Franche-Comté (FR)
Mitacs, Alberta Innovates, Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 8%
Microfluidic and Capillary Electrophoresis Applications
3.37
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