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Related Concept Videos

Renal Clearance01:23

Renal Clearance

492
The glomerular filtration rate (GFR) is a critical marker of kidney function, reflecting the efficiency of filtration by the glomeruli. Renal clearance of specific substances, such as inulin or creatinine, is commonly used to measure GFR.
Renal clearance refers to the volume of plasma cleared of a specific substance, such as creatinine, per unit of time. To measure clearance, urine samples are collected over a 24-hour period during each bladder voiding, followed by a single blood sample at the...
492

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A passive flow microreactor for urine creatinine test.

Dumitru Tomsa1, Yang Liu1, Amanda Stefanson1

  • 1Department of Physics and Astronomy, University of Manitoba, Winnipeg, MB, R3T 2N2, Canada.

Microsystems & Nanoengineering
|April 2, 2025
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Summary
This summary is machine-generated.

A new microfluidic chip (uCR-Chip) enables rapid, point-of-care urine creatinine measurement for chronic kidney disease (CKD) assessment. This low-cost, accurate assay integrates with existing albumin tests, offering a viable alternative to lab-based diagnostics.

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Area of Science:

  • Biomarker detection and microfluidics
  • Point-of-care diagnostics for chronic kidney disease (CKD)

Background:

  • Chronic kidney disease (CKD) poses a significant global health and economic burden.
  • Current CKD diagnostic methods rely on lab-based tests for biomarkers like creatinine.
  • Existing tests are regulated and lack point-of-care (PoC) accessibility for routine monitoring.

Purpose of the Study:

  • To develop a passive flow microreactor for colorimetric urine creatinine measurement (uCR-Chip).
  • To create a PoC assay for CKD assessment by integrating with a microfluidic urine albumin assay.
  • To enable rapid, accurate, and accessible CKD biomarker quantification.

Main Methods:

  • Developed a passive flow microreactor (uCR-Chip) utilizing a 2-phase pressure compensation (2-PPC) technique.
  • Employed microfluidic channel network design and an optimized observation window (OW) for fluidic control and signal stability.
  • Utilized custom photomask production and dry-film photoresist lithography for precise chip fabrication; detection via USB microscope platform.

Main Results:

  • Achieved a uniform and stable detection signal within 7 minutes.
  • Demonstrated a dynamic linear detection range up to 40 mM with a lower limit of detection (LOD) of 0.521 mM.
  • Validated the assay with artificial urine, showing acceptable recovery and low matrix effects, comparable to commercial PoC systems.

Conclusions:

  • The developed uCR-Chip offers a viable PoC test for chronic kidney disease (CKD) assessment.
  • The microreactor provides accurate creatinine quantification, meeting clinical precision requirements.
  • This technology platform has potential for measuring various disease biomarkers at the point of care.