Creatinine-On Colorimetric Elisa-Based Serum Creatinine Detection in a Microfluidic Device
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Date
2025
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Royal Soc Chemistry
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Abstract
Chronic kidney diseases (CKDs), which often end in kidney failure for many people around the world, have an important place in public health given that they also trigger other diseases. Therefore, the development of fast and cost-effective diagnostic technologies enables effective monitoring of patients and early diagnosis. Here, using the Enzyme-Linked Immunosorbent Assay (ELISA) principle, serum creatinine concentrations were determined using the developed lab-on-a-chip (LOC) platform. In this system, which was termed "creatinine-on-a-chip", colorimetric ELISA protocol was applied to determine creatinine levels in a microfluidic chip functionalized with creatinine-specific antibodies. Creatinine detection was performed by quantifying the absorbance difference between the detection and reference channels, normalized to the reference signal within the microfluidic chip. The detection signal intensity varied depending on the region selected along the microfluidic channel. The adsorption of the capture antibody used for surface functionalization, which was particularly more pronounced near the inlet region, played a critical role in the detection signal. These findings suggest that random selection of the detection area can lead to significant signal variability, and that careful selection of a well-characterized region is essential for improving detection performance. With this developed system, creatinine was detected with high sensitivity in the linear range of 1-20 mu g mL-1, both spiked in phosphate buffered saline (PBS) and fetal bovine serum (FBS). Using the creatinine-on-a-chip, serum creatinine analysis can be performed rapidly (similar to 15 min) in a cost-effective manner ($1.05 per test).
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Karakuzu, Betul/0000-0001-6517-7251
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Q2
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Q2
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Analyst
Volume
150
Issue
19
Start Page
4395
End Page
4403