Tomsa Dumitru, Liu Yang, Stefanson Amanda, Ren Xiaoou, Sokoro AbdulRazaq A H, Komenda Paul, Tangri Navdeep, Zahedi Rene P, Rigatto Claudio, Lin Francis
Department of Physics and Astronomy, University of Manitoba, Winnipeg, MB, R3T 2N2, Canada.
Institute of Health Sciences and Technology, Institutes of Material Science and Information Technology, Anhui University, Hefei, 230601, China.
Microsyst Nanoeng. 2025 Apr 2;11(1):56. doi: 10.1038/s41378-025-00880-z.
Chronic kidney disease (CKD) significantly affects people's health and quality of life and presents a high economic burden worldwide. There are well-established biomarkers for CKD diagnosis. However, the existing routine standard tests are lab-based and governed by strict regulations. Creatinine is commonly measured as a filtration biomarker in blood to determine estimated Glomerular Filtration Rate (eGFR), as well as a normalization factor to calculate urinary Albumin-to-Creatinine Ratio (uACR) for CKD evaluation. In this study, we developed a passive flow microreactor for colorimetric urine creatinine measurement (uCR-Chip), which is highly amenable to integration with our previously developed microfluidic urine albumin assay. The combination of the 2-phase pressure compensation (2-PPC) technique and microfluidic channel network design accurately controls the fluidic mixing ratio and chemical reaction. Together with an optimized observation window (OW) design, a uniform and stable detection signal was achieved within 7 min. The color signal was measured by a simple USB microscope-based platform to quantify creatinine concentration in the sample. The combination of the custom in-house photomask production techniques and dry-film photoresist-based lithography enabled rapid iterative design optimization and precise chip fabrication. The developed assay achieved a dynamic linear detection range up to 40 mM and a lower limit of detection (LOD) of 0.521 mM, meeting the clinical precision requirements (comparable to existing point-of-care (PoC) systems). The microreactor was validated using creatinine standards spiked into commercial artificial urine that mimics physiological matrix. Our results showed acceptable recovery rate and low matrix effect, especially for the low creatinine concentration range in comparison to a commercial PoC uACR test. Altogether, the developed uCR-Chip offers a viable PoC test for CKD assessment and provides a potential platform technology to measure various disease biomarkers.
慢性肾脏病(CKD)严重影响人们的健康和生活质量,并在全球范围内带来高昂的经济负担。目前已有成熟的CKD诊断生物标志物。然而,现有的常规标准检测基于实验室且受严格法规约束。肌酐通常作为血液中的滤过生物标志物来测定估算的肾小球滤过率(eGFR),同时也作为计算尿白蛋白与肌酐比值(uACR)的标准化因子用于CKD评估。在本研究中,我们开发了一种用于比色法检测尿肌酐的被动流动微反应器(uCR芯片),它非常适合与我们之前开发的微流控尿白蛋白检测方法集成。两相压力补偿(2-PPC)技术与微流控通道网络设计相结合,精确控制了流体混合比和化学反应。再加上优化的观察窗口(OW)设计,在7分钟内实现了均匀稳定的检测信号。通过一个简单的基于USB显微镜的平台测量颜色信号,以量化样品中的肌酐浓度。定制的内部光掩模生产技术与基于干膜光刻胶的光刻技术相结合,实现了快速迭代的设计优化和精确的芯片制造。所开发的检测方法实现了高达40 mM的动态线性检测范围和0.521 mM的检测下限(LOD),满足临床精度要求(与现有的即时检测(PoC)系统相当)。使用添加到模拟生理基质的商业人工尿液中的肌酐标准品对微反应器进行了验证。我们的结果显示出可接受的回收率和低基质效应,特别是与商业PoC uACR检测相比,在低肌酐浓度范围内更是如此。总之,所开发的uCR芯片为CKD评估提供了一种可行的PoC检测方法,并为测量各种疾病生物标志物提供了一个潜在的平台技术。