A Point‐of‐Care Sensing Platform for Multiplexed Detection of Chronic Kidney Disease Biomarkers Using Molecularly Imprinted Polymers

Author:

Li Yixuan1ORCID,Luo Liuxiong2,Kong Yingqi1,George Sophiamma3,Li Yujia1,Guo Xiaotong4,Li Xin5,Yeatman Eric4,Davenport Andrew36,Li Ying7,Li Bing189ORCID

Affiliation:

1. Institute for Materials Discovery Department of Chemistry University College London London WC1E 7JE UK

2. School of Materials Science and Engineering Central South University Changsha 410083 P. R. China

3. Department of Nephrology Royal Free Hospital London NW3 2QG UK

4. Department of Electrical and Electronic Engineering Imperial College London London SW7 2AZ UK

5. School of Finance & Accounting University of Westminster London NW1 5LS UK

6. Department of Renal Medicine University College London London NW3 2PF UK

7. Department of Brain Repair and Rehabilitation UCL Institute of Neurology London WC1N 3BG UK

8. Care Research & Technology Centre UK Dementia Research Institute London W12 0BZ UK

9. Department of Brain Science Imperial College London London W12 0BZ UK

Abstract

AbstractChronic kidney disease (CKD) is one of the most serious non‐communicable diseases affecting the population. In the early‐stages patients have no obvious symptoms, until it becomes life‐threatening leading end‐stage kidney failure. Therefore, it is important to early diagnose CKD to allow therapeutic interventions and progression monitoring. Here, a point‐of‐care (POC) sensing platform is reported for the simultaneous detection of three CKD biomarkers, namely creatinine, urea, and human serum albumin (HSA), using reduced graphene oxide/polydopamine‐molecularly imprinted polymer (rGO/PDA‐MIP) fabricated with novel surface‐molecularly imprinting technology. A multi‐channel electrochemical POC readout system with differential pulse voltammetry (DPV) function is developed, allowing the simultaneous detection of the three biomarkers, in combination with the surface‐MIP electrodes. This sensing platform achieves the record low limit‐of‐detection (LoD) at a femtomolar level for all three analytes, with wide detection ranges covering their physiological concentrations. Clinical validation is performed by measuring these analytes in serum and urine from healthy controls and patients with CKD. The average recovery rate is 81.8–119.1% compared to the results obtained from the hospital, while this platform is more cost‐effective, user‐friendly, and requires less sample‐to‐result time, showing the potential to be deployed in resource‐limited settings for the early diagnosis and tracking progression of CKD.

Funder

Royal Society

Medical Research Council

Engineering and Physical Sciences Research Council

Alzheimer’s Research UK

China Scholarship Council

Publisher

Wiley

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