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Continuous and quantitative measurement of toxin biomarkers in biological fluids constitutes a significant advancement in the proactive management of chronic kidney diseases (CKD). Although sweat analysis presents a promising non-invasive strategy, conventional detection methods suffer from inherent limitations, including low sensitivity, poor specificity, high cost, and inadequate long-term durability. Herein, we constructed a novel molecularly imprinted portable biosensor that can simultaneously detect three critical biomarkers (urea, creatinine, and uric acid) for CKD in human sweat. The sensor was fabricated on flexible polyethylene terephthalate (PET) film using screen-printing technology to form a five-electrode array consisting of one counter electrode, one reference electrode and three working electrodes. The ternary composite electrodes (NiCoMOF/MWCNTs/NCDs) were designed as sensing substrate, the porous structure derived from metal-organic frameworks provides abundant active sites for analyte sensing and in synergy with the conductivity of MWCNTs and NCDs, endows the ternary composite electrode with a high electrochemically active surface area (A) of 0.062 cm, a rapid electron transfer rate (k) of 6.685 × 10 cm s, and a low electron transfer resistance of 52.79 Ω, significantly enhancing its electrochemical properties (Bare carbon, A: 0.0161 cm, k: 0.613 × 10 cm s). Molecular imprinting technology generates highly specific recognition cavities with enhanced rebinding efficiency by removing template molecules from each working electrode. The portable sensing platform exhibits sensitivities of 6.2 μA mM cm, 134 nA μM cm, and 1870 nA μM cm for the detection of urea, creatinine, and uric acid, respectively, with detection limits of 0.048 mM, 0.032 μM, and 0.024 μM. The linear ranges encompass the physiological concentrations of these analytes in sweat, with corresponding correlation coefficients (R) of 0.9959, 0.9952, and 0.9981. The non-enzymatic mechanism ensures that the signal retention rate remains above 95.8 % after 60 days of storage. The results from various scenario tests demonstrated that the sensing system successfully achieved synchronous dynamic monitoring of three biomarkers in sweat samples. Hence, this work shows high development prospects for a continuous, convenient, non-invasive sensing platform for point-of-care diagnosis and personalized management of chronic kidney diseases.
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http://dx.doi.org/10.1016/j.talanta.2025.128227 | DOI Listing |
Ann Intern Med
September 2025
NYU Grossman School of Medicine, New York, New York (M.E.G., M.L.M.).
Nearly 14% of Americans have chronic kidney disease (CKD), which includes persistent decrements in glomerular filtration rate or the presence of albuminuria. Although CKD is commonly attributed to diabetes or hypertension, there is growing awareness of the interplay among cardiovascular, kidney, and metabolic health. Progression of CKD can result in metabolic abnormalities and end-stage kidney disease, but cardiovascular events are even more common.
View Article and Find Full Text PDFPLoS One
September 2025
Chilean Invasive Mycosis Network, Santiago, Chile.
Background: Invasive mold diseases (IMDs) are a severe complication of immunocompromised subjects and an emerging problem among severely ill, apparently immunocompetent patients. The aim of this study was to describe the epidemiological and clinical features of IMDs in Chile.
Methods: Prospective study of IMD cases in children and adults from 11 reference hospitals in Chile from May 2019 to May 2021.
Am J Physiol Regul Integr Comp Physiol
September 2025
Department of Health, Nutrition, and Food Sciences, Florida State University, Tallahassee, FL, USA.
Cystathionine γ-lyase (CSE) produces hydrogen sulfide (HS), a vasodilator critical for vascular function. While its systemic effects are well-documented, its role in erectile physiology remains unclear. This study investigated the impact of CSE deletion on vascular and erectile tissue reactivity.
View Article and Find Full Text PDFJ Infect Dev Ctries
August 2025
Division of Infectious Disease, Department of Internal Medicine, Phramongkutklao Hospital and Phramongkutklao College of Medicine, Bangkok 10400, Thailand.
Introduction: Clostridioides difficile often causes hospital-acquired diarrhea, leading to unfavorable treatment outcomes. This study investigates CDI treatment outcomes and factors affecting severity and mortality at a university hospital in Thailand.
Methodology: A retrospective study was conducted from June 2019 to December 2021.
Introduction: The residual risk of chronic kidney disease (CKD) progression remains high in clinical trials of kidney protective drugs in patients with diabetic kidney disease (DKD).
Methods: In a prospective study, we assessed whether 16 plasma and 10 urine cytokine levels can inform the residual risk of CKD progression in 93 incident patients with DKD treated by Nephrology according to clinical guidelines.
Results: Plasma and urine levels of 12 plasma and 7 urinary cytokines differed between patients with DKD and from healthy controls.