Issue 11, 2025

A dual turn-on–off fluorometric probe based on silver sulfide quantum dots for simultaneous assay of creatinine and calcium in complex matrices

Abstract

Biomarkers like creatinine (CRE) and calcium ions (Ca2+) are vital for detecting several disorders like chronic kidney disease (CKD). Hypocalcemia affects bones, the heart, and other organs. The main limitations of traditional CRE/Ca2+ monitoring protocols in biological samples are their invasiveness and time consumption. The present work aims at developing a rapid, highly sensitive, and selective fluorescent probe for the simultaneous determination of CRE and Ca2+ in pure and complex samples. The probe is based on Ag2S quantum dots (QDs) modified with polyethyleneimine and imidazole dicarboxylic acid. The interaction of the analytes with the modified Ag2S QDs causes a quenching in their fluorescence intensity at λem of 485 nm (λex: 240 nm) and 605 nm (λex: 300 nm) for CRE and Ca2+, respectively. The system was characterized with high-resolution transmission electron microscopy, FTIR spectroscopy, dynamic light scattering, and zeta potential measurement. The influence of solution pH, incubation time, amount of modified QDs, and interfering species was investigated. The probe demonstrated a limit of detection of 0.48 and 0.45 μg mL−1, a linear range of 0.7–9.0 and 0.5–4.0 μg mL−1, and recovery values in the ranges of 93.8–98.4 and 94.2–103.6% for CRE and Ca2+, respectively. The developed system can help in the early diagnosis of several renal disorders.

Graphical abstract: A dual turn-on–off fluorometric probe based on silver sulfide quantum dots for simultaneous assay of creatinine and calcium in complex matrices

Article information

Article type
Paper
Submitted
07 Jan 2025
Accepted
07 Mar 2025
First published
20 Mar 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 8707-8718

A dual turn-on–off fluorometric probe based on silver sulfide quantum dots for simultaneous assay of creatinine and calcium in complex matrices

H. A. Moustafa, A. S. Abo Dena and I. M. El-Sherbiny, RSC Adv., 2025, 15, 8707 DOI: 10.1039/D5RA00164A

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