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Nitrogen doped carbon dots and gold nanoparticles mediated FRET for the detection of creatinine in human urine samples

Authors
Chhillar, MonikaKukkar, DeepakKumar Yadav, AshokKim, Ki-Hyun
Issue Date
Nov-2024
Publisher
Pergamon-Elsevier Sciencd Ltd.
Keywords
Chronic kidney disease; Diabetic nephropathy; Diagnosis; Forster mechanism; Nanomaterials; Sensor
Citation
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v.321, pp 1 - 8
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
Volume
321
Start Page
1
End Page
8
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211213
DOI
10.1016/j.saa.2024.124752
ISSN
1386-1425
1873-3557
Abstract
Serum creatinine (CR) is regarded as one of the most sought out prognostic biomarkers in medical evaluation of chronic kidney disease (CKD). In light of the diagnostic significance of CR, the utility of a fluorescence biosensor for its detection in human urine specimens has been explored based on Förster resonance energy transfer (FRET) across nitrogen-doped carbon dots (N-CDs) and gold nanoparticles (GNPs). A straightforward microwave-assisted synthesis procedure has been adopted to prepare N-CDs (λexcitation = 400 nm, λemission = 540 ± 5 nm) with bright green emissions. On addition of pre-synthesized GNPs, the radiative emanation of the N-CDs is completely suppressed on account of FRET across the N-CDs and the GNPs. About 77 % of their fluorescence intensity is recovered after adding CR to GNPs@N-CDs nanocomposite. The limit of detection for CR sensing is estimated as 0.02 µg•mL−1. This biosensor is selective enough to recognize CR in the existence of potential interfering substances (e.g., ascorbic acid, glucose, glutathione, urea, and electrolytes). Its practical utility for CR detection has been validated further on the basis of satisfactory correlation with the benchmark Jaffe method, as observed in artificial/human urine specimens. Consequently, this manuscript marks a pioneering report on employing CDs and GNPs-based FRET for identifying CR in urine specimens of CKD patients.
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