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Carbon dot-copper nanocomposite-based fluorescent sensor for detection of creatinine in urine samples of CKD patients

Authors
Bhatt, PoornimaKukkar, DeepakYadav, Ashok KumarKim, Ki-Hyun
Issue Date
Feb-2024
Publisher
Pergamon-Elsevier Sciencd Ltd.
Keywords
Biomarker; Biosensing; Chronic kidney disease; Fluorescence assay; Quenching
Citation
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v.307, pp 1 - 9
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
Volume
307
Start Page
1
End Page
9
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/193268
DOI
10.1016/j.saa.2023.123666
ISSN
1386-1425
1873-3557
Abstract
Creatinine (CR) is accepted as a clinical biomarker of chronic kidney disease (CKD) such as renal injury and kidney failure. To help facilitate the prognosis of CKD, a highly luminescent carbon dot (CD)-based fluorescent (FL) sensor has been built and employed for CR detection in diverse media (e.g., artificial and human urine). CDs, synthesized from sucrose precursor by a rapid microwave-assisted method (average diameter 20 nm), exhibited highly luminescent green emission upon UV exposure (λexcitation = 390 nm, λemission = 453 nm) with excellent temporal stability over three months. The nanocomposites are formed between CDs and metal ions (e.g., Cu2+) to realize the optimum biosensing of CR. Although Cu2+ ions showcases a maximum quenching (73 %) of the CDs, Cu2+/CDs system restores 77 % of the original FL intensity upon the addition of CR. The linear detection range and limit of detection for CR are estimated as 10-5 to 0.1 mg·dL-1 (R2 = 0.936) and 5.1 × 10-16 mg·dL-1, respectively. Furthermore, our biosensor shows excellent reproducibility and selectivity for CR in urine samples of healthy subjects and CKD patients. The Bland-Altman analysis for urine samples (n = 30) showcased an excellent agreement (R2 = 0.95) between our method and the gold standard ‘Jaffe’ method. These observations supported the practical utility of our method proposed for detection of CR in clinical samples.
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