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

被引:7
|
作者
Bhatt, Poornima [1 ,2 ]
Kukkar, Deepak [1 ,2 ]
Yadav, Ashok Kumar [3 ]
Kim, Ki-Hyun [4 ]
机构
[1] Chandigarh Univ, Dept Biotechnol, Mohali 140413, Punjab, India
[2] Univ Ctr Res & Dev, Chandigarh Univ, Mohali 140413, Punjab, India
[3] Post Grad Inst Med Educ & Res, Dept Expt Med & Biotechnol, Sect 12, Chandigarh, India
[4] Hanyang Univ, Dept Civil & Environm Engn, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
Biomarker; Biosensing; Chronic kidney disease; Fluorescence assay; Quenching; QUANTUM DOTS; PROBE; IONS;
D O I
10.1016/j.saa.2023.123666
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
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 (lambda excitation = 390 nm, lambda emission = 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 & sdot;dL-1 (R2 = 0.936) and 5.1 x 10-16 mg & sdot;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.
引用
收藏
页数:9
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