Vanin-1-Activated Chemiluminescent Probe: Help to Early Diagnosis of Acute Kidney Injury with High Signal-to-Noise Ratio through Urinalysis

被引:8
|
作者
Feng, Yurong [1 ]
Xu, Shuai [1 ]
Guo, Haowei [1 ]
Ren, Tian-Bing [1 ]
Huan, Shuang-Yan [1 ]
Yuan, Lin [1 ]
Zhang, Xiao-Bing [1 ]
机构
[1] Hunan Univ, Mol Sci & Biomed Lab, State Key Lab Chemo Biosensing & Chemometr, Coll Chem & Chem Engn,Collaborat Innovation Ctr C, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
URINARY BIOMARKERS; POTENTIAL BIOMARKER; FLUORESCENT-PROBE; RENAL INJURY; VANIN-1; PANTETHEINASE; DISEASE; IDENTIFICATION; DEFINITION; MARKER;
D O I
10.1021/acs.analchem.3c02875
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Acute kidney injury (AKI) is a common medical condition with high morbidity and mortality. Although urinalysis provides a noninvasive and convenient diagnostic method for AKI at the molecular level, the low sensitivity of current chemical probes used in urinalysis hinders the time diagnosis of AKI. Herein, we achieved the sensitive and early diagnosis of AKI by the development of a chemiluminescent probe CL-Pa suitable for detection of urinary Vanin-1. Vanin-1 is considered as an early and sensitive biomarker for AKI, while few chemical probes have been applied to for its efficient detection. By virtue of the low autofluorescence interference during urine imaging in the chemiluminescence model, CL-Pa could realize the monitoring of the up-regulated urinary Vanin-1 with a high signal-to-noise ratio (similar to 588). Importantly, under the help of CL-Pa, the up-regulation of urinary Vanin-1 of cisplatin-induced AKI mice at 12 h post cisplatin injection was detected, which was much earlier than clinical biomarkers (sCr and BUN) and change of kidney histology (48 h post cisplatin injection). Furthermore, using this probe, the fluctuation of urinary Vanin-1 of mice with different degrees of AKI was monitored. This study demonstrated the ability of CL-Pa in sensitively detecting drug-induced AKI through urinalysis and suggested the great potential of CL-Pa for early diagnosis of AKI and evaluate the efficiency of anti-AKI drugs clinically.
引用
收藏
页码:14754 / 14761
页数:8
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