Niu Lisong, Li Lanya, Li Jinshan, Chen Zhitian, Lin Jiayuan, Zhang Bo, Fu Xiaoling
The No. 4 People' Hospital of Hengshui, Hengshui, Hebei, 053000, People's Republic of China.
Shuyang Hospital of Traditional Chinese Medicine, Suqian, Jiangsu, 223600, People's Republic of China.
J Fluoresc. 2023 May;33(3):1191-1200. doi: 10.1007/s10895-022-03120-z. Epub 2023 Jan 11.
Liver fatty acid binding protein (L-FABP) is an intercellular lipid chaperone protein that selectively combines with unsaturated free fatty acids and transports them to mitochondria or peroxisomes. L-FABP is a promising biomarker for the early detection of renal diseases in humans. Herein a chemiluminescence method (CLIA) was demonstrated to measure the level of urinary L-FABP in the urinary samples. An anti-(L-FABP)-magnetic beads complex was prepared to capture the analyte target. Sensitivity, precision, accuracy, interference effect, high-dose hook effect of the developed assay were evaluated. Under the suitable experimental parameters, the established method have a wide linear range (0.01-10 ng/mL) and also showed a sufficiently low limit of detection of 0.0060 ng/mL. Besides, the satisfactory recoveries of the method in the urinary were ranged from 97.74%-112.32%, which was well within the requirement of clinical analysis. Furthermore, this proposed method has been successfully applied to the clinical determination of L-FABP in patients who have been diagnosed with kidney disease. The results showed that CLIA could accurately and rapidly determine the urinary level of L-FABP with high-throughput, which could be useful as a new tool to predict complications in patients with kidney disease. The clinical trial was approved by Shuyang Hospital of Traditional Chinese Medicine Ethics Committee: 20,210,202-001 at February 2, 2021.
肝脏脂肪酸结合蛋白(L-FABP)是一种细胞内脂质伴侣蛋白,它能选择性地与不饱和游离脂肪酸结合,并将其转运至线粒体或过氧化物酶体。L-FABP是早期检测人类肾脏疾病的一种很有前景的生物标志物。本文展示了一种化学发光法(CLIA)来测定尿液样本中尿L-FABP的水平。制备了抗(L-FABP)磁珠复合物以捕获分析物靶标。对所开发检测方法的灵敏度、精密度、准确度、干扰效应、高剂量钩状效应进行了评估。在合适的实验参数下,所建立的方法具有较宽的线性范围(0.01 - 10 ng/mL),并且检测限足够低,为0.0060 ng/mL。此外,该方法在尿液中的回收率令人满意,范围为97.74% - 112.32%,完全符合临床分析的要求。此外,该方法已成功应用于已确诊肾病患者的L-FABP临床测定。结果表明,CLIA能够高通量、准确且快速地测定尿L-FABP水平,可作为预测肾病患者并发症的一种新工具。该临床试验于2021年2月2日获得沭阳中医院伦理委员会批准:20,210,202 - 001。