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用于快速定量检测人血浆中他克莫司的明亮纳米颗粒标记侧流免疫分析法。

Bright nanoparticle-labeled lateral flow immunoassay for rapid quantitative detection of tacrolimus in human plasma.

作者信息

Bian Lun, Fu Yu, Xu Zihao, Wu Biru, Liang Junyu, Guo Wei, Lin Guanfeng, Hu Fang

机构信息

Biomaterials Research Center, School of Biomedical Engineering, Southern Medical University, Guangzhou, 510515, China.

Department of Clinical Laboratory, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510150, China.

出版信息

Mikrochim Acta. 2025 May 13;192(6):349. doi: 10.1007/s00604-025-07200-2.

Abstract

Tacrolimus (Tac), a macrolide immunosuppressant widely employed in organ transplantation, requires therapeutic drug monitoring owing to the narrow treatment window. In this study, we established an innovative ultrabright nanoparticle-based lateral flow immunoassay (LFIA) for one-step rapid quantitative detection of Tac in human plasma. The aggregation-induced emission (AIE) luminogen, AIE490, was embedded in polystyrene nanoparticles to assemble the ultrabright AIE490NP as a highly sensitive fluorescence marker. Carboxyl-modified Tac was used to couple with carrier proteins to synthesize complete antigens coated on the test line. Under optimized conditions, the limit of detection for Tac is 0.589 ng/mL in human plasma. The linear range was 1-1000 ng/mL, completely covering the safe plasma concentration of Tac, 5-15 ng/mL. The intra- and inter-assay precisions of the established method are below 17.99% and 19.94%, respectively. In addition, for measuring the plasma concentration of Tac in 139 clinical samples, the results of the LFIA are consistent with those of LC-MS/MS (R = 0.8520, P < 0.0001). Therefore, the established LFIA demonstrates comparable reliability to the LC-MS/MS and holds great potential as a rapid quantitative detection method of Tac in human plasma.

摘要

他克莫司(Tac)是一种广泛应用于器官移植的大环内酯类免疫抑制剂,由于其治疗窗狭窄,需要进行治疗药物监测。在本研究中,我们建立了一种基于超亮纳米颗粒的创新型侧向流动免疫分析方法(LFIA),用于一步快速定量检测人血浆中的他克莫司。将聚集诱导发光(AIE)发光团AIE490嵌入聚苯乙烯纳米颗粒中,组装成超亮的AIE490NP作为高灵敏度荧光标记物。用羧基修饰的他克莫司与载体蛋白偶联,合成包被在检测线上的完全抗原。在优化条件下,人血浆中他克莫司的检测限为0.589 ng/mL。线性范围为1 - 1000 ng/mL,完全覆盖他克莫司的安全血浆浓度5 - 15 ng/mL。所建立方法的批内和批间精密度分别低于17.99%和19.94%。此外,对于139份临床样本中他克莫司血浆浓度的测定,LFIA结果与LC-MS/MS结果一致(R = 0.8520,P < 0.0001)。因此,所建立的LFIA与LC-MS/MS具有相当的可靠性,作为人血浆中他克莫司的快速定量检测方法具有巨大潜力。

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