Bian Lun, Liang Junyu, Zhao Hui, Ye Ke, Li Zhaoyue, Liu Tiancai, Peng Jie, Wu Yingsong, Lin Guanfeng
Key Laboratory of Antibody Engineering of Guangdong Higher Education Institutes, Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
Department of Clinical Laboratory, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Front Chem. 2021 Oct 18;9:763686. doi: 10.3389/fchem.2021.763686. eCollection 2021.
Establishing personalized medication plans for patients to maximize therapeutic efficacy and minimize the toxicity of vancomycin (VAN) requires rapid, simple, and accurate monitoring of VAN concentration in body fluid. In this study, we have developed a simple and rapid analytical method by integrating Eu (III) chelate nanoparticles (CN-EUs) and lateral flow immunoassay (LFIA) to achieve the real-time monitoring of VAN concentration in serum within 15 min. This approach was performed on nitrocellulose (NC) membrane assembled LFIA strips via indirect competitive immunoassay and exhibited a wide linear range of detection (0.1-80 μgml) with a low limit of detection (69.2 ngml). The coefficients of variation (CV) of the intra- and inter-assay in the detection of VAN were 7.12-8.53% and 8.46-11.82%, respectively. The dilution test and specificity indicated this method had a stability that was not affected by the serum matrix and some other antibiotics. Furthermore, the applicability of the proposed method was assessed by comparing the determined results with those measured by LC-MS/MS, showing a satisfactory correlation ( = 0.9713). The proposed CN-EUs-based LFIA manifested promising analytical performance, which showed potential value in the real-time monitoring of VAN and could help optimize the clinical use of more antibiotics.
为患者制定个性化用药方案以最大化万古霉素(VAN)的治疗效果并最小化其毒性,需要对体液中的VAN浓度进行快速、简便且准确的监测。在本研究中,我们通过整合铕(III)螯合纳米颗粒(CN-EUs)和侧向流动免疫分析(LFIA)开发了一种简单快速的分析方法,以在15分钟内实现血清中VAN浓度的实时监测。该方法通过间接竞争免疫分析在硝酸纤维素(NC)膜组装的LFIA试纸条上进行,检测线性范围宽(0.1 - 80 μgml),检测下限低(69.2 ngml)。检测VAN时批内和批间变异系数(CV)分别为7.12 - 8.53%和8.46 - 11.82%。稀释试验和特异性表明该方法具有不受血清基质和其他一些抗生素影响的稳定性。此外,通过将测定结果与LC-MS/MS测量结果进行比较评估了该方法的适用性,显示出令人满意的相关性( = 0.9713)。所提出的基于CN-EUs的LFIA表现出有前景的分析性能,在VAN的实时监测中显示出潜在价值,并有助于优化更多抗生素的临床使用。