School of Biology and Biological Engineering, South China University of Technology, Guangzhou, 510006, China.
Shimadzu (China) Corporation, Guangzhou Branch, 510010, China.
J Pharm Biomed Anal. 2019 Sep 10;174:330-339. doi: 10.1016/j.jpba.2019.06.004. Epub 2019 Jun 6.
A fully automatic system, which integrated cross used solid-phase extraction with ultra-high performance liquid chromatography-tandem mass spectrometry, was developed and validated for the simultaneous determination of multi-class pharmaceuticals (62 in total) in Milli-Q water, tap water, lake water, and ground water. The online system allowed the cross-utilization of two SPE columns without significant carryover and achieved an automatic, sensitive and fast analysis, requiring about 14 min per analysis. The features of the online system were systematically investigated and the analytical conditions were fully optimized. Sixty-two pharmaceuticals were divided into two groups (acidic and basic) under different extraction conditions to increase the extraction efficiency. Under optimal conditions, all the correlation coefficients were greater than 0.9929. The LODs and the LOQs were in the range of 0.00119-0.623 ng L and 0.00475-2.49 ng L, respectively. The RSDs% for the intra-/inter-day precision were less than 10.6% and 15.6%, respectively. The system recoveries ranged from 80.7 to 119.9%. Compared with the offline SPE method, the online cross used SPE-UHPLC-MS/MS method obtained higher sensitivity and reduced manual operations. Compared with the existing online SPE systems, this system can reduce the time per analysis. Finally, this online system was applied to the analyses of three real water samples. Based on the results, the online cross used SPE-UHPLC-MS/MS system as an automatic, sensitive and efficient technique showed great promise for the future in the trace analysis of multi-class pharmaceuticals in complex aqueous samples.
建立并验证了一种完全自动化的系统,该系统集成了交叉使用固相萃取与超高效液相色谱-串联质谱法,可同时测定 Milli-Q 水、自来水、湖水和地下水中的多类药物(共 62 种)。该在线系统允许两个 SPE 柱的交叉使用,且不存在明显的交叉污染,实现了自动、灵敏、快速的分析,每分析一次约需 14 分钟。系统地研究了在线系统的特点,并对分析条件进行了全面优化。将 62 种药物分为两组(酸性和碱性),采用不同的提取条件,以提高提取效率。在最佳条件下,所有相关系数均大于 0.9929。LOD 和 LOQ 的范围分别为 0.00119-0.623ng/L 和 0.00475-2.49ng/L。日内和日间精密度的 RSD%均小于 10.6%和 15.6%。系统回收率在 80.7%至 119.9%之间。与离线 SPE 方法相比,在线交叉使用 SPE-UHPLC-MS/MS 方法具有更高的灵敏度和更少的人工操作。与现有的在线 SPE 系统相比,该系统可缩短每次分析的时间。最后,将该在线系统应用于三种实际水样的分析。结果表明,在线交叉使用 SPE-UHPLC-MS/MS 系统作为一种自动、灵敏、高效的技术,在未来痕量分析复杂水样中的多类药物方面具有广阔的应用前景。