Urine Self-Sampling Kit Combined with an Automated Preparation-Sampler Device for Convenient and Reliable Analysis of Arsenic Metabolites by HPLC–ICPMS

• Published in: Analytical chemistry (Washington) Vol. 96; no. 4; pp. 1742 - 1749
• Main Authors: Zhang, Xiao, Jiang, Xin-Yi, Zhao, Lin, Chen, Shuai, Yu, Yong-Liang, Wang, Jian-Hua
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 30.01.2024
• Subjects: Anaerobic conditions; Argon; Arsenic; Arsenicals; Automation; Biological effects; Detection limits; High performance liquid chromatography; Inductively coupled plasma mass spectrometry; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Metabolites; Oxidation; Samplers; Sampling; Sampling methods; Speciation; Urine
• ISSN: 0003-2700; 1520-6882; 1520-6882
• DOI: 10.1021/acs.analchem.3c04881

Speciation analysis of arsenic in urine is essential for the studies of arsenic metabolism and biological effects, but the unstable arsenic species represented by MMAIII and DMAIII pose a huge challenge to analytical accuracy. Herein, a novel urine self-sampling (USS) kit combined with an automated preparation-sampler (APS) device is rationally designed and used for convenient analysis of arsenic metabolites by high-performance liquid chromatography–inductively coupled plasma mass spectrometry (HPLC–ICPMS). The subject can collect urine into a sampling vial at home and use a homemade syringe to pump argon to displace oxygen in the vial, thereby inhibiting the oxidation of MMAIII and DMAIII. After USS and transportation, the sampling vial is loaded directly onto the APS device, where the urine sample can be automatically mixed with diluent, filtered, and loaded into HPLC–ICPMS for arsenic speciation analysis under anaerobic conditions. For a single sample, the sampling time and the analysis time are <8 and <18 min, respectively. The recoveries of MMAIII and DMAIII in urine over 24 h at 4 °C are 86 and 67%, surpassing the conventional sampling method by 28 and 67%, respectively. When the APS is coupled to HPLC–ICPMS, the detection limits of AsC, iAsIII, MMAIII, DMAV, MMAV, DMAIII, and iAsV are 0.03–0.10 μg L–1 with precisions of <10%. The present method provides a convenient and reliable tool for the storage and analysis of unstable arsenic species in urine and lays the foundation for studying the metabolic and biological effects of methylated trivalent arsenicals.