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Precise determination of the molybdenum isotopic composition of urine by multiple collector inductively coupled plasma mass spectrometry
Author(s) -
Zhang Jing,
Li Jie,
Zhang Le,
Wang Zhibing,
Sun Shengling,
Luo Zhenyu
Publication year - 2020
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.8658
Subject(s) - chemistry , urine , inductively coupled plasma mass spectrometry , molybdenum , urinalysis , isotope , chromatography , mass spectrometry , isotope dilution , analytical chemistry (journal) , inorganic chemistry , biochemistry , physics , quantum mechanics
Rationale Molybdenum (Mo) is predominantly expelled from the human body in urine. Consequently, urinary variability in the concentration and isotopic composition of Mo may encode valuable clinical information. To access this information, however, it is first necessary to develop and demonstrate a rapid, accurate and precise methodology capable of concentrating Mo from urine for isotope analysis. Methods The utility of N ‐benzoyl‐ N ‐phenylhydroxylamine (BPHA) to effectively separate and purify Mo from urine samples without the need for acid digestion was tested. Following this approach, applying a double‐spike mass bias correction, we determined the Mo isotopic compositions of a set of urine samples by multiple collector inductively coupled plasma mass spectrometry (MC‐ICP‐MS). Results Based on replicate analyses of an in‐house urine standard, this approach demonstrates an external precision on δ 98/95 Mo values of better than 0.08‰ (2SD, n = 15). Application to a sample set collected from healthy individuals in Guangzhou, China, provides the first suite of δ 98/95 Mo measurements from urine samples. Samples from the female participants show δ 98/95 Mo (‰) values (1.31 ± 0.19‰, Ave ± 2SD, n = 14) that are consistently lower than those from the male participants (1.55 ± 0.16‰, Ave ± 2SD, n = 17). Conclusions The employed methodology is suitable for rapid, low‐blank and high‐throughput Mo isotope analysis of urine samples. Although resolvable δ 98/95 Mo variability is seen in this preliminary dataset, the mechanism driving this variability is unknown. High‐precision Mo isotopic analysis might be added to the urinalysis tool‐kit, with the potential to provide valuable clinical information in the future.