Deciphering the human urine matrix: a new approach to simultaneously quantify the main ions and organic compounds by ion chromatography/mass spectrometry (IC-MS)

• Published in: Analytical and bioanalytical chemistry 2023-09, Vol.415 (22), p.5337-5352
• Main Authors: Hopsort, Guillaume, Latapie, Laure, Groenen Serrano, Karine, Loubière, Karine, Tzedakis, Theodore
• Format: Article
• Language: English
• Subjects: Ammonium; Analysis; Analytical Chemistry; Biochemistry; Biochemistry, Molecular Biology; Calcium phosphates; Characterization and Evaluation of Materials; Chemical Sciences; Chemistry; Chemistry and Materials Science; Chlorides; Chromatography; Composition; Correlation coefficient; Correlation coefficients; Creatine; Creatinine; Food Science; Human wastes; Ions; Laboratory Medicine; Life Sciences; Magnesium; Mass spectrometry; Mass spectroscopy; Methods; Monitoring/Environmental Analysis; Organic chemistry; Organic compounds; Oxalic acid; Research Paper; Sulfates; Urea; Ureas; Urine
• ISSN: 1618-2642; 1618-2650; 1618-2650
• DOI: 10.1007/s00216-023-04808-2

Analyzing the composition of (human) urine plays a major role in the fields of biology and medicine. Organic molecules (such as urea, creatine) and ions (such as chloride, sulfate) are the major compounds present in urine, the quantification of which allows for the diagnosis of a subject’s health condition. Various analytical methods have been reported for studying urine components and validated on the basis of known and referenced compounds. The present work introduces a new method able to simultaneously determine both major organic molecules and ions contained in urine, by combining ion chromatography using a conductimetric detector with mass spectroscopy. The analysis of organic and ionized compounds (anionic and cationic) was achieved in double injections. For quantification, the standard addition method was used. Human urine samples were pre-treated (diluted and filtered) for IC-CD/MS analysis. The analytes were separated in 35 min. Calibration ranges (0–20 mg.L −1 ) and correlation coefficients (> 99.3%) as well as detection (LODs < 0.75 mg.L −1 ) and quantification (LOQs < 2.59 mg.L −1 ) limits were obtained for the main organic molecules (lactic, hippuric, citric, uric, oxalic acids, urea, creatine, and creatinine) and ions (chloride, sulfate, phosphate, sodium, ammonium, potassium, calcium, and magnesium) contained in urine. The intra- and inter-day accuracies of the analytes consistently ranged from 0.1 to 5.0%, and the precision was within 4.0%. For all analytes, no significant matrix effects were observed, and recoveries ranged from 94.9 to 102.6%. Finally, quantitative results of analytes were obtained from 10 different human urine samples. Graphical abstract