Glycosaminoglycans (GAGs) are long linear sulfated polysaccharides implicated in processes linked to disease development such as mucopolysaccharidosis, respiratory failure, cancer, and viral infections, thereby serving as potential biomarkers. A successful clinical translation of GAGs as biomarkers depends on the availability of standardized GAG measurements. However, owing to the analytical complexity associated with the quantification of GAG concentration and structural composition, a standardized method to simultaneously measure multiple GAGs is missing. In this study, we sought to characterize the analytical performance of a ultra-high-performance liquid chromatography coupled with triple-quadrupole tandem mass spectrometry (UHPLC-MS/MS)-based kit for the quantification of 17 free GAG disaccharides. The kit showed acceptable linearity, selectivity and specificity, accuracy and precision, and analyte stability in the absolute quantification of 15 disaccharides. In native human samples, here using urine as a reference matrix, the analytical performance of the kit was acceptable for the quantification of CS disaccharides. Intra- and inter-laboratory tests performed in an external laboratory demonstrated robust reproducibility of GAG measurements showing that the kit was acceptably standardized. In conclusion, these results indicated that the UHPLC-MS/MS kit was standardized for the simultaneous measurement of free GAG disaccharides allowing for comparability of measurements and enabling translational research.

Analytical performance of a standardized kit for mass spectrometry-based measurements of human glycosaminoglycans / Tamburro, D.; Bratulic, S.; Abou Shameh, S.; Soni, N. K.; Bacconi, A.; Maccari, F.; Galeotti, F.; Mattsson, K.; Volpi, N.; Nielsen, J.; Gatto, F.. - In: JOURNAL OF CHROMATOGRAPHY. B. - ISSN 1570-0232. - 1177:(2021), pp. 1-9. [10.1016/j.jchromb.2021.122761]

Analytical performance of a standardized kit for mass spectrometry-based measurements of human glycosaminoglycans

Maccari F.;Volpi N.;Gatto F.
2021

Abstract

Glycosaminoglycans (GAGs) are long linear sulfated polysaccharides implicated in processes linked to disease development such as mucopolysaccharidosis, respiratory failure, cancer, and viral infections, thereby serving as potential biomarkers. A successful clinical translation of GAGs as biomarkers depends on the availability of standardized GAG measurements. However, owing to the analytical complexity associated with the quantification of GAG concentration and structural composition, a standardized method to simultaneously measure multiple GAGs is missing. In this study, we sought to characterize the analytical performance of a ultra-high-performance liquid chromatography coupled with triple-quadrupole tandem mass spectrometry (UHPLC-MS/MS)-based kit for the quantification of 17 free GAG disaccharides. The kit showed acceptable linearity, selectivity and specificity, accuracy and precision, and analyte stability in the absolute quantification of 15 disaccharides. In native human samples, here using urine as a reference matrix, the analytical performance of the kit was acceptable for the quantification of CS disaccharides. Intra- and inter-laboratory tests performed in an external laboratory demonstrated robust reproducibility of GAG measurements showing that the kit was acceptably standardized. In conclusion, these results indicated that the UHPLC-MS/MS kit was standardized for the simultaneous measurement of free GAG disaccharides allowing for comparability of measurements and enabling translational research.
2021
1177
1
9
Analytical performance of a standardized kit for mass spectrometry-based measurements of human glycosaminoglycans / Tamburro, D.; Bratulic, S.; Abou Shameh, S.; Soni, N. K.; Bacconi, A.; Maccari, F.; Galeotti, F.; Mattsson, K.; Volpi, N.; Nielsen, J.; Gatto, F.. - In: JOURNAL OF CHROMATOGRAPHY. B. - ISSN 1570-0232. - 1177:(2021), pp. 1-9. [10.1016/j.jchromb.2021.122761]
Tamburro, D.; Bratulic, S.; Abou Shameh, S.; Soni, N. K.; Bacconi, A.; Maccari, F.; Galeotti, F.; Mattsson, K.; Volpi, N.; Nielsen, J.; Gatto, F....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1248439
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