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Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine

Methylmalonic acid (MMA) is a very short dicarboxylic acid (methylpropanedioic acid; CH(3)CH(COOH)(2); pK(a1), 3.07; pK(a2), 5.76) associated with vitamin B(12) deficiency and many other patho-physiological conditions. In this work, we investigated several carboxylic groups-specific derivatization r...

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Autores principales: Bollenbach, Alexander, Baskal, Svetlana, Mels, Catharina, Kruger, Ruan, Tsikas, Dimitrios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416772/
https://www.ncbi.nlm.nih.gov/pubmed/36014446
http://dx.doi.org/10.3390/molecules27165202
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author Bollenbach, Alexander
Baskal, Svetlana
Mels, Catharina
Kruger, Ruan
Tsikas, Dimitrios
author_facet Bollenbach, Alexander
Baskal, Svetlana
Mels, Catharina
Kruger, Ruan
Tsikas, Dimitrios
author_sort Bollenbach, Alexander
collection PubMed
description Methylmalonic acid (MMA) is a very short dicarboxylic acid (methylpropanedioic acid; CH(3)CH(COOH)(2); pK(a1), 3.07; pK(a2), 5.76) associated with vitamin B(12) deficiency and many other patho-physiological conditions. In this work, we investigated several carboxylic groups-specific derivatization reactions and tested their utility for the quantitative analysis of MMA in human urine and plasma by gas chromatography-mass spectrometry (GC-MS). The most useful derivatization procedure was the reaction of unlabeled MMA (d(0)-MMA) and trideutero-methyl malonic acid (d(3)-MMA) with 2,3,4,5,6-pentafluorobenzyl bromide (PFB-Br) in acetone. By heating at 80 °C for 60 min, we observed the formation of the dipentafluorobenzyl (PFB) ester of MMA (CH(3)CH(COOPFB)(2)). In the presence of N,N-diisopropylamine, heating at 80 °C for 60 min resulted in the formation of a tripentafluorobenzyl derivative of MMA, i.e., CH(3)CPFB(COOPFB)(2)). The retention time was 5.6 min for CH(3)CH(COOPFB)(2) and 7.3 min for CH(3)CPFB(COOPFB)(2)). The most intense ions in the negative-ion chemical ionization (NICI) GC-MS spectra of CH(3)CH(COOPFB)(2) were mass-to-charge (m/z) 233 for d(0)-MMA and m/z 236 for d(3)-MMA. The most intense ions in the NICI GC-MS spectra of CH(3)CPFB(COOPFB)(2) were mass-to-charge (m/z) 349 for d(0)-MMA and m/z 352 for d(3)-MMA. These results indicate that the H at C atom at position 2 is C-H acidic and is alkylated by PFB-Br only in the presence of the base N,N-diisopropylamine. Method validation and quantitative analyses in human urine and plasma were performed by selected ion monitoring (SIM) of m/z 349 for d(0)-MMA and m/z 352 for the internal standard d(3)-MMA in the NICI mode. We used the method to measure the urinary excretion rates of MMA in healthy black (n = 39) and white (n = 41) boys of the Arterial Stiffness in Offspring Study (ASOS). The creatinine-corrected excretion rates of MMA were 1.50 [0.85–2.52] µmol/mmol in the black boys and 1.34 [1.02–2.18] µmol/mmol in the white boys (P = 0.85; Mann–Whitney). The derivatization procedure is highly specific and sensitive for MMA and allows its accurate and precise measurement in 10-µl of human urine by GC-MS.
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spelling pubmed-94167722022-08-27 Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine Bollenbach, Alexander Baskal, Svetlana Mels, Catharina Kruger, Ruan Tsikas, Dimitrios Molecules Article Methylmalonic acid (MMA) is a very short dicarboxylic acid (methylpropanedioic acid; CH(3)CH(COOH)(2); pK(a1), 3.07; pK(a2), 5.76) associated with vitamin B(12) deficiency and many other patho-physiological conditions. In this work, we investigated several carboxylic groups-specific derivatization reactions and tested their utility for the quantitative analysis of MMA in human urine and plasma by gas chromatography-mass spectrometry (GC-MS). The most useful derivatization procedure was the reaction of unlabeled MMA (d(0)-MMA) and trideutero-methyl malonic acid (d(3)-MMA) with 2,3,4,5,6-pentafluorobenzyl bromide (PFB-Br) in acetone. By heating at 80 °C for 60 min, we observed the formation of the dipentafluorobenzyl (PFB) ester of MMA (CH(3)CH(COOPFB)(2)). In the presence of N,N-diisopropylamine, heating at 80 °C for 60 min resulted in the formation of a tripentafluorobenzyl derivative of MMA, i.e., CH(3)CPFB(COOPFB)(2)). The retention time was 5.6 min for CH(3)CH(COOPFB)(2) and 7.3 min for CH(3)CPFB(COOPFB)(2)). The most intense ions in the negative-ion chemical ionization (NICI) GC-MS spectra of CH(3)CH(COOPFB)(2) were mass-to-charge (m/z) 233 for d(0)-MMA and m/z 236 for d(3)-MMA. The most intense ions in the NICI GC-MS spectra of CH(3)CPFB(COOPFB)(2) were mass-to-charge (m/z) 349 for d(0)-MMA and m/z 352 for d(3)-MMA. These results indicate that the H at C atom at position 2 is C-H acidic and is alkylated by PFB-Br only in the presence of the base N,N-diisopropylamine. Method validation and quantitative analyses in human urine and plasma were performed by selected ion monitoring (SIM) of m/z 349 for d(0)-MMA and m/z 352 for the internal standard d(3)-MMA in the NICI mode. We used the method to measure the urinary excretion rates of MMA in healthy black (n = 39) and white (n = 41) boys of the Arterial Stiffness in Offspring Study (ASOS). The creatinine-corrected excretion rates of MMA were 1.50 [0.85–2.52] µmol/mmol in the black boys and 1.34 [1.02–2.18] µmol/mmol in the white boys (P = 0.85; Mann–Whitney). The derivatization procedure is highly specific and sensitive for MMA and allows its accurate and precise measurement in 10-µl of human urine by GC-MS. MDPI 2022-08-15 /pmc/articles/PMC9416772/ /pubmed/36014446 http://dx.doi.org/10.3390/molecules27165202 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bollenbach, Alexander
Baskal, Svetlana
Mels, Catharina
Kruger, Ruan
Tsikas, Dimitrios
Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title_full Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title_fullStr Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title_full_unstemmed Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title_short Unusual Derivatization of Methylmalonic Acid with Pentafluorobenzyl Bromide to a Tripentafluorobenzyl Derivative and Its Stable-Isotope Dilution GC-MS Measurement in Human Urine
title_sort unusual derivatization of methylmalonic acid with pentafluorobenzyl bromide to a tripentafluorobenzyl derivative and its stable-isotope dilution gc-ms measurement in human urine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416772/
https://www.ncbi.nlm.nih.gov/pubmed/36014446
http://dx.doi.org/10.3390/molecules27165202
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