Dehydroascorbic acid quantification in human plasma: Simultaneous direct measurement of the ascorbic acid/dehydroascorbic acid couple by UPLC/MS-MS

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
P.-C. Violet , N. Munyan , H.F. Luecke , Y. Wang , J. Lloyd , K. Patra , K. Blakeslee , I.C. Ebenuwa , M. Levine
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引用次数: 0

Abstract

Ascorbic acid (AA, vitamin C) and dehydroascorbic acid (DHA) constitute a biological couple. No technique can accurately, independently, and simultaneously quantify both members of the couple in animal and human samples, thereby constraining advances in physiology and pathophysiology. Here we describe a new UPLC/MS/MS method to measure both compounds directly and independently in human plasma. Lower limits of quantification were 16 nM, with linear coefficients >0.99 over a 100-fold concentration range. The method was stable and reproducible with <10 % injection-to-injection variation. Use of isotopic labeled internal standards for both compounds ensured precision and accuracy. Plasma preparation required only 2 steps. In plasma samples from 14 anonymized subjects who met criteria for blood donation, mean concentrations were 6±2 μmol/L (mean ± SD) and 56 ± 14 μmol/L for DHA and AA respectively, with (DHA)/(AA + DHA) ratio of 9.8 %. This method represents a pioneering approach to measuring the AA/DHA couple in human plasma.
人体血浆中的脱氢抗坏血酸定量:利用 UPLC/MS-MS 同时直接测定抗坏血酸/脱氢抗坏血酸偶联物
抗坏血酸(AA,维生素 C)和脱氢抗坏血酸(DHA)是一对生物组合。目前还没有一种技术能准确、独立地同时定量测定动物和人体样本中的这两种成分,因此制约了生理学和病理生理学的发展。在此,我们介绍一种新的超高效液相色谱/质谱/质谱(UPLC/MS/MS)方法,可直接、独立地测定人体血浆中的这两种化合物。该方法的定量下限为 16 nM,在 100 倍浓度范围内的线性系数为 0.99。该方法稳定且重现性好,注射与注射之间的差异为 10%。两种化合物均使用同位素标记的内标,确保了精确度和准确性。血浆制备只需两个步骤。在 14 名符合献血标准的匿名受试者的血浆样本中,DHA 和 AA 的平均浓度分别为 6±2 μmol/L(平均 ± SD)和 56±14 μmol/L,(DHA)/(AA + DHA)比值为 9.8%。该方法开创了测量人体血浆中 AA/DHA 偶联物的先河。
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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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