Measurement of plasma 25-hydroxyvitamin D2, 25-hydroxyvitamin D3 and 3-epi-25-hydroxyvitamin D3 in population of patients with cardiovascular disease by UPLC-MS/MS method

被引:23
作者
Abouzid, Mohamed [1 ]
Karazniewicz-Lada, Marta [1 ]
Pawlak, Kornel [1 ]
Burchardt, Pawel [2 ,3 ]
Kruszyna, Lukasz [4 ]
Glowka, Franciszek [1 ]
机构
[1] Poznan Univ Med Sci, Dept Phys Pharm & Pharmacokinet, 6 Swiecickiego St, PL-60781 Poznan, Poland
[2] J Strus Hosp, Dept Cardiol, Szwajcarska 3, PL-61285 Poznan, Poland
[3] Poznan Univ Med Sci, Biol Lipid Disorders Dept, Rokietnicka 8, PL-60806 Poznan, Poland
[4] Poznan Univ Med Sci, Dept Vasc & Endovasc Surg Angiol & Phlebol, Dluga 1-2, PL-60848 Poznan, Poland
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2020年 / 1159卷
关键词
Epi-hydroxyvitamin D; Deuterated internal standard; Liquid-liquid extraction; MS/MS detection; Validation; TANDEM MASS-SPECTROMETRY; VITAMIN-D; HUMAN-SERUM; C-3; EPIMER; D-3; ACCURATE; INFANTS; RISK; HPLC;
D O I
10.1016/j.jchromb.2020.122350
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin D has a potential role in protecting against cardiovascular disease (CVD). Serum 25-hydroxyvitamin D (25D) is the most widely used indicator of vitamin D status in the human body. 25D is estimated as total of 25-hydroxyvitamin D2 (25D2) and 25-hydroxyvitamin D3 (25D3). However, the presence of 3-epi-25-hydroxyvitamin D3 (3epi25D3) can affect 25D measurement. In this research a novel validated UPLC-MS/MS technique was developed to measure three vitamin D metabolites, 25D2, 25D3 and 3epi25D3 in human plasma. A liquid-liquid extraction using hexane was applied for isolation of the analytes from the samples. A chromatographic separation was achieved in a Kinetex F5 analytical column with isocratic elution (water and methanol with 0.1% methanoic acid, 20:80 v/v). Mass spectrometry detection of the metabolites was performed in a triple quadruple tandem mass spectrometer under positive ion mode. Concentrations of the analytes were estimated in plasma samples of 54 patients. Validation parameters of the UPLC-MS/MS method, including linearity, precision, accuracy, and stability, fulfilled the requirements for bioanalytical assays. The deficient concentration of 25D (< 20 ng/mL) was stated in over 60% of patients. 3epi25D3 was present in 78% of samples and its relative amount ranged from 0 to 54.1% of 25D concentration. The analysis of 25D2, 25D3 and 3epi25D3 by the validated UPLC-MS/MS method in plasma of patients with CVD permitted the classification of the patients with insufficient levels of 25D. 3epi25D3 might be relevant in the classification of vitamin D status.
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页数:7
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