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Simultaneous Determination of Underivatized Vitamin B1 and B6 in Whole Blood by Reversed Phase Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry

机译:反相超高效液相色谱串联质谱法同时测定全血中未衍生的维生素B1和B6

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Background Vitamin B1 (thiamine-diphosphate) and B6 (pyridoxal-5’phosphate) are micronutrients. Analysis of these micronutrients is important to diagnose potential deficiency which often occurs in elderly people due to malnutrition, in severe alcoholism and in gastrointestinal compromise due to bypass surgery or disease. Existing High Performance Liquid Chromatography (HPLC) based methods include the need for derivatization and long analysis time. We developed an Ultra High Performance Liquid Chromatography Tandem Mass spectrometry (UHPLC-MS/MS) assay with internal standards for simultaneous measurement of underivatized thiamine-diphosphate and pyridoxal-5’phosphate without use of ion pairing reagent. Methods Whole blood, deproteinized with perchloric acid, containing deuterium labelled internal standards thiamine-diphosphate(thiazole-methyl-D3) and pyridoxal-5’phosphate(methyl-D3), was analyzed by UHPLC-MS/MS. The method was validated for imprecision, linearity, recovery and limit of quantification. Alternate (quantitative) method comparisons of the new versus currently used routine HPLC methods were established with Deming regression. Results Thiamine-diphosphate and pyridoxal-5’phosphate were measured within 2.5 minutes instrumental run time. Limits of detection were 2.8 nmol/L and 7.8 nmol/L for thiamine-diphosphate and pyridoxal-5’phosphate respectively. Limit of quantification was 9.4 nmol/L for thiamine-diphosphate and 25.9 nmol/L for pyridoxal-5’phosphate. The total imprecision ranged from 3.5–7.7% for thiamine-diphosphate (44–157 nmol/L) and 6.0–10.4% for pyridoxal-5’phosphate (30–130 nmol/L). Extraction recoveries were 101–102% ± 2.5% (thiamine-diphosphate) and 98–100% ± 5% (pyridoxal-5’phosphate). Deming regression yielded slopes of 0.926 and 0.990 in patient samples (n = 282) and national proficiency testing samples (n = 12) respectively, intercepts of +3.5 and +3 for thiamine-diphosphate (n = 282 and n = 12) and slopes of 1.04 and 0.84, intercepts of -2.9 and +20 for pyridoxal-5’phosphate (n = 376 and n = 12). Conclusion The described UHPLC-MS/MS method allows simultaneous determination of underivatized thiamine-diphosphate and pyridoxal-5’phosphate in whole blood without intensive sample preparation.
机译:背景维生素B1(硫胺素二磷酸)和B6(吡py醛-5'磷酸)是微量营养素。这些微量营养素的分析对于诊断潜在的缺乏症很重要,这种缺陷通常发生在营养不良的老年人,严重的酒精中毒和因搭桥手术或疾病引起的胃肠道损害中。现有的基于高效液相色谱(HPLC)的方法包括需要衍生化和较长的分析时间。我们开发了具有内标的超高效液相色谱串联质谱(UHPLC-MS / MS)测定法,可在不使用离子配对试剂的情况下同时测量未衍生的硫胺素二磷酸和5x磷酸吡ido醛。方法用UHPLC-MS / MS分析全血,经高氯酸脱蛋白,其中含有氘标记的内标硫胺素二磷酸(噻唑-甲基-D3)和吡ido醛-5’磷酸(甲基-D3)。验证了该方法的不精确性,线性,回收率和定量限。通过Deming回归建立了新方法与当前使用的常规HPLC方法的替代(定量)方法比较。结果在仪器运行的2.5分钟内测量了硫胺二磷酸和5'磷酸吡ido醛。硫胺素二磷酸和吡ido醛-5’磷酸的检出限分别为2.8 nmol / L和7.8 nmol / L。硫胺二磷酸的定量下限为9.4 nmol / L,吡pyr醛-5’磷酸的定量下限为25.9 nmol / L。硫胺二磷酸(44-157 nmol / L)的总不准确性范围为3.5–7.7%,吡ido醛-5’磷酸(30–130 nmol / L)的总不准确性范围为6.0–10.4%。提取回收率为101–102%±2.5%(硫胺素二磷酸)和98–100%±5%(吡rid醛-5’磷酸)。通过Deming回归,患者样本(n = 282)和国家能力验证样本(n = 12)的斜率分别为0.926和0.990,硫胺素二磷酸酯(n = 282和n = 12)的截距分别为+3.5和+3。分别为1.04和0.84,吡ido醛-5'磷酸酯的截距为-2.9和+20(n = 376,n = 12)。结论所描述的UHPLC-MS / MS方法可同时测定全血中未衍生的硫胺素二磷酸和5'磷酸吡ido醛,而无需进行大量的样品前处理。

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