Puts Johan, de Groot Monique, Haex Martin, Jakobs Bernadette
Department of Clinical Chemistry and Haematology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
Life Science group, Agilent Technologies, Amstelveen, The Netherlands.
PLoS One. 2015 Jul 2;10(7):e0132018. doi: 10.1371/journal.pone.0132018. eCollection 2015.
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.
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.
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).
The described UHPLC-MS/MS method allows simultaneous determination of underivatized thiamine-diphosphate and pyridoxal-5'phosphate in whole blood without intensive sample preparation.
维生素B1(硫胺二磷酸)和B6(磷酸吡哆醛)是微量营养素。对这些微量营养素进行分析对于诊断潜在缺乏症很重要,这种缺乏症常因营养不良在老年人中出现,在严重酗酒者以及因旁路手术或疾病导致胃肠道功能受损的人群中也会出现。现有的基于高效液相色谱(HPLC)的方法需要衍生化且分析时间长。我们开发了一种超高效液相色谱串联质谱(UHPLC-MS/MS)测定法,使用内标物同时测定未衍生化的硫胺二磷酸和磷酸吡哆醛,无需使用离子对试剂。
用含有氘标记内标物硫胺二磷酸(噻唑 - 甲基 - D3)和磷酸吡哆醛(甲基 - D3)的高氯酸对全血进行脱蛋白处理,然后通过UHPLC-MS/MS进行分析。该方法针对不精密度、线性、回收率和定量限进行了验证。采用戴明回归法对新方法与当前使用的常规HPLC方法进行了替代(定量)方法比较。
硫胺二磷酸和磷酸吡哆醛在仪器运行时间2.5分钟内即可测定。硫胺二磷酸和磷酸吡哆醛的检测限分别为2.8 nmol/L和7.8 nmol/L。硫胺二磷酸的定量限为9.4 nmol/L,磷酸吡哆醛的定量限为25.9 nmol/L。硫胺二磷酸(44 - 157 nmol/L)的总不精密度范围为3.5 - 7.7%,磷酸吡哆醛(30 - 130 nmol/L)的总不精密度范围为6.0 - 10.4%。提取回收率为硫胺二磷酸101 - 102% ± 2.5%,磷酸吡哆醛98 - 100% ± 5%。在患者样本(n = 282)和国家能力验证样本(n = 12)中,戴明回归分别得出硫胺二磷酸的斜率为0.926和0.990,截距分别为 +3.5和 +3(n = 282和n = 12),磷酸吡哆醛的斜率为1.04和0.84,截距分别为 -2.9和 +20(n = 376和n = 12)。
所描述的UHPLC-MS/MS方法无需复杂的样品制备即可同时测定全血中未衍生化的硫胺二磷酸和磷酸吡哆醛。