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液相色谱-串联质谱法同时测定小生物体液中的维生素 A、25-羟维生素 D α-生育酚

Simultaneous determination of Vitamin A, 25-hydroxyl vitamin D α-tocopherol in small biological fluids by liquid chromatography-tandem mass spectrometry.

机构信息

Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing 100020, China.

Beijing Municipal Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing 100020, China; Institute of Molecular Medicine, Peking University, Beijing 100871, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Mar 15;1079:1-8. doi: 10.1016/j.jchromb.2017.12.017. Epub 2017 Dec 15.

Abstract

A sensitive method for the simultaneous analysis of vitamin A (VA), 25-hydroxyl vitamin D (25-OH VD) and α-tocopherol (VE) in children plasma by liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed and validated. Sample preparation chose the solid phase extraction. 100 μL of plasma was mixed with 300 μL ethanol contained 4 μL isotope-labelled analytes. After a series operation, the supernatant was applied to the solid phase extraction (SPE) plate (HLB μElution plate). The eluate was evaporated, and reconstituted in 100 μL methanol. And then, 6 μL reconstituted sample was injected into LC-MS/MS. Quantitative analysis was carried out by multiple reaction monitoring (MRM) with a positive mode electrospray (ESi + ). Separations of VA, 25-OH VD and VE were performed on an Acquity UPLC reversed-phase Phenyl-Hexyl analytical column (CSH, 2.1 × 50 mm, 1.7 μm). Gradient elution was used at a flow rate of 0.4 mL/min with a mobile phase consisting of 0.1% formic acid solution and 0.1% formic acid, 5 mM ammonium formate in acetonitrile. The total time of analysis was 10 min. The method had a limit of quantification (LOQ) of 10.03, 1.20, and 0.04 ng/mL for VA, 25-OH VD and VE in methanol, respectively. The linear calibration curves were fitted over the range of 0.14-14.32 μg/mL, 1.80-180.29 ng/mL, and 6.03-602.99 ng/mL for VA, 25-OH VD and VE in methanol. The correlation coefficients were greater than 0.998 for all analytes. The recoveries for all analytes were between 80 and 120% with the inter- and intra-day precisions (presented as relative standard deviation, RSD%) less than 10.0%. Analysis of VA, 25-OH VD and VE in recurrent respiratory tract infection children plasma and anemic infants' fingertip blood was then carried out using this method and statistical analysis of the data with statistic package for social science 20.0 (SPSS 20.0). Using this method, multiple fat-soluble vitamins could be detected at the same time. Solid phase extraction was used to simplify sample pretreatment. μElution plate used here could reduce the sample volume, only 100 μL sample was used in this method, and 6 μL reconstituted sample was injected into LC-MS/MS. This makes the method appropriate for larger sample pretreatment, and suitable for children, especially infants and newborns' sample detection, in whom the circulation blood was low.

摘要

一种灵敏的液相色谱-串联质谱(LC-MS/MS)法用于同时分析儿童血浆中的维生素 A(VA)、25-羟维生素 D(25-OH VD)和α-生育酚(VE),并对其进行了验证。样品制备选择固相萃取。将 100 μL 血浆与 300 μL 含 4 μL 同位素标记分析物的乙醇混合。经过一系列操作后,上清液应用于固相萃取(SPE)板(HLB μElution 板)。洗脱液蒸发后,用 100 μL 甲醇重新溶解。然后,将 6 μL 重新溶解的样品注入 LC-MS/MS。采用正离子电喷雾(ESI+)多反应监测(MRM)进行定量分析。VA、25-OH VD 和 VE 的分离在 Acquity UPLC 反相苯基-己基分析柱(CSH,2.1×50mm,1.7μm)上进行。以流速 0.4mL/min,流动相为 0.1%甲酸溶液和 0.1%甲酸、5mM 甲酸铵的乙腈进行梯度洗脱。分析总时间为 10min。该方法在甲醇中对 VA、25-OH VD 和 VE 的定量限(LOQ)分别为 10.03、1.20 和 0.04ng/mL。VA、25-OH VD 和 VE 在甲醇中的线性校准曲线拟合范围分别为 0.14-14.32μg/mL、1.80-180.29ng/mL 和 6.03-602.99ng/mL。所有分析物的相关系数均大于 0.998。所有分析物的回收率在 80%至 120%之间,日内和日间精密度(以相对标准偏差表示,RSD%)小于 10.0%。然后使用该方法分析复发性呼吸道感染儿童血浆和贫血婴儿指尖血中的 VA、25-OH VD 和 VE,并使用社会科学统计软件包 20.0(SPSS 20.0)对数据进行统计分析。该方法可同时检测多种脂溶性维生素。固相萃取用于简化样品预处理。这里使用的 μElution 板可以减少样品体积,该方法仅使用 100 μL 样品,6 μL 重新溶解的样品注入 LC-MS/MS。这使得该方法适用于更大的样品预处理,适用于儿童,特别是婴儿和新生儿的样品检测,因为他们的循环血量较低。

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