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化学衍生化法改进高效液相色谱-串联质谱法测定人尿液中多元羧酸。邻-苄基羟胺和 2-吡啶基乙胺的比较。

Improving liquid chromatography-tandem mass spectrometry determination of polycarboxylic acids in human urine by chemical derivatization. Comparison of o-benzyl hydroxylamine and 2-picolyl amine.

机构信息

Integrative Pharmacology and Systems Neuroscience Group (FINS), IMIM, Hospital del Mar, Doctor Aiguader 88, Barcelona, Spain; Universitat Pompeu Fabra (CEXS-UPF), Doctor Aiguader 88, Barcelona, Spain.

Integrative Pharmacology and Systems Neuroscience Group (FINS), IMIM, Hospital del Mar, Doctor Aiguader 88, Barcelona, Spain.

出版信息

J Pharm Biomed Anal. 2019 Feb 5;164:382-394. doi: 10.1016/j.jpba.2018.10.055. Epub 2018 Nov 3.

Abstract

Due to its high sensitivity and specificity, liquid chromatography-electrospray tandem mass spectrometry (LC-MS/MS) could be considered as the gold-standard in targeted metabolomics. Although LC-MS/MS allows for the direct detection of a large number of molecules, the proper quantification of highly polar compounds such as poly-carboxylic acids in complex matrices like urine is still a challenge. Chemical derivatization offers a suitable way to improve chromatographic behavior and sensitivity for these compounds. Several derivatizing agents have been proposed for the LC-MS/MS determination of carboxylic acids but studies dealing with their comparison in challenging scenarios are scarce. Here we present the evaluation of two different derivatization agents; o-benzylhydroxyl amine (oBHA) and 2-picolyl amine (2-PA); for the quantification of the (poly)-carboxylic acids belonging to the tricarboxylic acid cycle in urine. The suitability of both derivatizating agents was compared by validation of the two approaches. Derivatization with oBHA showed important advantages against 2-PA derivatization such as (i) providing better sensitivity, (ii) more stable derivatives and (iii) allowing for the proper validation of a larger number of analytes. Moreover, while 2-PA derivatization failed in the determination of the target analytes in some stored urine samples, oBHA derivatization successfully allowed for their appropriate determination in the same samples. A comparison between the concentrations obtained using oBHA derivatization and those provided by an external laboratory using UV and GC-MS detection revealed a satisfactory agreement between both results. Additionally, the concentrations obtained by the oBHA method for a set of 38 urines are in agreement with those previously reported in the literature. As a conclusion, our results show that the use of oBHA is preferred against 2-PA for the detection and quantification of (poly)-carboxylic acids in urine.

摘要

由于其高灵敏度和特异性,液相色谱-电喷雾串联质谱(LC-MS/MS)可被视为靶向代谢组学的金标准。尽管 LC-MS/MS 允许直接检测大量分子,但在尿液等复杂基质中对高度极性化合物(如多羧酸)进行适当定量仍然是一个挑战。化学衍生化提供了一种改善这些化合物色谱行为和灵敏度的合适方法。已经提出了几种衍生化试剂用于 LC-MS/MS 测定羧酸,但在具有挑战性的情况下对它们进行比较的研究很少。在这里,我们评估了两种不同的衍生化试剂;邻-苄基羟胺(oBHA)和 2-吡啶基胺(2-PA);用于尿液中三羧酸循环中(多)羧酸的定量。通过两种方法的验证比较了两种衍生化试剂的适用性。与 2-PA 衍生化相比,oBHA 衍生化具有重要优势,如(i)提供更好的灵敏度,(ii)更稳定的衍生物和(iii)允许对更多分析物进行适当验证。此外,虽然 2-PA 衍生化在一些储存的尿液样本中无法测定目标分析物,但 oBHA 衍生化成功地允许在相同样本中对其进行适当测定。使用 oBHA 衍生化获得的浓度与使用外部实验室的 UV 和 GC-MS 检测提供的浓度之间的比较显示出两者之间的结果令人满意的一致性。此外,oBHA 方法获得的一组 38 个尿液的浓度与文献中先前报道的浓度一致。总之,我们的结果表明,与 2-PA 相比,oBHA 用于尿液中(多)羧酸的检测和定量更优。

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