Suppr超能文献

从均相标记前体中制备同位素标记标准品用于定量挥发性代谢组学研究。

Production of isotopically labeled standards from a uniformly labeled precursor for quantitative volatile metabolomic studies.

机构信息

Division of Nutritional Sciences, Cornell University, Ithaca, New York 14853, USA.

出版信息

Anal Chem. 2012 Jun 19;84(12):5400-6. doi: 10.1021/ac300933d. Epub 2012 Jun 4.

Abstract

Optimal accuracy and precision in small-molecule profiling by mass spectrometry generally requires isotopically labeled standards chemically representative of all compounds of interest. However, preparation of mixed standards from commercially available pure compounds is often prohibitively expensive and time-consuming, and many labeled compounds are not available in pure form. We used a single-prototype uniformly labeled [U-(13)C]compound to generate [U-(13)C]-labeled volatile standards for use in subsequent experimental profiling studies. [U-(13)C]-α-Linolenic acid (18:3n-3, ALA) was thermally oxidized to produce labeled lipid degradation volatiles which were subsequently characterized qualitatively and quantitatively. Twenty-five [U-(13)C]-labeled volatiles were identified by headspace solid-phase microextraction-gas chromatography/time-of-flight mass spectrometry (HS-SPME-GC/TOF-MS) by comparison of spectra with unlabeled volatiles. Labeled volatiles were quantified by a reverse isotope dilution procedure. Using the [U-(13)C]-labeled standards, limits of detection comparable to or better than those of previous HS-SPME reports were achieved, 0.010-1.04 ng/g. The performance of the [U-(13)C]-labeled volatile standards was evaluated using a commodity soybean oil (CSO) oxidized at 60 °C from 0 to 15 d. Relative responses of n-decane, an unlabeled internal standard otherwise absent from the mixture, and [U-(13)C]-labeled oxidation products changed by up to 8-fold as the CSO matrix was oxidized, demonstrating that reliance on a single standard in volatile profiling studies yields inaccurate results due to changing matrix effects. The [U-(13)C]-labeled standard mixture was used to quantify 25 volatiles in oxidized CSO and low-ALA soybean oil with an average relative standard deviation of 8.5%. Extension of this approach to other labeled substrates, e.g., [U-(13)C]-labeled sugars and amino acids, for profiling studies should be feasible and can dramatically improve quantitative results compared to use of a single standard.

摘要

通过质谱法进行小分子分析时,要获得最佳的准确度和精密度,通常需要使用与所有感兴趣化合物在化学上具有代表性的同位素标记标准品。然而,从商业上可获得的纯化合物中制备混合标准品通常非常昂贵且耗时,并且许多标记化合物无法以纯形式获得。我们使用单一原型的均一标记 [U-(13)C]化合物来生成用于后续实验分析研究的 [U-(13)C]-标记挥发性标准品。[U-(13)C]-α-亚麻酸(18:3n-3,ALA)经热氧化产生标记的脂质降解挥发物,随后对其进行定性和定量分析。通过与未标记挥发物的光谱比较,通过顶空固相微萃取-气相色谱/飞行时间质谱法(HS-SPME-GC/TOF-MS)鉴定出 25 种 [U-(13)C]-标记挥发物。通过反向同位素稀释程序对标记挥发物进行定量。使用 [U-(13)C]-标记标准品,实现了与之前 HS-SPME 报告相当或更好的检测限,为 0.010-1.04 ng/g。使用 60°C 下从 0 到 15 天氧化的商品大豆油(CSO)评估 [U-(13)C]-标记挥发性标准品的性能。非标记内部标准正癸烷和 [U-(13)C]-标记氧化产物的相对响应在 CSO 基质氧化时变化高达 8 倍,表明在挥发性分析研究中依赖单一标准会导致由于基质效应变化而产生不准确的结果。使用 [U-(13)C]-标记的标准混合物在氧化的 CSO 和低 ALA 大豆油中定量分析了 25 种挥发物,平均相对标准偏差为 8.5%。将这种方法扩展到其他标记底物,例如 [U-(13)C]-标记的糖和氨基酸,用于分析研究应该是可行的,并且与使用单一标准相比,可以显著提高定量结果。

相似文献

本文引用的文献

6
Protocol for solid-phase microextraction method development.固相微萃取方法开发方案。
Nat Protoc. 2010 Jan;5(1):122-39. doi: 10.1038/nprot.2009.179. Epub 2010 Jan 7.
9
Demonstration of the ethylmalonyl-CoA pathway by using 13C metabolomics.利用13C代谢组学对乙基丙二酰辅酶A途径的证明。
Proc Natl Acad Sci U S A. 2009 Mar 24;106(12):4846-51. doi: 10.1073/pnas.0810932106. Epub 2009 Mar 4.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验