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冷冻脂质沉淀和强阳离子交换固相萃取联用技术在高效液相色谱-电喷雾串联质谱法测定高脂食品中吡咯里西啶生物碱的有效应用

Effective application of freezing lipid precipitation and SCX-SPE for determination of pyrrolizidine alkaloids in high lipid foodstuffs by LC-ESI-MS/MS.

作者信息

Yoon Soo Hwan, Kim Min-Sun, Kim Sang Hoon, Park Hyun Mee, Pyo Heesoo, Lee Yong Moon, Lee Kyung-Tae, Hong Jongki

机构信息

College of Pharmacy, Kyung Hee University, Seoul 130-701, Republic of Korea.

Department of Biology, Kyung Hee University, Seoul 130-701, Republic of Korea.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jun 15;992:56-66. doi: 10.1016/j.jchromb.2015.04.007. Epub 2015 Apr 25.

Abstract

Pyrrolizidine alkaloids (PAs) are naturally occurring plant toxins associated with serious hepatic disease in humans and animals. In this study, rapid and sensitive analytical method was developed for the determination of 9 toxic PAs in popularly high lipid foodstuffs by liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). PAs in lipid foodstuff were effectively purified by freezing lipid precipitation (FLP) and strong cation exchange (SCX)-solid-phase extraction (SPE). Especially, FLP could easily remove the large amounts of triacylglycerols in the lipid sample extract and effectively combine with SPE cleanup. During the FLP procedure, over 77% of the lipids in the foodstuff extracts were rapidly eliminated without any significant loss of the PAs with over 81% recovery. The elimination efficiency of lipids by FLP was tested with LC-atmospheric chemical ionization (APCI)-MS. For further purification, SCX-SPE cartridge could successfully purify PAs from the remaining interfering substances by the variation pH with 5% NH4OH in methanol. For precise quantification and confirmation of PAs in complicate sample matrices, appropriate transition ions in LC-MS/MS-multiple-ion reaction monitoring (MRM) mode were selected on the basis of MS/MS fragmentation pathways of PAs. The established analytical method was validated in terms of the linearity, limits of detection (LOD), and quantification (LOQ), precision, and accuracy. The method was deemed satisfactory by inter- and intra-day validation and exhibited both high accuracy and precision (relative standard deviation<11.06%). Overall limits of detection and quantitation of PAs were approximately 0.06-0.60ng/mL at a signal-to-noise ratio (S/N) of 3 and were about 0.20-1.99ng/mL at a S/N of 10 for all foodstuffs. The established method was successfully applied for the monitoring of toxic PAs in several types of high lipid foodstuffs such as soybeans, seed oil, milk, and margarine.

摘要

吡咯里西啶生物碱(PAs)是天然存在的植物毒素,与人类和动物的严重肝脏疾病有关。在本研究中,建立了一种快速灵敏的分析方法,用于通过液相色谱-电喷雾电离-串联质谱(LC-ESI-MS/MS)测定常见高脂食品中的9种有毒PAs。脂质食品中的PAs通过冷冻脂质沉淀(FLP)和强阳离子交换(SCX)-固相萃取(SPE)进行有效纯化。特别是,FLP可以轻松去除脂质样品提取物中的大量三酰甘油,并有效地与SPE净化相结合。在FLP过程中,食品提取物中超过77%的脂质被快速去除,而PAs没有任何显著损失,回收率超过81%。通过LC-大气压化学电离(APCI)-MS测试了FLP对脂质的去除效率。为了进一步纯化,SCX-SPE柱可以通过在甲醇中加入5%氢氧化铵改变pH值,成功地从剩余的干扰物质中纯化PAs。为了在复杂样品基质中对PAs进行精确的定量和确证,根据PAs的MS/MS裂解途径,在LC-MS/MS-多离子反应监测(MRM)模式下选择了合适的过渡离子。所建立的分析方法在线性、检测限(LOD)、定量限(LOQ)、精密度和准确度方面进行了验证。通过日内和日间验证,该方法被认为是令人满意的,并且具有高准确度和精密度(相对标准偏差<11.06%)。所有食品中PAs的总体检测限和定量限在信噪比(S/N)为3时约为0.06-0.60ng/mL,在S/N为10时约为0.20-1.99ng/mL。所建立的方法成功应用于监测几种高脂食品中的有毒PAs,如大豆、种子油、牛奶和人造黄油。

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