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基于环糊精的超交联聚合物涂层纤维顶空固相微萃取-气相色谱-质谱联用分析植物油中的邻苯二甲酸酯类化合物

[Analysis of phthalate esters from vegetable oils by gas chromatography-mass spectrometry coupled with headspace solid-phase microextraction using cyclodextrin-based hypercrosslinked polymer coated fiber].

作者信息

Zhang Peng-Cheng, Wang Yuan, Liu Kun-Ling, Sun Ya-Ming, He Li-Jun, Zhao Wen-Jie

机构信息

School of Chemistry and Chemical Engineering, Henan University of Technology, Zhengzhou 450001, China.

Ningxia Academy of Metrology and Quality Inspection, Yinchuan 750411, China.

出版信息

Se Pu. 2024 Sep;42(9):881-890. doi: 10.3724/SP.J.1123.2024.01019.

Abstract

Phthalate esters (PAEs) are used as additives to enhance the pliability and malleability of plastics. These substances frequently migrate from packaging materials to vegetable oils because of the absence of covalent bonds. Over time, this migration could result in the accumulation of PAEs in the human body through ingestion, contributing to various diseases. Therefore, accurate qualitative and quantitative analyses of PAEs in vegetable oils are imperative to assess the origins of contamination and investigate their toxicity, degradation, migration, and transformation patterns. However, the concentration of PAEs in most samples is low, and the composition of vegetable oils is complex. Thus, PAEs must be enriched and purified using appropriate sample pretreatment procedures before analysis. Common methods for pretreating PAEs in oil include solid-phase extraction (SPE), dispersive SPE, and magnetic SPE. These techniques require time-consuming and labor-intensive procedures such as oil dissolution, solvent extraction, and degreasing. These approaches also require numerous solvents and containers, increasing the risk of sample cross-contamination. Solid-phase microextraction (SPME) integrates sampling, extraction, purification, concentration, and injection into a single process, significantly accelerating analytical testing and reducing the potential for sample cross-contamination. In headspace (HS) mode, the analytes achieve equilibrium on the coating and are extracted in the gas phase. The fibers are shielded from nonvolatile and high-relative molecular mass substances in the sample matrix. Thus, SPME is an ideal method for extracting volatile compounds in vegetable oils. When HS-SPME coupled with gas chromatography-mass spectrometry (GC-MS), it can achieve the rapid screening of PAEs in vegetable oil. In this study, an SPME with cyclodextrin-based hypercrosslinked polymers (BnCD-HCP) coated on stainless steel fibers was employed to extract PAEs from vegetable oil. The structure and morphology of the polymers were characterized using Fourier-transform infrared spectroscopy, nuclear magnetic spectroscopy, and scanning electron microscopy. BnCD-HCP exhibited high stability and diverse interactions, including , hydrophobic, and host-guest interactions. The oil samples were incubated with methanol, and the PAEs were extracted from the headspace using the probe. The optimal extraction parameters included an extraction time of 20 min, extraction temperature of 50 ℃, desorption time of 4 min, and desorption temperature of 275 ℃. The BnCD-HCP/HS-SPME method was evaluated under optimized experimental conditions. The limits of detection (LODs) and quantification (LOQs) were determined by applying signal-to-noise ratios () of 3 and 10, respectively. Method accuracy was evaluated using relative standard deviations (RSDs). Single-needle precision was evaluated by conducting three consecutive analyses at 3 h intervals within a day. Inter-needle precision was assessed by conducting the same analyses (three replicates) with differently coated fibers. The 12 PAE compounds exhibited good linearity with correlation coefficients () of at least 0.99. The LODs and LOQs ranged from 0.21 to 3.74 μg/kg and from 0.69 to 12.34 μg/kg, respectively. The RSDs were in the range of 1.8%-11.4% and 5.1%-13.9% for the single-needle and needle-to-needle methods, respectively. The proposed method was applied to soybean, peanut, and sunflower oils, and two PAEs were found in all three oils. Moreover, the method demonstrated good precision (RSD=1.17%-11.73%) and recoveries (72.49%-124.43%). Compared with other methods, the developed method was able to extract many target analytes and had a low or comparable LOD and high recovery. More importantly, this method does not require tedious operations such as solvent extraction and purification. Consequently, the developed method can be used to extract not only PAEs in oils but also other substances with a high lipid content.

摘要

邻苯二甲酸酯(PAEs)用作添加剂以提高塑料的柔韧性和延展性。由于不存在共价键,这些物质经常从包装材料迁移到植物油中。随着时间的推移,这种迁移可能会导致人体通过摄入而积累PAEs,从而引发各种疾病。因此,准确地对植物油中的PAEs进行定性和定量分析对于评估污染来源以及研究其毒性、降解、迁移和转化模式至关重要。然而,大多数样品中PAEs的浓度较低,并且植物油的成分复杂。因此,在分析之前必须使用适当的样品预处理程序对PAEs进行富集和纯化。油中PAEs预处理的常用方法包括固相萃取(SPE)、分散固相萃取和磁性固相萃取。这些技术需要耗时且费力的程序,如油溶解、溶剂萃取和脱脂。这些方法还需要大量的溶剂和容器,增加了样品交叉污染的风险。固相微萃取(SPME)将采样、萃取、纯化、浓缩和进样整合为一个过程,显著加快了分析测试速度并降低了样品交叉污染的可能性。在顶空(HS)模式下,分析物在涂层上达到平衡并在气相中被萃取。纤维免受样品基质中不挥发和高相对分子质量物质的影响。因此,SPME是萃取植物油中挥发性化合物的理想方法。当HS-SPME与气相色谱-质谱联用(GC-MS)时,它可以实现植物油中PAEs的快速筛查。在本研究中,采用涂覆有基于环糊精的超交联聚合物(BnCD-HCP)的不锈钢纤维固相微萃取从植物油中萃取PAEs。使用傅里叶变换红外光谱、核磁共振光谱和扫描电子显微镜对聚合物的结构和形态进行了表征。BnCD-HCP表现出高稳定性和多种相互作用,包括疏水相互作用和主客体相互作用。将油样与甲醇孵育,然后使用探针从顶空中萃取PAEs。最佳萃取参数包括萃取时间20分钟、萃取温度50℃、解吸时间4分钟和解吸温度275℃。在优化的实验条件下对BnCD-HCP/HS-SPME方法进行了评估。检测限(LODs)和定量限(LOQs)分别通过应用信噪比(S/N)为3和10来确定。方法准确性通过相对标准偏差(RSDs)进行评估。单针精密度通过在一天内每隔3小时进行三次连续分析来评估。针间精密度通过使用不同涂层的纤维进行相同分析(三次重复)来评估。12种PAE化合物表现出良好的线性,相关系数(r)至少为0.99。LODs和LOQs分别为0.21至3.74μg/kg和0.69至12.34μg/kg。单针方法和针间方法的RSDs分别在1.8% - 11.4%和5.1% - 13.9%范围内。所提出的方法应用于大豆油、花生油和葵花籽油,在所有三种油中都发现了两种PAEs。此外,该方法表现出良好的精密度(RSD = 1.17% - 11.73%)和回收率(72.49% - 124.43%)。与其他方法相比,所开发的方法能够萃取多种目标分析物,并且具有较低或相当的检测限和高回收率。更重要的是,该方法不需要诸如溶剂萃取和纯化等繁琐操作。因此,所开发的方法不仅可用于萃取油中的PAEs,还可用于萃取其他高脂肪含量的物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0c4/11358874/6f785a1a7b21/img_1.jpg

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