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采用加速溶剂萃取辅助基质固相分散结合气相色谱 - 电子捕获检测器快速分析巴戟天中的多种农药,并通过气相色谱 - 质谱联用进行阳性确证。

Rapid analysis of multi-pesticides in Morinda officinalis by GC-ECD with accelerated solvent extraction assisted matrix solid phase dispersion and positive confirmation by GC-MS.

作者信息

Liu Hongmei, Kong Weijun, Gong Bao, Miao Qing, Qi Yun, Yang Meihua

机构信息

Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100193, China.

Hainan Branch Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Wanning 571533, Hainan, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jan 1;974:65-74. doi: 10.1016/j.jchromb.2014.10.017. Epub 2014 Oct 22.

DOI:10.1016/j.jchromb.2014.10.017
PMID:25463199
Abstract

In this work, 33 organochlorine pesticides (OCPs) and 9 pyrethroid pesticides (PYPs) in Morinda officinalis were effectively and selectively extracted and cleaned up by accelerated solvent extraction assisted matrix solid phase dispersion (ASE/MSPD) method, followed by gas chromatography-electron capture detection (GC-ECD). Carbophenothion was selected as the internal standard and added into the final extracts to improve the precision and accuracy of the method. Parameters for ASE/MSPD procedure including ratio of acetone to n-hexane, temperature and amount of Florisil were optimized to improve the performance of the method through orthogonal experimental design. Under the optimized conditions, the average recoveries (six replicates) for all pesticides (spiked at 0.05, 0.5 and 1.0 mg kg(-1)) ranged from 69.3% to 112% with RSD less than 14.14%. A wide linear range of 10-1000 ng mL(-1) was observed with r values of 0.9963-0.9999. Meanwhile, the method gave high selectivity and sensitivity (LODs<3 μg kg(-1) and LOQs<8.0 μg kg (-1)), good repeatability (RSD of 9.64%, on average) and precision (RSD of 5.48%, averagely) and excellent stability (RSD <9.47%). The feasibility of the proposed method was demonstrated by applying it for preconcentration and determination of OCPs and PYPs in 40 batches of real samples. Four kinds of pesticides (beta-endosulfan, tecnazene, hexachlorobenzene and alpha-BHC) were detected in three batches of samples, which were successfully confirmed by GC-MS. The results indicated that ASE/MSPD is a reliable and half-automated extraction and purification technique, with many advantages over traditional techniques. The combination of ASE/MSPD and GC-ECD could be especially useful for trace analysis of pesticide residues in complex matrices.

摘要

本研究采用加速溶剂萃取辅助基质固相分散(ASE/MSPD)法,对巴戟天中的33种有机氯农药(OCPs)和9种拟除虫菊酯类农药(PYPs)进行了有效、选择性的萃取和净化,随后采用气相色谱 - 电子捕获检测法(GC - ECD)进行分析。选用三硫磷作为内标物并添加到最终提取物中,以提高方法的精密度和准确性。通过正交实验设计优化了ASE/MSPD过程的参数,包括丙酮与正己烷的比例、温度以及弗罗里硅土的用量,以提高方法的性能。在优化条件下,所有农药(添加水平为0.05、0.5和1.0 mg kg⁻¹)的平均回收率(六次重复)在69.3%至112%之间,相对标准偏差(RSD)小于14.14%。观察到线性范围为10 - 1000 ng mL⁻¹,相关系数(r)值为0.9963 - 0.9999。同时,该方法具有高选择性和灵敏度(检测限<3 μg kg⁻¹,定量限<8.0 μg kg⁻¹)、良好的重复性(平均RSD为9.64%)和精密度(平均RSD为5.48%)以及出色的稳定性(RSD<9.47%)。将该方法应用于40批实际样品中OCPs和PYPs的预浓缩和测定,证明了该方法的可行性。在三批样品中检测到四种农药(β - 硫丹、四氯硝基苯、六氯苯和α - 六六六),并通过GC - MS成功确认。结果表明,ASE/MSPD是一种可靠的半自动化萃取和净化技术,与传统技术相比具有许多优势。ASE/MSPD与GC - ECD的结合对于复杂基质中农药残留的痕量分析尤其有用。

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