Dispersive solid‐phase extraction for the determination of organochlorine pesticides in fruit juice samples using iron‐doped zinc oxide nanoparticles supported with silica as a sorbent

IF 1.3 Q4 CHEMISTRY, ANALYTICAL SEPARATION SCIENCE PLUS Pub Date : 2023-12-10 DOI:10.1002/sscp.202300161
Bereket Tesfaye, A. Gure, Tsegaye Girma Asere, Toleshi Teshome, Yerosan Buzayo
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Abstract

An efficient analytical method has been developed based on dispersive solid‐phase extraction followed by gas chromatography‐mass spectrometry for the determinations of 13 organochlorine pesticides in fruit juice samples. In this method, dispersive solid phase extraction was used for the extraction of target analye using iron‐doped zinc oxide nanoparticles supported with silica as a sorbent. Different experimental parameters affecting the extraction efficiencies the proposed method were carefully optimized. Under the optimum conditions, the calibration graphs were linear in the concentration range of 0.6–100 ng/mL with coefficients of determinations in the range of 0.9927–0.9991. The limits of detection and quantification determined as 3 and 10 times the signal‐to‐noise ratio were in the range of 0.01–0.03 and 0.6–1.0 ng/mL, respectively. Intra‐ and inter‐day precision studies of the proposed method, expressed as relative standard deviations, were in the range of 2.1%–9.2% and 2.2%–9.7%, respectively. The recoveries of the spiked fruit juices samples were in the range of 81.4%–105.1% with the corresponding relative standard deviations ranging from 1.0%–8.8%. In general, the proposed method demonstrated satisfactory analytical performance. Thus,it could be used as simple and attracive alternative method for the extraction of organochlorine pesticides from fruit juice sample and other related matrices.
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使用以二氧化硅为吸附剂的掺铁氧化锌纳米颗粒进行分散固相萃取,测定果汁样品中的有机氯农药含量
建立了一种基于分散固相萃取-气相色谱-质谱联用的高效分析方法,用于测定果汁样品中的 13 种有机氯农药。该方法采用掺铁氧化锌纳米颗粒作为吸附剂,以分散固相萃取法萃取目标化合物。对影响该方法萃取效率的不同实验参数进行了细致的优化。在最佳条件下,校准图在 0.6-100 ng/mL 浓度范围内线性关系良好,测定系数在 0.9927-0.9991 之间。检测限和定量限分别为信噪比的 3 倍和 10 倍,范围分别为 0.01-0.03 纳克/毫升和 0.6-1.0 纳克/毫升。该方法的日内和日间精密度(以相对标准偏差表示)分别为 2.1%-9.2%和 2.2%-9.7%。加标果汁样品的回收率为 81.4%-105.1%,相对标准偏差为 1.0%-8.8%。总体而言,该方法的分析性能令人满意。因此,该方法可作为果汁样品和其他相关基质中有机氯农药提取的简便而有效的替代方法。
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来源期刊
SEPARATION SCIENCE PLUS
SEPARATION SCIENCE PLUS CHEMISTRY, ANALYTICAL-
CiteScore
1.90
自引率
9.10%
发文量
111
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