Greener and rapid magnetic solid phase microextraction method using Fe3O4@Al2O3/AC for chromatographic determination of neonicotinoid pesticides in vegetable oils

IF 6.5 Q1 CHEMISTRY, ANALYTICAL
Musiiwa V. Sengane , Masixole Sihlahla , Philiswa N. Nomngongo , Nomvano Mketo
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Abstract

A greener sample preparation method based on magnetic solid phase microextraction (MSPμE) was developed for the preconcentration of neonicotinoid pesticides (acetamiprid, imidacloprid, thiacloprid and thiamethoxam) in vegetable oil samples followed by separation and quantification using high performance liquid chromatography with diode array detector (HPLC-DAD). Different characterisation techniques such as Fourier Transform Infrared Spectroscopy (FTIR), Powder X-ray diffraction analysis (PXRD), Thermogravimetric Analysis (TGA), Transmission electron microscopy (TEM), and scanning electron microscope and energy-dispersive X-ray spectroscopy (SEM-EDS) confirmed the synthesised magnetic nano adsorbents (Fe3O4, Fe3O4@Al2O3 and Fe3O4@Al2O3/AC). The most influential parameters affecting MSPμE of NEOs by Fe3O4@Al2O3/AC were examined using a multivariate optimisation approach and 8 min extraction time, 13 pH, 9 mg adsorbent mass, and 0.5 mL eluent volume were optimal parameters. The proposed Fe3O4@Al2O3/AC method showed high accuracy (80–119.21%) and precision (≤10 %) for all the investigated NEOs. Additionally, the obtained limit of detection (LOD) ranged from 0.5–1.76 ng µL-1, the limit of quantification (LOQ) ranged from 1.87–6.62 ng µL-1 and satisfactory high preconcentration factors (73.02- 407.0) were comparable with literature reported studies. The Analytical GREEness calculator AGREE, BAGI and NEMI analysis confirmed greenness of MSPμE. After that, the validated MSPμE method was applied to real vegetable oil samples (avocado, canola, olive and sunflower), and fortunately, all the investigated NEOs were below LODs of the proposed MSPμE /HPLC-DAD methods.

Abstract Image

绿色快速的Fe3O4@Al2O3/AC磁固相微萃取法测定植物油中新烟碱类农药
建立了一种基于磁固相微萃取(MSPμE)的绿色样品制备方法,用于植物油样品中新烟碱类农药(啶虫脒、吡虫啉、噻虫啉和噻虫嗪)的预富集,并采用高效液相色谱二极管阵列检测器(HPLC-DAD)进行分离和定量。不同的表征技术,如傅里叶变换红外光谱(FTIR),粉末x射线衍射分析(PXRD),热重分析(TGA),透射电子显微镜(TEM),扫描电子显微镜和能量色散x射线能谱(SEM-EDS)证实了合成的磁性纳米吸附剂(Fe3O4, Fe3O4@Al2O3和Fe3O4@Al2O3/AC)。采用多元优化方法考察了Fe3O4@Al2O3/AC法提取neo的MSPμE的影响因素,确定提取时间为8 min, pH为13,吸附剂质量为9 mg,洗脱液体积为0.5 mL。所提出的Fe3O4@Al2O3/AC方法对所研究的近地天体具有较高的准确度(80-119.21%)和精密度(≤10%)。检出限(LOD)为0.5 ~ 1.76 ngµL-1,定量限(LOQ)为1.87 ~ 6.62 ngµL-1,高富集系数(73.02 ~ 407.0)与文献报道的研究相当。分析绿色计算器AGREE、BAGI和NEMI分析证实了MSPμE的绿色度。然后,将验证的MSPμE方法应用于实际植物油样品(牛油果、菜籽油、橄榄和向日葵),幸运的是,所有检测的neo都低于所建立的MSPμE /HPLC-DAD方法的lod。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.50
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