Polymethyldopamin@Fe3O4 for Magnetic Solid Phase Extraction of Polycyclic Aromatic Hydrocarbons Combined with DES as Desorption Solvent and High-Performance Liquid Chromatography-Ultraviolet Detection

被引:16
作者
Ghani, Milad [1 ]
Maleki, Behrooz [2 ]
Jafari, Zahra [1 ]
Veisi, Hojat [3 ]
机构
[1] Univ Mazandaran, Fac Chem, Dept Analyt Chem, Babolsar, Iran
[2] Univ Mazandaran, Fac Chem, Dept Organ Chem, Babolsar, Iran
[3] Payame Noor Univ, Dept Chem, Tehran, Iran
关键词
Polycyclic aromatic hydrocarbons; PMDP@Fe3O4; magnetic solid phase extraction; response surface; HPLC-UV; deep eutectic solvent; tap water; river water; smoked fish; smoked rice; DEEP EUTECTIC SOLVENT; SAMPLES PRIOR; MICROEXTRACTION; WATER; ACID;
D O I
10.1080/10406638.2023.2216835
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, Polymethyldopamin@Fe3O4 (PMDP@Fe3O4) has been synthesized using a very simple, easy, cost-effective, efficient, and fast method. First, magnetic nanoparticles (Fe3O4) were synthesized. It was followed by accommodating polymethyldopamin (PMDP) on the prepared Fe3O4. The prepared PMDP@Fe3O4 was utilized as a sorbent in the Magnetic Solid Phase Extraction (MSPE) of six selected Polycyclic Aromatic Hydrocarbons (PAHs) including anthracene, fluoranthene, fluorene, naphthalene, phenanthrene, and pyrene. The extracted model analytes were desorbed by a Deep Eutectic Solvent (DES) and were analyzed by High-Performance Liquid Chromatography-Ultraviolet detection (HPLC-UV). The method is validated according to ICH guidelines with respect to precision, accuracy, linearity, specificity, robustness, and limits of detection and quantification. Under the optimized condition, the linearity of the method was in the range of 0.1-500 mu g L-1 for the selected analytes. The calibration curves showed a determination of coefficient (r(2)) higher than 0.9986. The limits of detection (LODs) and limits of quantification (LOQs) were calculated to be between 0.03-0.14 and 0.09-0.46 mu g L-1, respectively. The inter-day and intra-day relative standard deviations (RSDs%) were determined to be in the range of 1.7-4.2% in three concentrations. Furthermore, the enrichment factors were found to be 76, 61, 65, 78, 69, and 67 for anthracene, fluoranthene, fluorene, naphthalene, phenanthrene, and pyrene, respectively. Moreover, the calculated absolute recoveries were between 61 and 78%. The results of the real sample analysis and the obtained recoveries indicated that the method was useful and applicable in complicated real samples.
引用
收藏
页码:2381 / 2393
页数:13
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