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Nano-sized FeO@SiO-molecular imprinted polymer as a sorbent for dispersive solid-phase microextraction of melatonin in the methanolic extract of , biological, and water samples

化学 吸附剂 检出限 吸附 色谱法 分子印迹聚合物 固相萃取 洗脱 固相微萃取 萃取(化学) 柱色谱法 吸附 气相色谱-质谱法 质谱法 选择性 有机化学 催化作用
作者
Ebrahim Alipanahpour Dil,Amir Hossein Doustimotlagh,Hamedreza Javadian,Arash Asfaram,Mehrorang Ghaedi
出处
期刊:Talanta [Elsevier]
卷期号:221: 121620-121620 被引量:92
标识
DOI:10.1016/j.talanta.2020.121620
摘要

In this study, a magnetic molecularly imprinted polymer (MMIP (Fe3O4@SiO2-MIP)) was used for the dispersive magnetic solid-phase microextraction (d-MSP-μ-E) to design an easy and effective method for melatonin (MLT) extraction in the methanolic extract of Portulaca oleracea, human urine and plasma, and water samples. HPLC with UV detection was utilized, and pH, the type and volume of eluent, MMIP mass, and contact time were considered as effective factors in the study of MLT separation and pre-concentration. These factors were optimized by Plackett–Burman and multi-objective response surface methodology (RSM). The values were 10 mg, 14 min, 4.2, methanol, 0.180 mL, 2.5 min, for the MMIP mass, time of sorption, sample pH, eluent type, eluent volume, and time of elution, respectively. At the optimum conditions, the limit of detection (LOD) was 0.046 ng mL−1, and the limit of quantification (LOQ) was 0.156 ng mL−1. The sorption capacity of the proposed MMIP sorbent was 109.1 mg g−1 at the optimum conditions. Besides, linear dynamic range (LDR) was 0.2–4200 ng mL−1, and the precision of the method (RSD %) for triplicate measurements was <6.1%. The MMIP showed saturation magnetization of 19.75 emu g−1, resulting in fast separation of the sorbent. The sorption test revealed the high sorption capacity of the MMIP for MLT and its homogeneous binding sites. In all spiked levels (50, 100, 200, and 500 ng mL−1), 93.07–104.1% was the range obtained for the recovery of MLT. The relative selectivity factor (β) values of MLT/tryptophan, MLT/serotonin, MLT/ferulic acid, MLT/mefenamic acid, MLT/quercetin, MLT/luteolin, and MLT/chlorogenic acid were 1.60, 1.68, 2.02, 2.38, 2.32, 2.40, and 2.50, respectively. The results of desorption–regeneration cycles (seven times) by employing the MMIP showed the high stability of the resultant material. In conclusion, the MMIP combined with the magnetic separation showed a specific sorption behavior for MLT and suggested a simple, flexible, selective, and powerful analytical tool.
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