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纳米级FeO@SiO分子印迹聚合物作为一种吸附剂,用于马齿苋甲醇提取物、生物样品和水样中褪黑素的分散固相微萃取。

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

作者信息

Dil Ebrahim Alipanahpour, Doustimotlagh Amir Hossein, Javadian Hamedreza, Asfaram Arash, Ghaedi Mehrorang

机构信息

Department of Chemistry, Yasouj University, Yasouj, 75918-74831, Iran.

Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

出版信息

Talanta. 2021 Jan 1;221:121620. doi: 10.1016/j.talanta.2020.121620. Epub 2020 Sep 5.

Abstract

In this study, a magnetic molecularly imprinted polymer (MMIP (FeO@SiO-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, and the limit of quantification (LOQ) was 0.156 ng mL. The sorption capacity of the proposed MMIP sorbent was 109.1 mg g at the optimum conditions. Besides, linear dynamic range (LDR) was 0.2-4200 ng mL, and the precision of the method (RSD %) for triplicate measurements was <6.1%. The MMIP showed saturation magnetization of 19.75 emu g, 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), 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.

摘要

在本研究中,磁性分子印迹聚合物(MMIP(FeO@SiO - MIP))用于分散磁固相微萃取(d - MSP - μ - E),以设计一种简便有效的方法,用于从马齿苋甲醇提取物、人尿液和血浆以及水样中提取褪黑素(MLT)。采用配有紫外检测的高效液相色谱法,在MLT分离和预浓缩研究中,将pH、洗脱剂类型和体积、MMIP质量以及接触时间视为有效因素。通过Plackett - Burman法和多目标响应面法(RSM)对这些因素进行了优化。MMIP质量、吸附时间、样品pH、洗脱剂类型、洗脱剂体积和洗脱时间的值分别为10 mg、14 min、4.2、甲醇、0.180 mL、2.5 min。在最佳条件下,检测限(LOD)为0.046 ng/mL,定量限(LOQ)为0.156 ng/mL。所提出的MMIP吸附剂在最佳条件下的吸附容量为109.1 mg/g。此外,线性动态范围(LDR)为0.2 - 4200 ng/mL,该方法重复测量的精密度(RSD%)<6.1%。MMIP的饱和磁化强度为19.75 emu/g,使得吸附剂能够快速分离。吸附试验表明MMIP对MLT具有高吸附容量及其均匀的结合位点。在所有加标水平(50、100、200和500 ng/mL)下,MLT的回收率范围为93.07 - 104.1%。MLT/色氨酸、MLT/血清素、MLT/阿魏酸、MLT/甲芬那酸、MLT/槲皮素、MLT/木犀草素和MLT/绿原酸的相对选择性因子(β)值分别为1.60、1.68、2.02、2.38、2.32、2.40和2.50。采用MMIP进行解吸 - 再生循环(七次)的结果表明所得材料具有高稳定性。总之,MMIP与磁分离相结合对MLT表现出特异性吸附行为,是一种简单、灵活、选择性强且功能强大的分析工具。

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