Fe3O4@p-Naphtholbenzein as a novel nano-sorbent for highly effective removal and recovery of Berberine: Response surface methodology for optimization of ultrasound assisted dispersive magnetic solid phase extraction

被引:34
作者
Aghaie, Ali B. G. [1 ]
Hadjmohammadi, Mohammad Reza [1 ]
机构
[1] Univ Mazandaran, Fac Chem, Dept Analyt Chem, Babol Sar, Iran
关键词
Ultrasound-assisted dispersive magnetic solid phase extraction; Response surface methodology; Berberine; Biological samples; p-Naphtholbenzein coating; Surface modification; CHROMATOGRAPHY-MASS-SPECTROMETRY; AQUEOUS-SOLUTIONS; COPTIDIS-RHIZOMA; HUMAN PLASMA; NANOPARTICLES; PALMATINE; ALKALOIDS; URINE; JATRORRHIZINE; FUNCTIONALIZATION;
D O I
10.1016/j.talanta.2016.04.034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A hydrophobic surface modified iron oxide magnetic nano-sorbent was successfully synthesized, characterized and utilized for highly effective removal and recovery of Berberine (Brb) by Ultrasound Assisted Dispersive Magnetic Solid Phase Extraction (UADM-SPE). Fabrication of p-Naphtholbenzein-coated magnetic nanoparticles (PNB-MNPs) was certified by characteristic analyses such as: Fourier transform infrared spectroscopy (FT-IR), X-ray Diffraction (XRD), thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The characterized PNB-MNPs were utilized to develop a UADM-SPE method for Brb, a well-known isoquinoline alkaloid with a highlighted chemical skeleton for designing selective and powerful bioactive molecules. Affecting parameters on the extraction of Brb were optimized through an orthogonal rotatable central composite design (CCD). The optimum condition is obtained when the variables are set to: pH=4, amount of MNPs=20 mg, sample volume=30 ml, sonication time=1 min at room temperature, and desorbing solvent=500 mu L, of methanol. Under the mentioned condition, an extraction recovery of 98.2%, with relative standard deviation of 3.7%, was obtained via five replicated measurements on a 0.1 mg L-1 Brb standard solution. Finally, the method was successfully applied for determination of Brb in human plasma and urine samples. Regarding the method calibration graphs in plasma and urine matrices, spiked in the range of 0.01-200.00 mu g L-1, pre-concentration factors of 134 and 122, method detection limit (MDL) of 0.17 and 0.19 mu g L-1, and lower limit of quantification of 0.57 and 0.63 mu g L-1 were obtained for plasma and urine samples, respectively. The method exhibits good potentials to be a fast, efficient and reliable method for determination of Brb in human biological samples. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 28
页数:11
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