Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV

作     者：Yadollah Yamini Meysam Safari Maryam Shamsayei 

作者机构：Department of Chemistry Tarbiat Modares University Department of Chemical Engineering Kermanshah University of Technology 

出 版 物：《Journal of Pharmaceutical Analysis》 (药物分析学报（英文版）)

年 卷 期：2018年第8卷第4期

页      面：250-257页

核心收录：

学科分类：0710[理学-生物学] 1008[医学-中药学(可授医学、理学学位)] 1007[医学-药学(可授医学、理学学位)] 1006[医学-中西医结合] 1002[医学-临床医学] 0817[工学-化学工程与技术] 0703[理学-化学] 0702[理学-物理学] 100602[医学-中西医结合临床] 10[医学] 

基　　金：supported by grants from Tarbiat Modares University 

主　　题：Magnetic nanoparticles Steroid drug Ointment High performance liquid chromatography Self-assembled monolayer 

摘      要：The copper-coated iron oxide nanoparticles with core-shell were produced by deposition of a Cu shell on Fe3 O4 NPs through reduction of Cu2 tions in solution using NaB H4. Subsequently, the organosulfur compound, bis-（2,4,4-trimethylpentyl）-dithiophosphinic acid（b-TMP-DTPA）, was used to form self-assembled monolayer in order to modify sorbent＇s surface via covalent bonding between Cu and thiol（–SH）terminal groups. The prepared magnetic nanoparticles were characterized by using Fourier transform infrared（FT-IR） spectroscopy, scanning electron microscopy（SEM）, transmission electron microscope（TEM）, vibrating sample magnetometer（VSM） and thermo gravimetric analysis（TGA）. Then, the application of this new sorbent was investigated to extract the steroid drugs in ointment samples with the aid of ultrasound. An external magnetic field was applied to collect the magnetic nanoparticles（MNPs）. The extracted analytes were desorbed using acetonitrile. The obtained extraction solution was analyzed by HPLC-UV. The main affecting factors on the extraction efficiency including p H, sonication time, amount of sorbent, salt concentration, and desorption conditions were optimized in detail. Under the optimum conditions, good linearity was obtained in the range of 2.5–250.0 mg/L with reasonable linearity（R24 0.99） and the limits of detection（LODs） ranged between 0.5 and 1.0 mg/L（based on S/N ？ 3）.Repeatability（intra-day precision） based on five replicates and preconcentration factors were calculated to be 3.6%–4.7% and 87–116, respectively. Relative recoveries in ointment samples at two spiked levels of the target analytes were obtained in the range of 90.0%–103.2%. The results illustrated that the Fe3 O4@Cu@ b-TMP-DTPA NPs have the capability of extraction of steroid drugs from ointment samples.