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

The copper-coated iron oxide nanoparticles with core-shell were produced by deposition of a Cu shell on Fe(3)O(4) NPs through reduction of Cu(2+) ions in solution using NaBH(4). Subsequently, the organosulfur compound, bis-(2,4,4-trimethylpentyl)-dithiophosphinic acid (b-TMP-DTPA), was used to form...

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Autores principales: Yamini, Yadollah, Safari, Meysam, Shamsayei, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104151/
https://www.ncbi.nlm.nih.gov/pubmed/30140489
http://dx.doi.org/10.1016/j.jpha.2018.05.005
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author Yamini, Yadollah
Safari, Meysam
Shamsayei, Maryam
author_facet Yamini, Yadollah
Safari, Meysam
Shamsayei, Maryam
author_sort Yamini, Yadollah
collection PubMed
description The copper-coated iron oxide nanoparticles with core-shell were produced by deposition of a Cu shell on Fe(3)O(4) NPs through reduction of Cu(2+) ions in solution using NaBH(4). 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 pH, 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 µg/ L with reasonable linearity (R(2) > 0.99) and the limits of detection (LODs) ranged between 0.5 and 1.0 µg/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 Fe(3)O(4)@Cu@ b-TMP-DTPA NPs have the capability of extraction of steroid drugs from ointment samples.
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spelling pubmed-61041512018-08-23 Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV Yamini, Yadollah Safari, Meysam Shamsayei, Maryam J Pharm Anal Original Article The copper-coated iron oxide nanoparticles with core-shell were produced by deposition of a Cu shell on Fe(3)O(4) NPs through reduction of Cu(2+) ions in solution using NaBH(4). 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 pH, 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 µg/ L with reasonable linearity (R(2) > 0.99) and the limits of detection (LODs) ranged between 0.5 and 1.0 µg/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 Fe(3)O(4)@Cu@ b-TMP-DTPA NPs have the capability of extraction of steroid drugs from ointment samples. Xi'an Jiaotong University 2018-08 2018-05-27 /pmc/articles/PMC6104151/ /pubmed/30140489 http://dx.doi.org/10.1016/j.jpha.2018.05.005 Text en © 2018 Xi'an Jiaotong University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Yamini, Yadollah
Safari, Meysam
Shamsayei, Maryam
Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title_full Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title_fullStr Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title_full_unstemmed Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title_short Simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by HPLC-UV
title_sort simultaneous determination of steroid drugs in the ointment via magnetic solid phase extraction followed by hplc-uv
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104151/
https://www.ncbi.nlm.nih.gov/pubmed/30140489
http://dx.doi.org/10.1016/j.jpha.2018.05.005
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