Determination of Tianeptine Using Mg/Fe Layered Double Hydroxide-Based Dispersive Solid-Phase Extraction Combined with High-Performance Liquid Chromatography

IF 1 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Weiwei Yang
{"title":"Determination of Tianeptine Using Mg/Fe Layered Double Hydroxide-Based Dispersive Solid-Phase Extraction Combined with High-Performance Liquid Chromatography","authors":"Weiwei Yang","doi":"10.1134/S1061934824701399","DOIUrl":null,"url":null,"abstract":"<p>The efficient extraction of tianeptine from environmental matrices has been a matter of concern issue due to the amphiphilic ionic organic substance property of tianeptine. A magnesium-iron layered double hydroxide (<b>Mg/Fe-LDH</b>) was successfully synthesized using hydrothermal synthesis and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy techniques. The as-prepared nanocomposite was used as an effective adsorbent to extract tianeptine from water samples <i>via</i> a dispersive solid-phase extraction (<b>DSPE</b>) procedure before high-performance liquid chromatography-ultraviolet detection (<b>HPLC</b>-<b>UV</b>). Experimental parameters affecting extraction efficiency, such as agitation type, pH, absorbent amount, elution solvent type, and absorption/elution time, were studied and optimized. The developed tianeptine analysis method, based on adsorption-release extraction using Mg/Fe-LDH and detection by HPLC-UV, exhibited a wide quantitative linear range of 10 to 1000 μg/L (<i>r</i><sup>2</sup> = 0.9986, <i>p</i> = 2.49 × 10<sup>–14</sup>) by plotting chromatography peak height versus tianeptine concentration. The limits of detection and quantification were 4.6 and 15 μg/L, respectively. The developed tianeptine analysis method was applied to analyze tianeptine spiked in water samples. An ideal recovery range of 94.1 to 103.5%, with a narrow relative standard deviation of 1.63–4.34%, was obtained. The proposed analysis method, which combined Mg/Fe-LDH-based DSPE with HPLC-UV detection, was reliable for determining tianeptine in environmental water samples.</p>","PeriodicalId":606,"journal":{"name":"Journal of Analytical Chemistry","volume":"79 12","pages":"1818 - 1825"},"PeriodicalIF":1.0000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1061934824701399","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The efficient extraction of tianeptine from environmental matrices has been a matter of concern issue due to the amphiphilic ionic organic substance property of tianeptine. A magnesium-iron layered double hydroxide (Mg/Fe-LDH) was successfully synthesized using hydrothermal synthesis and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy techniques. The as-prepared nanocomposite was used as an effective adsorbent to extract tianeptine from water samples via a dispersive solid-phase extraction (DSPE) procedure before high-performance liquid chromatography-ultraviolet detection (HPLC-UV). Experimental parameters affecting extraction efficiency, such as agitation type, pH, absorbent amount, elution solvent type, and absorption/elution time, were studied and optimized. The developed tianeptine analysis method, based on adsorption-release extraction using Mg/Fe-LDH and detection by HPLC-UV, exhibited a wide quantitative linear range of 10 to 1000 μg/L (r2 = 0.9986, p = 2.49 × 10–14) by plotting chromatography peak height versus tianeptine concentration. The limits of detection and quantification were 4.6 and 15 μg/L, respectively. The developed tianeptine analysis method was applied to analyze tianeptine spiked in water samples. An ideal recovery range of 94.1 to 103.5%, with a narrow relative standard deviation of 1.63–4.34%, was obtained. The proposed analysis method, which combined Mg/Fe-LDH-based DSPE with HPLC-UV detection, was reliable for determining tianeptine in environmental water samples.

Abstract Image

Mg/Fe层状双氢氧化物分散固相萃取-高效液相色谱法测定天奈汀
由于噻奈普汀具有两亲性离子有机物的特性,如何从环境基质中高效提取噻奈普汀一直是一个值得关注的问题。本研究采用水热合成法成功合成了一种镁铁双层氢氧化物(Mg/Fe-LDH),并利用 X 射线衍射、傅立叶变换红外光谱和扫描电子显微镜技术对其进行了表征。在高效液相色谱-紫外检测(HPLC-UV)前,将制备的纳米复合材料作为一种有效的吸附剂,通过分散固相萃取(DSPE)方法从水样中提取噻奈普汀。对影响萃取效率的实验参数,如搅拌方式、pH值、吸收剂用量、洗脱溶剂类型和吸收/洗脱时间等进行了研究和优化。通过绘制色谱峰高与噻奈普汀浓度的关系曲线,该方法的线性范围为10~1000 μg/L(r2 = 0.9986, p = 2.49 × 10-14)。检出限和定量限分别为 4.6 μg/L 和 15 μg/L。应用所开发的噻奈普汀分析方法对水样中添加的噻奈普汀进行了分析。该方法的理想回收率范围为94.1%~103.5%,相对标准偏差为1.63%~4.34%。该方法结合了基于镁/铁-LDH的DSPE和高效液相色谱-紫外检测技术,能可靠地测定环境水样中的噻奈丁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Analytical Chemistry
Journal of Analytical Chemistry 化学-分析化学
CiteScore
2.10
自引率
9.10%
发文量
146
审稿时长
13 months
期刊介绍: The Journal of Analytical Chemistry is an international peer reviewed journal that covers theoretical and applied aspects of analytical chemistry; it informs the reader about new achievements in analytical methods, instruments and reagents. Ample space is devoted to problems arising in the analysis of vital media such as water and air. Consideration is given to the detection and determination of metal ions, anions, and various organic substances. The journal welcomes manuscripts from all countries in the English or Russian language.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信