Polyvinyl alcohol/citric acid/β-cyclodextrin/CuONP composite nanofibers as an effective and green absorbent for the simultaneous extraction of three antidepressant drugs in biological fluids prior to GC-FID analysis

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Farbod Kharazmi, Fatemeh Sadat Hosseini, Homeira Ebrahimzadeh
{"title":"Polyvinyl alcohol/citric acid/β-cyclodextrin/CuONP composite nanofibers as an effective and green absorbent for the simultaneous extraction of three antidepressant drugs in biological fluids prior to GC-FID analysis","authors":"Farbod Kharazmi,&nbsp;Fatemeh Sadat Hosseini,&nbsp;Homeira Ebrahimzadeh","doi":"10.1007/s00604-023-05800-4","DOIUrl":null,"url":null,"abstract":"<div><h2>Abstract\n</h2><div><p>Composite nanofibers, namely, polyvinyl alcohol (PVA), citric acid (CA), β-cyclodextrin (β–CD), and copper oxide nanoparticles (PVA/CA/β-cyclodextrin/CuO NPs), were developed as a novel, green, and efficient adsorbent in the pipette tip-micro-solid-phase extraction method (PT-µSPE), for the simultaneous extraction of three antidepressants drugs namely imipramine (IMP), citalopram (CIT), and clozapine (CLZ) in biological fluids before quantification by gas chromatography (GC-FID). Based on the obtained results from field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD), the successful synthesis of composite nanofibers was approved. Due to the presence of β-cyclodextrins and CuO NPs rich of functional groups on their surface, the nanofibers have high extraction efficiency. Under the optimal conditions, the linear range for imipramine, citalopram, and clozapine was 0.1 to 1000.0 ng mL<sup>−1</sup> with a determination coefficient ≥ 0.99. The limits of detection (LODs) were in the range 0.03 to 0.15 ng mL<sup>−1</sup>. The relative standard deviation was 4.8 to 8.7% (within-day, <i>n</i> = 4) and 5.1 to 9.2% (between-day, <i>n</i> = 3) for 3 consecutive days. In addition, excellent clean-up was achieved which is a great advantage over other sample preparation methods. Finally, the ability of the developed method to extract the target analytes from the biological samples was evaluated.</p><h3>Graphical Abstract</h3>\n <figure><div><div><div><picture><source><img></source></picture></div></div></div></figure>\n </div></div>","PeriodicalId":705,"journal":{"name":"Microchimica Acta","volume":"190 6","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2023-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microchimica Acta","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00604-023-05800-4","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 3

Abstract

Abstract

Composite nanofibers, namely, polyvinyl alcohol (PVA), citric acid (CA), β-cyclodextrin (β–CD), and copper oxide nanoparticles (PVA/CA/β-cyclodextrin/CuO NPs), were developed as a novel, green, and efficient adsorbent in the pipette tip-micro-solid-phase extraction method (PT-µSPE), for the simultaneous extraction of three antidepressants drugs namely imipramine (IMP), citalopram (CIT), and clozapine (CLZ) in biological fluids before quantification by gas chromatography (GC-FID). Based on the obtained results from field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD), the successful synthesis of composite nanofibers was approved. Due to the presence of β-cyclodextrins and CuO NPs rich of functional groups on their surface, the nanofibers have high extraction efficiency. Under the optimal conditions, the linear range for imipramine, citalopram, and clozapine was 0.1 to 1000.0 ng mL−1 with a determination coefficient ≥ 0.99. The limits of detection (LODs) were in the range 0.03 to 0.15 ng mL−1. The relative standard deviation was 4.8 to 8.7% (within-day, n = 4) and 5.1 to 9.2% (between-day, n = 3) for 3 consecutive days. In addition, excellent clean-up was achieved which is a great advantage over other sample preparation methods. Finally, the ability of the developed method to extract the target analytes from the biological samples was evaluated.

Graphical Abstract

Abstract Image

聚乙烯醇/柠檬酸/β-环糊精/CuONP 复合纳米纤维作为一种有效的绿色吸收剂,用于在 GC-FID 分析前同时提取生物液体中的三种抗抑郁药物
摘要 开发了聚乙烯醇(PVA)、柠檬酸(CA)、β-环糊精(β-CD)和氧化铜纳米颗粒(PVA/CA/β-环糊精/CuO NPs)复合纳米纤维,作为一种新型、绿色、高效的吸附剂,在移液管吸头-微固相萃取法(PT-µSPE)中用于同时萃取三种抗抑郁药物,即丙咪嗪(IMP)、丙咪嗪(CMP)和丙咪嗪(CMP)、吸头-微固相萃取法(PT-µSPE)同时萃取生物液体中的三种抗抑郁药物,即丙咪嗪(IMP)、西酞普兰(CIT)和氯氮平(CLZ),然后用气相色谱法(GC-FID)进行定量。根据场发射扫描电子显微镜(FE-SEM)、能量色散 X 射线光谱(EDX)、傅立叶变换红外光谱(FT-IR)和 X 射线衍射(XRD)的结果,成功合成了复合纳米纤维。由于β-环糊精和表面富含官能团的 CuO NPs 的存在,纳米纤维具有很高的萃取效率。在最佳条件下,丙咪嗪、西酞普兰和氯氮平的线性范围为0.1~1000.0 ng mL-1,测定系数≥0.99。检出限为 0.03 至 0.15 纳克/毫升。连续 3 天的相对标准偏差为 4.8%至 8.7%(日内,n = 4)和 5.1%至 9.2%(日间,n = 3)。此外,与其他样品制备方法相比,该方法的净化效果极佳。最后,评估了所开发方法从生物样品中提取目标分析物的能力。
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
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
×
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:604180095
Book学术官方微信