Electrodeposition of Zn–Al-Layered Double Hydroxides With Interlayer Modification by Ibuprofen as Fiber Coating for Solid Phase Microextraction of Nonsteroidal Anti-Inflammatory Drugs

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL Journal of separation science Pub Date : 2024-11-06 DOI:10.1002/jssc.70011
Qasim Chyad Abdulzahra Al-Furaiji, Fatemeh Darvishnejad, Jahan Bakhsh Raoof, Milad Ghani
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Abstract

In this study, in situ electrodeposition of Zn─Al-layered double hydroxides (Zn─Al-LDHs) on the surface of pencil graphite substrate were practiced with interlayer modification by ibuprofen. The prepared composite increases the efficiency of the proposed method by increasing the level of interaction between the sorbent and the selected analytes including acetylsalicylic acid and naproxen (NAP) in real sample. Eventually, the extracted target analytes were injected into high-performance liquid chromatography ultraviolet (HPLC-UV) for their measurement. The experimental design including PBD and BBD was implemented to obtain the maximize efficiency and optimal condition for extraction of the target analytes. Therefore, in optimal conditions, limits of detection of 0.33–0.64 µg L−1, linear dynamic range (LDR) of 1–100 µg L−1 (with r2 > 0.9934), and limits of quantification (LOQs) of 1.1–2.1 µg L−1 were obtained for target analytes by SPME-HPLC-UV. The intra-day relative standard deviation (RSD%) were found to range in 3.90%–5.30% (4.90%–6.80%) at concentration of 5–50 µg L−1 (2–10 µg L−1). According to obtained result, the relative recovery was calculated between 90% and 109%. Therefore, the obtained results showed that the selected method has a suitable performance for the preconcentration and extraction of acetylsalicylic acid and NAP in biological samples.

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电沉积层间有布洛芬修饰的锌-铝层双氢氧化物作为固相微萃取非甾体抗炎药物的纤维涂层
本研究将 Zn─Al 层状双氢氧化物(Zn─Al-LDHs)原位电沉积在铅笔状石墨基底表面,并用布洛芬对其进行层间修饰。所制备的复合材料提高了吸附剂与所选分析物(包括实际样品中的乙酰水杨酸和萘普生(NAP))之间的相互作用水平,从而提高了拟议方法的效率。最后,将提取的目标分析物注入高效液相色谱紫外检测器(HPLC-UV)进行测定。实验设计包括 PBD 和 BBD,以获得目标分析物萃取的最大效率和最佳条件。因此,在最佳条件下,SPME-HPLC-UV 对目标分析物的检出限为 0.33-0.64 µg L-1,线性动态范围为 1-100 µg L-1(r2 > 0.9934),定量限为 1.1-2.1 µg L-1。在 5-50 µg L-1 (2-10 µg L-1) 浓度范围内,日内相对标准偏差 (RSD%) 为 3.90%-5.30% (4.90%-6.80%) 。根据计算结果,相对回收率在 90% 至 109% 之间。因此,该方法适用于生物样品中乙酰水杨酸和 NAP 的预富集和萃取。
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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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