Development of a Novel Ultrasound Vacuum-Assisted Headspace Solid-Phase Microextraction Approach for Determination of Solvent Residuals in Pharmaceuticals and Comparison with Traditional Headspace Solid-Phase Microextraction Method.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Somayeh Hajipour, Alireza Ghiasvand, Mohammad Hajipour
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引用次数: 0

Abstract

In this report, an ultrasonication and vacuum-assisted headspace solid-phase microextraction procedure followed by gas chromatography-flame ionization detection (UVA-HS-SPME-GC-FID) was proposed for direct extraction of solvent residuals, including benzene, toluene, ethyl benzene, m,p-xylene and o-xylene, in pharmaceutical matrices. A novel robust, reliable and durable nanocomposite solid-phase microextraction (SPME) fiber was prepared by layer-by-layer coating of 3-aminopropyltriethoxysilane-functionalized graphene on a stainless-steel wire. Then, the proposed fiber was used for headspace SPME and trapping of toluene as a residual solvent in solid penicillin, ampicillin and cefazolin vials followed by gas chromatography-flame ionization detection. UVA-HS-SPME-GC-FID achieves better validation parameters, including the limit of detection, limit of quantification, linearity, recovery and repeatability, in comparison with conventional HS-SPME-GC-FID. The UVA-HS-SPME-GC-FID strategy is very effective for quantitatively tracing volatile and semivolatile solvent residuals in various pharmaceutical drugs.

超声真空辅助顶空固相微萃取法测定药品中溶剂残留量及其与传统顶空固相微萃取法的比较
本文提出了一种超声和真空辅助顶空固相微萃取-气相色谱-火焰电离检测(UVA-HS-SPME-GC-FID)的方法,用于直接提取药物基质中的溶剂残留物,包括苯、甲苯、乙苯、间苯、对二甲苯和邻二甲苯。将3-氨基丙基三乙氧基硅烷功能化石墨烯逐层涂覆在不锈钢丝上,制备了一种坚固、可靠、耐用的纳米复合固相微萃取(SPME)纤维。然后,将该纤维用于固相青霉素、氨苄西林和头孢唑林小瓶中残留溶剂甲苯的顶空SPME和捕集,并进行气相色谱-火焰电离检测。与传统的HS-SPME-GC-FID相比,UVA-HS-SPME-GC-FID具有更好的验证参数,包括检出限、定量限、线性度、回收率和可重复性。UVA-HS-SPME-GC-FID方法对各种药物中挥发性和半挥发性溶剂残留量的定量追踪是非常有效的。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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