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微芯片等速电泳与表面增强拉曼光谱联用在药物分析中的应用。

Microchip isotachophoresis coupled to surface-enhanced Raman spectroscopy for pharmaceutical analysis.

机构信息

Department of Analytical Chemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Mlynská dolina CH2, Ilkovičova 6, 842 15, Bratislava, Slovakia.

Department of Medical and Clinical Biophysics, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Trieda SNP 1, 04011, Košice, Slovakia.

出版信息

Mikrochim Acta. 2020 Jul 16;187(8):448. doi: 10.1007/s00604-020-04436-y.

Abstract

A novel online coupling of microchip isotachophoresis (μITP) with surface-enhanced Raman spectroscopy (SERS) for the analysis of complex samples is presented. Polymeric microchip with coupled channels was used for μITP-SERS analysis of four structurally similar Raman active synthetic dyes (brilliant black BN, carmoisine, ponceau 4R, and sunset yellow FCF) in pharmaceuticals. The μITP separation and simultaneous pre-concentration of the analytes were performed in the first channel of the microchip at pH 6.0 with the aid of non-Raman active discrete spacers (acetate, butyrate, glutarate, pantothenate, and valerate). Silver nanoparticles used for Raman enhancement were present in the second channel, and individual SERS spectra of the dyes were acquired by a mini Raman spectrometer operating at 532 nm. The analytical enhancement factors for silver nanoparticles were 1-5 × 10. The microchip with coupled channels enabled independent μITP separation and SERS detection, and eliminated any adverse impact of nanoparticles on the separation. The developed approach allowed reliable online SERS identification and detection of dyes with limits of detection ranging from 12 to 62 nM. Synthetic dyes were successfully separated, identified, and quantified in pharmaceutical preparations within 7 min without the need for complex or time-consuming sample pretreatment. The results were in good agreement with those obtained by an independent analytical method reported for studied dyes. Graphical abstract.

摘要

提出了一种新颖的在线微芯片等速电泳(μITP)与表面增强拉曼光谱(SERS)联用技术,用于分析复杂样品。采用带有耦合通道的聚合物微芯片对四种结构相似的拉曼活性合成染料(亮黑 BN、胭脂红、丽春红 4R 和日落黄 FCF)在药物中的μITP-SERS 分析。μITP 分离和同时预浓缩在微芯片的第一个通道中进行,在 pH 6.0 下,借助非拉曼活性离散间隔物(乙酸盐、丁酸盐、戊二酸盐、泛酸盐和缬氨酸盐)进行。用于拉曼增强的银纳米粒子存在于第二个通道中,通过在 532nm 处工作的小型拉曼光谱仪获得染料的个体 SERS 光谱。银纳米粒子的分析增强因子为 1-5×10。带有耦合通道的微芯片能够实现独立的μITP 分离和 SERS 检测,并消除纳米粒子对分离的任何不利影响。所开发的方法允许对染料进行可靠的在线 SERS 识别和检测,检测限范围从 12 到 62nm。在无需复杂或耗时的样品预处理的情况下,在 7 分钟内成功分离、鉴定和定量了药物制剂中的合成染料。结果与报道的用于研究染料的独立分析方法获得的结果非常吻合。

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