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采用静电纺丝复合纳米纤维的小分子药物和高分子合成/生物聚合物的表面辅助激光解吸/电离飞行时间质谱法。

Surface-assisted laser desorption/ionization time-of-flight mass spectrometry of small drug molecules and high molecular weight synthetic/biological polymers using electrospun composite nanofibers.

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210, USA.

出版信息

Analyst. 2017 Mar 27;142(7):1125-1132. doi: 10.1039/c6an02444k.

DOI:10.1039/c6an02444k
PMID:28294237
Abstract

Polyacrylonitrile/Nafion®/carbon nanotube (PAN/Nafion®/CNT) composite nanofibers were prepared using electrospinning. These electrospun nanofibers were studied as possible substrates for surface-assisted laser desorption/ionization (SALDI) and matrix-enhanced surface-assisted laser desorption/ionization time-of-flight mass spectrometry (ME-SALDI/TOF-MS) for the first time in this paper. Electrospinning provides this novel substrate with a uniform morphology and a narrow size distribution, where CNTs were evenly and firmly immobilized on polymeric nanofibers. The results show that PAN/Nafion®/CNT nanofibrous mats are good substrates for the analysis of both small drug molecules and high molecular weight polymers with high sensitivity. Markedly improved reproducibility was observed relative to MALDI. Due to the composite formation between the polymers and the CNTs, no contamination of the carbon nanotubes to the mass spectrometer was observed. Furthermore, electrospun nanofibers used as SALDI substrates greatly extended the duration of ion signals of target analytes compared to the MALDI matrix. The proposed SALDI approach was successfully used to quantify small drug molecules with no interference in the low mass range. The results show that verapamil could be detected with a surface concentration of 220 femtomoles, indicating the high detection sensitivity of this method. Analysis of peptides and proteins with the electrospun composite substrate using matrix assisted-SALDI was improved and a low limit of detection of approximately 6 femtomoles was obtained for IgG. Both SALDI and ME-SALDI analyses displayed high reproducibility with %RSD ≤ 9% for small drug molecules and %RSD ≤ 14% for synthetic polymers and proteins.

摘要

聚丙稀腈/全氟磺酸(PAN/Nafion®/CNT)复合纳米纤维是通过静电纺丝制备的。本文首次将这些静电纺纳米纤维作为表面辅助激光解吸/电离(SALDI)和基质增强表面辅助激光解吸/电离飞行时间质谱(ME-SALDI/TOF-MS)的可能基底进行了研究。静电纺丝为这种新型基底提供了均匀的形态和狭窄的尺寸分布,其中 CNT 均匀且牢固地固定在聚合物纳米纤维上。结果表明,PAN/Nafion®/CNT 纳米纤维垫是分析小分子药物和高分子量聚合物的良好基底,具有较高的灵敏度。与 MALDI 相比,观察到明显提高的重现性。由于聚合物和 CNT 之间的复合形成,没有观察到碳纳米管对质谱仪的污染。此外,与 MALDI 基质相比,静电纺纳米纤维用作 SALDI 基底大大延长了目标分析物离子信号的持续时间。所提出的 SALDI 方法成功地用于定量分析小分子药物,在低质量范围内没有干扰。结果表明,维拉帕米可以在表面浓度为 220 飞摩尔的情况下被检测到,表明该方法具有较高的检测灵敏度。使用基质辅助-SALDI 对肽和蛋白质进行分析时,静电纺复合基底的分析得到了改善,对于 IgG,得到了约 6 飞摩尔的低检测限。SALDI 和 ME-SALDI 分析均显示出高重现性,对于小分子药物,%RSD≤9%,对于合成聚合物和蛋白质,%RSD≤14%。

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