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用于小分子基质辅助激光解吸电离质谱分析的紫外线吸收配体包覆金纳米粒子

UV-Absorbing Ligand Capped Gold Nanoparticles for the SALDI-MS Analysis of Small Molecules.

作者信息

Kakuta Tomomi, Manyuan Nichayanan, Kawasaki Hideya

机构信息

Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Osaka, Japan.

出版信息

Mass Spectrom (Tokyo). 2022;11(1):A0107. doi: 10.5702/massspectrometry.A0107. Epub 2022 Dec 15.

DOI:10.5702/massspectrometry.A0107
PMID:36713807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9853113/
Abstract

We report that modifying the surface of gold nanoparticles (Au NPs) with 2-mercaptopyridine-3-carboxylic acid (MPyCA) enhances surface-assisted laser desorption/ionization (SALDI) performance in the analysis of small molecules. The MPyCA ligand has a strong UV absorbance at the wavelengths of the typical MALDI laser at 337 nm, resulting in efficient thermal/energy transfer from the Au NPs to analytes during pulse-laser irradiation. In addition, the MPyCA ligand contains carboxylic acid and pyridine groups, providing affinity to various analytes through acid-base interactions. Irganox1010, glucose and meropenem were utilized as model analytes to evaluate SALDI performance because these molecules are generally ionized with difficulty by conventional MALDI-MS. Our results demonstrate that the MPyCA-Au NP based SALDI-MS could detect Irganox1010, glucose and meropenem with stronger ion peaks for these molecules compared to MALDI-MS using CHCA. The limit of detection (LOD) for meropenem was much lower in the case of SALDI (LOD=1 ng/mL) compared to MALDI (LOD=10 μg/mL).

摘要

我们报道,用2-巯基吡啶-3-羧酸(MPyCA)修饰金纳米颗粒(Au NPs)的表面,可增强小分子分析中的表面辅助激光解吸/电离(SALDI)性能。MPyCA配体在典型基质辅助激光解吸电离(MALDI)激光的波长337 nm处具有很强的紫外吸收,导致在脉冲激光照射期间从金纳米颗粒到分析物的有效热/能量转移。此外,MPyCA配体含有羧酸和吡啶基团,通过酸碱相互作用对各种分析物具有亲和力。选用抗氧剂1010、葡萄糖和美罗培南作为模型分析物来评估SALDI性能,因为这些分子通常难以通过传统的基质辅助激光解吸电离质谱(MALDI-MS)进行电离。我们的结果表明,与使用α-氰基-4-羟基肉桂酸(CHCA)的MALDI-MS相比,基于MPyCA-Au NP的SALDI-MS能够检测到抗氧剂1010、葡萄糖和美罗培南,且这些分子的离子峰更强。与MALDI(检测限=10μg/mL)相比,美罗培南在SALDI情况下的检测限(LOD)要低得多(LOD=1 ng/mL)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/3509d65c4d04/massspectrometry-11-1-A0107-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/526ad3dfc5ed/massspectrometry-11-1-A0107-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/41ac7d8709e0/massspectrometry-11-1-A0107-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/6468ad554f88/massspectrometry-11-1-A0107-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/3509d65c4d04/massspectrometry-11-1-A0107-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/526ad3dfc5ed/massspectrometry-11-1-A0107-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/41ac7d8709e0/massspectrometry-11-1-A0107-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/6468ad554f88/massspectrometry-11-1-A0107-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ea/9853113/3509d65c4d04/massspectrometry-11-1-A0107-figure04.jpg

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