4.8 Article

Cysteine Modified Small Ligament Au Nanoporous Film: An Easy Fabricating and Highly Efficient Surface-Assisted Laser Desorption/Ionization Substrate

期刊

ANALYTICAL CHEMISTRY
卷 83, 期 10, 页码 3668-3674

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac103222p

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资金

  1. National Science Fund for Distinguished Young Scholars of China [21025729]
  2. National Basic Research Program of China [2010CB933502]
  3. National Natural Science Foundation of China [20921063, 20977101]

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Au nanoporous films (NPFs) with different surface modification and morphology were fabricated and utilized as substrates for the analysis of a series of compounds, including amino acids, drug, cyclodextrins, peptides, and polyethylene glycols, using surface-assisted laser desorption/ionization time-of-flight mass spectrometry (SALDI-TOF MS). It was found that the size and interconnection state of the NPF ligament as well as the surface modification are key parameters that affect the laser desorption/ionization performance. Compared with 2,5-dihydroxybenzoic acid, pristine NPF, and aminobenzenethiol or 3-mercaptopropanoic acid modified Au NPFs, cysteine modified Au NPF generated intense and background-suppressing mass spectra. Regarding the effect of Au NPF morphology, the Au NPF with nanopores in the range of 10-30 nm, ligament size of 5 nm, and electrochemistry surface area of 26.1 m(2)/g exhibited the highest performance as a substrate. This high-performance NPFs can be easily fabricated by capping agent replacement induced self-organization of ultrathin nanowires, followed by self-assembling of a monolayer (SAM) of cysteine. The good thermal/electroconductivity and uniformity of Au NPFs avoided the fragmentation of analytes, eliminated the intrinsic matrix ions interference, and provided good reproducibility (RSD <= 10%). Additionally, the fabricated NPFs can be easy divided into microarrys (a similar to 4 x 4 array from a 1 cm x 1 cm NPF). This work provides a simple and cost-effective route for acquiring an Au nanostructure as a SALDI substrate, which offers a new technique for high-speed analysis of low-molecular weight compounds.

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