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金纳米粒子修饰的纤维素膜与激光解吸/电离质谱联用检测尿液中的碘化物。

Gold-nanoparticles-modified cellulose membrane coupled with laser desorption/ionization mass spectrometry for detection of iodide in urine.

机构信息

Institute of Bioscience and Biotechnology and ‡Center of Excellence for the Oceans, National Taiwan Ocean University , Keelung, 20224, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2013 Sep 25;5(18):9161-6. doi: 10.1021/am4025824. Epub 2013 Sep 9.

Abstract

We report an efficient method for the determination of iodide (I(-)) ions by using gold-iodide hybrid cluster ions on gold nanoparticles (Au NPs) modified mixed cellulose ester membrane (Au NPs-MCEM) by pulsed laser desorption/ionization mass spectrometry (LDI-MS). When I(-) ions were deposited and concentrated on the surfaces of Au NPs (32 nm) via strong Au(+)-I(-) interaction on the MECM, the Au NPs-MCEM was observed to function as an efficient surface-assisted LDI substrate with very low background noise. When pulsed laser radiation (355 nm) was applied, I(-) binding to Au NPs ions induced the enhancement of the desorption and ionization efficiency of gold-iodide hybrid cluster ions from the Au NPs surfaces. The reproducibility of the probe for both shot-to-shot and sample-to-sample (both less than 10%) ion production was also improved by the homogeneous nature of the substrate surface. Thus, it allows the accurate and precise quantification of I(-) ions in high-salinity real samples (i.e., edible salt samples and urine) at the nanomolar range. This novel LDI-MS approach provides a simple route for the high-speed analysis of I(-) ions with high sensitivity and selectivity in real biological samples.

摘要

我们报告了一种通过使用金纳米粒子(Au NPs)上的金-碘化物杂化簇离子(Au NPs-MCEM)修饰的混合纤维素酯膜(MCEM),利用脉冲激光解吸/电离质谱(LDI-MS)测定碘化物(I(-))离子的有效方法。当 I(-)离子通过在 MCEM 上的强 Au(+)-I(-)相互作用沉积并浓缩在 Au NPs(32nm)的表面上时,Au NPs-MCEM 被观察为具有非常低背景噪声的有效表面辅助 LDI 基底。当施加脉冲激光辐射(355nm)时,I(-)与 Au NPs 离子的结合诱导 Au NPs 表面上的金-碘化物杂化簇离子的解吸和电离效率增强。通过基质表面的均匀性,还提高了探针对单次和样品间(均小于 10%)离子产生的重现性。因此,它允许在纳摩尔范围内对高盐真实样品(即食用盐样品和尿液)中的 I(-)离子进行准确和精确的定量。这种新型 LDI-MS 方法为在真实生物样品中进行高灵敏度和选择性的 I(-)离子高速分析提供了一种简单的途径。

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