Hoang Tiffany T, Chen Yenfeng, May Sheldon W, Browner Richard F
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332-0400, USA.
Anal Chem. 2004 Apr 1;76(7):2062-70. doi: 10.1021/ac020707z.
Laser desorption/ionization time-of-flight mass spectra of three thermally labile low molecular weight organoselenium compounds (selenomethionine, selenoethionine, trimethylselenonium iodide) in human urine matrix have been obtained by using surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS). Four active layers, active carbon, silica sol-gel, and silica sol-gel impregnated with crown ether and with active carbon, were deposited on three different support substrates: (i) microscope slide coverslips; (ii) Al foil; and (iii) Cu tapes. Primarily protonated molecular ions and alkali metal adducts were observed in the mass spectra. A mixed-silica sol-gel and active carbon substrate active layer gave the best signal response for all compounds. Sol-gel substrates offered very clean backgrounds compared to the pure active carbon layers; however, the mass spectral signal intensities acquired were substantially lower for the sol-gel surfaces than those of the pure active carbon under the same conditions. Cu tape and Al foil support materials gave strong mass spectra of molecular ions and alkali metal molecular ion adducts, with lower Na and K adducts found with the Cu tape than with Al foil. Glass coverslips gave no response under all experimental conditions examined. Aerosol deposition was used to prepare SALDI substrates to avoid the localized "sweet spot" phenomenon encountered in conventional SALDI substrate preparation. Various nebulizers were examined and found to be effective in producing SALDI films with controlled and reproducible thicknesses. We were able to obtain exact mass identification of all three selenium species by high-resolution TOF-MS. To the best of our knowledge, this is the first time low molecular weight organoselenium compounds have been identified by SALDI-high-resolution TOF-MS.
通过表面辅助激光解吸/电离质谱法(SALDI-MS)获得了人尿基质中三种热不稳定的低分子量有机硒化合物(硒代蛋氨酸、硒代乙硫氨酸、碘化三甲基硒)的激光解吸/电离飞行时间质谱。将四个活性层,即活性炭、硅溶胶-凝胶以及浸渍有冠醚和活性炭的硅溶胶-凝胶,沉积在三种不同的支撑基底上:(i)显微镜载玻片盖玻片;(ii)铝箔;(iii)铜带。在质谱中主要观察到质子化分子离子和碱金属加合物。混合的硅溶胶-凝胶和活性炭基底活性层对所有化合物给出了最佳信号响应。与纯活性炭层相比,溶胶-凝胶基底提供了非常干净的背景;然而,在相同条件下,溶胶-凝胶表面获得的质谱信号强度明显低于纯活性炭的信号强度。铜带和铝箔支撑材料给出了分子离子和碱金属分子离子加合物的强质谱,在铜带上发现的钠和钾加合物比铝箔上的低。在所有检查的实验条件下,玻璃盖玻片均无响应。采用气溶胶沉积法制备SALDI基底,以避免传统SALDI基底制备中遇到的局部“亮点”现象。对各种雾化器进行了检查,发现它们能有效制备出厚度可控且可重现的SALDI薄膜。我们能够通过高分辨率TOF-MS对所有三种硒物种进行精确质量鉴定。据我们所知,这是首次通过SALDI-高分辨率TOF-MS鉴定低分子量有机硒化合物。