2004
DOI: 10.1002/rcm.1742
|View full text |Cite
|
Sign up to set email alerts
|

Evaluation of a hydrogen laser vacuum ultraviolet source for photoionization mass spectrometry of pharmaceuticals

Abstract: A photoionization hydrogen laser time-of-flight mass spectrometer system (H2-TOFMS) has been evaluated for the rapid analysis of drugs of abuse and pharmaceutical agents extracted from prescription tablets and spiked urine samples. The spectra obtained using the H2-TOFMS showed primarily intact molecular ions (M+*) after introduction by a heated probe and irradiation with vacuum ultraviolet (VUV) photons from the laser. Samples analyzed by this technique required only a simple solid-phase extraction step; no c… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
19
0

Year Published

2005
2005
2016
2016

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(19 citation statements)
references
References 31 publications
(39 reference statements)
0
19
0
Order By: Relevance
“…Maier et al [33] found that silene was stable only under argon matrix isolation at 10 K and it dimerized to 1,3-disilacyclobutane upon thawing of the matrix at 35 K. In a study of thermal decomposition of 1,1-dimethyl-1-silacyclobutane [34], although kinetic evidence supports the existence of an unstable intermediate, 1,1-dimethyl-1-silene, the only products detected are ethene and 1,1,3,3-tetramethyl-1,3-disilacyclobutane. 1,1-Dimethylsilene, an analog of silene, was found to undergo similar dimerization reactions to yield 1,1,3,3-tetramethyl-1,3-disilacyclobutane: (16) Our study of the hot wire decomposition of silacyclobutane [35] also showed that silene (H 2 Si CH 2 ) was produced, supported by the observation of its dimer signal, 1,3-disilacyclobutane. For the pyrolysis of TMS, 1,1,3,3-tetramethyl-1,3-disilacyclobutane (m/z = 144) [24,29] were previously observed as a product from the analysis by gas chromatography (GC) or GC-MS.…”
Section: Gas-phase Reaction Products From the Hwcvd Reactormentioning
confidence: 69%
See 1 more Smart Citation
“…Maier et al [33] found that silene was stable only under argon matrix isolation at 10 K and it dimerized to 1,3-disilacyclobutane upon thawing of the matrix at 35 K. In a study of thermal decomposition of 1,1-dimethyl-1-silacyclobutane [34], although kinetic evidence supports the existence of an unstable intermediate, 1,1-dimethyl-1-silene, the only products detected are ethene and 1,1,3,3-tetramethyl-1,3-disilacyclobutane. 1,1-Dimethylsilene, an analog of silene, was found to undergo similar dimerization reactions to yield 1,1,3,3-tetramethyl-1,3-disilacyclobutane: (16) Our study of the hot wire decomposition of silacyclobutane [35] also showed that silene (H 2 Si CH 2 ) was produced, supported by the observation of its dimer signal, 1,3-disilacyclobutane. For the pyrolysis of TMS, 1,1,3,3-tetramethyl-1,3-disilacyclobutane (m/z = 144) [24,29] were previously observed as a product from the analysis by gas chromatography (GC) or GC-MS.…”
Section: Gas-phase Reaction Products From the Hwcvd Reactormentioning
confidence: 69%
“…Non-resonant SPI using VUV wavelengths (100 nm ≤ λ ≤ 200 nm) is generally considered to be a soft ionization method [16][17][18]. Efficient ionization of the chemical species of interest can be achieved by this method with little or no fragmentation.…”
Section: Introductionmentioning
confidence: 99%
“…In Figure , the available ionization energies (IEs) of biomass vapors are shown as a function of their molecular mass along with the VUV emission profiles of a commonly used light source, and most of them are distributed in the energy range of 7.8–10.0 eV. Some convenient VUV sources, such as a molecular fluorine laser (F 2 laser) and hydrogen laser (H 2 laser), can emit short pulses at 7.87 and 7.75 eV, respectively. , However, these low photon energies are below the IEs of most biomass vapors (see Figure ). Photon energies of VUV light from an Ar- or Kr-excimer lamp and from a Nd:YAG laser (9.0–10.5 eV) well cover the IEs of most biomass vapors .…”
Section: Introductionmentioning
confidence: 99%
“…[8]. Postionization of laser desorbed neutrals with 7.87 eV photons from a molecular fluorine laser will single photon ionize various low ionization potential compounds including secondary, tertiary, and aromatic amines as well as various fused ring aromatics, tryptophan containing peptides, and pharmaceuticals [9-11]. Selectivity for specific higher ionization potential species can be achieved by derivatizing a molecular analyte with an appropriate chemical tag to lower the ionization potential of the resultant complex below 7.87 eV, thereby permitting postionization with the fluorine laser [12].…”
Section: Introductionmentioning
confidence: 99%