Electron monochromator-mass spectrometer instrument for negative ion analysis of electronegative compounds

1996 ◽  
Vol 15 (1) ◽  
pp. 15-42 ◽  
Author(s):  
J. A. Laramée ◽  
P. Mazurkiewicz ◽  
V. Berkout ◽  
M. L. Deinzer
2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S386-S387
Author(s):  
Sydney C Povilaitis ◽  
Ashish D Chakraborty ◽  
Rachel D Downey ◽  
Sarmistha Bhaduri Hauger ◽  
Livia Eberlin

Abstract Background In the age of antimicrobial resistance, rapid identification of infectious agents is critical for antimicrobial stewardship and effective therapy. To this end, ambient ionization mass spectrometry techniques have been applied for rapid identification of microbes directly from culture isolates. We have developed a handheld, mass spectrometry-based device, the MasSpec Pen, that permits direct molecular analysis of a biological sample in seconds (Scheme 1). Here, we employ the MasSpec Pen to identify clinically relevant microbes directly from culture isolates. Methods Staphylococcus aureus, Staphylococcus epidermidis, Group A and B Streptococcus, Kingella kingae (K.k), and Pseudomonas aeruginosa (P.a) were cultured on 5% sheep’s blood nutrient agar at 37 °C overnight. Colonies were transferred to a glass slide where they were analyzed directly with the MasSpec Pen coupled to a Q Exactive mass spectrometer (Thermo Scientific) in negative ion mode. For MasSpec Pen analysis, a 10 µL droplet of water was held in contact with the sample surface for 3 seconds and then aspirated to the mass spectrometer for analysis. Data was normalized and the molecular features resulting from the analysis solvent and nutrient medium were removed. The least absolute shrinkage and selection operator (lasso) statistical method was used to build classification models for prediction of bacterial identity. Model performance was evaluated by leave-one-out cross-validation and a validation set of samples. Scheme 1: MasSpec Pen workflow Results Various small molecules were detected including metabolites and glycerophospholipid species. The mass spectral profiles for each species exhibited qualitative differences among them (Figure 1). Additionally, several quorum-sensing molecules were observed in P.a. including hydroxy-heptyl-quinoline (m/z 242.155). Lasso statistical classifiers were created to differentiate organisms at the level of Gram type, genus, and species with each model comprised of a sparse set of molecular features. Accuracies of 90% or greater were achieved for all lasso models and as high as 98% for the differentiation of Staphylococcus (Staph.) and Streptococcus (Strep.). Figure 1: Molecular profiles of species analyzed Figure 2: Statistical classification results Conclusion These results demonstrate the potential of the MasSpec Pen as a tool for clinical analysis of infected biospecimens. Disclosures Sydney C. Povilaitis, BA, MS Pen Technologies, Inc. (Other Financial or Material Support, Patent) Livia Eberlin, PhD, MS Pen Technolpogies, Inc. (Board Member, Shareholder)


2021 ◽  
Vol 22 ◽  
Author(s):  
Shan Jiang ◽  
Haoran Li ◽  
Ailin Yang ◽  
Hongbing Zhang ◽  
Pingping Dong ◽  
...  

Background : Astilbin, a dihydroflavonoid compound widely found in plants, exhibits a variety of pharmacological activities and biological effects. However, little is known about the metabolism of this active compound in vivo, which is very helpful for elucidating the pharmacodynamic material basis and application of astilbin. Objective: To establish a rapid profiling and identification method for metabolites in rat urine, faeces and plasma using a UHPLC-Q-Exactive mass spectrometer in negative ion mode. Methods: In this study, a simple and rapid systematic strategy and 7 metabolite templates, which were established based on previous reports, were utilized to screen and identify astilbin metabolites. Results: As a result, a total of 72 metabolites were detected and characterized, among which 33 metabolites were found in rat urine, while 28 and 38 metabolites were characterized from rat plasma and faeces, respectively. These metabolites were presumed to be generated through ring cleavage, sulfation, dehydrogenation, methylation, hydroxylation, glucuronidation, dehydroxylation and their composite reactions. Conclusion: This study illustrated the capacity of the sensitive UHPLC-Q-Exactive mass spectrometer analytical system combined with the data-mining methods to rapidly elucidate the unknown metabolism. Moreover, the comprehensive metabolism study of astilbin provided an overall metabolic profile, which will be of great help in predicting the in vivo pharmacokinetic profiles and understanding the action mechanism of this active ingredient.


2018 ◽  
Author(s):  
Qian Xiao ◽  
Mei Li ◽  
Huan Liu ◽  
Fanyuan Deng ◽  
Mingliang Fu ◽  
...  

Abstract. Emissions from ships at berth played an important role in the exposure of atmospheric pollutants to high density population in port areas, but these emissions were not understood very well. In this study, volatile organic compounds (VOCs) and particle emissions from 20 container ships at berth were sampled and analyzed during the fuel switch period at Jingtang Port in Hebei Province, China. VOCs and particles were analyzed by gas chromatography-mass spectrometer (GC-MS) and the Single Particle Aerosol Mass Spectrometer (SPAMS), respectively. VOCs analysis showed that alkanes and aromatics, especially benzene, toluene and heavier compounds e.g. n-heptane, n-octane, n-nonane, dominated the total identified species. Secondary organic aerosol yields and ozone forming potential were 0.017 ± 0.007 g SOA/g VOCs and 2.63 ± 0.37 g O3/g VOCs, respectively. Both positive and negative ion mass spectra from individual ship were derived and intensity of specific ions could be quantified. Results showed that element carbon (35.74 %), element carbon-organic carbon mixture (33.95 %) and Na-rich particles (21.12 %) were major classes with a total number ratio of 90.7 %. Particles from ship auxiliary engines were in a size range of 0.2 to 2.5 μm, with a peak occurring at around 0.4 μm. The issue of vanadium as tracer element was discussed that V was not a proper tracer when using low sulfur content diesel oil. The average percentage of sulfate particles from shipping emissions before and after switching to marine diesel oil were 23.82 % and 23.61 % respectively. The total results provide robust evidences in port area air quality assessment and source apportionment.


2003 ◽  
Vol 13 (4) ◽  
pp. 959-971 ◽  
Author(s):  
Yasuto MACHII ◽  
Osamu KUMAZAKI ◽  
Kenji MIZUNO ◽  
Mitsugu NAGANO ◽  
Yoshio HAYASAKA ◽  
...  

1976 ◽  
Vol 29 (10) ◽  
pp. 2219 ◽  
Author(s):  
JW Clark-Lewis ◽  
GL Aldous ◽  
MJ Thompson

The previously proposed structure (2) for the compound named in the title is confirmed by spectroscopic methods and by synthesis of related compounds. The barbituric acid undergoes a very facile thermal fragmentation in the mass spectrometer into 1,3-dimethyl-5-(4-ethylamino-3-nitrobenzy1)-barbituric acid (3) (which was also prepared by unambiguous synthesis) and 1,3-dimethyl-5-methylenebarbituric acid (4). The electron-impact, chemical-ionization, and negative-ion mass spectrometric behaviour of the barbituric acid (2) was examined.


2015 ◽  
Vol 15 (14) ◽  
pp. 7765-7776 ◽  
Author(s):  
F. D. Lopez-Hilfiker ◽  
C. Mohr ◽  
M. Ehn ◽  
F. Rubach ◽  
E. Kleist ◽  
...  

Abstract. We measured a large suite of gas- and particle-phase multi-functional organic compounds with a Filter Inlet for Gases and AEROsols (FIGAERO) coupled to a high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS) developed at the University of Washington. The instrument was deployed on environmental simulation chambers to study monoterpene oxidation as a secondary organic aerosol (SOA) source. We focus here on results from experiments utilizing an ionization method most selective towards acids (acetate negative ion proton transfer), but our conclusions are based on more general physical and chemical properties of the SOA. Hundreds of compounds were observed in both gas and particle phases, the latter being detected by temperature-programmed thermal desorption of collected particles. Particulate organic compounds detected by the FIGAERO–HR-ToF-CIMS are highly correlated with, and explain at least 25–50 % of, the organic aerosol mass measured by an Aerodyne aerosol mass spectrometer (AMS). Reproducible multi-modal structures in the thermograms for individual compounds of a given elemental composition reveal a significant SOA mass contribution from high molecular weight organics and/or oligomers (i.e., multi-phase accretion reaction products). Approximately 50 % of the HR-ToF-CIMS particle-phase mass is associated with compounds having effective vapor pressures 4 or more orders of magnitude lower than commonly measured monoterpene oxidation products. The relative importance of these accretion-type and other extremely low volatility products appears to vary with photochemical conditions. We present a desorption-temperature-based framework for apportionment of thermogram signals into volatility bins. The volatility-based apportionment greatly improves agreement between measured and modeled gas-particle partitioning for select major and minor components of the SOA, consistent with thermal decomposition during desorption causing the conversion of lower volatility components into the detected higher volatility compounds.


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