Detection of chemical warfare agent simulants and hydrolysis products in biological samples by paper spray mass spectrometry

Literature Information

Publication Date 2017-03-17
DOI 10.1039/C7AN00144D
Impact Factor 4.616
Authors

Josiah McKenna, Elizabeth S. Dhummakupt, Theresa Connell, Paul S. Demond, Dennis B. Miller, J. Michael Nilles, Nicholas E. Manicke, Trevor Glaros


View Original

Abstract

Paper spray ionization coupled to a high resolution tandem mass spectrometer (a quadrupole orbitrap) was used to identify and quantitate chemical warfare agent (CWA) simulants and their hydrolysis products in blood and urine. Three CWA simulants, dimethyl methylphosphonate (DMMP), trimethyl phosphate (TMP), and diisopropyl methylphosphonate (DIMP), and their isotopically labeled standards were analyzed in human whole blood and urine. Calibration curves were generated and tested with continuing calibration verification standards. Limits of detection for these three compounds were in the low ng mL−1 range for the direct analysis of both blood and urine samples. Five CWA hydrolysis products, ethyl methylphosphonic acid (EMPA), isopropyl methylphosphonic acid (IMPA), isobutyl methylphosphonic acid (iBuMPA), cyclohexyl methylphosphonic acid (CHMPA), and pinacolyl methylphosphonic acid (PinMPA), were also analyzed. Calibration curves were generated in both positive and negative ion modes. Limits of detection in the negative ion mode ranged from 0.36 ng mL−1 to 1.25 ng mL−1 in both blood and urine for the hydrolysis products. These levels were well below those found in victims of the Tokyo subway attack of 2 to 135 ng mL−1. Improved stability and robustness of the paper spray technique in the negative ion mode was achieved by the addition of chlorinated solvents. These applications demonstrate that paper spray mass spectrometry (PS-MS) can be used for rapid, sample preparation-free detection of chemical warfare agents and their hydrolysis products at physiologically relevant concentrations in biological samples.

Related Literature

The fast Z-scan method for studying working catalytic reactors with high energy X-ray diffraction: ZSM-5 in the methanol to gasoline process

David S. Wragg, Francesca L. Bleken, Matthew G. O'Brien, Marco Di Michiel, Helmer Fjellvåg, Unni Olsbye

2013-03-18 Paper

DOI: 10.1039/C3CP44343D

Structure of Nb2O5–NaPO3 glasses by X-ray and neutron diffraction

U. Hoppe, L. Delevoye, L. Montagne, M. v. Zimmermann, A. C. Hannon

2012-12-03 Paper

DOI: 10.1039/C2CP42772A

Sieving di-branched from mono-branched and linear alkanes using ZIF-8: experimental proof and theoretical explanation

Marjo C. Mittelmeijer-Hazeleger, Miguel Angelo Granato, Vanessa F. Duarte Martins, Alírio E. Rodrigues, Gadi Rothenberg

2013-05-02 Paper

DOI: 10.1039/C3CP44381G

Unraveling the atomic structure of Ge-rich sulfide glasses

Gabriel J. Cuello, Shinji Kohara, Chris J. Benmore, David L. Price, Eugene Bychkov

2013-04-08 Paper

DOI: 10.1039/C3CP50536G

Back cover

Cover

DOI: 10.1039/C3CP90065G

Ultra-slow dynamics in low density amorphous ice revealed by deuteron NMR: indication of a glass transition

Florian Löw, Katrin Amann-Winkel, Thomas Loerting, Franz Fujara, Burkhard Geil

2013-05-10 Paper

DOI: 10.1039/C3CP50818H

Free volume in ionic liquids: a connection of experimentally accessible observables from PALS and PVT experiments with the molecular structure from XRD data‡

Yang Yu, Günter Dlubek, Reinhard Krause-Rehberg, Jürgen Pionteck, Dirk Pfefferkorn, Safak Bulut, Dana Bejan, Christian Friedrich

2013-04-10 Paper

DOI: 10.1039/C3CP43306D

Controlled electrochemical deposition and transformation of hetero-nanoarchitectured electrodes for energy storage

Jonathon Duay, Eleanor Gillette, Junkai Hu

2013-04-17 Perspective

DOI: 10.1039/C3CP50724F

Comparison of the performance of an array of nanoband electrodes with a macro electrode with similar overall area

Reshma Sultana, Naser Reza, Helena Woodvine, Jonathan G. Terry, Anthony J. Walton, Charlotte L. Brady, Ilka Schmueser, Andrew R. Mount

2013-04-05 Paper

DOI: 10.1039/C3CP50759A

Charge carrier separation in nanostructured TiO2 photoelectrodes for water splitting

Alexander J. Cowan, Wenhua Leng, Piers R. F. Barnes, David R. Klug, James R. Durrant

2013-04-17 Paper

DOI: 10.1039/C3CP50318F

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Analyst

Analyst
CiteScore: 7.8
Self-citation Rate: 5.6%
Articles per Year: 653

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.