This paper is based on work presented at the 12th Symposium of the Japanese Arsenic Scientists' Society (JASS) held 5–6 November 2005 in Takizawa, Iwate Prefecture, Japan.
Environment, Biology and Toxicology
Determination of degradation compounds derived from Lewisite by high performance liquid chromatography/inductively coupled plasma-mass spectrometry†
Article first published online: 17 AUG 2006
DOI: 10.1002/aoc.1104
Copyright © 2006 John Wiley & Sons, Ltd.
Issue
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Applied Organometallic Chemistry
Special Issue: Special issue including information from the 12th Symposium of the Japanese Arsenic Scientists' Society (JASS) held 5–6 November 2005 in Takizawa, Iwate Prefecture, Japan
Volume 20, Issue 9, pages 591–596, September 2006
Additional Information
How to Cite
Kinoshita, K., Shikino, O., Seto, Y. and Kaise, T. (2006), Determination of degradation compounds derived from Lewisite by high performance liquid chromatography/inductively coupled plasma-mass spectrometry. Appl. Organometal. Chem., 20: 591–596. doi: 10.1002/aoc.1104
- †
Publication History
- Issue published online: 17 AUG 2006
- Article first published online: 17 AUG 2006
- Manuscript Accepted: 29 JUN 2006
- Manuscript Received: 10 MAY 2006
- Abstract
- References
- Cited By
Keywords:
- chemical warfare agents;
- Lewisite;
- 2-chlorovinylarsenous acid (CVAA);
- 2-chlorovinylarsonic acid (CVAOA);
- HPLC/ICP-MS;
- speciation analysis
Abstract
A method for determination of 2-chlorovinylarsenous acid (CVAA) and 2-chlorovinylarsonic acid (CVAOA), which are degradation compounds of the chemical warfare agent Lewisite, was examined by high-performance liquid chromatography/inductively coupled plasma-mass spectrometry (HPLC/ICP-MS). Inertsil C8 was suitable as the column and the mobile phase was consisted of 0.1% formic acid-acetonitrile (80:20). These compounds were detected sensitively in a short time and separated from inorganic arsenicals and diphenylarsinic acid (DPAA) and phenylarsonic acid (PAA), which are degradation compounds of diphenylchloroarsine and phenyldichloroarsine, respectively. The detection limits of CVAA and CVAOA were 0.2 and 0.1 ngAs/ml, respectively. In addition, a dynamic reaction cell and oxygen as the reaction gas were applied, and then arsenic was detected as AsO+ (m/z 91) in order to prevent interference by ArCl+ (m/z 75). This method was applied to the analysis of urine obtained from a CVAA-administered mouse and CVAOA was detected as the main metabolite. Thus, the speciation analysis of arsenic compounds derived from chemical warfare agents was achieved by HPLC/ICP-MS. Copyright © 2006 John Wiley & Sons, Ltd.

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