References
- Bakke J., Gustafsson J. -A. Mercapturic acid pathway metabolites of xenobiotics: generation of potentially toxic metabolites during enterohepatic circulation. Trends in Pharmacological Sciences 1984; 5: 517–521
- Black R. M., Read R. W. Detection of trace levels of thiodiglycol in blood, plasma and urine using gas chromatography-electron-capture negative ion chemical ionisation mass spectrometry. Journal of Chromatography 1988; 449: 261–270
- Black R. M., Read R. W. Methods for the analysis of thiodiglycol sulphoxide, a metabolite of sulphur mustard, in urine using gas chromatography-mass spectrometry. Journal of Chromatography 1991a; 558: 393–404
- Black R. M., Brewster K., Harrison J. M., Stansfield N. The chemistry of 1,1′-thiobis(2-chloroethane) (sulphur mustard). Part 1. Some simple derivatives. Submitted to Phosphorus and Sulphur 1992a
- Black R. M., Brewster K., Clarke R. J., Harrison J. M. The chemistry of 1,1′-thiobis(2-chloroethane) (sulphur mustard). Part 2. The synthesis of some conjugates with cysteine, N-acetylcysteine and methyl N-acetylcysteine. Submitted to Phosphorus and Sulphur 1992b
- Black R. M., Hambrook J. L., Howells D. J., Read R. W. Biological fate of sulphur mustard, 1,1′-thiobis(2-chloroethane). Urinary excretion profiles of hydrolysis products and β-lyase metabolites of sulphur mustard after cutaneous application in the rat. Journal of Analytical Toxicology 1992c, In press
- Black R. M., Clarke R. J., Read R. W. A method for the analysis of 1,1′-sulphonylbis[2-(methylsulphinyl)ethane] and 1-methyisulphinyl-2-[2-(methylthio)ethylsulphonyl]ethane, metabolites of sulphur mustard, in urine using gas chromatography-mass spectrometry. Journal of Chromatography 1991b; 558: 405–414
- Davison C., Rozman R. S., Smith P. K. Metabolism of bis-β-chloroethyl sulphide (sulphur mustard gas). Biochemical Pharmacology 1961; 7: 65–74
- Elfarra A. A., Anders M. W. Renal processing of glutathione conjugates. Role in nephrotoxicity. Biochemical Pharmacology 1984; 33: 3729–3732
- Gray P. J. A literature review on the mechanism of action of sulphur and nitrogen mustard. Materials Research Laboratory, Maribyrnong, VictoriaAustralia 1989, Materials Research Laboratory Technical Report No. MRL-TR-89–24, DRIC P-284131
- Hambrook J. L., Harrison J. M., Howells D. J., Schock C. Biological fate of sulphur mustard, 1,1′-thiobis-(2-chloroethane). Urinary and faecal excretion of 35S by rat after injection or cutaneous application of 35S-labelled sulphur mustard. Xenobiotica 1992; 22: 65–75
- Harrison J. M. The synthesis of isotopically labelled 1,1′-thiobis[2-chloroethane] and some related compounds. Journal of Labelled Compounds and Radiopharmaceuticals 1991; XXIX: 1175–1180
- Roberts J. J., Warwick G. P. Studies of the mode of action of alkylating agents—IV. The metabolism of bis-2-chloroethylsulphide (mustard gas) and related compounds. Biochemical Pharmacology 1963; 12: 1329–1334
- Somani S. M., Babu S. R. Toxicodynamics of sulphur mustard. International Journal of Clinical Pharmacology, Therapy and Toxicology 1989; 27: 419–435
- United Nations Security Council. Report of the specialists appointed by the Security-General to investigate allegations by the Islamic Republic of Iran concerning the use of chemical weapons. New York 1984, Report S-16433
- United Council Nations Security. Report of the mission dispatched by the Security-General to investigate allegations of the use chemical weapons in the conflict between the Islamic Republic of Iran and Iraq. New York 1986, Report S-17911
- United Council Nations Security. Report of the mission dispatched by the Security-General to investigate allegations of the use of chemcial weapons in the conflict between the Islamic Republic of Iran and Iraq. New York 1988, Report S-20134
- Van Bladeren P. J. Formation of toxic metabolites from drugs and other xenobiotics by glutathione conjugation. Trends in Pharmacological Sciences 1988; 9: 295–299
- Warwick G. P. The mechanism of action of alkylating agents. Cancer Research 1963; 23: 1315–1333