Spontaneous formation of thiuram disulfides in solutions of iron(III) dithiocarbamates

被引:33
作者
Bergendorff, O [1 ]
Hansson, C [1 ]
机构
[1] Lund Univ, Univ Hosp, Dept Dermatol, SE-22185 Lund, Sweden
关键词
contact allergy; cross-reactivity; dermatitis; disulfiram; ferbam; ferric compounds; HPLC; oxidation; pesticides; rubber chemicals; thiocarbamates; thiram;
D O I
10.1021/jf011143n
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Dithiocarbamates are used as pesticides and rubber additives. Dithiocarbamates are the reduced forms of thiuram disulfides and both of these groups of substances induce allergic contact dermatitis. The allergic cross-reactivity pattern between dithiocarbamates and thiurams is unclear. The aim of this study was to investigate why these cross-reactions occur sometimes but not always. HPLC-analysis of buffer solutions of iron(III) dithiocarbamates demonstrated that thiuram disulfides were formed spontaneously and rapidly in high yield. No such oxidation was observed in solutions of copper(II), zinc(II), or sodium dithiocarbamates. However, sodium diethyldithiocarbamate and zinc diethyldithiocarbamate were oxidized in buffer solution when ferric salt was added. The influence of different metal ions on the oxidation reaction is probably an explanation for the cross-reactivity patterns seen between dithiocarbamates and thiurams. These findings also show that careful handling is necessary in analytical and biological studies with solutions of iron(III) dithiocarbamates. Oxidation of dithiocarbamates in aqueous buffer at physiological pH has not been shown before.
引用
收藏
页码:1092 / 1096
页数:5
相关论文
共 32 条
[1]   SERUM-ALBUMIN AND THE METABOLISM OF DISULFIRAM [J].
AGARWAL, RP ;
PHILLIPS, M ;
MCPHERSON, RA ;
HENSLEY, P .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (19) :3341-3347
[2]  
Belsito DV, 2000, HDB OCCUPATIONAL DER, P701
[3]   Stability of thiuram disulfides in patch test preparations and formation of asymmetric disulfides [J].
Bergendorff, O ;
Hansson, C .
CONTACT DERMATITIS, 2001, 45 (03) :151-157
[4]   Dithiocarbamate toxicity toward thymocytes involves their copper-catalyzed conversion to thiuram disulfides, which oxidize glutathione in a redox cycle without the release of reactive oxygen species [J].
Burkitt, MJ ;
Bishop, HS ;
Milne, L ;
Tsang, SY ;
Provan, GJ ;
Nobel, CSI ;
Orrenius, S ;
Slater, AFG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 353 (01) :73-84
[5]   Oxidation of dithiocarbamates and synthesis of a stable sulfine [J].
Chevrie, D ;
Metzner, P .
TETRAHEDRON LETTERS, 1998, 39 (49) :8983-8986
[6]   THE REACTION OF TETRAMETHYLTHIURAMDISULPHIDE WITH ACETONE .2. THE EFFECTS OF ADDITIVES [J].
CRAIG, D ;
ROBINSON, JR ;
FOWLER, RB .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1956, 34 (11) :1601-1610
[7]   Disulfiram generates a stable N,N-diethylcarbamoyl adduct on Cys-125 of rat hemoglobin β-chains in vivo [J].
Erve, JCL ;
Jensen, ON ;
Valentine, HS ;
Amarnath, V ;
Valentine, WM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2000, 13 (04) :237-244
[8]   Hapten synthesis for the development of a competitive inhibition enzyme-immunoassay for thiram [J].
Gueguen, F ;
Boisdé, F ;
Queffelec, AL ;
Haelters, JP ;
Thouvenot, D ;
Corbel, B ;
Nodet, P .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (10) :4492-4499
[9]   THE STABILITY OF SODIUM DIETHYLDITHIOCARBAMATE IN BIOCHEMICAL EXPERIMENTS [J].
HALLAWAY, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1959, 36 (02) :538-540
[10]   Extraction of mercaptobenzothiazole compounds from rubber products [J].
Hansson, C ;
Bergendorff, O ;
Ezzelarab, M ;
Sterner, O .
CONTACT DERMATITIS, 1997, 36 (04) :195-200