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Hemoglobin adduct biomonitoring

Zwimer-Baier I, Neumann HG. 1994. Biomonitoring of aromatic amines FV Use of hemoglobin adducts to demonstrate the bioavailability of cleavage products from diaiylide azo pigments in vivo. Arch Toxicol 68(1) 8-14. [Pg.166]

Landin, H.H., Osterman-Golkar, S., Zorcec. V. Tomqvist, M. (1996) Biomonitoring of epichlorohydrin by hemoglobin adducts. Anal. Biochem., 240, 1-6... [Pg.623]

It has been proposed to use hemoglobin adducts in biomonitoring, as a dosimeter for the biologically active dose of arylamines/arylacetamides. This may also provide information about the individual susceptibility to the toxic and carcinogenic effects of these chemicals30,31. Field workers exposed to Propanil (38), a major herbicide in rice paddies,... [Pg.649]

Zhou QX, Ye CL (2008) Ionic liquid for improved single-drop microextraction of aromatic amines in water samples. Microchim Acta 162(1-2) 153-159. doi 10.1007/s00604-007-0857-l Zwimer-Baier 1, Deckart K, Jackh R, Neumann HG (2003) Biomonitoring of aromatic amines VI determination of hemoglobin adducts after feeding aniline hydrochloride in the diet of rats for 4 weeks. Arch Toxicol 77 672-677. doi 10.1007/s00204-003-0473-8... [Pg.346]

Neumann, H. G. 1988. Biomonitoring of aromatic amines and alkylating agents by measuring hemoglobin adducts. Int. Arch. Occup. Environ. Health 60 151-155. [Pg.150]

Acrylamide is genotoxic in a number of test systems. It induces gene mutation, structural chromosomal aberrations, sister chromatid exchange, and cell transformation. Furthermore, acrylamide forms covalent adducts with DNA in rodents and covalent adducts with hemoglobin in humans. Flemoglobin adducts have been used for biomonitoring of acrylamide. Studies indicate that the adducts are useful predictors of acrylamide-induced peripheral neuropathy. ... [Pg.26]

Figure 4. Persistence of sulfur mustard adduct to N-terminal valine residue of hemoglobin in blood of a marmoset after sulfur mustard administration (4.1 mg/kg, i.v.) at t = 0. At the time points indicated blood samples were collected, globin was isolated and analyzed by using the modified Edman degradation for determination of the N-terminal valine adduct. Globin from human blood exposed to ris-sulfur mustard (10 iM) was used as an internal standard. (Reprinted from Toxicology and Applied Pharmacology, Vol. 184, D. Noort, H.P. Benschop and R.M. Black, Biomonitoring of Exposure to Chemical Warfare Agents A Review, pages 116-126 (2002), with permission from Elsevier Science.)... Figure 4. Persistence of sulfur mustard adduct to N-terminal valine residue of hemoglobin in blood of a marmoset after sulfur mustard administration (4.1 mg/kg, i.v.) at t = 0. At the time points indicated blood samples were collected, globin was isolated and analyzed by using the modified Edman degradation for determination of the N-terminal valine adduct. Globin from human blood exposed to ris-sulfur mustard (10 iM) was used as an internal standard. (Reprinted from Toxicology and Applied Pharmacology, Vol. 184, D. Noort, H.P. Benschop and R.M. Black, Biomonitoring of Exposure to Chemical Warfare Agents A Review, pages 116-126 (2002), with permission from Elsevier Science.)...
Fidder A, Noort D, Hulst AG, de Jong LPA, Benschop HP. Biomonitoring of exposure to lewisite based on adducts to hemoglobin. Arch Toxicol, 2000 74 207-214. [Pg.543]

See other pages where Hemoglobin adduct biomonitoring is mentioned: [Pg.305]    [Pg.317]    [Pg.338]    [Pg.204]    [Pg.434]    [Pg.51]    [Pg.72]    [Pg.76]    [Pg.113]   
See also in sourсe #XX -- [ Pg.649 , Pg.667 ]



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