Identification and characterisation of adducts between serum albumin and 4,4'-methylenediphenyl diisocyanate (MDI) in human plasma

• Published in: Archives of toxicology Vol. 78; no. 7; pp. 378 - 383
• Main Authors: JOHANNESSON, G, SENNBRO, C. J, WILLIX, P, LINDH, C. H, JÖNSSON, B. A. G
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.07.2004; Springer Nature B.V
• Subjects: Basic Medicine; Biological and medical sciences; Chromatography, Gel; Chromatography, Ion Exchange; Farmakologi och toxikologi; Female; Humans; Immunoblotting; Immunoglobulin G - blood; Isocyanates - blood; Isocyanates - immunology; Male; Mass Spectrometry; Medical and Health Sciences; Medical sciences; Medicin och hälsovetenskap; Medicinska och farmaceutiska grundvetenskaper; Occupational Exposure; Pharmacology and Toxicology; Protein Binding; Proteins; Serum Albumin - metabolism; Toxicology; Trypsin - metabolism; Human; Isocyanates; Organic diisocyanate; Antibody; Isocyanate; Polyurethane; Albumin; Serum albumin; Molecular adduct; Adduct; Blood plasma
• ISSN: 0340-5761; 1432-0738
• DOI: 10.1007/s00204-004-0555-2

Diisocyanates are potent inducers of airways disease. Methylenediphenyl diisocyanate (MDI) is a widely used diisocyanate in the chemical industry. The aim of this study was to identify major and also immunologically relevant protein conjugates of MDI in plasma. Plasma was obtained from an MDI-exposed worker. The plasma was dialysed and then fractionated using ion exchange chromatography (IEC) and gel filtration. These fractions and also aliquots of unfractioned plasma were hydrolysed, derivatised and analysed for isocyanate adduct content using gas chromatography-mass spectrometry. In addition, immunologically relevant proteins were identified through specific IgG immunoblotting using pooled sera from two exposed workers. It was shown by dialysis that 96% of the hydrolysed MDI derivatives were protein bound and that 95% of the MDI adducts co-eluted with serum albumin in plasma using IEC. All MDI-protein adducts co-eluted with serum albumin using gel filtration. IgG immunoblotting showed a major 66 kDa protein and also some intermolecular reactions in serum albumin. This study shows serum albumin to be the major protein in plasma that forms adducts in vivo with MDI. Thus, a quick and simple quantitative method for biological monitoring may be developed for MDI exposure. The results also showed that MDI-specific IgG antibodies preferentially bind to the serum albumin in in-vitro-synthesised MDI-plasma protein conjugates.