Toxicology and Applied Pharmacology 1984-06-30

Experimental delayed hypersensitivity following inhalation of dicyclohexylmethane-4,4'-diisocyanate: a concentration-response relationship.

J Stadler, M H Karol

Index: Toxicol. Appl. Pharmacol. 74(2) , 244-9, (1984)

Full Text: HTML

Abstract

Exposure of workers to low-molecular-weight chemicals has been associated with delayed-onset hypersensitivity reactions in both the skin and the respiratory tract. The use of two animal models to examine factors affecting the production of delayed hypersensitivity to dicyclohexylmethane-4,4'-diisocyanate (HMDI) is described. Guinea pigs were exposed to HMDI by a "head-only" method and mice in a "nose-only" procedure. All animals were subsequently tested for dermal sensitivity by topical challenge with the isocyanate. In both species, a concentration-response relationship and "no-effect" concentration was observed between chamber concentration of HMDI and (a) severity of the dermal response and (b) number of animals responding. Guinea pigs developed skin sensitivity following inhalation of 3 micrograms/liter or greater HMDI for 2 hr/day on 3 consecutive days. Inhalation of 1.25 micrograms/liter did not result in sensitization. Contact sensitivity was detected in BALB/cBy mice following inhalation of 17 micrograms/liter or greater HMDI. No reactions occurred as a result of exposure to 7 micrograms/liter or less HMDI. Dermal contact of the head, as would occur during inhalation exposures, also resulted in contact sensitization. Identification of the concentration-response relationship for contact sensitization following inhalation exposure implies that safe exposure levels can be proposed to prevent cases of dermal sensitization to HMDI.


Related Compounds

Related Articles:

Multiple shape memory polymers based on laminates formed from thiol-click chemistry based polymerizations.

2015-09-14

[Soft Matter 11 , 6852-8, (2015)]

Functionalization of graphene oxide nanostructures improves photoluminescence and facilitates their use as optical probes in preclinical imaging.

2015-06-21

[Nanoscale 7 , 10410-20, (2015)]

Fabrication of chiral amino acid ionic liquid modified magnetic multifunctional nanospheres for centrifugal chiral chromatography separation of racemates.

2015-06-26

[J. Chromatogr. A. 1400 , 40-6, (2015)]

Degradation studies on segmented polyurethanes prepared with HMDI, PCL and different chain extenders.

2010-06-01

[Acta Biomater. 6(6) , 2035-44, (2010)]

Preparation and surface characterization of HMDI-activated 316L stainless steel for coronary artery stents.

2008-06-01

[J. Biomed. Mater. Res. A 85(3) , 722-30, (2008)]

More Articles...