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U.S. Department of Energy
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Medical Research and Evaluation Facility (MREF) and studies supporting the medical chemical defense program on task 89-03: Test up to 20 candidate topical protectants. Final report, October 1989-February 1992

Technical Report ·
OSTI ID:544426
Fourteen candidate topical skin protectants (TSPs) were examined in a multiple-phase testing regimen that included a variety of testing models designed to assess different aspects of TSP efficacy. Phase I initial efficacy tests were performed using both in vitro and in vivo models. The Phase I in vitro model involved determining the penetration profile of a challenge dose of chemical surety materiel (CSM), either soman (GD), VX, or thickened soman (TGD), through a 0.1 mm thick film of TSP layered between two disks of synthetic membrane. The in vivo models were performed in New Zealand White rabbits pretreated with 0.1 mm thick layers of TSP. Following topical application of an organophosphonate challenge (TGD) on rabbits, the end point for determining TSP efficacy was erythrocyte acetylcholinesterase inhibition profiles. Following topical application of a vesicant challenge (HD), the end point for TSP efficacy was the size of the lesion resulting after prescribed exposure periods.
Research Organization:
Battelle Memorial Inst., Columbus, OH (United States)
OSTI ID:
544426
Report Number(s):
AD-B--162425/3/XAB; CNN: Contract DAMD17-89-C-9050
Country of Publication:
United States
Language:
English