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1.
J Hazard Mater ; 196: 115-22, 2011 Nov 30.
Artigo em Inglês | MEDLINE | ID: mdl-21944706

RESUMO

Bench-scale testing was used to evaluate the efficacy of four decontamination formulations on typical indoor surfaces following exposure to the liquid chemical warfare agents sarin (GB), soman (GD), sulfur mustard (HD), and VX. Residual surface contamination on coupons was periodically measured for up to 24h after applying one of four selected decontamination technologies [0.5% bleach solution with trisodium phosphate, Allen Vanguard Surface Decontamination Foam (SDF™), U.S. military Decon Green™, and Modec Inc. and EnviroFoam Technologies Sandia Decontamination Foam (DF-200)]. All decontamination technologies tested, except for the bleach solution, performed well on nonporous and nonpermeable glass and stainless-steel surfaces. However, chemical agent residual contamination typically remained on porous and permeable surfaces, especially for the more persistent agents, HD and VX. Solvent-based Decon Green™ performed better than aqueous-based bleach or foams on polymeric surfaces, possibly because the solvent is able to penetrate the polymer matrix. Bleach and foams out-performed Decon Green for penetrating the highly polar concrete surface. Results suggest that the different characteristics needed for an ideal and universal decontamination technology may be incompatible in a single formulation and a strategy for decontaminating a complex facility will require a range of technologies.


Assuntos
Clareadores/química , Substâncias para a Guerra Química/análise , Descontaminação/métodos , Poluentes Ambientais/análise , Habitação/normas , Oxirredução , Projetos Piloto , Propriedades de Superfície
2.
Hum Ecol Risk Assess ; 17(1): 2-56, 2011 Feb 13.
Artigo em Inglês | MEDLINE | ID: mdl-21390292

RESUMO

In the event of a chemical terrorist attack on a transportation hub, post-event remediation and restoration activities necessary to attain unrestricted facility reuse and re-entry could require hours to multiple days. While restoration timeframes are dependent on numerous variables, a primary controlling factor is the level of pre-planning and decision-making completed prior to chemical terrorist release. What follows is the first of a two-part analysis identifying key considerations, critical information, and decision criteria to facilitate post-attack and post-decontamination consequence management activities. A conceptual site model and human health-based exposure guidelines are developed and reported as an aid to site-specific pre-planning in the current absence of U.S. state or Federal values designated as compound-specific remediation or re-entry concentrations, and to safely expedite facility recovery to full operational status. Chemicals of concern include chemical warfare nerve and vesicant agents and the toxic industrial compounds phosgene, hydrogen cyanide, and cyanogen chloride. This work has been performed as a national case study conducted in partnership with the Los Angeles International Airport and The Bradley International Terminal. All recommended guidelines have been selected for consistency with airport scenario release parameters of a one-time, short-duration, finite airborne release from a single source followed by compound-specific decontamination.

3.
Bioorg Chem ; 35(1): 50-8, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16949126

RESUMO

A systematically generated series of hydrazones were analyzed as potential inhibitors of anthrax lethal factor. The hydrazones were screened using one UV-based and two fluorescence-based in vitro assays. The study identified several inhibitors with IC50 values in the micromolar range, and importantly, significant differences in the types of inhibition were observed with the different assays.


Assuntos
Antígenos de Bactérias/química , Toxinas Bacterianas/química , Inibidores Enzimáticos/química , Hidrazonas/química , Aldeídos/química , Bacillus anthracis/química , Bacillus anthracis/enzimologia , Toxinas Bacterianas/antagonistas & inibidores , Catálise , Inibidores Enzimáticos/farmacologia , Hidrazinas/química , Hidrazonas/farmacologia , Cinética , Quinases de Proteína Quinase Ativadas por Mitógeno/antagonistas & inibidores , Quinases de Proteína Quinase Ativadas por Mitógeno/química , Estrutura Molecular , Relação Estrutura-Atividade
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