-
Something wrong with this record ?
In vivo decontamination of the nerve agent VX using the domestic swine model
J. Misik, M. Pavlik, L. Novotny, R. Pavlikova, RP. Chilcott, J. Cabal, K. Kuca,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Chemical Warfare Agents poisoning MeSH
- Cholinesterases metabolism MeSH
- Decontamination methods MeSH
- Organothiophosphorus Compounds poisoning MeSH
- Sus scrofa MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The purpose of this in vivo study was to assess a new, putatively optimised method for mass casualty decontamination ("ORCHIDS protocol") for effectiveness in removing the chemical warfare agent VX from the skin of anaesthetised, domestic white pigs. ORCHIDS protocol consists of a 1.5-minute shower with a mild detergent (Argos™) supplemented by physical removal. A standard method of wet decontamination was used for comparison. Experimental animals were divided into four groups (A-D). Two groups were exposed to a supra-lethal percutaneous dose (5 × LD(50); 300 μg kg(-1)) of VX for 1 h prior to decontamination with either the ORCHIDS (C) or standard protocol (D). A third (B, positive control) group was exposed but not subject to decontamination. Blank controls (A) received anaesthesia and the corresponding dose of normal saline instead of VX. Observations of the clinical signs of intoxication were supplemented by measurements of whole blood cholinesterase (ChE) performed on samples of arterial blood acquired at 30-minute intervals for the duration of the study (up to 6 h). Untreated (B) animals displayed typical cholinergic signs consistent with VX intoxication (local fasciculation, mastication, salivation, pilo-erection and motor convulsions) and died 165-240 min post exposure. All animals in both decontamination treatment groups (C, D) survived the duration of the study and exhibited less severe signs of cholinergic poisoning. Thus, both the standard and ORCHIDS protocol were demonstrably effective against exposure to the potent nerve agent VX, even after a delay of 1 h. A critical advantage of the ORCHIDS protocol is the relatively short shower duration (1½ min compared to 3 min). In practice, this could substantially improve the rate at which individuals could be decontaminated by emergency responders following exposure to toxic materials such as chemical warfare agents.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13000591
- 003
- CZ-PrNML
- 005
- 20130109112034.0
- 007
- ta
- 008
- 130108s2012 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3109/15563650.2012.720986 $2 doi
- 035 __
- $a (PubMed)22963275
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Misik, Jan $u Faculty of Military Health Sciences, Department of Toxicology, University of Defence, Trebesska, Hradec Kralove, Czech Republic. misik@pmfhk.cz
- 245 10
- $a In vivo decontamination of the nerve agent VX using the domestic swine model / $c J. Misik, M. Pavlik, L. Novotny, R. Pavlikova, RP. Chilcott, J. Cabal, K. Kuca,
- 520 9_
- $a The purpose of this in vivo study was to assess a new, putatively optimised method for mass casualty decontamination ("ORCHIDS protocol") for effectiveness in removing the chemical warfare agent VX from the skin of anaesthetised, domestic white pigs. ORCHIDS protocol consists of a 1.5-minute shower with a mild detergent (Argos™) supplemented by physical removal. A standard method of wet decontamination was used for comparison. Experimental animals were divided into four groups (A-D). Two groups were exposed to a supra-lethal percutaneous dose (5 × LD(50); 300 μg kg(-1)) of VX for 1 h prior to decontamination with either the ORCHIDS (C) or standard protocol (D). A third (B, positive control) group was exposed but not subject to decontamination. Blank controls (A) received anaesthesia and the corresponding dose of normal saline instead of VX. Observations of the clinical signs of intoxication were supplemented by measurements of whole blood cholinesterase (ChE) performed on samples of arterial blood acquired at 30-minute intervals for the duration of the study (up to 6 h). Untreated (B) animals displayed typical cholinergic signs consistent with VX intoxication (local fasciculation, mastication, salivation, pilo-erection and motor convulsions) and died 165-240 min post exposure. All animals in both decontamination treatment groups (C, D) survived the duration of the study and exhibited less severe signs of cholinergic poisoning. Thus, both the standard and ORCHIDS protocol were demonstrably effective against exposure to the potent nerve agent VX, even after a delay of 1 h. A critical advantage of the ORCHIDS protocol is the relatively short shower duration (1½ min compared to 3 min). In practice, this could substantially improve the rate at which individuals could be decontaminated by emergency responders following exposure to toxic materials such as chemical warfare agents.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a chemické bojové látky $x otrava $7 D002619
- 650 _2
- $a cholinesterasy $x metabolismus $7 D002802
- 650 _2
- $a dekontaminace $x metody $7 D003666
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a organothiofosforové sloučeniny $x otrava $7 D009946
- 650 _2
- $a Sus scrofa $7 D034421
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pavlik, Michal
- 700 1_
- $a Novotny, Ladislav
- 700 1_
- $a Pavlikova, Ruzena
- 700 1_
- $a Chilcott, Robert P
- 700 1_
- $a Cabal, Jiri
- 700 1_
- $a Kuca, Kamil
- 773 0_
- $w MED00013938 $t Clinical toxicology (Philadelphia, Pa.) $x 1556-9519 $g Roč. 50, č. 9 (2012), s. 807-11
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22963275 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20130108 $b ABA008
- 991 __
- $a 20130109112139 $b ABA008
- 999 __
- $a ok $b bmc $g 963373 $s 798755
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 50 $c 9 $d 807-11 $i 1556-9519 $m Clinical toxicology $n Clin Toxicol (Phila) $x MED00013938
- LZP __
- $a Pubmed-20130108