نتایج جستجو برای: sarin

تعداد نتایج: 592  

Journal: :Forensic science review 2014
A T Tu

The radical religious group Aum Shinrikyo was founded in Japan in the 1980s and grew rapidly in the 1990s. Aum members perpetrated a mass murder in Matsumoto City in 1994, where they used sarin as a chemical weapon to poison approximately 500 civilians. On March 20, 1995, Aum deployed sarin in an even larger terrorist attack on the Tokyo Subway System, which poisoned some 6,000 people. After th...

2015
Yong Pan Ning Mu Shengyu Shao Liu Yang Wen Wang Xiao Xie Shitang He

Self-assembly and molecular imprinting technologies are very attractive technologies for the development of artificial recognition systems and provide chemical recognition based on need and not happenstance. In this paper, we employed a b-cyclodextrin derivative surface acoustic wave (SAW) chemical sensor for detecting the chemical warfare agents (CWAs) sarin (O-Isoprophyl methylphosphonofluori...

2015
Yong Pan Shengyu Shao Wen Wang Xiao Xie Shitang He

Self-assembly and molecular imprinting technologies are very attractive technologies for the development of artificial recognition systems and provide chemical recognition based on need and not happenstance. In this paper, we employed a β-cyclodextrin derivative surface acoustic wave (SAW) chemical sensor for detecting the chemical warfare agents (CWAs) sarin (O-Isoprophyl methylphosphonofluori...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2015
A Gore R Brandeis I Egoz J Turetz U Nili E Grauer E Bloch-Shilderman

Eye exposure to the extremely toxic organophosphorus sarin results in long-term miosis and visual impairment. As current treatment using atropine or homatropine eye drops may lead to considerable visual side effects, alternative combined treatments of intramuscular (im) oximes (16.8 µmol/kg, im) with atropine (0.5 mg/kg, im) or with the short acting antimuscarinic tropicamide (0.5%; w/v) eye dr...

Journal: :Arhiv za higijenu rada i toksikologiju 2009
Ante Vucemilović Mirko Hadzija Ivan Jukić

Our Institute's nuclear, biological, and chemical defense research team continuously investigates and develops preparations for skin decontamination against nerve agents. In this in vivo study, we evaluated skin decontamination efficacy against sarin by a synthetic preparation called Mineral Cationic Carrier (MCC) with known ion exchange, absorption efficacy and bioactive potential. Mice were t...

Journal: :Lab on a chip 2008
Hsih Yin Tan Weng Keong Loke Yong Teng Tan Nam-Trung Nguyen

Sarin (C(4)H(10)FO(2)P,O-isopropyl methylphosphonofluoridate) is a colourless, odourless and highly toxic phosphonate that acts as a cholinesterase inhibitor and disrupts neuromuscular transmission. Sarin and related phosphonates are chemical warfare agents, and there is a possibility of their application in a military or terrorist attack. This paper reports a lab-on-a-chip device for detecting...

Journal: :Toxicology letters 2011
Manojkumar Valiyaveettil Yonas Alamneh Peter Rezk Michael W Perkins Alfred M Sciuto Bhupendra P Doctor Madhusoodana P Nambiar

To explore the efficacy of paraoxonase 1 (PON1) as a catalytic bioscavenger, we evaluated human recombinant PON1 (rePON1) expressed in Trichoplusia ni larvae against sarin and soman toxicity using microinstillation inhalation exposure in guinea pigs. Animals were pretreated intravenously with catalytically active rePON1, followed by exposure to 1.2 X LCt₅₀ sarin or soman. Administration of 5 un...

Journal: :Journal of Synthetic Organic Chemistry, Japan 1995

Journal: :Nihon Shuchu Chiryo Igakukai zasshi 1997

2003
TJERK J. H. BUETERS MARLOES J. A. JOOSEN MEINDERT DANHOF

The objective of the present study was to develop a kinetics of pharmacodynamics model to properly describe and investigate the in vivo interaction between the selective adenosine A1 agonist N-cyclopentyladenosine (CPA), acetylcholinesterase (AChE) in blood and brain, and the AChE-inhibitor sarin (isopropylmethylphosphonofluoridate). The direct interaction of CPA (2 M) on the inhibition of AChE...

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