-
Je něco špatně v tomto záznamu ?
Efficacy of structural homoloques and isomers of pralidoxime in reactivation of immobilised acetylcholinesterase inhibited with sarin, cyclosarin and soman
M. Hoskovcova, E. Halamek, Z. Kobliha
Jazyk angličtina Země Švédsko
Typ dokumentu časopisecké články
PubMed
20027163
Knihovny.cz E-zdroje
- MeSH
- acetylcholinesterasa metabolismus MeSH
- biosenzitivní techniky MeSH
- cholinesterasové inhibitory chemie toxicita MeSH
- enzymy imobilizované antagonisté a inhibitory metabolismus MeSH
- isomerie MeSH
- organofosforové sloučeniny chemie farmakologie MeSH
- oximy chemie farmakologie MeSH
- pralidoximové sloučeniny chemie farmakologie MeSH
- reaktivátory cholinesterázy chemie farmakologie MeSH
- sarin toxicita MeSH
- soman toxicita MeSH
- Publikační typ
- časopisecké články MeSH
OBJECTIVES: Quantification of efficacy of monopyridinium isomers and homologs derived from clinically used Pralidoxime within reactivation of acetylcholinesterase inhibited with organophosphorus nerve agents. METHODS: This work uses the colorimetric biosensor called Detehit - cotton cloth with immobilized enzyme acetylcholinesterase. Biosensor is based on the modificated Ellman's method. RESULTS: The highest reactivation was observed with sarin-inhibited acetylcholinesterase. Substantially lower reactivation was found with the cyclosarin-inhibited enzyme whereas AChE, inhibited by soman could not be effectively reactivated under the given conditions (enzyme inhibition for 2 minutes and subsequent treatment with the reactivator for 15 minutes). CONCLUSION: Our work gives comparison of efficacy of reactivators in dependence on the length of alkylene chain and position of aldoxime functional group. Evaluation of effectivity of aldoxime reactivators is provided by simple means. The method allows rapid in vitro evaluation of the reactivators without being disturbed by excess of the organophosphate or reactivator.
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12025379
- 003
- CZ-PrNML
- 005
- 20130129065418.0
- 007
- ta
- 008
- 120816s2009 sw f 000 0#eng||
- 009
- AR
- 035 __
- $a (PubMed)20027163
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sw
- 100 1_
- $a Hoskovcová, Monika $7 xx0128579 $u University of Defence, Institute od NBC Defence, Czech Republic. monika.hoskovcova@unob.cz
- 245 10
- $a Efficacy of structural homoloques and isomers of pralidoxime in reactivation of immobilised acetylcholinesterase inhibited with sarin, cyclosarin and soman / $c M. Hoskovcova, E. Halamek, Z. Kobliha
- 520 9_
- $a OBJECTIVES: Quantification of efficacy of monopyridinium isomers and homologs derived from clinically used Pralidoxime within reactivation of acetylcholinesterase inhibited with organophosphorus nerve agents. METHODS: This work uses the colorimetric biosensor called Detehit - cotton cloth with immobilized enzyme acetylcholinesterase. Biosensor is based on the modificated Ellman's method. RESULTS: The highest reactivation was observed with sarin-inhibited acetylcholinesterase. Substantially lower reactivation was found with the cyclosarin-inhibited enzyme whereas AChE, inhibited by soman could not be effectively reactivated under the given conditions (enzyme inhibition for 2 minutes and subsequent treatment with the reactivator for 15 minutes). CONCLUSION: Our work gives comparison of efficacy of reactivators in dependence on the length of alkylene chain and position of aldoxime functional group. Evaluation of effectivity of aldoxime reactivators is provided by simple means. The method allows rapid in vitro evaluation of the reactivators without being disturbed by excess of the organophosphate or reactivator.
- 650 _2
- $a acetylcholinesterasa $x metabolismus $7 D000110
- 650 _2
- $a biosenzitivní techniky $7 D015374
- 650 _2
- $a cholinesterasové inhibitory $x chemie $x toxicita $7 D002800
- 650 _2
- $a reaktivátory cholinesterázy $x chemie $x farmakologie $7 D002801
- 650 _2
- $a enzymy imobilizované $x antagonisté a inhibitory $x metabolismus $7 D004800
- 650 _2
- $a isomerie $7 D007536
- 650 _2
- $a organofosforové sloučeniny $x chemie $x farmakologie $7 D009943
- 650 _2
- $a oximy $x chemie $x farmakologie $7 D010091
- 650 _2
- $a pralidoximové sloučeniny $x chemie $x farmakologie $7 D011220
- 650 _2
- $a sarin $x toxicita $7 D012524
- 650 _2
- $a soman $x toxicita $7 D012999
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Halámek, Emil $7 xx0001011
- 700 1#
- $a Kobliha, Zbyněk. $7 _AN043412
- 773 0_
- $w MED00168352 $t Neuro endocrinology letters $x 0172-780X $g Roč. 30 Suppl 1(2009), s. 152-155
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/20027163 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m
- 990 __
- $a 20120816 $b ABA008
- 991 __
- $a 20130129065554 $b ABA008
- 999 __
- $a ok $b bmc $g 947421 $s 782725
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2009 $b 30 Suppl 1 $d 152-155 $i 0172-780X $m Neuro-endocrinology letters $n Neuro-endocrinol. lett. $x MED00168352
- LZP __
- $a Pubmed-20120816/10/02