Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr

Objective: The lethal dose 50 (LD50) of  lorazepam in albino mice (Musmusculus), swiss ICR strain, was determined as a first step in the study of the conjoint toxicity of admixtures of scopolamine and benzodiazepines ("new burundanga"). Method: Sixty adult male mice were randomly assigned...

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Main Authors: Francisco Alejandro Múnera G., Miguel Eduardo Martínez S., Manuel Joaquín Rojas B., Ana Janeth Mora C., Carlos Moreno B.
Format: Article
Language:English
Published: Universidad Nacional de Colombia 2000-10-01
Series:Revista de la Facultad de Medicina
Subjects:
Online Access:https://revistas.unal.edu.co/index.php/revfacmed/article/view/19629
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spelling doaj-7d73a82470aa4cb5a69b69d89b8f84652020-11-24T23:46:20ZengUniversidad Nacional de ColombiaRevista de la Facultad de Medicina0120-00112357-38482000-10-0148419019417872Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icrFrancisco Alejandro Múnera G.Miguel Eduardo Martínez S.Manuel Joaquín Rojas B.Ana Janeth Mora C.Carlos Moreno B.Objective: The lethal dose 50 (LD50) of  lorazepam in albino mice (Musmusculus), swiss ICR strain, was determined as a first step in the study of the conjoint toxicity of admixtures of scopolamine and benzodiazepines ("new burundanga"). Method: Sixty adult male mice were randomly assigned to five experimental groups and to a control one. The dose of lorazepam administered intraperitoneally to each group was: group 1,10 mg kg_1; group 11,20 mg kgI; group 111,40mg kgL; group IV,80mgkg'; group V,160mg kg-l.The control group received only the vehicle solution. Mortality was recorded during 15 days after injection. Necropsies were performed to all the mice dead during the assay and to the survivors. Data were processed using probit analysis and survival analysis. Results: Estimated LD50 were 90.71 mg kg- 1, with 95% confidence range of 65,02to 150,13mg kg- 1.Deaths occurred within the first six days after injection of doses higher than 80 mg kg:', mostly during the first 48 hours. Conclusions: The estimated LD50 of  lorazepam in this experiment almost doubles the reported one, this finding suggests a higher resistance of the mice strain used in this experiment The critic period for lorazepam poisoning spans the first 48 hours.https://revistas.unal.edu.co/index.php/revfacmed/article/view/19629DL50 lorazepamdosis letalratonesmortalidadescopolaminafármacosintoxicaciones
collection DOAJ
language English
format Article
sources DOAJ
author Francisco Alejandro Múnera G.
Miguel Eduardo Martínez S.
Manuel Joaquín Rojas B.
Ana Janeth Mora C.
Carlos Moreno B.
spellingShingle Francisco Alejandro Múnera G.
Miguel Eduardo Martínez S.
Manuel Joaquín Rojas B.
Ana Janeth Mora C.
Carlos Moreno B.
Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
Revista de la Facultad de Medicina
DL50 lorazepam
dosis letal
ratones
mortalidad
escopolamina
fármacos
intoxicaciones
author_facet Francisco Alejandro Múnera G.
Miguel Eduardo Martínez S.
Manuel Joaquín Rojas B.
Ana Janeth Mora C.
Carlos Moreno B.
author_sort Francisco Alejandro Múnera G.
title Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
title_short Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
title_full Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
title_fullStr Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
title_full_unstemmed Dosis letal 50 de lorazepam en ratón (Mus musculus) Albino, cepa suizo-icr
title_sort dosis letal 50 de lorazepam en ratón (mus musculus) albino, cepa suizo-icr
publisher Universidad Nacional de Colombia
series Revista de la Facultad de Medicina
issn 0120-0011
2357-3848
publishDate 2000-10-01
description Objective: The lethal dose 50 (LD50) of  lorazepam in albino mice (Musmusculus), swiss ICR strain, was determined as a first step in the study of the conjoint toxicity of admixtures of scopolamine and benzodiazepines ("new burundanga"). Method: Sixty adult male mice were randomly assigned to five experimental groups and to a control one. The dose of lorazepam administered intraperitoneally to each group was: group 1,10 mg kg_1; group 11,20 mg kgI; group 111,40mg kgL; group IV,80mgkg'; group V,160mg kg-l.The control group received only the vehicle solution. Mortality was recorded during 15 days after injection. Necropsies were performed to all the mice dead during the assay and to the survivors. Data were processed using probit analysis and survival analysis. Results: Estimated LD50 were 90.71 mg kg- 1, with 95% confidence range of 65,02to 150,13mg kg- 1.Deaths occurred within the first six days after injection of doses higher than 80 mg kg:', mostly during the first 48 hours. Conclusions: The estimated LD50 of  lorazepam in this experiment almost doubles the reported one, this finding suggests a higher resistance of the mice strain used in this experiment The critic period for lorazepam poisoning spans the first 48 hours.
topic DL50 lorazepam
dosis letal
ratones
mortalidad
escopolamina
fármacos
intoxicaciones
url https://revistas.unal.edu.co/index.php/revfacmed/article/view/19629
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