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The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom
In Iran intramuscular (IM) administration of antivenoms is used for the treatment of human scorpion envenoming of six medically dangerous scorpion species, including Odonthubuthus doriae (O. doriae). The purpose of the current study is to investigate the efficiency of the intramuscular route and the...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Library Publishing Media
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086193/ https://www.ncbi.nlm.nih.gov/pubmed/21544182 |
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author | Jalali, Amir Moazen, Sara Babaee, Mohammad Dadashzade, Simin Droudi, Alireza |
author_facet | Jalali, Amir Moazen, Sara Babaee, Mohammad Dadashzade, Simin Droudi, Alireza |
author_sort | Jalali, Amir |
collection | PubMed |
description | In Iran intramuscular (IM) administration of antivenoms is used for the treatment of human scorpion envenoming of six medically dangerous scorpion species, including Odonthubuthus doriae (O. doriae). The purpose of the current study is to investigate the efficiency of the intramuscular route and the delay of injection on the neutralizing effect of the available polyvalent antivenom. We compared the pharmacokinetics parameters of O. doriae venom and its antivenom. 5µg (131)I-labeled venom and 0.2µl of antivenom were administered via subcutaneous (SC) or IM into rats. Blood samples were taken at various predetermined time intervals during a 24hr period for the venom and a 360min period for the antivenom. The radio-iodination was carried out using the chloramin-T method. The results showed that pharmacokinetic parameters of the venom were T(1/2) = 496.53min; V(d) = 1522ml/kg; Cl = 2.12 ml/kg/min; mean resident residual time (MRT) = 555.77min, and for the antivenom T(1/2) = 902.13min, V(d) = 666.66 ml/kg , Cl = 0.512 ml/kg/min and MRT = 1292min. The total body clearance of the venom is relatively low in agreement with a high mean residence time. Higher AUC and C(max) values for the antivenom as well as its longer residence time indicate that the venom and antivenom are expected to have enough opportunity to interact in the tissue compartments. Over, this study suggests that the intramuscular administration of a single dose of antivenom (2 vials each of 5ml) based on current protocol in Iran is a suitable route for the treatment of envenomation with O. doriae. Prudently, further clinical studies with similar aims need to be carried out to confirm these findings in human victims. |
format | Text |
id | pubmed-3086193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Library Publishing Media |
record_format | MEDLINE/PubMed |
spelling | pubmed-30861932011-05-04 The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom Jalali, Amir Moazen, Sara Babaee, Mohammad Dadashzade, Simin Droudi, Alireza J Venom Res Research Report In Iran intramuscular (IM) administration of antivenoms is used for the treatment of human scorpion envenoming of six medically dangerous scorpion species, including Odonthubuthus doriae (O. doriae). The purpose of the current study is to investigate the efficiency of the intramuscular route and the delay of injection on the neutralizing effect of the available polyvalent antivenom. We compared the pharmacokinetics parameters of O. doriae venom and its antivenom. 5µg (131)I-labeled venom and 0.2µl of antivenom were administered via subcutaneous (SC) or IM into rats. Blood samples were taken at various predetermined time intervals during a 24hr period for the venom and a 360min period for the antivenom. The radio-iodination was carried out using the chloramin-T method. The results showed that pharmacokinetic parameters of the venom were T(1/2) = 496.53min; V(d) = 1522ml/kg; Cl = 2.12 ml/kg/min; mean resident residual time (MRT) = 555.77min, and for the antivenom T(1/2) = 902.13min, V(d) = 666.66 ml/kg , Cl = 0.512 ml/kg/min and MRT = 1292min. The total body clearance of the venom is relatively low in agreement with a high mean residence time. Higher AUC and C(max) values for the antivenom as well as its longer residence time indicate that the venom and antivenom are expected to have enough opportunity to interact in the tissue compartments. Over, this study suggests that the intramuscular administration of a single dose of antivenom (2 vials each of 5ml) based on current protocol in Iran is a suitable route for the treatment of envenomation with O. doriae. Prudently, further clinical studies with similar aims need to be carried out to confirm these findings in human victims. Library Publishing Media 2010-10-15 /pmc/articles/PMC3086193/ /pubmed/21544182 Text en ©The Authors http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an open access article, published under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/). This license permits non-commercial use, distribution and reproduction of the article, provided the original work is appropriately acknowledged with correct citation details. |
spellingShingle | Research Report Jalali, Amir Moazen, Sara Babaee, Mohammad Dadashzade, Simin Droudi, Alireza The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title | The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title_full | The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title_fullStr | The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title_full_unstemmed | The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title_short | The pharmacokinetics of Iranian scorpion Odonthubuthus doriae venom and the available antivenom |
title_sort | pharmacokinetics of iranian scorpion odonthubuthus doriae venom and the available antivenom |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3086193/ https://www.ncbi.nlm.nih.gov/pubmed/21544182 |
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