Enzyme immunoassays in brown snake (Pseudonaja spp.) envenoming:: Detecting venom, antivenom and venom-antivenom complexes

被引:38
作者
O'Leary, Margaret A.
Isbister, Geoffrey K.
Schneider, Jennifer J.
Brown, Simon G. A.
Currie, Bart J.
机构
[1] Newcastle Mater Hosp, Dept Clin Toxicol & Pharmacol, Waratah, NSW 2298, Australia
[2] Univ Newcastle, Discipline Clin Pharmacol, Newcastle, NSW 2308, Australia
[3] Charles Darwin Univ, Menzies Sch Hlth Res, Trop & Emergency Infect Dis Div, Darwin, NT, Australia
[4] Univ Newcastle, Sch Biomed Sci, Newcastle, NSW 2308, Australia
[5] Univ Western Australia, Discipline Emergency Med, Perth, WA 6009, Australia
[6] Fremantle Hosp, Perth, WA 6009, Australia
[7] Flinders Univ S Australia, Royal Darwin Hosp, No Terr Clin Sch, Adelaide, SA 5001, Australia
基金
英国医学研究理事会;
关键词
venom; Pseudonaja; ELISA; antivenom; envenoming;
D O I
10.1016/j.toxicon.2006.04.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although a commercial snake venom detection kit (SVDK) is available to distinguish between the five major snake groups in Australia, there is no assay for quantifying venom or antivenom concentrations in envenomed patients. Serum samples were obtained from patients with brown snake (Pseudonaja spp.) envenoming before and after the administration of antivenom and patients with suspected brown snake bites but no evidence of envenoming. Enzyme immunoassays (EIAs) were developed for free venom, free antivenom and the venom-antivenom complex. Standard samples measured in duplicate had a coefficient of variation of less than 10%. The EIA for venom was able to detect brown snake venom down to concentrations of 3ng/mL. A high baseline absorbance was measured in some patients that did not change with the addition of excess antivenom to the samples. In these patients, the baseline absorbance was subtracted from all measurements to calculate the true venom concentration. The EIA for brown snake antivenom had a limit of detection of 20 mu g/mL, but 50 mu g/mL was used as a cut-off based on assays in patients who had not received antivenom. The EIA for venom-antivenom complexes was unable to detect these at the low venom concentrations that occurred in patients. Quantification of venom and antivenom will help to determine the dose of antivenom required to bind venom and to establish appropriate end points for antivenom treatment. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4 / 11
页数:8
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