The pre-clinical assessment of QT interval prolongation:: a comparison of in vitro and in vivo methods

被引:21
作者
Davis, AS [1 ]
机构
[1] Zeneca Pharmaceut, Anim Welf Grp, Macclesfield SK10 4TG, Cheshire, England
来源
HUMAN & EXPERIMENTAL TOXICOLOGY | 1998年 / 17卷 / 12期
关键词
QT interval; action potential duration; dog; in vivo; in vitro;
D O I
10.1177/096032719801701205
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The literature was searched for in vivo dog studies reporting QT prolongation and in vitro studies reporting increased myocardial action potential duration, which indicates the potential to prolong QT interval, for nine non-cardiac drugs that have been reported to produce QT prolongation in man. The drugs were: astemizole; terfenadine; erythromycin; sparfloxacin; cisapride; probucol; terodiline; risperidone and sertindole. 1 There were reports of the appropriate finding with in vitro methods for six of the drugs and with in vivo methods for seven of the drugs. No reports were found concerning the remaining drugs with each method. This indicates that both methods are effective and each method would have correctly identified the drugs in question as having the potential to prolong the QT interval in man in all cases for which studies were reported. 2 This suggests that, if properly conducted, either method alone is sufficient for the pre-clinical assessment of QT interval prolongation. This does not support the routine use of both methods before the administration of new drugs to man.
引用
收藏
页码:677 / 680
页数:4
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