摘要
目的观察速效抗晕胶囊对小鼠的急性毒性表现以评价药物的安全性。方法通过对ICR小鼠单次灌胃观察速效抗晕胶囊对小鼠的急性毒性表现,根据死亡率用综合分析法计算药物的半致死剂量(LD50)值。结果小鼠服药后呈现与浓度正相关的兴奋性神经症状。症状初始时间为服药后10min左右,高浓度组(1461.6mg/kg)小鼠快速死亡,死亡时间集中在1~2h。速效抗晕胶囊对小鼠的LD50为1043.3mg/kg,LD50的95%可信区间为972.8~1113.8mg/kg。结论速效抗晕胶囊灌胃给药小鼠的LD50为1043.3mg/kg,相当于临床推荐剂量的298~596倍。
Objective To observe and determine the medial lethal dose ( LDso ) of quick-effective antimotion capsule for mice to evaluate it' s safety. Methods The toxicity response of ICR mice were observed and recorded after the mice were lavaged with the capsule once. LD50 and 95% reliability limit were calculated by aggregate analysis according to death rate. Results The mice showed exciting nerval syndrome with a positive correlation to the medicine concentration. The earliest syndrome emerged about 10 vain after treatment. The mice in the high dosage groups died quickly and the death time focused within 1-2 h. LD50 of quick-effective anti-motion capsule for mice was 1043.3 mg/kg, 95% reliability limi of LD50 was 972.8-1113.8 mg/kg. Conclusions LD40 of quick-effective anti-motion capsule for mice is 1043.3 mg/kg, which is 298-596 times of recommended clinic dosage.
出处
《中华航海医学与高气压医学杂志》
CAS
CSCD
2008年第2期97-98,共2页
Chinese Journal of Nautical Medicine and Hyperbaric Medicine
基金
总后科研基金项目(06A202)
关键词
速效抗晕胶囊
急性毒性
半致死剂量
运动病
Quick-effective anti-motion capsule
Acute toxicity
LD50
Motion sickness