Venkataramana D, Krishna D R
University College of Pharmaceutical Sciences, Kakatiya University, Warangal, India.
Eur J Drug Metab Pharmacokinet. 1993 Apr-Jun;18(2):161-3. doi: 10.1007/BF03188791.
The pharmacokinetics of usnic acid, a lichen antitubercular, antitumor and enzyme inhibiting agent, was studied in normal male rabbits after administration of 5 mg/kg dose by intravenous route. Plasma samples were collected up to 48 h. The plasma usnic acid levels showed a triexponential decay with a terminal half life of 10.69 h. The mean volume of distribution of the central compartment was 43.93 ml/kg. The pharmacokinetic parameters obtained from a three-compartment body model and a noncompartment body model gave close values. The mean steady-state volume of distribution was 167.17 and 163.29 ml/kg, systemic clearance was 12.17 and 12.25 ml/h/kg and AUC was 428.51 and 426.69 micrograms.ml/h following three-compartmental and noncompartmental analyses respectively.
地衣芽孢杆菌的抗结核、抗肿瘤和酶抑制因子松萝酸,在以5mg/kg剂量静脉给药后,对正常雄性家兔的药代动力学进行了研究。采集血浆样本长达48小时。血浆松萝酸水平呈三指数衰减,终末半衰期为10.69小时。中央室的平均分布容积为43.93ml/kg。从三室模型和非房室模型获得的药代动力学参数值相近。三室分析和非房室分析后,平均稳态分布容积分别为167.17和163.29ml/kg,全身清除率分别为12.17和12.25ml/h/kg,AUC分别为428.51和426.69μg·ml/h。