Böcker R, Estler C J, Maywald M, Weber D
Arzneimittelforschung. 1981;31(12):2116-7.
Doxycycline levels in various organs of mice after i.v. and p.o. administration were measured by a high-performance liquid chromatography method. When given as a single dose (50 mg/kg) i.v. doxycycline accumulated in the lung. High concentrations were also measured in liver and kidneys. When 50 mg/kg doxycycline were administered by stomach tube to fed mice the antibiotic accumulated to a lesser degree in the lung. On the other hand, the antibiotic levels in the liver and the kidneys were higher as after i.v. injection. The absorption of doxycycline administered p.o. was about 92% and seemed not to be influenced by food in the stomach. The elimination half-life in mice was 170 min independent of the route of administration.
采用高效液相色谱法测定小鼠静脉注射和口服给药后各器官中的强力霉素水平。静脉注射单剂量(50mg/kg)强力霉素后,其在肺中蓄积。在肝脏和肾脏中也检测到高浓度。当给喂食的小鼠经胃管给予50mg/kg强力霉素时,抗生素在肺中的蓄积程度较小。另一方面,肝脏和肾脏中的抗生素水平高于静脉注射后。口服强力霉素的吸收约为92%,似乎不受胃内食物的影响。小鼠体内的消除半衰期为170分钟,与给药途径无关。