Matsui H, Komiya M, Ikeda C, Tachibana A
Antimicrob Agents Chemother. 1984 Aug;26(2):204-7. doi: 10.1128/AAC.26.2.204.
The pharmacokinetics of YM-13115, ceftriaxone, and ceftazidime were studied in rats, dogs, and rhesus monkeys (only YM-13115 and ceftriaxone were studied in rhesus monkeys). The plasma half-lives in rats were 48 min for YM-13115, 34 min for ceftriaxone, and 14 min for ceftazidime. In dogs, they were 21.9 min for YM-13115, 50.7 min for ceftriaxone, and 49.0 min for ceftazidime. In monkeys, they were 5.30 h for YM-13115 and 3.40 h for ceftriaxone. The 24-h urinary recoveries in rats were 26.7% of the dose for YM-13115, 32.0% for ceftriaxone, and 97.1% for ceftazidime. In dogs, they were 13.3% for YM-13115, 62.5% for ceftriaxone, and 86.3% for ceftazidime. In monkeys, they were 22.5% for YM-13115 and 29.3% for ceftriaxone. The 24-h biliary recoveries in rats were 72.2% for YM-13115, 61.8% for ceftriaxone, and 0.63% for ceftazidime.
对YM - 13115、头孢曲松和头孢他啶在大鼠、犬和恒河猴体内的药代动力学进行了研究(在恒河猴体内仅研究了YM - 13115和头孢曲松)。在大鼠体内,YM - 13115的血浆半衰期为48分钟,头孢曲松为34分钟,头孢他啶为14分钟。在犬体内,YM - 13115的血浆半衰期为21.9分钟,头孢曲松为50.7分钟,头孢他啶为49.0分钟。在猴体内,YM - 13115的血浆半衰期为5.30小时,头孢曲松为3.40小时。在大鼠体内,YM - 13115、头孢曲松和头孢他啶24小时尿液回收率分别为给药剂量的26.7%、32.0%和97.1%。在犬体内,YM - 13115、头孢曲松和头孢他啶24小时尿液回收率分别为13.3%、62.5%和86.3%。在猴体内,YM - 13115和头孢曲松24小时尿液回收率分别为22.5%和29.3%。在大鼠体内,YM - 13115、头孢曲松和头孢他啶24小时胆汁回收率分别为72.2%、61.8%和0.63%。