McNulty C A, Garden G M, Wise R, Andrews J M
J Antimicrob Chemother. 1985 Dec;16(6):743-9. doi: 10.1093/jac/16.6.743.
The pharmacokinetics of teicoplanin were studied following a 440 mg intravenous dose in six male volunteers. The levels of the compound were measured in serum, blister fluid and urine. The mean serum level 0.5 h after injection was 44.6 mg/l falling to 3.6 mg/l at 49 h. The elimination half-life of teicoplanin from serum was 34.2 h and the apparent distribution half-life 1.5 h. Penetration into blister fluid was moderately fast, the mean maximum concentration (14.8 mg/l) occurring at 2.7 h, and the mean percentage penetration being 77.4%. Urinary recovery of the drug was 48.3% by 96 h.
在六名男性志愿者静脉注射440毫克替考拉宁后,对其药代动力学进行了研究。在血清、水疱液和尿液中测量了该化合物的水平。注射后0.5小时的平均血清水平为44.6毫克/升,在49小时时降至3.6毫克/升。替考拉宁从血清中的消除半衰期为34.2小时,表观分布半衰期为1.5小时。进入水疱液的速度适中,平均最大浓度(14.8毫克/升)出现在2.7小时,平均渗透百分比为77.4%。到96小时时,药物的尿回收率为48.3%。