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头孢噻肟的药代动力学。

Pharmacokinetics of cefotaxime.

作者信息

Fu K P, Aswapokee P, Ho I, Matthijssen C, Neu H C

出版信息

Antimicrob Agents Chemother. 1979 Nov;16(5):592-7. doi: 10.1128/AAC.16.5.592.

Abstract

The pharmacokinetics of cefotaxime after intramuscular injection and intravenous infusion were determined. The mean peak serum level after the 500-mg intramuscular dose was 11.7 micrograms/ml, and it was 20.5 micrograms/ml after a 1,000-mg dose. The serum half-life was 1.2 and 1.3 h, respectively for the two doses. The apparent fractional volumes of distribution of 32 and 37 liters were not significantly different for the two doses, and the fractional serum clearance was approximately 315 ml/min per 1.73 m2 for both doses. The mean peak serum level after 1,000 mg administered by intravenous infusion over 30 min was 41.1 micrograms/ml. The half-life was 1.13 h, apparent volume of distribution was 33 liters, serum clearance 341 ml/min per 1.73 m2, and renal clearance was 130 ml/min per 1.73 m2. The pharmacology of cefotaxime is similar to the pharmacology of other cephalosporin antibiotics, but the low inhibitory levels which it has against gram-positive and gram-negative bacteria suggest that lower dosage regimens should be possible.

摘要

测定了头孢噻肟肌内注射和静脉输注后的药代动力学。500mg肌内注射剂量后的平均血清峰值水平为11.7微克/毫升,1000mg剂量后为20.5微克/毫升。两剂量的血清半衰期分别为1.2小时和1.3小时。两剂量的表观分布分数容积分别为32升和37升,无显著差异,两剂量的血清清除分数约为每1.73平方米315毫升/分钟。30分钟内静脉输注1000mg后的平均血清峰值水平为41.1微克/毫升。半衰期为1.13小时,表观分布容积为33升,血清清除率为每1.73平方米341毫升/分钟,肾清除率为每1.73平方米130毫升/分钟。头孢噻肟的药理作用与其他头孢菌素抗生素相似,但其对革兰氏阳性菌和革兰氏阴性菌的低抑制水平表明可能采用较低的给药方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc3c/352911/71c11cdebaa3/aac00281-0072-a.jpg

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