Barbhaiya R H, Shukla U A, Gleason C R, Shyu W C, Pittman K A
Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Company, Syracuse, New York 13221-4755.
Antimicrob Agents Chemother. 1990 Jun;34(6):1210-3. doi: 10.1128/AAC.34.6.1210.
The objective of this study was to assess the effects of food on the pharmacokinetics of cefprozil and cefaclor. A group of 12 healthy male volunteers received a single 250-mg dose of cefprozil or cefaclor under fasting conditions as well as after the intake of food. There was a 1-week washout period between each treatment. Serial blood samples were collected and assayed for cefprozil or cefaclor by specific high-pressure liquid chromatographic methods. The mean +/- standard deviation peak concentration (Cmax) of cefprozil in plasma was 6.13 +/- 1.22 micrograms/ml under the fasting condition and 5.27 +/- 1.06 micrograms/ml after breakfast, and these values were not significantly different from each other. The corresponding median time to reach Cmax was prolonged after food intake, but this difference was not significant. The mean Cmax values of cefaclor decreased significantly from 8.70 +/- 2.72 micrograms/ml under the fasting condition to 4.29 +/- 1.52 micrograms/ml after breakfast, and the corresponding median times to reach Cmax were significantly prolonged. The mean half-lives of cefprozil and cefaclor were nearly identical for the two treatments, suggesting that the elimination kinetics of these cephalosporins remained unaltered when the drugs were administered with food. The area under the plasma-concentration-versus-time curves for fasted and fed conditions were not significantly different for both drugs. The results of this study indicate that the extent of absorption and rate of elimination of both cephalosporins remain unaltered in the presence of food. However, the absorption rate of cefaclor is significantly reduced in the presence of food, while that of cefprozil remains unaltered. As a result, the Cmax of cefaclor is significantly reduced in the presence of food, whereas that of cefprozil is not significantly affected. Cefprozil can be administered with a meal without markedly affecting levels in blood.
本研究的目的是评估食物对头孢丙烯和头孢克洛药代动力学的影响。一组12名健康男性志愿者在禁食条件下以及进食后接受了单次250毫克剂量的头孢丙烯或头孢克洛。每次治疗之间有1周的洗脱期。采集系列血样,并用特定的高压液相色谱法测定头孢丙烯或头孢克洛。空腹条件下血浆中头孢丙烯的平均±标准差峰浓度(Cmax)为6.13±1.22微克/毫升,早餐后为5.27±1.06微克/毫升,这些值彼此无显著差异。进食后达到Cmax的相应中位时间延长,但这种差异不显著。头孢克洛的平均Cmax值从禁食条件下的8.70±2.72微克/毫升显著降至早餐后的4.29±1.52微克/毫升,达到Cmax的相应中位时间显著延长。两种治疗中头孢丙烯和头孢克洛的平均半衰期几乎相同,这表明当药物与食物一起给药时,这些头孢菌素的消除动力学保持不变。两种药物在禁食和进食条件下的血浆浓度-时间曲线下面积无显著差异。本研究结果表明,两种头孢菌素在有食物存在时的吸收程度和消除速率保持不变。然而,食物存在时头孢克洛的吸收速率显著降低,而头孢丙烯的吸收速率保持不变。结果,食物存在时头孢克洛的Cmax显著降低,而头孢丙烯的Cmax不受显著影响。头孢丙烯可以与食物一起给药,而不会显著影响血液中的水平。