Jovanovich J F, Saravolatz L D, Burch K, Pohlod D J
Antimicrob Agents Chemother. 1981 Oct;20(4):530-2. doi: 10.1128/AAC.20.4.530.
This investigation evaluated the effect of probenecid on ceforanide concentrations in eight healthy volunteers. Each volunteer was given 1 or 2 g of ceforanide either alone or with 1 g of probenecid. Concentrations of ceforanide in plasma, urine, and saliva were then measured. Probenecid did not alter the plasma concentrations of ceforanide, nor did it affect the urinary excretion of this agent. Ceforanide was not secreted into saliva in any detectable amount either when administered alone or with probenecid. It is not clear why probenecid has a negligible effect on ceforanide concentrations in plasma. It may be that tubular secretion plays less of a role in the excretion of ceforanide than expected, or that the physical properties of ceforanide prevent probenecid from affecting its excretion.
本研究评估了丙磺舒对8名健康志愿者体内头孢乙腈浓度的影响。每位志愿者单独服用1或2克头孢乙腈,或与1克丙磺舒一起服用。然后测量血浆、尿液和唾液中头孢乙腈的浓度。丙磺舒并未改变头孢乙腈的血浆浓度,也未影响该药物的尿排泄。单独给药或与丙磺舒合用时,头孢乙腈均未以任何可检测到的量分泌到唾液中。尚不清楚为什么丙磺舒对血浆中头孢乙腈浓度的影响可忽略不计。可能是肾小管分泌在头孢乙腈排泄中所起的作用比预期的要小,或者是头孢乙腈的物理性质使丙磺舒无法影响其排泄。