Baber N, Halliday L, Sibeon R, Littler T, Orme M L
Clin Pharmacol Ther. 1978 Sep;24(3):298-307. doi: 10.1002/cpt1978243298.
The interaction between indomethacin and probenecid has been studied in 17 patients with rheumatoid arthritis with the use of a specific gas-liquid chromatographic method for the assay of indomethacin in plasma and urine. Probenecid in a dose of 0.5 gm twice daily improved the therapeutic response to indomethacin administered in a dose of 25 mg 3 times daily for a 3-wk period. There was an increase in the mean AUC of indomethacin in plasma from 2,553 +/- 213 hr ng/ml to 4,181 +/- 384 hr ng/ml when probenecid was given, but there was no change in the plasma half-life of indomethacin. There was a reduction in the mean plasma clearance of indomethacin from 174 +/- 21 ml/kg/hr to 107 +/- 14 ml/kg/hr when probenecid was added to the indomethacin therapy and a decrease in the apparent volume of distribution from 0,927 +/- 0.16 L/kg to 0.613 +/- 0.13 L/kg. There was no change in the amount of free indomethacin excreted in the urine during probenecid therapy but there was a reduction in the urinary excretion of free plus glucuronide conjugate of indomethacin from 8,967 +/- 867 microgram/day to 4,760 +/- 674 microgram/day, with a fall in the mean renal clearance of indomethacin glucuronide from 271 +/- 48 ml/min to 126 +/- 57.0 ml/min. The changes in the plasma indomethacin concentration profile during probenecid therapy are due to a decrease in the nonrenal clearance of indomethacin possibly because of reduced biliary clearance.
采用一种测定血浆和尿液中吲哚美辛的特定气液色谱法,对17例类风湿性关节炎患者中吲哚美辛与丙磺舒之间的相互作用进行了研究。丙磺舒剂量为每日两次,每次0.5克,在为期3周的时间里,可改善患者对每日3次、每次25毫克吲哚美辛的治疗反应。给予丙磺舒后,血浆中吲哚美辛的平均曲线下面积(AUC)从2553±213小时纳克/毫升增至4181±384小时纳克/毫升,但吲哚美辛的血浆半衰期无变化。在吲哚美辛治疗中加用丙磺舒后,吲哚美辛的平均血浆清除率从174±21毫升/千克/小时降至107±14毫升/千克/小时,表观分布容积从0.927±0.16升/千克降至0.613±0.13升/千克。丙磺舒治疗期间,尿液中排泄的游离吲哚美辛量无变化,但吲哚美辛游离型加葡糖醛酸结合物的尿排泄量从8967±867微克/天降至4760±674微克/天,吲哚美辛葡糖醛酸的平均肾清除率从271±48毫升/分钟降至126±57.0毫升/分钟。丙磺舒治疗期间血浆吲哚美辛浓度曲线的变化,可能是由于吲哚美辛非肾清除率降低,原因可能是胆汁清除率下降。