Caraco Y, Zylber-Katz E, Granit L, Levy M
Clinical Pharmacology Unit, Hadassah University Hospital, Jerusalem, Israel.
Arzneimittelforschung. 1993 Nov;43(11):1204-8.
Plasma and saliva pharmacokinetics of dipyrone (CAS 5907-38-0) metabolites, 4-methylaminoantipyrine (MAA), 4-aminoantipyrine (AA), 4-formylaminoantipyrine (FAA) and 4-acetylaminoantipyrine (AAA), has been studied in 10 healthy volunteers, after oral administration of 1.0 g dipyrone, MAA, AA, FAA and AAA saliva concentrations correlated significantly with the respective plasma concentrations (r = 0.81, r = 0.62, r = 0.83 and r = 0.91, p < 0.001). MAA and AA concentrations in saliva were lower than in plasma while the FAA and AAA saliva concentrations were similar to the respective plasma concentrations. The saliva/plasma concentration ratios were highly dependent on sampling time. The elimination half-life of the final metabolites FAA and AAA can be equally evaluated from plasma and saliva data. For MAA, plasma and saliva t1/2 values were significantly correlated despite a substantial intra-subject difference. No correlation was found for AA plasma and saliva derived pharmacokinetic parameters. Similar to the plasma AAA/AA ratio, the saliva AAA/AA ratio in spot sample 6 h following oral dose might be proven to be a reliable discriminatory index for acetylation phenotyping.
在10名健康志愿者口服1.0 g安乃近(CAS 5907-38-0)后,对其代谢产物4-甲基氨基安替比林(MAA)、4-氨基安替比林(AA)、4-甲酰氨基安替比林(FAA)和4-乙酰氨基安替比林(AAA)的血浆和唾液药代动力学进行了研究。MAA、AA、FAA和AAA的唾液浓度与各自的血浆浓度显著相关(r = 0.81、r = 0.62、r = 0.83和r = 0.91,p < 0.001)。唾液中MAA和AA的浓度低于血浆,而FAA和AAA的唾液浓度与各自的血浆浓度相似。唾液/血浆浓度比高度依赖于采样时间。最终代谢产物FAA和AAA的消除半衰期可以从血浆和唾液数据中同等评估。对于MAA,尽管个体内存在显著差异,但血浆和唾液的t1/2值显著相关。未发现AA血浆和唾液衍生的药代动力学参数之间存在相关性。与血浆AAA/AA比值相似,口服给药6小时后即时样本中的唾液AAA/AA比值可能被证明是乙酰化表型分型的可靠鉴别指标。