Zylber-Katz E, Granit L, Levy M
Eur J Clin Pharmacol. 1985;29(1):67-71. doi: 10.1007/BF00547371.
Four metabolites of dipyrone, 4-methylaminoantipyrine (MAA), 4-aminoantipyrine (AA), 4-formylaminoantipyrine (FAA) and 4-acetylaminoantipyrine (AAA) can be identified in human plasma after its oral administration. The plasma protein binding of the metabolites in samples from 20 healthy volunteers was determined by ultrafiltration. None of the metabolites were found to be extensively bound to plasma proteins. The binding of MAA and AA was relatively higher than of FAA and AAA, as expected from their chemical structure. The mean percentage plasma protein binding was 57.6% for MAA, 47.9 for AA, 17.8 for FAA and 14.2% for AAA. The correlation between the unbound concentration in plasma and the total concentrations of MAA, AA, FAA and AAA was linear. No association was evident between the total protein plasma concentration and the extent of binding. The possible therapeutic implications related to protein binding of several analgesic and non-steroidal anti-inflammatory drugs are discussed.
口服双氯芬酸后,可在人体血浆中鉴定出其四种代谢产物,即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)。通过超滤法测定了20名健康志愿者样本中代谢产物的血浆蛋白结合率。未发现任何一种代谢产物与血浆蛋白有广泛结合。正如从其化学结构所预期的那样,MAA和AA的结合率相对高于FAA和AAA。MAA的平均血浆蛋白结合率为57.6%,AA为47.9%,FAA为17.8%,AAA为14.2%。血浆中游离浓度与MAA、AA、FAA和AAA总浓度之间的相关性呈线性。血浆总蛋白浓度与结合程度之间无明显关联。讨论了几种镇痛和非甾体抗炎药的蛋白结合可能产生的治疗意义。