Nelson E B, Egan J M, Abernethy D R
Clin Pharmacol Ther. 1987 May;41(5):571-3. doi: 10.1038/clpt.1987.73.
To evaluate the potential interaction of propylene glycol on hepatic drug oxidation, antipyrine disposition was measured in 10 healthy subjects who received 1.2 gm antipyrine alone on one occasion and 1.2 gm antipyrine with propylene glycol on a second occasion. Propylene glycol was given as a 5 ml dose every 4 hours during the 48 hours of the study. Propylene glycol had no effect on antipyrine half life (11.7 hours control vs. 12.1 hours treatment), clearance (42.6 vs. 39.2 ml/min), or volume of distribution (42.1 vs 41.9 L). At a dose similar to that used as a vehicle for administration of other drugs, propylene glycol had no significant effect on antipyrine clearance in humans.
为评估丙二醇对肝脏药物氧化的潜在相互作用,对10名健康受试者进行了安替比林处置测定,这些受试者一次单独接受1.2克安替比林,另一次接受1.2克安替比林与丙二醇。在研究的48小时内,每4小时给予5毫升丙二醇。丙二醇对安替比林半衰期(对照为11.7小时,治疗为12.1小时)、清除率(42.6对39.2毫升/分钟)或分布容积(42.1对41.9升)均无影响。在与用作其他药物赋形剂的剂量相似时,丙二醇对人体安替比林清除率无显著影响。