Speth P A, Vree T B, Neilen N F, de Mulder P H, Newell D R, Gore M E, de Pauw B E
Department of Haematology, St. Radboud University Hospital, Nijmegen, The Netherlands.
Ther Drug Monit. 1987 Sep;9(3):255-8. doi: 10.1097/00007691-198709000-00001.
Knowledge of the pharmacokinetics of propylene glycol (PG) is scarce, though it is used in a number of preparations for intravenous use. Although systemic toxicity appears to be uncommon, PG has been reported to cause lactic acidosis and other adverse effects. We describe a rapid gas chromatographic assay method for PG and the plasma pharmacokinetics after intravenous administration to six patients on nine occasions. The pharmacokinetics were nonlinear, based on a saturable clearance. The apparent first-order half-life was 2.3 +/- 0.7 h. There was no evidence of lactic acidosis, hemolysis, or increase in osmolality at 3-15 g/m2 PG infused over periods of 4 h.
尽管丙二醇(PG)被用于多种静脉制剂中,但其药代动力学方面的知识却很匮乏。虽然全身毒性似乎并不常见,但已有报道称PG可导致乳酸性酸中毒及其他不良反应。我们描述了一种快速气相色谱法,用于测定PG,并研究了六名患者在九次静脉给药后的血浆药代动力学。基于饱和清除率,其药代动力学呈非线性。表观一级半衰期为2.3±0.7小时。在4小时内输注3 - 15 g/m²的PG时,没有证据表明存在乳酸性酸中毒、溶血或渗透压升高。