Jonkman J H, Van Bork L E, Wijsbeek J, De Zeeuw R K, Orie N G
Clin Pharmacol Ther. 1977 Apr;21(4):457-63. doi: 10.1002/cpt1977214457.
Bioavailability after oral administration of the anticholinergic drug thiazinamium methylsulfate (Multergan), a phenothiazine derivative with a quaternary ammonium group in the molecule, has been studied in patients and volunteers by measuring the drug concentrations in plasma or the excretion of the parent drug in urine. The relative bioavailability as compared to intramuscular injection seems to be of the order of 10%. Much more of the drug is absorbed, however, but is metabolized during the first liver passage. Moreover, there seems to be a substantial interindividual variation in the bioavailability of the drug. Studies in a group of eight volunteers showed that there is also a substantial intraindividual variation, but its magnitude is smaller than that of the interindividual variation.
抗胆碱能药物甲硫酸噻嗪铵(Multergan)是一种分子中带有季铵基团的吩噻嗪衍生物,通过测量血浆中的药物浓度或母体药物在尿液中的排泄情况,已在患者和志愿者中研究了其口服后的生物利用度。与肌肉注射相比,其相对生物利用度似乎约为10%。然而,更多的药物被吸收,但在首次经过肝脏时会被代谢。此外,该药物的生物利用度似乎存在很大的个体间差异。对一组八名志愿者的研究表明,个体内也存在很大差异,但其幅度小于个体间差异。