Hidvegi S, Ecobichon D J
Can J Physiol Pharmacol. 1986 Jan;64(1):72-6. doi: 10.1139/y86-011.
The biotransformation of single acute oral doses of acetaminophen (100 mg/kg body weight) in adult male guinea pigs was studied by collecting serial blood, urine, and bile samples post-treatment and identifying and quantitating the concentrations of parent drug and excretory products by high performance liquid chromatography. The plasma half-life (beta t/2) (mean +/- SD) of acetaminophen was 1.87 +/- 0.30 h, while that of the only metabolite detected in plasma, the glucuronide, was 2.41 +/- 0.64 h. In 24-h urine samples, the predominant product was the glucuronide (90%) with a small amount of the sulphate conjugate (7.0%) and approximately 3.0% acetaminophen. In bile, the glucuronide was the major metabolite detected initially but, with time, this product decreased concomitantly with an increase in the cysteinyl conjugate. No sulphate was detected in bile but two unidentified metabolites were detected, having distinct column retention times and comprising approximately 6-10% of the total excretory products. The results demonstrated that glucuronidation is a high capacity biotransformation pathway for acetaminophen in this species, only small amounts of other conjugated products being detectable under usual circumstances.
通过在成年雄性豚鼠单次口服对乙酰氨基酚(100毫克/千克体重)后,收集连续的血液、尿液和胆汁样本,并采用高效液相色谱法鉴定和定量母体药物及排泄产物的浓度,研究了对乙酰氨基酚在成年雄性豚鼠体内的生物转化。对乙酰氨基酚的血浆半衰期(βt/2)(平均值±标准差)为1.87±0.30小时,而血浆中检测到的唯一代谢物葡糖醛酸苷的血浆半衰期为2.41±0.64小时。在24小时尿液样本中,主要产物是葡糖醛酸苷(90%),少量为硫酸酯共轭物(7.0%),对乙酰氨基酚约为3.0%。在胆汁中,葡糖醛酸苷是最初检测到的主要代谢物,但随着时间推移,该产物减少,同时半胱氨酸共轭物增加。胆汁中未检测到硫酸酯,但检测到两种未鉴定的代谢物,它们具有不同的柱保留时间,约占总排泄产物的6 - 10%。结果表明,葡糖醛酸化是该物种中对乙酰氨基酚的一种高容量生物转化途径,在通常情况下只能检测到少量其他共轭产物。