Johansen M, Rasmussen K E, Christophersen A S, Skuterud B
Institute of Pharmacy, University of Oslo, Norway.
Acta Pharm Nord. 1991;3(2):91-4.
A study of pholcodine metabolism in man is reported. Three subjects received a single therapeutic oral dose of 50 mg pholcodine and urine samples were collected as long as a positive opiate response could be detected by EMIT (16-26 days). Pholcodine was found to conjugate with glucuronic acid and 15% (13-17%) of the pholcodine dose was excreted in urine as the glucuronide, and 29% (24-35%) as unconjugated pholcodine. Morphine was detected to be a metabolite of pholcodine and 0.5-1% of the pholcodine dose was excreted as morphine glucuronide. The identity of morphine was confirmed by capillary gas chromatography-mass spectroscopy (GC-MS).
本文报道了一项关于人身体中福可定代谢的研究。三名受试者口服了50毫克的单一治疗剂量福可定,只要能通过酶放大免疫测定技术(EMIT)检测到阳性阿片反应(持续16 - 26天),就收集尿液样本。研究发现福可定与葡萄糖醛酸结合,给药剂量的15%(13% - 17%)以葡萄糖醛酸苷的形式随尿液排出,29%(24% - 35%)以未结合的福可定形式排出。检测到吗啡是福可定的一种代谢产物,给药剂量的0.5% - 1%以吗啡葡萄糖醛酸苷的形式排出。吗啡的身份通过毛细管气相色谱 - 质谱联用仪(GC - MS)得以确认。