Metabolic study of pholcodine in urine using enzyme multiplied immunoassay technique (EMIT) and capillary gas chromatography.

Acta pharmaceutica Nordica Pub Date : 1991-01-01
M Johansen, K E Rasmussen, A S Christophersen, B Skuterud
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Abstract

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).

利用酶倍增免疫分析技术(EMIT)和毛细管气相色谱法研究尿中福可定的代谢。
报道了一项关于人体内福尔可定代谢的研究。3名受试者接受单次口服氟可定治疗剂量50 mg,只要通过EMIT检测到阿片类药物阳性反应,就采集尿样(16-26天)。结果表明,15%(13-17%)的剂量以葡萄糖醛酸的形式排出体外,29%(24-35%)的剂量以未结合的形式排出体外。吗啡是福可定的代谢物,0.5-1%的福可定以吗啡葡萄糖醛酸盐的形式排出体外。采用毛细管气相色谱-质谱联用技术(GC-MS)对吗啡进行鉴定。
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