Jonsson J
Res Commun Chem Pathol Pharmacol. 1977 Oct;18(2):189-99.
m-Hydroxyamphetamine (mOHA) was found as a metabolite of amphetamine in rat urine, liver perfusate and bile. The identity was established with a gas chromatograph-mass spectrometer (GC/MS) by its retention time, mass spectrum and selective-ion-monitoring of fragments representing both the side chain and the aromatic moiety. Furthermore, deuterium-labelled amphetamine was used in order to circumvent the possibility of interference by substances with similar structure of endogenous or exogenous origin. The amount of mOHA was low, about 10% of the ring hydroxylation could be accounted for as metahydroxylation.
间羟基苯丙胺(mOHA)在大鼠尿液、肝脏灌流液和胆汁中被发现是苯丙胺的一种代谢产物。通过气相色谱 - 质谱联用仪(GC/MS)依据其保留时间、质谱以及对代表侧链和芳香部分的碎片进行选择性离子监测来确定其身份。此外,使用氘标记的苯丙胺以避免内源性或外源性来源的结构相似物质产生干扰的可能性。mOHA的量很低,约10%的环羟基化可归因于间位羟基化。