Nyoni E C, Sitaram B R, Taylor D A
Department of Pharmaceutics, Monash University, Parkville, Victoria, Australia.
J Chromatogr B Biomed Appl. 1996 Apr 26;679(1-2):79-84. doi: 10.1016/0378-4347(96)00027-8.
delta 9-Tetrahydrocannabinol (delta 9-THC) is the major psychoactive component of cannabis. To assist in investigating the mechanism(s) of action of delta 9-THC, a convenient method for determining its levels in brain tissue is required. We now describe a method for determining nanogram quantities of delta 9-THC in rat brain tissue. The method employs solvent extraction with methanol-hexane-ethyl acetate, followed by analysis using liquid chromatography with electrochemical detection. Overall recoveries were greater than 80%. The relationship between the peak-height ratio for processed standards extracted in the presence of tissue (delta 9-THC/internal standard) and the amount of delta 9-THC added was shown to be linear within the range of concentrations examined. Quantitative measurements of delta 9-THC in different brain regions following the intravenous administration of delta 9-THC are presented as examples of the applications of this method.
δ9-四氢大麻酚(δ9-THC)是大麻的主要精神活性成分。为了有助于研究δ9-THC的作用机制,需要一种测定其在脑组织中含量的简便方法。我们现在描述一种测定大鼠脑组织中纳克量δ9-THC的方法。该方法采用甲醇 - 己烷 - 乙酸乙酯进行溶剂萃取,然后使用液相色谱 - 电化学检测进行分析。总体回收率大于80%。在存在组织的情况下提取的处理标准品(δ9-THC/内标)的峰高比与添加的δ9-THC量之间的关系在所研究的浓度范围内呈线性。静脉注射δ9-THC后不同脑区中δ9-THC的定量测量作为该方法应用的示例给出。