Midha K K, McGilveray I J, Bhatnagar S P, Cooper J K
J Pharm Sci. 1976 Feb;65(2):188-97. doi: 10.1002/jps.2600650205.
A GLC method for qualitative and quantitative determination of 3,4-methylenedioxyamphetamine in biological fluids is described. After extraction of the drug and the internal standard, 4-methoxyamphetamine, from plasma and urine, the solvent is evaporated and the residue is mixed with 20 mul of freshly distilled ether. Aliquots (1-2 mul) then are injected into the gas chromatograph. Both the drug and the internal standard give well-separated symmetrical peaks. Flame-ionization detection allows concentrations of 0.125 mug of 3,4-methylenedioxyamphetamine from plasma to be determined with a precision of 3.16%. The method is applicable to the estimation of 4-methoxyamphetamine, employing 3,4-methylenedioxyamphetamine as the internal standard. For identification purposes, various derivatives such as Schiff bases, isothiocyanates, trifluoroacetates, and heptafluorobutyrates of both compounds were formed following extraction from urine and their GLC behavior was investigated. Derivative formation was confirmed by GLC-mass spectrometry. Mass spectral data for these derivatives are presented.
本文描述了一种用于生物体液中3,4-亚甲基二氧基苯丙胺定性和定量测定的气相色谱法。从血浆和尿液中提取药物及其内标物4-甲氧基苯丙胺后,蒸发溶剂,残余物与20微升新蒸馏的乙醚混合。然后取1至2微升等分试样注入气相色谱仪。药物和内标物均给出分离良好的对称峰。火焰离子化检测可测定血浆中浓度为0.125微克的3,4-亚甲基二氧基苯丙胺,精密度为3.16%。该方法适用于以3,4-亚甲基二氧基苯丙胺为内标物来测定4-甲氧基苯丙胺。为了进行鉴定,从尿液中提取后,形成了两种化合物的各种衍生物,如席夫碱、异硫氰酸酯、三氟乙酸酯和七氟丁酸酯,并研究了它们的气相色谱行为。通过气相色谱-质谱联用确认了衍生物的形成。给出了这些衍生物的质谱数据。