Potts B D, Martin C A, Vore M
Clin Chem. 1984 Aug;30(8):1374-7.
The gas-chromatographic assay for methylphenidate described here involves isolation by solid-phase extraction and quantification by thermionic nitrogen-phosphorus detection. Methylphenidate and the internal standard, ethylphenidate, are extracted from plasma by partition onto C2 reversed-phase packing. Methylphenidate and ethylphenidate are eluted, dried, derivatized with trifluoroacetic anhydride, and gas-chromatographed, with nitrogen-sensitive detection. The standard curve for the assay is linear in the range 5-100 micrograms/L. The within-run CV is less than 4%, the between-run CV less than 6%. Mean analytical recovery of methylphenidate was greater than 90%. The smallest measurable concentration is 2 micrograms/L. The sensitivity, reproducibility, and economy of this assay make it suitable for clinical monitoring and pharmacokinetic studies.
本文所述的哌甲酯气相色谱测定法包括通过固相萃取进行分离以及通过热离子氮磷检测进行定量。哌甲酯和内标物乙哌甲酯通过分配到C2反相填料上从血浆中萃取出来。哌甲酯和乙哌甲酯被洗脱、干燥,用三氟乙酸酐衍生化,然后进行气相色谱分析,并采用氮敏感检测。该测定法的标准曲线在5 - 100微克/升范围内呈线性。批内变异系数小于4%,批间变异系数小于6%。哌甲酯的平均分析回收率大于90%。最小可测浓度为2微克/升。该测定法的灵敏度、重现性和经济性使其适用于临床监测和药代动力学研究。