Bouquillon A I, Freeman D, Moulin D E
Department of Clinical Neurological Sciences, University of Western Ontario, Victoria Hospital, London, Canada.
J Chromatogr. 1992 Jun 10;577(2):354-7. doi: 10.1016/0378-4347(92)80258-r.
High-performance liquid chromatography has become an important analytical tool for the quantitation of opioid drugs. Using solid-phase extraction and coulometric electrochemical detection, we have developed a chromatographic method for the simultaneous measurement of morphine and hydromorphone which is both sensitive and specific. Using 1 ml of plasma, intra-assay and inter-assay data show that the detection limit for accurate quantitation of these compounds is about 1.2 ng/ml (coefficient of variation 11.6%) for morphine and 2.5 ng/ml (coefficient of variation 10.5%) for hydromorphone. The method is simple and readily adaptable to most pharmacokinetic studies and toxic screens involving these drugs.