Keswani S R, Edfort M J, Wilhelm J A, Kvavlo L T, Venturella V S
Pharmaceutical Research Department, Anaquest (Division of The BOC, Inc.), Murray Hill, NJ 07974.
J Chromatogr. 1990 Dec 14;534:77-86. doi: 10.1016/s0378-4347(00)82150-7.
A liquid chromatographic-mass spectrometric method for the determination of 14-beta-n-pentylaminomorphinone (pentamorphone) and 14-beta-n-pentylaminocodeinone (PAC) as internal standard is developed. Concentration levels in serum were calculated by the ratio of the peak areas of pentamorphone to PAC versus the concentration of pentamorphone. Peak areas were measured using selected-ion-recording of the pseudo-molecular ions of pentamorphone and PAC (m/z 369 and m/z 383, respectively). Aliquots (50 microliters) of sample were injected on a C18 mu Bondapak column following solid-phase extraction. The lowest limit of quantitation observed was 43 pg/ml. The sensitivity, accuracy and reproducibility of the method were demonstrated to be satisfactory for application in pharmacokinetic study of pentamorphone.
开发了一种用于测定14-β-N-戊基氨基吗啡酮(戊吗啡)和作为内标的14-β-N-戊基氨基可待因酮(PAC)的液相色谱-质谱法。通过戊吗啡与PAC的峰面积比相对于戊吗啡的浓度来计算血清中的浓度水平。使用戊吗啡和PAC的准分子离子的选择离子记录(分别为m/z 369和m/z 383)来测量峰面积。在固相萃取后,将等分试样(50微升)注入C18 μ Bondapak柱。观察到的最低定量限为43 pg/ml。该方法的灵敏度、准确性和重现性被证明对于戊吗啡的药代动力学研究应用是令人满意的。