Ifa D R, Moraes M E, Moraes M O, Santagada V, Caliendo G, de Nucci G
Department of Pharmacology, ICB-University of São Paulo, Brazil.
J Mass Spectrom. 2000 Mar;35(3):440-5. doi: 10.1002/(SICI)1096-9888(200003)35:3<440::AID-JMS955>3.0.CO;2-8.
A liquid chromatographic atmospheric pressure chemical ionization tandem mass spectrometric method is described for the determination of 21-hydroxydeflazacort in human plasma using dexamethasone 21-acetate as an internal standard. The procedure requires a single diethyl ether extraction. After evaporation of the solvent under a nitrogen flow, the analytes are reconstituted in the mobile phase, chromatographed on a C18 reversed-phase column and analyzed by mass spectrometry via a heated nebulizer interface where they are detected by multiple reaction monitoring. The method has a chromatographic run time of less than 5 min and a linear calibration curve with a range of 1-400 ng ml(-1) (r>0.999). The between-run precision, based on the relative standard deviation for replicate quality controls, was < or =5.5% (10 ng ml(-1)), 1.0% (50 ng ml(-1)) and 2.7% (200 ng ml(-1)). The between-run accuracy was +/-7.1, 3.8 and 4.8% for the above concentrations, respectively. This method was employed in a bioequivalence study of two DFZ tablet formulations (Denacen from Marjan Industria e Comercio, Brazil, as a test formulation, and Calcort from Merrell Lepetit, Brazil, as a reference formulation) in 24 healthy volunteers of both sexes who received a single 30 mg dose of each formulation. The study was conducted using an open, randomized, two-period crossover design with a 7-day washout interval. The 90% confidence interval (CI) of the individual geometric mean ratio for Denacen/Calcort was 89.8-109.5% for area under the curve AUC(0-24 h) and 80.7-98.5% for Cmax. Since both the 90% CI for AUC(0-24 h) and Cmax were included in the 80-125% interval proposed by the US Food and Drug Administration, Denacen was considered bioequivalent to Calcort according to both the rate and extent of absorption.
描述了一种液相色谱-大气压化学电离串联质谱法,用于以醋酸地塞米松21-醋酸酯为内标物测定人血浆中的21-羟基去氟可的松。该方法只需用二乙醚进行一次萃取。在氮气流下蒸发溶剂后,将分析物用流动相复溶,在C18反相柱上进行色谱分离,并通过加热雾化器接口进行质谱分析,通过多反应监测进行检测。该方法的色谱运行时间少于5分钟,线性校准曲线范围为1 - 400 ng ml(-1)(r>0.999)。基于重复质量控制的相对标准偏差,批间精密度分别为≤5.5%(10 ng ml(-1))、1.0%(50 ng ml(-1))和2.7%(200 ng ml(-1))。上述浓度下的批间准确度分别为±7.1%、3.8%和4.8%。该方法用于24名男女健康志愿者的两种去氟可的松片剂制剂(来自巴西Marjan Industria e Comercio的Denacen作为受试制剂,来自巴西Merrell Lepetit的Calcort作为参比制剂)的生物等效性研究,每位志愿者单次服用每种制剂30 mg剂量。该研究采用开放、随机、两周期交叉设计,洗脱期为7天。Denacen/Calcort的个体几何平均比值的90%置信区间(CI),曲线下面积AUC(0 - 24 h)为89.8 - 109.5%,Cmax为80.7 - 98.5%。由于AUC(0 - 24 h)和Cmax的90% CI均包含在美国食品药品监督管理局提议的80 - 125%区间内,根据吸收速率和程度,Denacen被认为与Calcort生物等效。