Fox A R, McLoughlin D A
PharmaKinetics Laboratories, Inc., Baltimore, MD 21201.
J Chromatogr. 1993 Feb 12;631(1-2):255-9. doi: 10.1016/0021-9673(93)80530-l.
A method of analysis has been developed to quantify promethazine in human serum with a sensitivity that was suitable for bioavailability studies following a 50.0-mg rectal dose. The limit of quantification from 1.0 ml of serum for promethazine using electrochemical detection was 0.200 ng/ml. At this concentration, the total coefficient of variation obtained from seven replicates over the course of three days of validation was 7.53%. The amount of serum required, the ease of sample preparation and the precision of the method at the limit of quantification demonstrated an improvement over previous assays. A validation study was completed that included an evaluation of recovery, ruggedness, linearity of response, accuracy, precision, sensitivity, stability and selectivity. The method was then used to determine promethazine serum levels in a 36-subject bioavailability study following a 50.0-mg suppository dose.
已开发出一种分析方法,用于定量测定人血清中的异丙嗪,其灵敏度适用于50.0毫克直肠给药后的生物利用度研究。使用电化学检测法,1.0毫升血清中异丙嗪的定量限为0.200纳克/毫升。在此浓度下,在三天的验证过程中,七次重复测定得到的总变异系数为7.53%。所需血清量、样品制备的简便性以及该方法在定量限处的精密度均表明比以前的测定方法有所改进。完成了一项验证研究,包括对回收率、耐用性、响应线性、准确性、精密度、灵敏度、稳定性和选择性的评估。然后,该方法用于在一项36名受试者的生物利用度研究中,测定50.0毫克栓剂给药后的异丙嗪血清水平。