Young D, Evans P C, Paxton J W
Department of Pharmacology and Clinical Pharmacology, University of Auckland School of Medicine, New Zealand.
J Chromatogr. 1990 Jun 29;528(2):385-94. doi: 10.1016/s0378-4347(00)82396-8.
N-[2-(Dimethylamino)ethyl]acridine-4-carboxamide is a new experimental antitumour agent which has excellent in vivo activity against the Lewis lung tumour in mice. A reversed-phase high-performance liquid chromatographic method is described for the measurement of this agent in plasma. The internal standard was N-[2-(diethylamino)ethyl]acridine-4-carboxamide. The compounds of interest were extracted from plasma (0.2 ml) with acetonitrile and further purified on C18 solid-phase extraction Bond Elut columns. After elution with acetonitrile-ammonium acetate buffer and evaporation, the final separation was carried out on a C18 muBondapak column with fluorimetric detection. Over the plasma concentration range 100-5000 nM, the intra- and inter-assay coefficients of variation were less than 4.1 and 7.7%, respectively. The accuracy of the method varied from 97 to 105% of the theoretical values. The lowest concentration which could be measured with acceptable accuracy (+/- 10%) and precision (coefficient of variation less than 10%) was 10 nM. The method was sufficiently sensitive to allow pharmacokinetic analyses of 30 mumol/kg doses for more than six half-lives (t1/2) in rabbits (t1/2 = 4) and mice (t1/2 = 1.3 h).
N-[2-(二甲基氨基)乙基]吖啶-4-甲酰胺是一种新型实验性抗肿瘤药物,对小鼠Lewis肺癌具有优异的体内活性。本文描述了一种反相高效液相色谱法用于测定血浆中的该药物。内标为N-[2-(二乙氨基)乙基]吖啶-4-甲酰胺。将感兴趣的化合物从血浆(0.2 ml)中用乙腈萃取,并在C18固相萃取Bond Elut柱上进一步纯化。用乙腈-醋酸铵缓冲液洗脱并蒸发后,最终在C18 μBondapak柱上进行分离并采用荧光检测。在血浆浓度范围100 - 5000 nM内,批内和批间变异系数分别小于4.1%和7.7%。该方法的准确度在理论值的97%至105%之间。能够以可接受的准确度(±10%)和精密度(变异系数小于10%)进行测量的最低浓度为10 nM。该方法灵敏度足够高,能够对兔(t1/2 = 4小时)和小鼠(t1/2 = 1.3小时)中30 μmol/kg剂量进行超过六个半衰期(t1/2)的药代动力学分析。