Bullen W W, Whitfield L R, Walter G A, Brodfuehrer J I
Parke-Davis Pharmaceutical Research, Department of Pharmacokinetics and Drug Metabolism, Division of Warner-Lambert Company, Ann Arbor, MI 48105, USA.
J Chromatogr B Biomed Appl. 1995 Jun 9;668(1):141-51. doi: 10.1016/0378-4347(95)00067-s.
CI-980, a 1-deaza-7,8-dihydropteridine, is a novel anticancer agent that is a potent mitotic inhibitor acting as a tubulin binder similar to the vinca alkaloids. CI-980 has shown equivalent or superior anticancer activity in vitro compared to vincristine and retains full activity against vincristine resistant tumors in vitro. A high-performance liquid chromatographic (HPLC) assay was developed and validated for human plasma and urine to support Phase 1 clinical trials. CI-980 and PD 080658, internal standard, were isolated from 2-ml samples of human plasma and urine by solid-phase extraction with Bond-Elut C18 cartridges. Urine samples must be pretreated with bovine serum albumin (BSA) to minimize the binding of CI-980 to glass and some plastics. The eluate from the cartridges for both matrices was evaporated to dryness and taken up in mobile phase. Zorbax RX C18 columns, mobile phase buffer of 10 mM ammonium dihydrogen phosphate at pH 7.5 and a flow-rate of 0.75 ml/min were used for both matrices. Column dimensions, column temperature and mobile phase acetonitrile-buffer ratio were 300 mm x 4.6 mm I.D., 30 degrees C and 38:62 (v/v), respectively, for the plasma assay and 250 mm x 4.6 mm I.D., 35 degrees C and 40:60 (v/v), respectively, for the urine assay. Column effluent was monitored fluorometrically for the plasma method using excitation and emission wavelengths of 388 nm and 473 nm, respectively. Ultraviolet detection at 380 nm was used for the urine method. Peak-area ratios were proportional to CI-980 concentrations from 0.2 to 25 ng/ml and 1 to 100 ng/ml for plasma and urine, respectively. CI-980 in water will bind to glass and plastics but not PTFE or stainless steel. Urine calibration standards were frozen prior to use in order to compensate for loss of CI-980 due to freezing in this matrix. The accuracy of the assay was within 4.7%, with a precision of 5.6% for both matrices. Recoveries ranged from 93.8 to 102% and 90.7 to 92.3% for plasma and urine, respectively. CI-980 was stable in plasma and urine for at least 275 and 217 days, respectively, when stored at -70 degrees C. The assay is suitable for studying the clinical pharmacokinetics of CI-980.
CI-980是一种1-脱氮-7,8-二氢蝶啶,是一种新型抗癌剂,是一种强效的有丝分裂抑制剂,作用类似于长春花生物碱,可作为微管蛋白结合剂。与长春新碱相比,CI-980在体外显示出同等或更高的抗癌活性,并且在体外对长春新碱耐药肿瘤保持完全活性。开发并验证了一种用于人血浆和尿液的高效液相色谱(HPLC)测定法,以支持1期临床试验。通过使用Bond-Elut C18柱进行固相萃取,从2 ml人血浆和尿液样品中分离出CI-980和内标PD 080658。尿液样品必须用牛血清白蛋白(BSA)进行预处理,以尽量减少CI-980与玻璃和一些塑料的结合。两种基质的柱洗脱液均蒸发至干,并溶解于流动相中。血浆和尿液测定均使用Zorbax RX C18柱、pH 7.5的10 mM磷酸二氢铵流动相缓冲液和0.75 ml/min的流速。血浆测定的柱尺寸、柱温及流动相乙腈-缓冲液比例分别为300 mm×4.6 mm内径、30℃和38:62(v/v),尿液测定分别为250 mm×4.6 mm内径、35℃和40:60(v/v)。血浆方法采用荧光法监测柱流出物,激发波长和发射波长分别为388 nm和473 nm。尿液方法采用380 nm紫外检测。血浆和尿液的峰面积比分别与0.2至25 ng/ml和1至100 ng/ml的CI-980浓度成正比。水中的CI-980会与玻璃和塑料结合,但不会与聚四氟乙烯或不锈钢结合。尿液校准标准品在使用前冷冻,以补偿由于在此基质中冷冻导致的CI-980损失。该测定法的准确度在4.7%以内,两种基质的精密度均为5.6%。血浆和尿液的回收率分别为93.8%至102%和90.7%至92.3%。当在-70℃储存时,CI-980在血浆和尿液中分别至少稳定275天和217天。该测定法适用于研究CI-980的临床药代动力学。