Zimm S, Collins J M, Miser J, Chatterji D, Poplack D G
Clin Pharmacol Ther. 1984 Jun;35(6):826-30. doi: 10.1038/clpt.1984.120.
To better characterize the disposition of cytosine arabinoside (Ara-C) in cerebrospinal fluid (CSF), its kinetics were studied in seven patients with meningeal leukemia in complete remission. After intraventricular injection of 30 mg Ara-C, CSF and plasma samples were obtained over a 24-hr period. Ara-C levels were measured by a reverse-phase HPLC assay (with a sensitivity of 0.5 microM in CSF and 1.0 microM in plasma) that readily separated Ara-C from its major metabolite uracil arabinoside (Ara-U). Elimination of Ara-C from CSF followed a biphasic pattern, with an initial t1/2 of 1 hr and a terminal t1/2 of 3.4 hr. Ara-C clearance from CSF was 0.42 ml/min, suggesting that drug elimination was primarily by CSF bulk flow. The ratio of the AUC of Ara-U to the AUC of Ara-C was 0.08, indicating only minor metabolism of Ara-C to Ara-U in CSF, in contrast to that after systemic Ara-C. Despite initial CSF Ara-C concentrations exceeding 2 mM, Ara-C was not detectable in plasma in any patient. Intraventricular Ara-C results in very high levels in CSF, but systemic tissues are relatively spared from exposure to Ara-C.
为了更好地描述阿糖胞苷(Ara-C)在脑脊液(CSF)中的分布情况,对7例处于完全缓解期的脑膜白血病患者的阿糖胞苷动力学进行了研究。经脑室内注射30mg阿糖胞苷后,在24小时内采集脑脊液和血浆样本。阿糖胞苷水平通过反相高效液相色谱法测定(脑脊液中的灵敏度为0.5μM,血浆中的灵敏度为1.0μM),该方法能轻易地将阿糖胞苷与其主要代谢产物阿糖尿苷(Ara-U)分离。脑脊液中阿糖胞苷的消除呈双相模式,初始半衰期为1小时,终末半衰期为3.4小时。脑脊液中阿糖胞苷的清除率为0.42ml/min,表明药物消除主要通过脑脊液的整体流动。阿糖尿苷的AUC与阿糖胞苷的AUC之比为0.08,这表明与全身应用阿糖胞苷后相比,脑脊液中阿糖胞苷向阿糖尿苷的代谢作用较小。尽管脑脊液中阿糖胞苷的初始浓度超过2mM,但在任何患者的血浆中均未检测到阿糖胞苷。脑室内注射阿糖胞苷可使脑脊液中的药物水平非常高,但全身组织相对较少暴露于阿糖胞苷。