Bleyer W A, Dedrick R L
Cancer Treat Rep. 1977 Jul;61(4):703-8.
Cerebrospinal fluid (CSF) and plasma methotrexate (MTX) concentrations were measured in 76 children and adults who received intrathecal MTX, 12 mg/m2 body surface area, without developing symptoms of lumbar puncture syndrome or drug-induced neurotoxicity. After an initial rapid redistribution of the injected drug, the mean antifolate value in the lumbar CSF declined in a biphasic manner with half-lives of 4.5 and 14 hours. In the plasma the mean MTX concentration reached a peak of 2 X 10(-7) M between 3 and 12 hours after injection and decreased biexponentially thereafter with half-lives of 5.5 and 24 hours. Pharmacokinetic analysis suggested that the predominant mode of MTX transfer from the central nervous system to the systemic circulation is bulk flow absorption of CSF with entrained drug. The two phases of disappearance from the lumbar CSF appear to result from interaction of the convective transport and diffusion between the CSF and brain extracellular fluid (and perhaps some intracellular sites).
对76名接受鞘内注射甲氨蝶呤(MTX)(剂量为12 mg/m²体表面积)且未出现腰椎穿刺综合征症状或药物诱导神经毒性的儿童和成人,测定了其脑脊液(CSF)和血浆中甲氨蝶呤(MTX)的浓度。在注射药物最初快速重新分布后,腰椎脑脊液中的平均抗叶酸值呈双相下降,半衰期分别为4.5小时和14小时。在血浆中,MTX平均浓度在注射后3至12小时达到峰值2×10⁻⁷ M,此后呈双指数下降,半衰期分别为5.5小时和24小时。药代动力学分析表明,MTX从中枢神经系统向体循环转移的主要方式是夹带药物的脑脊液的大量流动吸收。腰椎脑脊液中药物消失的两个阶段似乎是脑脊液与脑细胞外液(可能还有一些细胞内位点)之间对流运输和扩散相互作用的结果。