Suppr超能文献

甲氨蝶呤在血浆和红细胞之间的体内分布。

The in vivo distribution of methotrexate between plasma and erythrocytes.

作者信息

Steele W H, Stuart J F, Lawrence J R, McNeill C A

出版信息

Cancer Chemother Pharmacol. 1982;9(2):110-3. doi: 10.1007/BF00265389.

Abstract
  1. The concentration of methotrexate in whole blood, plasma and erythrocytes was measured in three patients receiving 250 mg methotrexate by continuous intravenous infusion over 12 h for different malignant diseases. 2. Methotrexate was measured using a double-antibody radioimmunoassay which facilitated drug monitoring for 1--2 weeks. 3. The concentration of methotrexate in plasma was much higher than that in whole blood and erythrocytes during the period of infusion, but this profile was reversed during the elimination phase. 4. The concentration in erythrocytes fell rapidly immediately after the infusion ended, but thereafter, in contrast to plasma levels, methotrexate concentrations in erythrocytes did not appear to decay during the elimination phase. In one patient the concentration/time profiles differed between treatment days. On the first occasion, at the initiation of chemotherapy, erythrocytes progressively accumulated methotrexate in the elimination phase against an apparent concentration gradient. On the second occasion this progressive increase was not observed, but as in the other two patients, methotrexate levels in red cells remained many times higher than drug levels in plasma throughout the period of observation. 5. Folinic acid administration did not appear to influence the distribution of methotrexate between red cells and plasma. 6. It was concluded that while the distribution between plasma and erythrocytes was probably mediated by complex mechanisms, the results were consistent with the erythrocyte mass behaving as a slowly exchanging kinetic compartment. Accumulation and persistence of a drug such as methotrexate in red cells might be expected to promote resistance and perhaps influence the expression of toxicity.
摘要
  1. 对三名因不同恶性疾病接受12小时持续静脉输注250毫克甲氨蝶呤的患者,测定了全血、血浆和红细胞中甲氨蝶呤的浓度。2. 采用双抗体放射免疫分析法测定甲氨蝶呤,该方法便于进行1至2周的药物监测。3. 输注期间,血浆中甲氨蝶呤的浓度远高于全血和红细胞中的浓度,但在消除阶段这种情况则相反。4. 输注结束后,红细胞中的浓度立即迅速下降,但此后,与血浆水平不同,红细胞中甲氨蝶呤的浓度在消除阶段似乎并未衰减。在一名患者中,不同治疗日的浓度/时间曲线有所不同。第一次,在化疗开始时,红细胞在消除阶段逆着明显的浓度梯度逐渐积累甲氨蝶呤。第二次未观察到这种逐渐增加的情况,但与其他两名患者一样,在整个观察期间,红细胞中甲氨蝶呤的水平仍比血浆中的药物水平高许多倍。5. 给予亚叶酸似乎并未影响甲氨蝶呤在红细胞和血浆之间的分布。6. 得出的结论是,虽然血浆和红细胞之间的分布可能由复杂机制介导,但结果与红细胞群体表现为一个缓慢交换的动力学隔室一致。甲氨蝶呤等药物在红细胞中的积累和持续存在可能会导致耐药性增加,并可能影响毒性的表达。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验