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癌症患者静脉输注甲氨蝶呤后的蛋白质结合与消除情况。

The protein binding and elimination of methotrexate after intravenous infusions in cancer patients.

作者信息

Paxton J W

出版信息

Clin Exp Pharmacol Physiol. 1982 May-Jun;9(3):225-34. doi: 10.1111/j.1440-1681.1982.tb00800.x.

Abstract
  1. Total serum concentrations and protein binding of methotrexate (MTX) have been studied after fifty-eight 6 h MTX infusions in nineteen cancer patients. 2. There was a linear relationship between dose (mg/kg) and serum MTX concentration at termination of infusion. 3. The elimination of total serum and "free' MTX followed similar bi-exponential expressions during the 72 h studied after the infusion. 4. Of the eight occasions when total serum concentrations did not fall below 10(-7) mol/l on the third day, five were associated with toxicity. 5. Mean per cent MTX bound by sera from the nineteen patients was 47.2 (s.d. = 4.4) per cent and appeared to be independent of MTX concentration within the range studied. 6. This study suggests that the very high binding previously reported for MTX should be questioned and that measurement of total serum MTX concentration (bound plus free) is sufficient for the recognition of patients who might be at risk of developing toxicity.
摘要
  1. 在19例癌症患者接受58次6小时甲氨蝶呤(MTX)输注后,对其血清总浓度及蛋白结合情况进行了研究。2. 输注结束时,剂量(mg/kg)与血清MTX浓度之间存在线性关系。3. 在输注后的72小时研究期间,血清总MTX和“游离”MTX的消除遵循相似的双指数表达式。4. 在8次第三天血清总浓度未降至10⁻⁷mol/L以下的情况中,有5次与毒性相关。5. 19例患者血清结合MTX的平均百分比为47.2%(标准差=4.4%),在所研究范围内似乎与MTX浓度无关。6. 本研究表明,先前报道的MTX极高结合率值得怀疑,测定血清总MTX浓度(结合型加游离型)足以识别可能有发生毒性风险的患者。

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