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多发性骨髓瘤常规治疗期间口服和静脉注射美法仑的药代动力学

Pharmacokinetics of oral and intravenous melphalan during routine treatment of multiple myeloma.

作者信息

Bosanquet A G, Gilby E D

出版信息

Eur J Cancer Clin Oncol. 1982 Apr;18(4):355-62. doi: 10.1016/0277-5379(82)90006-2.

Abstract

Plasma melphalan levels have been measured in nine (mostly stage IIIA) multiple myeloma patients after therapeutic doses of drug had been given p.o. and i.v. A new isocratic high-pressure liquid chromatographic (HPLC) method with a sensitivity limit o 5 ng/ml was used to quantify the melphalan. Patients receiving 8-28.5 mg melphalan i.v. showed alpha and beta plasma decays with half-lives of 7.7 +/- 3.3 (mean +/- S.D.) and 83 +/- 14 min respectively. The apparent volume of the central compartment was 12.8 +/- 4.3 1, and the total volume of distribution was 0.62 +/- 0.21 l/kg. Very variable absorption was seen in the same patients after receiving 5-12 mg melphalan p.o. The half-life of the absorption phase varied from 2.1 to 62.1 min (22.8 +/- 18.1 min) with delays (before absorption started) of 0-113 min. The fraction of dose absorbed varied from 0.32 to 1.03 (0.72 +/- 0.23), and the half-life of the beta phase was 92 +/- 27 min. The type of breakfast eaten before p.o. melphalan was found to correlate with the fraction of drug absorbed.

摘要

在9名(大多为IIIA期)多发性骨髓瘤患者口服和静脉注射治疗剂量的药物后,测定了其血浆美法仑水平。采用一种灵敏度极限为5 ng/ml的新型等度高压液相色谱(HPLC)方法对美法仑进行定量。静脉注射8 - 28.5 mg美法仑的患者,其血浆α相和β相消除半衰期分别为7.7±3.3(均值±标准差)和83±14分钟。中央室的表观容积为12.8±4.3升,分布总体积为0.62±0.21升/千克。同一患者口服5 - 12 mg美法仑后,吸收情况差异很大。吸收相半衰期在2.1至62.1分钟之间变化(22.8±18.1分钟),吸收延迟时间(在吸收开始前)为0至113分钟。吸收的剂量分数在0.32至1.03之间变化(0.72±0.23),β相半衰期为92±27分钟。发现口服美法仑前吃的早餐类型与药物吸收分数相关。

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