Alberts D S, Chang S Y, Chen H S, Evans T L, Moon T E
Clin Pharmacol Ther. 1979 Dec;26(6):737-45. doi: 10.1002/cpt1979266737.
The systemic availability of melphalan after oral administration is not well known. Most patients are put on a fixed oral dosage regimen. We have studied the disposition of melphalan in 14 patients after single oral doses. Five were also studied after receiving the same dose intravenously. Oral melphalan had a mean plasma terminal phase half-life (t1/2) of 90 +/- 17 min. The mean area under the plasma concentration:time curve (CXT) was 53 +/- 33 micrograms . min/ml. Urinary excretion of oral melphalan averaged 10.9 +/- 4.9% during the first 24 hr. The CXT ratio (oral:intravenous) for the 5 patients studied after both oral and intravenous melphalal (0.6 mg/kg) ranged between 0.25 and 0.89 and averaged 0.56. After oral dosing in 14 fasting patients, the time at which melphalan first appeared in the plasma varied between 15 min and 6 hr. In a myeloma patient who took oral melphalan, no melphalan was found in plasma or urine up to 24 hr. Some instances of failure of tumor response to oral melphalan may be due to inadequate bioavailability rather than inherent tumor resistance.
口服美法仑后的全身可用性尚不清楚。大多数患者采用固定的口服给药方案。我们研究了14例患者单次口服美法仑后的处置情况。其中5例患者还在静脉注射相同剂量后进行了研究。口服美法仑的血浆终末相半衰期(t1/2)平均为90±17分钟。血浆浓度-时间曲线下面积(CXT)平均为53±33微克·分钟/毫升。口服美法仑在前24小时的尿排泄平均为10.9±4.9%。对5例口服和静脉注射美法仑(0.6毫克/千克)后进行研究的患者,其CXT比值(口服:静脉注射)在0.25至0.89之间,平均为0.56。在14例空腹患者口服给药后,美法仑首次出现在血浆中的时间在15分钟至6小时之间。在一名口服美法仑的骨髓瘤患者中,在长达24小时的时间里,血浆或尿液中均未发现美法仑。口服美法仑后肿瘤反应失败的一些情况可能是由于生物利用度不足而非肿瘤固有耐药性所致。