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口服美法仑的药代动力学:干扰素诱导发热的影响。

Oral melphalan pharmacokinetics: influence of interferon-induced fever.

作者信息

Ehrsson H, Eksborg S, Wallin I, Osterborg A, Mellstedt H

机构信息

Karolinska Pharmacy and Radiumhemmet, Karolinska Hospital, Stockholm, Sweden.

出版信息

Clin Pharmacol Ther. 1990 Jan;47(1):86-90. doi: 10.1038/clpt.1990.13.

Abstract

The influence of interferon-induced fever on oral melphalan pharmacokinetics has been studied in 10 myeloma patients in a randomized crossover design. The melphalan dose (0.25 mg/kg) was given alone and 5 hours after the administration of human interferon alpha (7 x 10(6) IU/m2), respectively. The plasma concentration of melphalan was determined by liquid chromatography with fluorometric detection after derivatization of melphalan with N-acetylcysteine. The area under the plasma concentration-time curve (AUC) was significantly lower (p = 0.02) when melphalan was given with interferon. There was a significant negative correlation (p = 0.008) between body temperature and dose normalized AUC, whereas no effect was noticed on the maximum plasma concentration (Cmax) and on the time to obtain Cmax. The rate of elimination showed a tendency (p = 0.06) to increase with increasing body temperature. It is suggested that the cytotoxicity of the drug is most probably enhanced because of the higher alkylating activity of the compound at elevated body temperatures.

摘要

采用随机交叉设计,在10例骨髓瘤患者中研究了干扰素诱导的发热对口服美法仑药代动力学的影响。美法仑剂量(0.25mg/kg)分别单独给药以及在给予人干扰素α(7×10⁶IU/m²)5小时后给药。用N - 乙酰半胱氨酸对美法仑进行衍生化后,通过荧光检测液相色谱法测定美法仑的血浆浓度。当美法仑与干扰素合用时,血浆浓度 - 时间曲线下面积(AUC)显著降低(p = 0.02)。体温与剂量标准化AUC之间存在显著负相关(p = 0.008),而对最大血浆浓度(Cmax)和达到Cmax的时间未观察到影响。消除速率有随体温升高而增加的趋势(p = 0.06)。提示由于该化合物在体温升高时具有更高的烷基化活性,药物的细胞毒性很可能增强。

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