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多柔比星在人为诱导产生酸性或碱性尿液情况下的药代动力学。

Pharmacokinetics of doxorubicin in man with induced acid or alkaline urine.

作者信息

Krarup-Hansen A, Wassermann K, Rasmussen S N, Dalmark M

机构信息

Department of Oncology A, Finsen Institute, Copenhagen, Denmark.

出版信息

Acta Oncol. 1988;27(1):25-30. doi: 10.3109/02841868809090314.

Abstract

The common side effects of doxorubicin (DOX) treatment, i.e. vomiting and diarrhoea, would be expected to alter the pharmacokinetics of DOX in man, the efficacy of treatment, and further aggravate the side effects through acid/base disturbances. The pharmacokinetics were therefore investigated in 4 anthracycline naive females with advanced mammary carcinoma in 2 series of DOX monotherapy 70 mg/m2 administered with an interval of 4 weeks between the treatments. Sequential loading either with acid or base was instituted 2 days before and continued for 2 days after DOX infusion. Median urine pH was 5.0 or 8.0, and median arterial blood pH 7.30 or 7.43 respectively. Plasma and urine samples were analyzed by high performance liquid chromatography (HPLC). No difference was seen between the acid and alkaline condition for DOX or doxorubicinol with regard to clearance from blood plasma, area under the curve, renal clearance, renal drug clearance/renal creatinine clearance. Thus moderate acid/base metabolic disturbances did not alter the pharmacokinetics of DOX up to 48 h after DOX infusion.

摘要

阿霉素(DOX)治疗的常见副作用,即呕吐和腹泻,预计会改变DOX在人体中的药代动力学、治疗效果,并通过酸碱紊乱进一步加重副作用。因此,在2组DOX单药治疗中,对4名未接受过蒽环类药物治疗的晚期乳腺癌女性患者进行了药代动力学研究,每次给予70mg/m²的DOX,治疗间隔为4周。在DOX输注前2天开始依次进行酸或碱负荷,并在DOX输注后持续2天。尿液pH中位数分别为5.0或8.0,动脉血pH中位数分别为7.30或7.43。通过高效液相色谱法(HPLC)分析血浆和尿液样本。在酸性和碱性条件下,DOX或阿霉素醇在血浆清除率、曲线下面积、肾清除率、肾药物清除率/肾肌酐清除率方面均未观察到差异。因此,在DOX输注后长达48小时内,中度酸碱代谢紊乱并未改变DOX的药代动力学。

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