Walle T, Walle U K, Kumar G N, Bhalla K N
Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston 29425, USA.
Drug Metab Dispos. 1995 Apr;23(4):506-12.
The objective of this study was to determine the metabolic fate and disposition of taxol in cancer patients. Five patients received 225 or 250 mg/m2 of taxol together with 100 microCi of [3H]taxol as a 3-hr infusion, followed by cisplatin and 5-fluorouracil. Urine, feces, and blood samples were collected for 120 hr and analyzed for total radioactivity, taxol, and metabolites by reversed-phase HPLC and tandem MS. Total urinary excretion was 14.3 +/- 1.4% (SE) of the dose, with unchanged taxol and an unknown polar metabolite as the main excretion products. Total fecal excretion was 71.1 +/- 8.2%, with 6 alpha-hydroxytaxol being the largest component by far. Unchanged taxol and four other metabolites could also be identified from fecal extracts. The plasma area under the curve for unchanged taxol was 20.5 +/- 2.3 microM.hr and that for total taxol metabolites was 14.2 +/- 4.5 microM.hr. The half-life of total metabolites (5.6 +/- 0.4 hr), however, greatly exceeded that of unchanged taxol (2.9 +/- 0.3 hr). Thus, at 5-hr posttaxol infusion, the plasma concentrations of the five metabolites together exceeded the taxol concentration by 2.4-fold. The findings from this study should be of importance as a guide to further therapeutic evaluation of this drug.
本研究的目的是确定紫杉醇在癌症患者体内的代谢转归和处置情况。5名患者接受了225或250mg/m²的紫杉醇,同时静脉输注100μCi的[³H]紫杉醇,持续3小时,随后给予顺铂和5-氟尿嘧啶。收集尿液、粪便和血液样本120小时,并通过反相高效液相色谱法和串联质谱法分析总放射性、紫杉醇及其代谢产物。尿中总排泄量为剂量的14.3±1.4%(标准误),排泄产物主要为原形紫杉醇和一种未知的极性代谢产物。粪便中总排泄量为71.1±8.2%,其中6α-羟基紫杉醇是迄今为止最大的成分。从粪便提取物中还可鉴定出原形紫杉醇和其他四种代谢产物。原形紫杉醇的血浆曲线下面积为20.5±2.3μM·小时,紫杉醇总代谢产物的血浆曲线下面积为14.2±4.5μM·小时。然而,总代谢产物的半衰期(5.6±0.4小时)大大超过原形紫杉醇的半衰期(2.9±0.3小时)。因此,在紫杉醇输注后5小时,五种代谢产物的血浆浓度之和超过紫杉醇浓度2.4倍。本研究结果对于进一步评估该药物的治疗效果具有重要指导意义。