Literature DB >> 7600920

Taxol metabolism and disposition in cancer patients.

T Walle1, U K Walle, G N Kumar, K N Bhalla.   

Abstract

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.

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Year:  1995        PMID: 7600920

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  18 in total

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Review 2.  The taxoids. Comparative clinical pharmacology and therapeutic potential.

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3.  Taxol suppresses dynamics of individual microtubules in living human tumor cells.

Authors:  A M Yvon; P Wadsworth; M A Jordan
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Review 5.  Methods to evaluate biliary excretion of drugs in humans: an updated review.

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6.  Formulating paclitaxel in nanoparticles alters its disposition.

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Journal:  Pharm Res       Date:  2005-06-08       Impact factor: 4.200

7.  A population pharmacokinetic model for paclitaxel in the presence of a novel P-gp modulator, Zosuquidar Trihydrochloride (LY335979).

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8.  Human liver microsomal metabolism of paclitaxel and drug interactions.

Authors:  P B Desai; J Z Duan; Y W Zhu; S Kouzi
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1998 Jul-Sep       Impact factor: 2.441

9.  Increased elimination of paclitaxel by magnesium isoglycyrrhizinate in epithelial ovarian cancer patients treated with paclitaxel plus cisplatin: a pilot clinical study.

Authors:  Kai Jie Chen; Wan Yi Chen; Xia Chen; Yi Ming Jia; Gui Qin Peng; Li Chen
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2013-05-17       Impact factor: 2.441

10.  Paclitaxel Enhances Carboplatin-DNA Adduct Formation and Cytotoxicity.

Authors:  Shuai Jiang; Amy W Pan; Tzu-yin Lin; Hongyong Zhang; Michael Malfatti; Kenneth Turteltaub; Paul T Henderson; Chong-xian Pan
Journal:  Chem Res Toxicol       Date:  2015-11-11       Impact factor: 3.739

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