Literature DB >> 536670

Determination of tamoxifen and an hydroxylated metabolite in plasma from patients with advanced breast cancer using gas chromatography-mass spectrometry.

C P Daniel, S J Gaskell, H Bishop, R I Nicholson.   

Abstract

An assay has been established for the selective measurement of tamoxifen and its monohydroxy derivative, metabolite B, in human plasma. The assay was used to examine the concentrations of these compounds, relative to oestradiol-17 beta, in the plasma of patients undergoing tamoxifen therapy for advanced breast cancer. Oral administration of the drug (20 mg twice a day) raised the level of tamoxifen in plasma to approximately 200 ng/ml 20 days after the commencement of treatment. This level was 3000-fold higher than the corresponding concentration of oestradiol which remained within the range for post-menopausal women. Metabolite B was present in plasma at a much lower concentration than tamoxifen although in considerable excess over oestradiol. The overall results are discussed in relation to the possible mechanism of action of the drug.

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Year:  1979        PMID: 536670     DOI: 10.1677/joe.0.0830401

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  15 in total

Review 1.  Clinical pharmacokinetics of endocrine agents used in advanced breast cancer.

Authors:  P E Lønning; E A Lien; S Lundgren; S Kvinnsland
Journal:  Clin Pharmacokinet       Date:  1992-05       Impact factor: 6.447

2.  The effect of adjuvant therapy with or without tamoxifen on the endocrine function of patients with breast cancer.

Authors:  T Yasumura; T Akami; M Mitsuo; T Oka; K Naitoh; T Yamamoto; H Honjyo; H Okada
Journal:  Jpn J Surg       Date:  1990-07

3.  Electrospray ionization mass spectrometry for analysis of low-molecular-weight anticancer drugs and their analogues.

Authors:  G K Poon; G M Bisset; P Mistry
Journal:  J Am Soc Mass Spectrom       Date:  1993-07       Impact factor: 3.109

4.  Anti-Tumoral Activity of a Short Decapeptide Fragment of the Alzheimer's Abeta Peptide.

Authors:  Daniel Paris; Nikunj Patel; Nowell J Ganey; Vincent Laporte; Amita Quadros; Michael J Mullan
Journal:  Int J Pept Res Ther       Date:  2010       Impact factor: 1.931

5.  The development of tamoxifen for breast cancer therapy: a tribute to the late Arthur L. Walpole.

Authors:  V C Jordan
Journal:  Breast Cancer Res Treat       Date:  1988-07       Impact factor: 4.872

Review 6.  Laboratory studies to develop general principles for the adjuvant treatment of breast cancer with antiestrogens: problems and potential for future clinical applications.

Authors:  V C Jordan
Journal:  Breast Cancer Res Treat       Date:  1983       Impact factor: 4.872

Review 7.  Tamoxifen. A reappraisal of its pharmacodynamic and pharmacokinetic properties, and therapeutic use.

Authors:  M M Buckley; K L Goa
Journal:  Drugs       Date:  1989-04       Impact factor: 9.546

8.  Effect of oestrogen receptor status and time on the intra-tumoural accumulation of tamoxifen and N-desmethyltamoxifen following short-term therapy in human primary breast cancer.

Authors:  S R Johnston; B P Haynes; N P Sacks; J A McKinna; L J Griggs; M Jarman; M Baum; I E Smith; M Dowsett
Journal:  Breast Cancer Res Treat       Date:  1993-12       Impact factor: 4.872

Review 9.  Metabolites of tamoxifen in animals and man: identification, pharmacology, and significance.

Authors:  V C Jordan
Journal:  Breast Cancer Res Treat       Date:  1982       Impact factor: 4.872

10.  Inhibition of cloned HERG potassium channels by the antiestrogen tamoxifen.

Authors:  Dierk Thomas; Bernd Gut; Syrus Karsai; Anna-Britt Wimmer; Kezhong Wu; Gunnar Wendt-Nordahl; Wei Zhang; Sven Kathöfer; Wolfgang Schoels; Hugo A Katus; Johann Kiehn; Christoph A Karle
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2003-06-25       Impact factor: 3.000

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