Literature DB >> 2611038

Pharmacokinetics of anthracyclines.

S Eksborg1.   

Abstract

The plasma pharmacokinetics of the two commonly used anthracyclines doxorubicin and 4'epi-doxorubicin have been studied by reversed phase liquid chromatography with photometric detection. After intravenous administration the plasma pharmacokinetics of doxorubicin and 4'epi-doxorubicin are characterized by the three compartment open model. Typically, the half-life time of the alpha-phase is 3-5 min and the terminal half-life time in the order 20-30 h. An almost 10-fold inter-individual variation of the dose normalized area under the plasma concentration time curve (AUC/mg/m2) has been observed, underlining the need for an individualization of the dose. The chemical structures of doxorubicin and 4'epi-doxorubicin are very similar. Comparative pharmacokinetic studies were carried out by simultaneous administration of the drugs using a highly selective analytical technique. By this approach it was possible to reduce the influence by the large intra- and inter-individual pharmacokinetic variations. The values of AUC and Cmax were on the average 1.6 and 1.2 times larger for doxorubicin than for 4'epi-doxorubicin. Side effects, reported to be related to the maximum plasma concentration (Cmax), include cardiac toxicity, nausea and vomiting, while the antitumour effect has been associated with the area under the plasma concentration time curve (AUC). A 10-fold decrease of Cmax without a decrease of AUC was observed when doxorubicin was administered as a 4-h infusion as compared to an intravenous bolus injection. A further increase of the administration time had only a minor effect on Cmax. Intrahepatic administration of doxorubicin reduced the values of AUC and Cmax by 1.5 and 1.7 (mean values) respectively. The combination of doxorubicin and 4'epi-doxorubicin with biodegradable starch microspheres (Spherex) resulted in a further decrease of Cmax, while AUC was unaffected. The observed increase of the mean residence time (MRT) supports the assumption of an increased drug exposure of the tumour caused by Spherex.

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Year:  1989        PMID: 2611038     DOI: 10.3109/02841868909092323

Source DB:  PubMed          Journal:  Acta Oncol        ISSN: 0284-186X            Impact factor:   4.089


  6 in total

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Authors:  J R Wade; A W Kelman; D J Kerr; J Robert; B Whiting
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2.  Overexpression of SERCA2a Alleviates Cardiac Microvascular Ischemic Injury by Suppressing Mfn2-Mediated ER/Mitochondrial Calcium Tethering.

Authors:  Feng Tian; Ying Zhang
Journal:  Front Cell Dev Biol       Date:  2021-04-01

3.  HDAC6 inhibition reverses long-term doxorubicin-induced cognitive dysfunction by restoring microglia homeostasis and synaptic integrity.

Authors:  Blake R McAlpin; Rajasekaran Mahalingam; Anand K Singh; Shruti Dharmaraj; Taylor T Chrisikos; Nabila Boukelmoune; Annemieke Kavelaars; Cobi J Heijnen
Journal:  Theranostics       Date:  2022-01-01       Impact factor: 11.600

Review 4.  Mitochondrial-Targeted Therapy for Doxorubicin-Induced Cardiotoxicity.

Authors:  Bin Bin Wu; Kam Tong Leung; Ellen Ngar-Yun Poon
Journal:  Int J Mol Sci       Date:  2022-02-09       Impact factor: 5.923

5.  Phase I dose escalation and pharmacokinetic study of pluronic polymer-bound doxorubicin (SP1049C) in patients with advanced cancer.

Authors:  S Danson; D Ferry; V Alakhov; J Margison; D Kerr; D Jowle; M Brampton; G Halbert; M Ranson
Journal:  Br J Cancer       Date:  2004-06-01       Impact factor: 7.640

6.  Doxorubicin induces large-scale and differential H2A and H2B redistribution in live cells.

Authors:  Péter Nánási; László Imre; Erfaneh Firouzi Niaki; Rosevalentine Bosire; Gábor Mocsár; Anett Türk-Mázló; Juan Ausio; Gábor Szabó
Journal:  PLoS One       Date:  2020-04-16       Impact factor: 3.240

  6 in total

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