Spectroscopic investigations of the molecular interaction of anticancer drug mitoxantrone with non-ionic surfactant micelles

J Pharm Pharmacol. 2012 May;64(5):688-96. doi: 10.1111/j.2042-7158.2012.01445.x. Epub 2012 Feb 7.

Abstract

Objectives: The aim of this study was to investigate the interaction of the anticancer drug mitoxantrone with non-ionic micelles, as simple model systems of biological membranes.

Methods: UV-VIS absorption spectroscopy was used to quantify the drug-surfactant micelle interactions in terms of the binding constant and the micelle-water partition coefficient of the drug.

Key findings: Interaction of mitoxantrone with non-ionic micelles reduces the dimerization process of mitoxantrone, the drug molecules being encapsulated into micelles as monomer. The strength of the interaction between mitoxantrone and non-ionic micelles is higher at pH10 than at pH7.4, and depends on the surfactant in the order Tween 80>Tween 20>Triton X-100. The higher partition coefficient at pH10 compared to pH7.4 suggests that at basic pH the deprotonated mitoxantrone is incorporated more efficiently into the hydrophobic medium of non-ionic micelles compared to physiological pH, when the protonated drug is predominant.

Conclusions: These results on simple model systems miming the drug-membrane interactions contribute to the elucidation of the behaviour of the drug in vivo, as well as the possible utilization of surfactant micelles as drug carriers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dimerization
  • Drug Carriers / chemistry
  • Hydrogen-Ion Concentration
  • Hydrophobic and Hydrophilic Interactions
  • Membranes / chemistry*
  • Micelles*
  • Mitoxantrone / administration & dosage
  • Mitoxantrone / chemistry*
  • Models, Biological
  • Spectrophotometry, Ultraviolet / methods
  • Surface-Active Agents / chemistry*
  • Water

Substances

  • Drug Carriers
  • Micelles
  • Surface-Active Agents
  • Water
  • Mitoxantrone