Tamoxifen-encapsulated vesicular systems: cytotoxicity evaluation in human epidermal keratinocyte cell line

Drug Dev Ind Pharm. 2010 Mar;36(3):350-4. doi: 10.1080/03639040903173549.

Abstract

Aim: Tamoxifen is a nonsteroidal estrogen receptor modulator indicated in the treatment of breast cancer. Apoptosis has been reported to be a major mechanism for its antitumor effect. Tamoxifen has also shown significant potential in treating various dermatological disorders including psoriasis, characterized by hyperproliferation of epidermal keratinocytes. An endeavor was made in the current studies to investigate the potency of vesicle-encapsulated tamoxifen on human epidermal keratinocyte cell lines.

Methods: Drug was encapsulated in the phospholipid-based vesicular systems, namely, conventional liposomes and flexible-membrane liposomes. In vitro cytotoxicity evaluation of the formulations was carried out employing MTT cell proliferation assay.

Results: A composition-dependent strong inhibition in the viability of epidermal keratinocyte cells was observed.

Conclusion: The encouraging findings of this work construe immense potential of the tamoxifen-encapsulated vesicular systems in the management of psoriasis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Cutaneous
  • Cell Line
  • Cell Proliferation / drug effects*
  • Cell Survival / drug effects
  • Cholesterol / chemistry
  • Drug Carriers / administration & dosage*
  • Drug Carriers / pharmacology
  • Hexoses / chemistry
  • Humans
  • Inhibitory Concentration 50
  • Keratinocytes / drug effects
  • Liposomes
  • Membrane Fluidity
  • Phosphatidylcholines / chemistry
  • Psoriasis / drug therapy
  • Selective Estrogen Receptor Modulators / administration & dosage*
  • Selective Estrogen Receptor Modulators / pharmacology
  • Surface-Active Agents / chemistry
  • Tamoxifen / administration & dosage*
  • Tamoxifen / pharmacology

Substances

  • Drug Carriers
  • Hexoses
  • Liposomes
  • Phosphatidylcholines
  • Selective Estrogen Receptor Modulators
  • Surface-Active Agents
  • sorbitan monooleate
  • Tamoxifen
  • Cholesterol