Efficiency of liposomes in the delivery of a photosensitizer controlled by the stereochemistry of a gemini surfactant component

Mol Pharm. 2010 Feb 1;7(1):130-7. doi: 10.1021/mp900173v.

Abstract

Liposomes formulated with dimyristoyl-sn-glycero-phosphatidylcholine, DMPC, and either one of the cationic gemini surfactants (S,S)-2,3-dimethoxy-1,4-bis(N-hexadecyl-N,N-dimethylammonio)butane bromide, 1a, and (S,R)-2,3-dimethoxy-1,4-bis(N-hexadecyl-N,N-dimethylammonio)butane bromide, 1b, were investigated as vehicles of the photosensitizer m-tetrahydroxyphenylchlorin, m-THPC, to cell models of malignant glioma. The delivery efficiency of DMPC/1a and DMPC/1b liposome formulations were evaluated on the murine glioblastoma cell line C6 and on the human glioblastoma cell line LN229 by flow cytometry and laser scanning confocal microscopy. The stereochemistry of the spacer of the gemini was found to strongly influence the delivery efficiency of m-THPC to cells, the mode of interaction with the cell membrane, and the intracellular distribution of m-THPC. The physicochemical features of liposomes were investigated with the aim of explaining the parameters that control their biological features. Differences that could account for the different biological activity of the formulations concern the values of surface potential and the environment of m-THPC at the water/liposome interface.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Dimyristoylphosphatidylcholine / chemistry
  • Drug Delivery Systems*
  • Glioblastoma / drug therapy
  • Glioblastoma / metabolism
  • Humans
  • Liposomes / chemistry
  • Mesoporphyrins / administration & dosage*
  • Mesoporphyrins / pharmacokinetics
  • Mice
  • Microscopy, Confocal
  • Molecular Structure
  • Photochemotherapy
  • Photosensitizing Agents / administration & dosage*
  • Photosensitizing Agents / pharmacokinetics
  • Stereoisomerism
  • Surface-Active Agents / chemistry

Substances

  • Liposomes
  • Mesoporphyrins
  • Photosensitizing Agents
  • Surface-Active Agents
  • temoporfin
  • Dimyristoylphosphatidylcholine