Differential scanning calorimetry in drug-membrane interactions

Biochem Biophys Res Commun. 2024 May 21:709:149806. doi: 10.1016/j.bbrc.2024.149806. Epub 2024 Mar 19.

Abstract

Differential Scanning Calorimetry (DSC) is a central technique in investigating drug - membrane interactions, a critical component of pharmaceutical research. DSC measures the heat difference between a sample of interest and a reference as a function of temperature or time, contributing essential knowledge on the thermally induced phase changes in lipid membranes and how these changes are affected by incorporating pharmacological substances. The manuscript discusses the use of phospholipid bilayers, which can form structures like unilamellar and multilamellar vesicles, providing a simplified yet representative membrane model to investigate the complex dynamics of how drugs interact with and penetrate cellular barriers. The manuscript consolidates data from various studies, providing a comprehensive understanding of the mechanisms underlying drug - membrane interactions, the determinants that influence these interactions, and the crucial role of DSC in elucidating these components. It further explores the interactions of specific classes of drugs with phospholipid membranes, including non-steroidal anti-inflammatory drugs, anticancer agents, natural products with antioxidant properties, and Alzheimer's disease therapeutics. The manuscript underscores the critical importance of DSC in this field and the need for continued research to improve our understanding of these interactions, acting as a valuable resource for researchers.

Keywords: Differential scanning calorimetry (DSC); Liposomes; Membrane; Multilamellar vesicles; Phospholipids.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents*
  • Calorimetry, Differential Scanning
  • Lipid Bilayers* / chemistry
  • Liposomes / chemistry
  • Membranes, Artificial
  • Phospholipids / chemistry

Substances

  • Lipid Bilayers
  • Phospholipids
  • Membranes, Artificial
  • Antineoplastic Agents
  • Liposomes