Determination of Nonspherical Morphology of Doxorubicin-Loaded Liposomes by Atomic Force Microscopy

J Pharm Sci. 2018 Feb;107(2):717-726. doi: 10.1016/j.xphs.2017.10.009. Epub 2017 Oct 13.

Abstract

The 3-D morphology of doxorubicin (DOX)-loaded liposomes with a size of circa 100 nm was characterized by atomic force microscopy in an aqueous environment. Prolate liposomes appear in accordance with linear expansion of DOX fiber bundles precipitated inside liposomes. Oblate and concave liposomes were simultaneously observed with increased DOX concentrations; however, their morphologies were not readily determined by 2-D cryo-TEM imaging. Precise data analysis of the 3-D parameters of each liposome allowed semiquantitative evaluation of the transformation of spherical liposomes into nonspherical-prolate, oblate, and concave liposomes. In addition, nonspherical liposomes became spherical on the replacement of the liposomal outer phase consisting of a sucrose solution, with water and subsequent water influx. All spherical liposomes transformed into oblate and concave liposomes with a return to hyperosmotic conditions, when transferred from water to sucrose solution. Furthermore, the concave liposomes did not appear under DOX incubation conditions (65°C), which could be due to the amorphous and supersaturated DOX inside the liposomes that restrained liposomal shrinkage. As atomic force microscopy has improved our ability to image 3-D morphologies of liposomes in various conditions, it is an alternative analytical tool to cryo-TEM and may have future applications in regulatory tests for quality control and assurance.

Keywords: Atomic force microscopy; Cryo-transmission electron microscopy; Doxorubicin-loaded liposome; Liposomal morphology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Doxorubicin / analogs & derivatives*
  • Doxorubicin / chemistry*
  • Drug Carriers / chemistry
  • Liposomes / chemistry*
  • Microscopy, Atomic Force / methods
  • Nanoparticles / chemistry*
  • Particle Size
  • Polyethylene Glycols / chemistry
  • Sucrose / chemistry
  • Water / chemistry

Substances

  • Drug Carriers
  • Liposomes
  • liposomal doxorubicin
  • Water
  • Polyethylene Glycols
  • Sucrose
  • Doxorubicin