Engineering thermosensitive liposome-nanoparticle hybrids loaded with doxorubicin for heat-triggered drug release

Research output: Contribution to journalArticle

Abstract

The engineering of responsive multifunctional delivery systems that combine therapeutic and diagnostic (theranostic) capabilities holds great promise and interest. We describe the design of thermosensitive liposome-nanoparticle (NP) hybrids that can modulate drug release in response to external heating stimulus. These hybrid systems were successfully engineered by the incorporation of gold, silver, and iron oxide NPs into the lipid bilayer of lysolipid-containing thermosensitive liposomes (LTSL). Structural characterization of LTSL-NP hybrids using cryo-TEM and AFM revealed the incorporation of metallic NPs into the lipid membranes without compromising doxorubicin loading and retention capability.
The presence of metallic NPs in the lipid bilayer reinforced bilayer retention and offered a nanoparticle concentration- dependent modulation of drug release in response to external heating. In conclusion, LTSL-NP hybrids represent a promising versatile platform based on LTSL liposomes that could be further utilize the properties of the embedded NPs for multifunctional theranostic applications.

Bibliographical metadata

Original languageEnglish
Pages (from-to)133-141
JournalInternational Journal of Pharmaceutics
Volume514
Issue number1
Early online date15 Nov 2016
DOIs
Publication statusPublished - 30 Nov 2016