Journal
JOURNAL OF CONTROLLED RELEASE
Volume 251, Issue -, Pages 82-91Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jconrel.2017.02.026
Keywords
Liposome; Aptamer; Doxorubicin; Encapsulation efficiency; Controlled release; Active loading
Funding
- Reseau Quebecois de Recherche sur le Medicament (RQRM)
- Hydro-Quebec
- University of Montreal
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Aptamer technology has shown much promise in cancer therapeutics for its targeting abilities. However, its potential to improve drug loading and release fromnanocarriers has not been thoroughly explored. In this study, we employed drug-binding aptamers to actively load drugs into liposomes. We designed a series of DNA aptamer sequences specific to doxorubicin, displayingmultiple binding sites and various binding affinities. The binding ability of aptamers was preserved when incorporated into cationic liposomes, binding up to 15 equivalents of doxorubicin per aptamer, therefore drawing the drug into liposomes. Optimization of the charge and drug/ aptamer ratios resulted in >= 80% encapsulation efficiency of doxorubicin, ten times higher than classical passively-encapsulating liposomal formulations and similar to a pH-gradient active loading strategy. In addition, kinetic release profiles and cytotoxicity assay on HeLa cells demonstrated that the release and therapeutic efficacy of liposomal doxorubicin could be controlled by the aptamer's structure. Our results suggest that the aptamer exhibiting a specific intermediate affinity is the best suited to achieve high drug loading while maintaining efficient drug release and therapeutic activity. This strategy was successfully applied to tobramycin, a hydrophilic drug suffering from low encapsulation into liposomes, where its loading was improved six-fold using aptamers. Overall, we demonstrate that aptamers could act, in addition to their targeting properties, asmultifunctional excipients for liposomal formulations. (C) 2017 Elsevier B.V. All rights reserved.
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