Article
Linear-dendritic polymeric amphiphiles as carriers of doxorubicin—In vitro evaluation of biocompatibility and drug delivery
Article first published online: 5 OCT 2011
DOI: 10.1002/pola.25008
Copyright © 2011 Wiley Periodicals, Inc.
Issue

Journal of Polymer Science Part A: Polymer Chemistry
Volume 50, Issue 2, pages 217–226, 15 January 2012
Additional Information
How to Cite
Wu, Z., Zeng, X., Zhang, Y., Feliu, N., Lundberg, P., Fadeel, B., Malkoch, M. and Nyström, A. M. (2012), Linear-dendritic polymeric amphiphiles as carriers of doxorubicin—In vitro evaluation of biocompatibility and drug delivery. J. Polym. Sci. A Polym. Chem., 50: 217–226. doi: 10.1002/pola.25008
Publication History
- Issue published online: 12 DEC 2011
- Article first published online: 5 OCT 2011
- Manuscript Accepted: 1 SEP 2011
- Manuscript Received: 8 AUG 2011
Funded by
- the Swedish Research Council for financial. Grant Numbers: 2006-3617, 2009-3259
- Åke Wiberg foundation
- Karolinska Institutet
- The Swedish Medical Nanoscience Center
- Carl Bennet AB
- Swedish Governmental Agency for Innovation Systems (Vinnova)
- Axel and Eva Wallström foundation
- Jeansson foundation
- the Knut and Alice Wallenberg Foundation (to A.M.N.)
Keywords:
- block copolymers;
- breast cancer;
- delivery vehicle;
- dendrimers;
- doxorubicin;
- drug delivery systems;
- linear dendrimer;
- primary macrophages
Abstract
In our recent work, we have explored the formation of chemotherapeutic delivery vehicles constructed from four different amphiphilic linear-dendritic hybrid block copolymers. These micelles were found to form about 100-nm-sized structures that were capable of sequestering doxorubicin at loading efficiencies up to 22%. Here, the cellular toxicity of these biocompatible and biodegradable linear-dendritic hybrid materials was evaluated on two breast cancer cell lines and primary human macrophages. The micelles were found not to affect the cellular viability at concentrations below 35 μg mL−1. After drug loading, these constructs could deliver an efficient dose of drugs, resulting in significant decreases in cell viability. Kinetic studies indicated that the drug formulation in the polymer micelles slowed down the cell uptake compared with the nonformulated drug, but similar efficacy in viability reduction and cell apoptosis were found. Taken together, these linear-dendritic hybrid materials represent an interesting novel architecture for the construction of drug delivery systems. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012

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