4.6 Review

Modulating the release kinetics through the control of the permeability of the layer-by-layer assembly: a review

Journal

EXPERT OPINION ON DRUG DELIVERY
Volume 6, Issue 6, Pages 585-597

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/17425240902967599

Keywords

controlled release of biomolecules; layer-by-layer assembly; polyelectrolyte multilayer film and shell; tuned permeability

Funding

  1. FRSQ
  2. National Research and Engineering Council of Canada
  3. Canadian Institutes for Health Research-regenerative Medicine/Nanomedicine
  4. Fonds Quebecois de la Recherche sur la Nature et les Technologies

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The layer-by-layer (LbL) self-assembly technique has emerged as a simple and versatile method for coating biological and non-biological templates for various biomedical applications. A promising avenue of this technique lies in the encapsulation of drugs and other biological substances for controlled release. Fundamental studies of LbL assembly on flat surfaces have provided a sound understanding of film deposition theory and its pertinence to ionic and molecular transport and diffusion through polyelectrolyte multilayer (PEM) films. However, there is a lack of information on the permeability of three-dimensional PEM shell systems. In either PEM films or shells, it has been shown that drug release is a function of the ionic strength, pH and/or multilayer thickness. This report aims to provide an overview of the physicochemical parameters affecting the permeability of two- and three-dimensional multilayer shells, including ionic strength, layer number and pH. Furthermore, their synergic effect on loading and release of biologically active molecules from LbL multilayers are discussed.

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