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Converging layer-by-layer polyelectrolyte microcapsule and cubic lyotropic liquid crystalline nanoparticle approaches for molecular encapsulation

Year: 2011

Journal: Soft Matter, 2011, 7, 4257-4266, 20120104

Authors: Driever CD 1 2, Mulet X 2 3, Johnston APR 1, Waddington LJ 4, Thissen H 2, Caruso F 1 *, Drummond CJ 2 *

Last authors: Calum J. Drummond

Organizations: 1 Department of Chemical and Biomolecular Engineering, The University of Melbourne, Parkville, VIC 3010, A ustralia. E-mail: fcaruso@unimelb.edu.au 2 CSIRO Materials Science and Engineering (CMSE), Bag 10, Clayton, VIC 3169, Australia. E-mail: calum.drummond@csiro.au 3 Monash Institute of Pharmaceutical Sciences, Department of Drug Delivery, Deposition and Dynamics, Faculty of Pharmacy and Pharmaceutical Science, Monash University, 381 Royal Parade, Parkville, VIC 3052, Australia 4 CSIRO Materials Science and Engineering (CMSE), 343 Royal Parade, Parkville, VIC 3052, Australia

Country: Australia

Microcapsules created by the layer-by-layer (LbL) polyelectrolyte adsorption technique have been sub-compartmentalised by embedding cubic mesophase lipid nanoparticles (cubosomes™) into the capsule shell wall. Monoolein and phytantriol cubosomes™ containing fluorescent lipid and/or positively charged surfactant were first analysed for stability via dynamic light scattering, microelectrophoresis, and small angle X-ray scattering techniques. Once nanoparticle stability was confirmed, cubosomes™ were embedded within a multilayer assembly of oppositely charged polyelectrolytes [poly(allylamine hydrochloride) and poly(styrene sulfonate)] on planar silica substrates. Deposition of each layer was monitored using a quartz crystal microbalance with dissipation monitoring. These findings were then correlated to the growth of polyelectrolyte films incorporating cubosomes™ onto silica microparticles, where ζ-potential measurements were used to monitor the deposition of each subsequent layer. Small angle X-ray scattering experiments provided verification that cubosomes™ remained structurally intact when embedded within the polyelectrolyte matrix. Upon removal of the silica core, stable microcapsules containing one layer of embedded cubic nanoparticles were obtained. A diversity of molecular encapsulation matrices is offered through the capsule core, polyelectrolyte layers, and the embedded cubosomes™ of these sub-compartmentalised, nanostructured microcapsules.