Journal article

Engineering advanced capsosomes: Maximizing the number of subcompartments, cargo retention, and temperature-triggered reaction

R Chandrawati, L Hosta-Rigau, D Vanderstraaten, SA Lokuliyana, B Städler, F Albericio, F Caruso

ACS Nano | Published : 2010

Abstract

Advanced mimics of cells require a large yet controllable number of subcompartments encapsulated within a scaffold, equipped with a trigger to initiate, terminate, and potentially restart an enzymatic reaction. Recently introduced capsosomes, polymer capsules containing thousands of liposomes, are a promising platform for the creation of artificial cells. Capsosomes are formed by sequentially layering liposomes and polymers onto particle templates, followed by removal of the template cores. Herein, we engineer advanced capsosomes and demonstrate the ability to control the number of subcompartments and hence the degree of cargo loading. To achieve this, we employ a range of polymer separation..

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University of Melbourne Researchers

Grants

Funding Acknowledgements

This work was supported by the Australian Research Council under the Federation Fellowship (F.C.) and Discovery Project (F.C.) schemes. We thank Dr. A. D. Price (The University of Melbourne) for assisting in cross-linking the PMASH using BM(PEG)<INF>2</INF> and labeling luciferase-FITC, Dr. A. Postma (CSIRO Molecular and Health Technologies) for his help in PMAc synthesis, and Dr. A. N. Zelikin (The University of Melbourne) and S.-F. Chong (The University of Melbourne) for their input in assembling the PMA hydrogel carrier capsules.