Self-assembled PAA-based nanoparticles as potential gene and protein delivery systems
Griffiths, Peter C. ORCID: 0000-0002-6686-1271, Mauro, Nicolo, Murphy, Damien M., Carter, Emma, Richardson, Simon C.W. ORCID: 0000-0002-7927-0649, Dyer, Paul and Ferruti, Paolo (2013) Self-assembled PAA-based nanoparticles as potential gene and protein delivery systems. Macromolecular Bioscience, 13 (5). pp. 641-649. ISSN 1616-5187 (Print), 1616-5195 (Online) (doi:https://doi.org/10.1002/mabi.201200462)
Full text not available from this repository.Abstract
A series of nanoparticles is prepared via layer-by-layer assembly of oppositely charged, synthetic biocompatible polyamidoamine polymers as potential carriers. Particle size, surface charge and internal chain mobility are quantified as a function of the polymer type and number of layers. The effect of addition of surfactant is examined to simulate the effects of nanoparticle dissolution. The cyctotoxicity of these particles (in epithelia and murine cell lines) are orders of magnitude lower than polyethyleneimine controls. Stable nanoparticles may be prepared from mixtures of strongly, oppositely charged
polymers, but less successfully from weakly charged polymers, and, given their acceptable toxicity characteristics, such modularly designed constructs show promise for drug and gene delivery.
Item Type: | Article |
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Additional Information: | [1] First published online: 19 March 2013. [2] Published in print: May 2013. |
Uncontrolled Keywords: | gene delivery, layer-by-layer assembly, nanoparticles, self-assembly, zeta-potential |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Faculty / School / Research Centre / Research Group: | Faculty of Education, Health & Human Sciences > School of Human Sciences (HUM) |
Related URLs: | |
Last Modified: | 09 Oct 2021 04:46 |
URI: | http://gala.gre.ac.uk/id/eprint/9698 |
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