Ioanna Danai Styliari
Nanoformulation-by-design: an experimental and molecular dynamics study for polymer coated drug nanoparticles
Styliari, Ioanna Danai; Taresco, Vincenzo; Theophilus, Andrew; Alexander, Cameron; Garnett, Martin; Laughton, Charles
Authors
Dr VINCENZO TARESCO VINCENZO.TARESCO@NOTTINGHAM.AC.UK
NOTTINGHAM RESEARCH FELLOW
Andrew Theophilus
Professor CAMERON ALEXANDER CAMERON.ALEXANDER@NOTTINGHAM.AC.UK
PROFESSOR OF POLYMER THERAPEUTICS
Martin Garnett
Professor CHARLES LAUGHTON CHARLES.LAUGHTON@NOTTINGHAM.AC.UK
PROFESSOR OF COMPUTATIONAL PHARMACEUTICAL SCIENCE
Abstract
© The Royal Society of Chemistry 2020. The formulation of drug compounds into nanoparticles has many potential advantages in enhancing bioavailability and improving therapeutic efficacy. However, few drug molecules will assemble into stable, well-defined nanoparticulate structures. Amphiphilic polymer coatings are able to stabilise nanoparticles, imparting defined surface properties for many possible drug delivery applications. In the present article we explore, both experimentally andin silico, a potential methodology to coat drug nanoparticles with an amphiphilic co-polymer. Monomethoxy polyethylene glycol-polycaprolactone (mPEG-b-PCL) diblock copolymers with different mPEG lengths (Mw350, 550, 750 and 2000), designed to give different levels of colloidal stability, were used to coat the surface of indomethacin nanoparticles. Polymer coating was achieved by a flow nanoprecipitation method that demonstrated excellent batch-to-batch reproducibility and resulted in nanoparticles with high drug loadings (up to 78%). At the same time, in order to understand this modified nanoprecipitation method at an atomistic level, large-scale all-atom molecular dynamics simulations were performed in parallel using the GROMOS53a6 forcefield parameters. It was observed that the mPEG-b-PCL chains act synergistically with the acetone molecules to dissolve the indomethacin nanoparticle while after the removal of the acetone molecules (mimicking the evaporation of the organic solvent) a polymer-drug nanoparticle was formed (yield 99%). This work could facilitate the development of more efficient methodologies for producing nanoparticles of hydrophobic drugs coated with amphiphilic polymers. The atomistic insight from the MD simulations in tandem with the data from the drug encapsulation experiments thus leads the way to ananoformulation-by-designapproach for therapeutic nanoparticles.
Citation
Styliari, I. D., Taresco, V., Theophilus, A., Alexander, C., Garnett, M., & Laughton, C. (2020). Nanoformulation-by-design: an experimental and molecular dynamics study for polymer coated drug nanoparticles. RSC Advances, 10(33), 19521-19533. https://doi.org/10.1039/d0ra00408a
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 8, 2020 |
Online Publication Date | May 21, 2020 |
Publication Date | May 21, 2020 |
Deposit Date | Apr 29, 2020 |
Publicly Available Date | May 21, 2020 |
Journal | RSC Advances |
Electronic ISSN | 2046-2069 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 10 |
Issue | 33 |
Pages | 19521-19533 |
DOI | https://doi.org/10.1039/d0ra00408a |
Public URL | https://nottingham-repository.worktribe.com/output/4359859 |
Publisher URL | https://pubs.rsc.org/en/content/articlelanding/2020/RA/D0RA00408A#!divAbstract |
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Nanoformulation-by-design: An experimental and molecular dynamics study for polymer coated drug nanoparticles
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Publisher Licence URL
https://creativecommons.org/licenses/by/3.0/
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