An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer

The recently proposed by the authors numerical approach to modelling of drug release from polymersome nanoparticles based on PNIPAM-g-PEO graft copolymer is generalized on the basis of different model dependent methods. It takes into account the specific features of the experimental procedure and eq...

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Main Authors: Rumiana Blagoeva, Assen Nedev, Victoria Michailova
Format: Article
Language:English
Published: Bulgarian Academy of Sciences 2017-06-01
Series:International Journal Bioautomation
Subjects:
Online Access:http://www.biomed.bas.bg/bioautomation/2017/vol_21.2/files/21.2_02.pdf
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spelling doaj-2f7d1a6ff9794ad98e93ee3da44256832020-11-25T03:05:37ZengBulgarian Academy of SciencesInternational Journal Bioautomation1314-19021314-23212017-06-01212179188An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft CopolymerRumiana Blagoeva0Assen NedevVictoria MichailovaInstitute of Mechanics, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., bl. 4, 1113 Sofia, BulgariaThe recently proposed by the authors numerical approach to modelling of drug release from polymersome nanoparticles based on PNIPAM-g-PEO graft copolymer is generalized on the basis of different model dependent methods. It takes into account the specific features of the experimental procedure and equipment used during the experimental study of the drug release kinetics. The rate parameters are numerically evaluated when fitting each model curve to the available experimental data for indomethacin. Numerical simulation of drug release for 5% and 20% ethanol content is performed and the reliability of the used approach is discussed. It is established that the drug release rate is strongly influenced by the ethanol content. The considered numerical approach enables modeling of different drugs release under the same experimental equipment as well as inclusion of some new model functions describing other mechanisms controlling the release kinetics.http://www.biomed.bas.bg/bioautomation/2017/vol_21.2/files/21.2_02.pdfPNIPAM-g-PEO polymersome nanoparticlesDrug releaseModel dependent methodsNumerical simulation
collection DOAJ
language English
format Article
sources DOAJ
author Rumiana Blagoeva
Assen Nedev
Victoria Michailova
spellingShingle Rumiana Blagoeva
Assen Nedev
Victoria Michailova
An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
International Journal Bioautomation
PNIPAM-g-PEO polymersome nanoparticles
Drug release
Model dependent methods
Numerical simulation
author_facet Rumiana Blagoeva
Assen Nedev
Victoria Michailova
author_sort Rumiana Blagoeva
title An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
title_short An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
title_full An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
title_fullStr An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
title_full_unstemmed An Approach to Modeling Drug Release from Polymersome Nanoparticles Based on PNIPAM-g-PEO Graft Copolymer
title_sort approach to modeling drug release from polymersome nanoparticles based on pnipam-g-peo graft copolymer
publisher Bulgarian Academy of Sciences
series International Journal Bioautomation
issn 1314-1902
1314-2321
publishDate 2017-06-01
description The recently proposed by the authors numerical approach to modelling of drug release from polymersome nanoparticles based on PNIPAM-g-PEO graft copolymer is generalized on the basis of different model dependent methods. It takes into account the specific features of the experimental procedure and equipment used during the experimental study of the drug release kinetics. The rate parameters are numerically evaluated when fitting each model curve to the available experimental data for indomethacin. Numerical simulation of drug release for 5% and 20% ethanol content is performed and the reliability of the used approach is discussed. It is established that the drug release rate is strongly influenced by the ethanol content. The considered numerical approach enables modeling of different drugs release under the same experimental equipment as well as inclusion of some new model functions describing other mechanisms controlling the release kinetics.
topic PNIPAM-g-PEO polymersome nanoparticles
Drug release
Model dependent methods
Numerical simulation
url http://www.biomed.bas.bg/bioautomation/2017/vol_21.2/files/21.2_02.pdf
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