University of Illinois Urbana-Champaign

Modeling of controlled-release drug delivery from autocatalytically degrading polymer microspheres

Ford Versypt, Ashlee

Content Files
derivDeff.f
deriv.f
derivH.f
diffn_ctr.f
diffn.f
diffn_int.f
driver_radau5.f
Fderiv.f
FordVersypt_Ashlee.pdf
initial.f
intpar.f
Jderiv.f
kraken.deck
makefile
rxn.f
rxn_half.f
rxn_pseudo.f
rxn_quad.f
rxn_uncat.f

Permalink

https://hdl.handle.net/2142/30970

Description

Title
Modeling of controlled-release drug delivery from autocatalytically degrading polymer microspheres
Author(s)
Ford Versypt, Ashlee
Issue Date
2012-05-22T00:19:10Z
Director of Research (if dissertation) or Advisor (if thesis)
Braatz, Richard D.
Doctoral Committee Chair(s)
Pack, Daniel W.
Committee Member(s)
  • Braatz, Richard D.
  • Aluru, Narayana R.
  • Rao, Christopher V.
Department of Study
Chemical & Biomolecular Engr
Discipline
Chemical Engineering
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Date of Ingest
2012-05-22T00:19:10Z
Keyword(s)
  • controlled-release drug delivery
  • mathematical modeling
  • PLGA microspheres
  • reaction-diffusion equation
  • hindered diffusion
  • polymorphous low-grade adenocarcinoma (PLGA)
Abstract
A mathematical model is developed for the simultaneous treatment of PLGA degradation and erosion and diffusive drug release with autocatalytic effects and nonconstant effective diffusivity of the drug. A mechanistic reaction-diffusion model with pore evolution coupled to hydrolysis and related to the effective diffusivity through hindered diffusion theory is proposed. Experimental background motivating the attention to the size-dependent effects of autocatalysis on drug release and a brief review of related mathematical models are presented. The model equations are derived, solved numerically with a computational code developed for this work and described in detail, and compared to the analytical solutions to the model in limiting cases. The model performance for the case of drug release from microspheres of different sizes is presented to highlight the capability of the model for predicting size-dependent, autocatalytic effects on the polymer and the release of drug.
Graduation Semester
2012-05
Permalink
http://hdl.handle.net/2142/30970
Copyright and License Information
Copyright 2012 Ashlee Nicole Ford Versypt

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Dissertations and Theses - Chemical and Biomolecular Engineering
Dissertations and Theses - Chemical and Biomolecular Engineering
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Graduate Theses and Dissertations at Illinois