D
Douglas R. Flanagan
Researcher at University of Iowa
Publications - 59
Citations - 4449
Douglas R. Flanagan is an academic researcher from University of Iowa. The author has contributed to research in topics: Solubility & Dissolution. The author has an hindex of 27, co-authored 59 publications receiving 3958 citations. Previous affiliations of Douglas R. Flanagan include Battelle Memorial Institute.
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Journal ArticleDOI
Solid-State Kinetic Models: Basics and Mathematical Fundamentals
Ammar Khawam,Douglas R. Flanagan +1 more
TL;DR: This work summarizes commonly employed models and presents their mathematical development as nucleation, geometrical contraction, diffusion, and reaction order.
Journal ArticleDOI
Drug transfer through mucus.
TL;DR: The study of the permeability of native or purified mucous gels is also important to understanding how it may alter the action or absorption of drugs that come in contact with epithelial surfaces.
Journal ArticleDOI
Basics and Applications of Solid-State Kinetics: A Pharmaceutical Perspective
Ammar Khawam,Douglas R. Flanagan +1 more
TL;DR: Controversies have arisen with regard to interpreting solid-state kinetic results, which include variable activation energy, calculation methods, and kinetic compensation effects.
Journal ArticleDOI
Role of isoconversional methods in varying activation energies of solid-state kinetics: II. Nonisothermal kinetic studies
Ammar Khawam,Douglas R. Flanagan +1 more
TL;DR: In this paper, the relationship between calculation methods and artifactual variation in activation energy was investigated by employing model-fitting and isoconversional methods to analyze both simulated and experimental nonisothermal data.
Journal ArticleDOI
Solid‐State Kinetic Models: Basics and Mathematical Fundamentals
Ammar Khawam,Douglas R. Flanagan +1 more
TL;DR: In this paper, the authors summarized commonly employed solid-state kinetic models and presented their mathematical development, and classified them according to their mechanistic basis as nucleation, geometrical contraction, diffusion, and reaction order.