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Geoff G. Z. Zhang

Researcher at AbbVie

Publications -  174
Citations -  6701

Geoff G. Z. Zhang is an academic researcher from AbbVie. The author has contributed to research in topics: Crystallization & Amorphous solid. The author has an hindex of 38, co-authored 154 publications receiving 5666 citations. Previous affiliations of Geoff G. Z. Zhang include Abbott Laboratories & University of Iowa.

Papers
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Phase transformation considerations during process development and manufacture of solid oral dosage forms

TL;DR: The basic principles of polymorphism are reviewed, the classes of phase transformation and the underlying transformation mechanisms are defined, and respective kinetic factors are discussed.
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Understanding the Behavior of Amorphous Pharmaceutical Systems during Dissolution

TL;DR: The dissolution advantage of amorphous solids can be negated either by crystallization of the isomorphous solid on contact with the dissolution medium or through rapid crystallizationof the supersaturated solution.
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Physical stability of amorphous pharmaceuticals: Importance of configurational thermodynamic quantities and molecular mobility

TL;DR: Crystallization studies under nonisothermal conditions revealed that compounds with the highest entropic barriers and lowest mobilities were most difficult to crystallize, regardless of the thermodynamic driving forces.
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Physical chemistry of supersaturated solutions and implications for oral absorption.

TL;DR: The concepts of solubility, supersaturation, and the connection to membrane transport rate are discussed and it is believed that formulations that rapidly supersaturate and subsequently undergo LLPS, with maintenance of the supersaturation at this maximum value throughout the absorption process, will give superior performance in terms of absorption.
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Dissolution and precipitation behavior of amorphous solid dispersions.

TL;DR: The supersaturation generated upon dissolution of the solid dispersions was maintained for biologically relevant timeframes for the HPMC dispersions, whereas PVP appeared to be a less effective crystallization inhibitor.