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Molecular Pharmaceutics|December 7, 2019
Modeling Recrystallization Kinetics Following the Dissolution of Amorphous DrugsPeter J Skrdla, Philip D Floyd, Philip C Dell'OrcoJournal of Pharmaceutical Sciences|January 14, 2020
Predicting the Solubility Advantage of Amorphous Drugs: Effect of pHPeter J Skrdla, Philip D Floyd, Philip C Dell'OrcoInternational Journal of Pharmaceutics|July 7, 2019
Predicting the solubility enhancement of amorphous drugs and related phenomena using basic thermodynamic principles and semi-empirical kinetic modelsPeter J Skrdla, Philip D Floyd, Philip C Dell'OrcoJournal of Pharmaceutical Sciences|July 4, 2016
Practical Estimation of Amorphous Solubility Enhancement Using Thermoanalytical Data: Determination of the Amorphous/Crystalline Solubility Ratio for Pure Indomethacin and FelodipinePeter J Skrdla, Philip D Floyd, Philip C Dell'orcoInternational Journal of Pharmaceutics|November 19, 2018
Predicted amorphous solubility and dissolution rate advantages following moisture sorption: Case studies of indomethacin and felodipinePeter J Skrdla, Philip D Floyd, Philip C Dell'OrcoPhysical Chemistry Chemical Physics : PCCP|July 22, 2017
The amorphous state: first-principles derivation of the Gordon-Taylor equation for direct prediction of the glass transition temperature of mixtures; estimation of the crossover temperature of fragile glass formers; physical basis of the "Rule of 2/3"Peter J Skrdla, Philip D Floyd, Philip C Dell'OrcoAnalytical Chemistry|April 14, 2012
Analytical characterization of an orally-delivered peptide pharmaceutical productWayne P Kelley, Shujun Chen, Philip D Floyd, et al.Pageof 1