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Pharmaceutical Research|June 28, 2000
What is the true solubility advantage for amorphous pharmaceuticals?B C Hancock, M ParksPharmaceutical Research|September 1, 1993
The use of solution theories for predicting water vapor absorption by amorphous pharmaceutical solids: a test of the Flory-Huggins and Vrentas modelsB C Hancock, G ZografiJournal of Pharmaceutical Sciences|January 1, 1997
Characteristics and significance of the amorphous state in pharmaceutical systemsB C Hancock, G ZografiPharmaceutical Research|April 1, 1994
The relationship between the glass transition temperature and the water content of amorphous pharmaceutical solidsB C Hancock, G ZografiPharmaceutical Development and Technology|February 23, 1999
The effect of temperature on water vapor sorption by some amorphous pharmaceutical sugarsB C Hancock, C R DaltonJournal of Pharmaceutical Sciences|February 1, 2006
Process simulation in the pharmaceutical industry: a review of some basic physical modelsD M Kremer, B C HancockJournal of the American Podiatric Medical Association|July 7, 2015
Lateral Ankle Stabilization Using Acellular Human Dermal Allograft AugmentationRobert M Parks, Stephanie M ParksPharmaceutical Research|June 1, 1999
Determination of the viscosity of an amorphous drug using thermomechanical analysis (TMA)B C Hancock, Y Dupuis, R ThibertJournal of Pharmaceutical Sciences|December 1, 1994
Crystallization of indomethacin from the amorphous state below and above its glass transition temperatureM Yoshioka, B C Hancock, G ZografiJournal of Pharmaceutical Sciences|August 1, 1995
Inhibition of indomethacin crystallization in poly(vinylpyrrolidone) coprecipitatesM Yoshioka, B C Hancock, G ZografiPageof 46