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Dive into the research topics where Matthew J. Mollan is active.

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Featured researches published by Matthew J. Mollan.


Aaps Pharmscitech | 2002

Crystal doping aided by rapid expansion of supercritical solutions

Chandra Vemavarapu; Matthew J. Mollan; Thomas E. Needham

The purpose of this study was to test the utility of rapid expansion of supercritical solution (RESS) based cocrystallizations in inducing polymorph conversion and crystal disruption of chlorpropamide (CPD). CPD crystals were recrystallized by the RESS process utilizing supercritical carbon dioxide as the solvent. The supercritical region investigated for solute extraction ranged from 45 to 100°C and 2000 to 8000 psi. While pure solute recrystallization formed stage I of these studies, stage II involved recrystallization of CPD in the presence of urea (model impurity). The composition, morphology, and crystallinity of the particles thus produced were characterized utilizing techniques such as microscopy, thermal analysis, x-ray powder diffractometry, and high-performance liquid chromatography. Also, comparative evaluation between RESS and evaporative crystallization from liquid solvents was performed. RESS recrystallizations of commercially available CPD (form A) resulted in polymorph conversion to metastable forms C and V, depending on the temperature and pressure of the recrystallizing solvent. Cocrystallization studies revealed the formation of eutectic mixtures and solid solutions of CPD+urea. Formation of the solid solutions resulted in the crystal disruption of CPD and subsequent amorphous conversion at urea levels higher than 40% wt/wt. Consistent with these results were the reductions in melting point (up to 9°C) and in the ΔHfvalues of CPD (up to 50%). Scanning electron microscopy revealed a particle size reduction of up to an order of magnitude upon RESS processing. Unlike RESS, recrystallizations from liquid organic solvents lacked the ability to affect polymorphic conversions. Also, the incorporation of urea into the lattice of CPD was found to be inadequate. In providing the ability to control both the particle and crystal morphologies of active pharmaceutical ingredients, RESS proved potentially advantageous to crystal engineering. Rapid crystallization kinetics were found vital in making RESS-based doping superior to conventional solvent-based cocrystallizations.


Archive | 2000

Continuous production of pharmaceutical granulation

Isaac Ghebre-Sellassie; Matthew J. Mollan; Nitin Pathak; Mayur Lodaya; Mebrahtu Fessehaie


International Journal of Pharmaceutics | 2005

Design and process aspects of laboratory scale SCF particle formation systems.

Chandra Vemavarapu; Matthew J. Mollan; Mayur Lodaya; Thomas E. Needham


Archive | 2001

Process and system for controlled-release drug delivery

Stephen Craig Dyar; Mebrahtu Fessehaie; Isaac Ghebre-Sellassie; Monzer Michael Mayassi; Matthew J. Mollan; Haimanot Woldegaber


Archive | 2005

Preparation of pharmaceutical compositions containing nanoparticles

Christopher J. Galli; Mayur Lodaya; Matthew J. Mollan; William Michael Polak; Umang Shah; Chandra Vemavarapu


Powder Technology | 2009

Coprecipitation of pharmaceutical actives and their structurally related additives by the RESS process

Chandra Vemavarapu; Matthew J. Mollan; Thomas E. Needham


Archive | 2003

Twin-Screw Wet Granulation

Isaac Ghebre-Sellassie; Mayur Lodaya; Matthew J. Mollan


Archive | 2005

Pharmaceutical compositions of amorphous atorvastatin and process for preparing same

Stephen Craig Dyar; Mayur Lodaya; Matthew J. Mollan; Umang Shah; Hei Jen Sun; Zeri Teweldemedhin


Archive | 2003

Melt-Extruded Particulate Dispersions

Isaac Ghebre-Sellassie; Matthew J. Mollan; S Craig Dyar


Archive | 2001

Process and system for uniform release drug delivery

Stephen Craig Dyar; Mebrahtu Fessehaie; Isaac Ghebre-Sellassie; Monzer Michael Mayassi; Matthew J. Mollan; Haimanot Woldegaber

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Thomas E. Needham

University of Rhode Island

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