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Phase transition and heterogeneous/epitaxial nucleation of hydrated and anhydrous theophylline crystals

dc.contributor.authorRodriguez-Hornedo, Nairen_US
dc.contributor.authorLechuga-Ballesteros, Daviden_US
dc.contributor.authorHsiu-Jean Wu,en_US
dc.date.accessioned2006-04-10T15:04:43Z
dc.date.available2006-04-10T15:04:43Z
dc.date.issued1992-09-20en_US
dc.identifier.citationRodriguez-Hornedo, Nair, Lechuga-Ballesteros, David, Hsiu-Jean Wu, (1992/09/20)."Phase transition and heterogeneous/epitaxial nucleation of hydrated and anhydrous theophylline crystals." International Journal of Pharmaceutics 85(1-3): 149-162. <http://hdl.handle.net/2027.42/29838>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T7W-4755417-10P/2/760b93c76c84c9116a3fe7cfd416b377en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29838
dc.description.abstractTheophylline crystallizes in the anhydrous or monohydrate form. The solubility of the anhydrous form exceeds the solubility of the monohydrate form below 60[deg]C. The anhydrous: hydrate phase transition of theophylline in buffered suspensions has been studied by measurement of the supersaturation profile and the crystal size distributions. The role of crystallographic parameters in the nucleation and growth of monohydrate crystals, during dissolution of the anhydrous phase, has been investigated. A solvent-mediated route has been identified and can be described in terms of the dissolution kinetics of the anhydrous phase and the nucleation and growth kinetics of the hydrated phase. The growth rate of the monohydrate crystals depends on the square of the supersaturation and is independent of the stirring rate, which suggests a surface-controlled growth process. The dissolution rate of the anhydrous crystals depends on the 1.5 order of the undersaturation and is inversely proportional to the square root of the crystal size. Anhydrous theophylline crystals act as heterogeneous nucleation substrates for the crystals of the monohydrate phase and these grow epitaxially on the anhydrous crystals. Based on the kinetic equations for dissolution of the anhydrous form and crystallization of the monohydrate form, a computer simulation has been developed that predicts the changes in the concentration of theophylline in solution during the phase transition.en_US
dc.format.extent1390187 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titlePhase transition and heterogeneous/epitaxial nucleation of hydrated and anhydrous theophylline crystalsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, MI 48109-1065, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, MI 48109-1065, USAen_US
dc.contributor.affiliationotherCollege of Pharmacy, The University of Arizona, Tucson, AZ 85721, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29838/1/0000185.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0378-5173(92)90144-Qen_US
dc.identifier.sourceInternational Journal of Pharmaceuticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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