Show simple item record

dc.contributor.authorWang, Mao
dc.contributor.authorRutledge, Gregory C.
dc.contributor.authorMyerson, Allan S.
dc.contributor.authorTrout, Bernhardt L.
dc.date.accessioned2013-07-11T18:22:03Z
dc.date.available2013-07-11T18:22:03Z
dc.date.issued2011-12
dc.date.submitted2011-11
dc.identifier.issn00223549
dc.identifier.urihttp://hdl.handle.net/1721.1/79583
dc.description.abstractIn this paper, an electrospray technique followed by annealing at high temperatures was developed to produce nanocrystals of carbamazepine (CBZ), a poorly water-soluble drug, for continuous pharmaceutical manufacturing process. Electrospraying solutions of CBZ in methanol obeys the expected scaling law of current, which is I ∼ Q[superscript 1/2] (I, electrical current; Q, flow rate), for liquids with sufficiently high conductivity and viscosity. Lower flow rates during electrospraying were preferred to produce smaller diameters of monodisperse, dense CBZ nanoparticles. CBZ nanoparticles were predominantly amorphous immediately after electrospraying. Crystallization of CBZ nanoparticles was accelerated by annealing at high temperatures. CBZ nanocrystals with the most stable polymorph, form III, were obtained by annealing at 90°C, which is above the transition temperature, 78°C, for the enantiotropic CBZ form III and form I. The solubility and dissolution rates of CBZ nanocrystals increased significantly as compared with those of CBZ bulk particles. Therefore, electrospray technology has the potential to produce pharmaceutical dosage forms with enhanced bioavailability and can readily be integrated in a continuous pharmaceutical manufacturing process.en_US
dc.description.sponsorshipNovartis-MIT Center for Continuous Manufacturingen_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/jps.23024en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceProf. Rutledge Via Erja Kajosaloen_US
dc.titleProduction and characterization of carbamazepine nanocrystals by electrospraying for continuous pharmaceutical manufacturingen_US
dc.typeArticleen_US
dc.identifier.citationWang, Mao, Gregory C. Rutledge, Allan S. Myerson, and Bernhardt L. Trout. Production and Characterization of Carbamazepine Nanocrystals by Electrospraying for Continuous Pharmaceutical Manufacturing. Journal of Pharmaceutical Sciences 101, no. 3 (March 20, 2012): 1178-1188.en_US
dc.contributor.departmentNovartis-MIT Center for Continuous Manufacturingen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.approverRutledge, Gregory C.en_US
dc.contributor.mitauthorWang, Maoen_US
dc.contributor.mitauthorRutledge, Gregory C.en_US
dc.contributor.mitauthorMyerson, Allan S.en_US
dc.contributor.mitauthorTrout, Bernhardt L.en_US
dc.relation.journalJournal of Pharmaceutical Sciencesen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsWang, Mao; Rutledge, Gregory C.; Myerson, Allan S.; Trout, Bernhardt L.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1417-9470
dc.identifier.orcidhttps://orcid.org/0000-0001-8137-1732
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record