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dc.contributor.authorYang, Xiaochuan
dc.contributor.authorOng, Ta-Chung
dc.contributor.authorMichaelis, Vladimir K.
dc.contributor.authorHeng, Scott N.
dc.contributor.authorGriffin, Robert Guy
dc.contributor.authorMyerson, Allan S.
dc.date.accessioned2017-06-26T19:11:17Z
dc.date.available2017-06-26T19:11:17Z
dc.date.issued2016-08
dc.identifier.issn1466-8033
dc.identifier.urihttp://hdl.handle.net/1721.1/110273
dc.description.abstractMethods to produce nano-sized organic molecular crystals in thin films are of great interest in the pharmaceutical industry due to the potential benefit of increased solubility of poorly soluble drugs and the advantages of film-based dosage forms over traditional tablet/capsule-based dosage forms. One method to directly form organic nanocrystals is by crystallization in confined environments where the overall crystallization volume is constrained. We report the use of a novel solution impregnation method to form nanocrystals in polymer matrices with various microstructures in order to study the structure of the confined nanocrystals and the role of soft confinement and polymer chemistry on the nucleation process of nano-sized crystals. The particle diameter correlates with the microstructure of the polymer matrices and the nucleation kinetics. In addition, by carefully choosing the experimental conditions and the polymer matrix, polymorph control of nanocrystals can be achieved. Solid-state nuclear magnetic resonance (ssNMR) was used to examine the local structure of nanocrystals inside the polymer matrices and crystal polymer interactions. This method may serve as a novel formulation method to obtain nanocrystals of poorly soluble active pharmaceutical ingredients (APIs) for pharmaceutical industry.en_US
dc.description.sponsorshipNovartis-MIT Center for Continuous Manufacturingen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant no. EB-002026)en_US
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canadaen_US
dc.description.sponsorshipGovernment of Canada (Banting Postdoctoral Fellowship)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistry, Theen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c5ce01202cen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleFormation of organic molecular nanocrystals under soft confinementen_US
dc.typeArticleen_US
dc.identifier.citationYang, Xiaochuan et al. “Formation of Organic Molecular Nanocrystals under Soft Confinement.” CrystEngComm 17.31 (2015): 6044–6052.en_US
dc.contributor.departmentNovartis-MIT Center for Continuous Manufacturingen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentFrancis Bitter Magnet Laboratory (Massachusetts Institute of Technology)en_US
dc.contributor.mitauthorYang, Xiaochuan
dc.contributor.mitauthorOng, Ta-Chung
dc.contributor.mitauthorMichaelis, Vladimir K.
dc.contributor.mitauthorHeng, Scott N.
dc.contributor.mitauthorGriffin, Robert Guy
dc.contributor.mitauthorMyerson, Allan S.
dc.relation.journalCrystEngCommen_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.orderedauthorsYang, Xiaochuan; Ong, Ta-Chung; Michaelis, Vladimir K.; Heng, Scott; Griffin, Robert G.; Myerson, Allan S.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6708-7660
dc.identifier.orcidhttps://orcid.org/0000-0003-1589-832X
dc.identifier.orcidhttps://orcid.org/0000-0002-7468-8093
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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