Show simple item record

dc.contributor.authorNi, Qing Zhe
dc.contributor.authorYang, Fengyuan
dc.contributor.authorCan, Thach V.
dc.contributor.authorSergeyev, Ivan V.
dc.contributor.authorD’Addio, Suzanne M.
dc.contributor.authorJawla, Sudheer K.
dc.contributor.authorLi, Yongjun
dc.contributor.authorLipert, Maya P.
dc.contributor.authorXu, Wei
dc.contributor.authorWilliamson, R. Thomas
dc.contributor.authorLeone, Anthony
dc.contributor.authorGriffin, Robert G.
dc.contributor.authorSu, Yongchao
dc.date.accessioned2018-07-30T16:00:41Z
dc.date.available2018-07-30T16:00:41Z
dc.date.issued2017-08
dc.date.submitted2017-07
dc.identifier.issn1520-6106
dc.identifier.issn1520-5207
dc.identifier.urihttp://hdl.handle.net/1721.1/117192
dc.description.abstractA principal advantage of magic angle spinning (MAS) NMR spectroscopy lies in its ability to determine molecular structure in a noninvasive and quantitative manner. Accordingly, MAS should be widely applicable to studies of the structure of active pharmaceutical ingredients (API) and formulations. However, the low sensitivity encountered in spectroscopy of natural abundance APIs present at low concentration has limited the success of MAS experiments. Dynamic nuclear polarization (DNP) enhances NMR sensitivity and can be used to circumvent this problem provided that suitable paramagnetic polarizing agent can be incorporated into the system without altering the integrity of solid dosages. Here, we demonstrate that DNP polarizing agents can be added in situ during the preparation of amorphous solid dispersions (ASDs) via spray drying and hot-melt extrusion so that ASDs can be examined during drug development. Specifically, the dependence of DNP enhancement on sample composition, radical concentration, relaxation properties of the API and excipients, types of polarizing agents and proton density, has been thoroughly investigated. Optimal enhancement values are obtained from ASDs containing 1% w/w radical concentration. Both polarizing agents TOTAPOL and AMUPol provided reasonable enhancements. Partial deuteration of the excipient produced 3× higher enhancement values. With these parameters, an ASD containing posaconazole and vinyl acetate yields a 32-fold enhancement which presumably results in a reduction of NMR measurement time by ∼1000. This boost in signal intensity enables the full assignment of the natural abundance pharmaceutical formulation through multidimensional correlation experiments.en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acs.jpcb.7b07213en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Griffinen_US
dc.titleIn Situ Characterization of Pharmaceutical Formulations by Dynamic Nuclear Polarization Enhanced MAS NMRen_US
dc.typeArticleen_US
dc.identifier.citationNi, Qing Zhe et al. “In Situ Characterization of Pharmaceutical Formulations by Dynamic Nuclear Polarization Enhanced MAS NMR.” The Journal of Physical Chemistry B 121, 34 (August 2017): 8132–8141 © 2017 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Plasma Science and Fusion Centeren_US
dc.contributor.mitauthorJawla, Sudheer K.
dc.relation.journalJournal of Physical Chemistry Ben_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.orderedauthorsNi, Qing Zhe; Yang, Fengyuan; Can, Thach V.; Sergeyev, Ivan V.; D’Addio, Suzanne M.; Jawla, Sudheer K.; Li, Yongjun; Lipert, Maya P.; Xu, Wei; Williamson, R. Thomas; Leone, Anthony; Griffin, Robert G.; Su, Yongchaoen_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_POLICYen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record