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dc.contributor.authorMaddux, Nathaniel R.
dc.contributor.authorJoshi, Sangeeta B.
dc.contributor.authorVolkin, David B.
dc.contributor.authorRalston, John P.
dc.contributor.authorMiddaugh, C. Russell
dc.date.accessioned2017-04-26T15:06:30Z
dc.date.available2017-04-26T15:06:30Z
dc.date.issued2011-10
dc.identifier.citationMaddux, N. R., Joshi, S. B., Volkin, D. B., Ralston, J. P., & Middaugh, C. R. (2011). Multidimensional Methods for the Formulation of Biopharmaceuticals and Vaccines. Journal of Pharmaceutical Sciences, 100(10), 4171–4197. http://doi.org/10.1002/jps.22618en_US
dc.identifier.urihttp://hdl.handle.net/1808/23779
dc.description.abstractDetermining and preserving the higher order structural integrity and conformational stability of proteins, plasmid DNA and macromolecular complexes such as viruses, virus-like particles and adjuvanted antigens is often a significant barrier to the successful stabilization and formulation of biopharmaceutical drugs and vaccines. These properties typically must be investigated with multiple lower resolution experimental methods, since each technique monitors only a narrow aspect of the overall conformational state of a macromolecular system. This review describes the use of empirical phase diagrams (EPDs) to combine large amounts of data from multiple high-throughput instruments and construct a map of a target macromolecule's physical state as a function of temperature, solvent conditions, and other stress variables. We present a tutorial on the mathematical methodology, an overview of some of the experimental methods typically used, and examples of some of the previous major formulation applications. We also explore novel applications of EPDs including potential new mathematical approaches as well as possible new biopharmaceutical applications such as analytical comparability, chemical stability, and protein dynamics.en_US
dc.publisherElsevieren_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectPhase diagramsen_US
dc.subjectFormulationen_US
dc.subjectStabilityen_US
dc.subjectProteinen_US
dc.subjectMonoclonal Antibodiesen_US
dc.subjectPlasmid DNAen_US
dc.subjectVaccinesen_US
dc.subjectCircular dichroismen_US
dc.subjectFluorescenceen_US
dc.subjectCalorimetryen_US
dc.subjectLight scatteringen_US
dc.titleMultidimensional Methods for the Formulation of Bipharmaceuticals and Vaccinesen_US
dc.typeArticleen_US
kusw.kuauthorMaddux, Nathaniel R.
kusw.kuauthorJoshi, Sangeeta B.
kusw.kuauthorVolkin, David B.
kusw.kuauthorRalston, John P.
kusw.kuauthorMiddaugh, C. Russell
kusw.kudepartmentPharmaceutical Chemistryen_US
kusw.kudepartmentPhysics and Astronomyen_US
dc.identifier.doi10.1002/jps.22618en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC3949199en_US
dc.rights.accessrightsopenAccess


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This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.