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dc.contributor.authorGajjar, P
dc.contributor.authorStyliari, I D
dc.contributor.authorNguyen, T T H
dc.contributor.authorCarr, J
dc.contributor.authorChen, X
dc.contributor.authorElliott, J A
dc.contributor.authorHammond, R B
dc.contributor.authorBurnett, T L
dc.contributor.authorRoberts, K
dc.contributor.authorWithers, P J
dc.contributor.authorMurnane, D
dc.date.accessioned2020-04-18T00:06:55Z
dc.date.available2020-04-18T00:06:55Z
dc.date.issued2020-06
dc.identifier.citationGajjar , P , Styliari , I D , Nguyen , T T H , Carr , J , Chen , X , Elliott , J A , Hammond , R B , Burnett , T L , Roberts , K , Withers , P J & Murnane , D 2020 , ' 3D Characterisation of Dry Powder Inhaler Formulations: Developing X-ray Micro Computed Tomography Approaches ' , European Journal of Pharmaceutics and Biopharmaceutics , vol. 151 , pp. 32-44 . https://doi.org/10.1016/j.ejpb.2020.02.013
dc.identifier.issn0939-6411
dc.identifier.otherORCID: /0000-0002-7476-2994/work/72308376
dc.identifier.urihttp://hdl.handle.net/2299/22606
dc.description© 2020 The Author(s). This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/).
dc.description.abstractCarrier-based dry powder inhaler (DPI) formulations need to be accurately characterised for their particle size distributions, surface roughnesses, fines contents and flow properties. Understanding the micro-structure of the powder formulation is crucial, yet current characterisation methods give incomplete information. Commonly used techniques like laser diffraction (LD) and optical microscopy (OM) are limited due to the assumption of sphericity and can give variable results depending on particle orientation and dispersion. The aim of this work was to develop new three dimensional (3D) powder analytical techniques using X-ray computed tomography (XCT) that could be employed for non-destructive metrology of inhaled formulations. α-lactose monohydrate powders with different characteristics have been analysed, and their size and shape (sphericity/aspect ratio) distributions compared with results from LD and OM. The three techniques were shown to produce comparable size distributions, while the different shape distributions from XCT and OM highlight the difference between 2D and 3D imaging. The effect of micro-structure on flowability was also analysed through 3D measurements of void volume and tap density. This study has demonstrated for the first time that XCT provides an invaluable, non-destructive and analytical approach to obtain number- and volume-based particle size distributions of DPI formulations in 3D space, and for unique 3D characterisation of powder micro-structure.en
dc.format.extent13
dc.format.extent14920514
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.title3D Characterisation of Dry Powder Inhaler Formulations: Developing X-ray Micro Computed Tomography Approachesen
dc.contributor.institutionDepartment of Clinical and Pharmaceutical Sciences
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionSchool of Health and Social Work
dc.contributor.institutionAirway Group
dc.contributor.institutionPharmaceutics
dc.contributor.institutionPharmaceutical Analysis and Product Characterisation
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1016/j.ejpb.2020.02.013
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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