Show simple item record

dc.contributor.authorPaluch, Krzysztof J.*
dc.contributor.authorTajber, L.*
dc.contributor.authorCorrigan, O.I.*
dc.contributor.authorHealy, A.M.*
dc.date.accessioned2018-01-03T14:47:49Z
dc.date.available2018-01-03T14:47:49Z
dc.date.issued2013-08
dc.identifier.citationPaluch KJ, Tajber L, Corrigan OI et al (2013) Impact of alternative solid state forms and specific surface area of high-dose, hydrophilic active pharmaceutical ingredients on tabletability. Molecular Pharmaceutics. 10(10): 3628-3639.en_US
dc.identifier.urihttp://hdl.handle.net/10454/14342
dc.descriptionYesen_US
dc.description.abstractIn order to investigate the effect of using different solid state forms and specific surface area (TBET) of active pharmaceutical ingredients on tabletability and dissolution performance, the mono- and dihydrated crystalline forms of chlorothiazide sodium and chlorothiazide potassium (CTZK) salts were compared to alternative anhydrous and amorphous forms, as well as to amorphous microparticles of chlorothiazide sodium and potassium which were produced by spray drying and had a large specific surface area. The tablet hardness and tensile strength, porosity, and specific surface area of single-component, convex tablets prepared at different compression pressures were characterized. Results confirmed the complexity of the compressibility mechanisms. In general it may be concluded that factors such as solid-state form (crystalline vs amorphous), type of hydration (presence of interstitial molecules of water, dehydrates), or specific surface area of the material have a direct impact on the tabletability of the powder. It was observed that, for powders of the same solid state form, those with a larger specific surface area compacted well, and better than powders of a lower surface area, even at relatively low compression pressures. Compacts prepared at lower compression pressures from high surface area porous microparticles presented the shortest times to dissolve, when compared with compacts made of equivalent materials, which had to be compressed at higher compression pressures in order to obtain satisfactory compacts. Therefore, materials composed of nanoparticulate microparticles (NPMPs) may be considered as suitable for direct compaction and possibly for inclusion in tablet formulations as bulking agents, APIs, carriers, or binders due to their good compactibility performanceen_US
dc.description.sponsorshipSolid State Pharmaceutical Cluster (SSPC), supported by Science Foundation Ireland under Grant No. 07/SRC/B1158.en_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttp://dx.doi.org/10.1021/mp400124zen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Molecular Pharmaceutics, copyright © 2013 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/mp400124zen_US
dc.subjectSolid state form; Micromeritic characterization; Tabletability; Dissolutionen_US
dc.titleImpact of alternative solid state forms and specific surface area of high-dose, hydrophilic active pharmaceutical ingredients on tabletabilityen_US
dc.status.refereedYesen_US
dc.date.Accepted2013-08-20
dc.date.application2013-08-20
dc.typeArticleen_US
dc.type.versionAccepted Manuscripten_US
refterms.dateFOA2018-07-29T03:28:17Z


Item file(s)

Thumbnail
Name:
Paluch_Molecular_Pharmaceutics ...
Size:
1.093Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record