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dc.contributor.authorElShaer, Amr
dc.contributor.authorKaialy, Waseem
dc.contributor.authorAkhtar, Noreen
dc.contributor.authorIyire, Affiong
dc.contributor.authorHussain, Tariq
dc.contributor.authorAlany, Raid
dc.contributor.authorMohammed, Afzal R.
dc.date.accessioned2016-03-14T15:32:57Zen
dc.date.available2016-03-14T15:32:57Zen
dc.date.issued2015-10
dc.identifier.citationElshaer, A., Kaialy, W., Akhtar, N., Iyire, A., Hussain, T., Alany, R.G., & Mohammed, A.R. (2015). A methodological evaluation and predictive in silico investigation into the multi-functionality of arginine in directly compressed tablets. European journal of pharmaceutics and biopharmaceutics, 96 (2015), pp 272-281. Doi: 10.1016/j.ejpb.2015.07.028
dc.identifier.issn0939-6411
dc.identifier.doi10.1016/j.ejpb.2015.07.028
dc.identifier.urihttp://hdl.handle.net/2436/601308
dc.description.abstractThe acceleration of solid dosage form product development can be facilitated by the inclusion of excipients that exhibit poly-/multi-functionality with reduction of the time invested in multiple excipient optimisations. Because active pharmaceutical ingredients (APIs) and tablet excipients present diverse densification behaviours upon compaction, the involvement of these different powders during compaction makes the compaction process very complicated. The aim of this study was to assess the macrometric characteristics and distribution of surface charges of two powders: indomethacin (IND) and arginine (ARG); and evaluate their impact on the densification properties of the two powders. Response surface modelling (RSM) was employed to predict the effect of two independent variables; Compression pressure (F) and ARG percentage (R) in binary mixtures on the properties of resultant tablets. The study looked at three responses namely; porosity (P), tensile strength (S) and disintegration time (T). Micrometric studies showed that IND had a higher charge density (net charge to mass ratio) when compared to ARG; nonetheless, ARG demonstrated good compaction properties with high plasticity (Y = 28.01 MPa). Therefore, ARG as filler to IND tablets was associated with better mechanical properties of the tablets (tablet tensile strength (r) increased from 0.2 ± 0.05 N/mm2 to 2.85 ± 0.36 N/mm2 upon adding ARG at molar ratio of 8:1 to IND). Moreover, tablets’ disintegration time was shortened to reach few seconds in some of the formulations. RSM revealed tablet porosity to be affected by both compression pressure and ARG ratio for IND/ARG physical mixtures (PMs). Conversely, the tensile strength (r) and disintegration time (T) for the PMs were influenced by the compression pressure, ARG ratio and their interactive term (FR); and a strong correlation was observed between the experimental results and the predicted data for tablet porosity. This work provides clear evidence of the multi-functionality of ARG as filler, binder and disintegrant for directly compressed tablets.
dc.language.isoen
dc.publisherElsevier
dc.relation.urlhttp://linkinghub.elsevier.com/retrieve/pii/S0939641115003318
dc.subjectIndomethacin
dc.subjectArginine
dc.subjectCompressibility
dc.subjectCompactibility
dc.subjectTabletability
dc.subjectDisintegration time
dc.subjectDisintegration time
dc.subjectMultifunctional excipient
dc.subjectDirect compression
dc.titleA methodological evaluation and predictive in silico investigation into the multi-functionality of arginine in directly compressed tablets
dc.typeJournal article
dc.identifier.journalEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.source.volume96
dc.source.issueOctober 2015
dc.source.beginpage272
dc.source.endpage281
refterms.dateFOA2016-10-01T00:00:00Z
html.description.abstractThe acceleration of solid dosage form product development can be facilitated by the inclusion of excipients that exhibit poly-/multi-functionality with reduction of the time invested in multiple excipient optimisations. Because active pharmaceutical ingredients (APIs) and tablet excipients present diverse densification behaviours upon compaction, the involvement of these different powders during compaction makes the compaction process very complicated. The aim of this study was to assess the macrometric characteristics and distribution of surface charges of two powders: indomethacin (IND) and arginine (ARG); and evaluate their impact on the densification properties of the two powders. Response surface modelling (RSM) was employed to predict the effect of two independent variables; Compression pressure (F) and ARG percentage (R) in binary mixtures on the properties of resultant tablets. The study looked at three responses namely; porosity (P), tensile strength (S) and disintegration time (T). Micrometric studies showed that IND had a higher charge density (net charge to mass ratio) when compared to ARG; nonetheless, ARG demonstrated good compaction properties with high plasticity (Y = 28.01 MPa). Therefore, ARG as filler to IND tablets was associated with better mechanical properties of the tablets (tablet tensile strength (r) increased from 0.2 ± 0.05 N/mm2 to 2.85 ± 0.36 N/mm2 upon adding ARG at molar ratio of 8:1 to IND). Moreover, tablets’ disintegration time was shortened to reach few seconds in some of the formulations. RSM revealed tablet porosity to be affected by both compression pressure and ARG ratio for IND/ARG physical mixtures (PMs). Conversely, the tensile strength (r) and disintegration time (T) for the PMs were influenced by the compression pressure, ARG ratio and their interactive term (FR); and a strong correlation was observed between the experimental results and the predicted data for tablet porosity. This work provides clear evidence of the multi-functionality of ARG as filler, binder and disintegrant for directly compressed tablets.


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