Literature DB >> 15661488

Compact size and mechanical strength of pharmaceutical diluents.

Kyriakos Kachrimanis1, Stavros Malamataris.   

Abstract

The effects of compact size and powder particle size on the axial compressive (sigma(C)) and diametral tensile (sigma(T)) strength were evaluated, for three compressed pharmaceutical diluents (microcrystalline cellulose, MCC, calcium hydrogen phosphate dihydrate, CHPD, and pregelatinized starch, PGS) differing in deformational behaviour during compaction and testing. Cylindrical specimens of similar aspect ratio ( approximately 1) but different diameter (13, 10 and 5mm) and total porosity (0.35-0.05) were employed and the extrapolated and interpolated strength values, at zero and 0.15 porosity (sigma(C0) or sigma(T0) and sigma(C0.15) or sigma(T0.15)), were predicted by applying an exponential relation. The ratio of sigma(C0.15)/sigma(T0.15) was correlated to the corresponding percent radial elastic recovery (%RR). It was found that the changes of compressive and tensile strength with compact size were not characteristic and general. Specimen's size affected both extrapolated and interpolated values of sigma(C) and sigma(T) most significantly in the case of MCC, for which sigma(T) increased while sigma(C) decreased, as the compact size became smaller. Less significant was the effect of compact size on the interpolated value of compressive strength (sigma(C)) and the extrapolated value of tensile strength (sigma(T)) for PGS. For CHPD, no significant and characteristic effect of compact size was observed. Particle size significantly affected the interpolated values of sigma(T) for MCC and both sigma(C) and sigma(T) for CHPD; they all increased with decreasing particle size. The sigma(C0.15)/sigma(T0.15) ratio was affected significantly by the compact size only in the case of MCC and seems to be an indication of material elasto-plasticity, since PGS has by far the highest ratio, followed by MCC and CHPD. A correlation between sigma(C0.15)/sigma(T0.15) and %RR was established as was its dependence upon deformational behaviour.

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Year:  2005        PMID: 15661488     DOI: 10.1016/j.ejps.2004.10.007

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  4 in total

1.  A study on in-line tablet coating--the influence of compaction and coating on tablet dimensional changes.

Authors:  C Cahyadi; B X Tan; L W Chan; P W S Heng
Journal:  AAPS PharmSciTech       Date:  2012-05-15       Impact factor: 3.246

2.  Effect of Porosity on Strength Distribution of Microcrystalline Cellulose.

Authors:  Özgür Keleṣ; Nicholas P Barcenas; Daniel H Sprys; Keith J Bowman
Journal:  AAPS PharmSciTech       Date:  2015-05-29       Impact factor: 3.246

3.  Anisotropic porous structure of pharmaceutical compacts evaluated by PGSTE-NMR in relation to mechanical property anisotropy.

Authors:  Patrice Porion; Virginie Busignies; Vincent Mazel; Bernard Leclerc; Pierre Evesque; Pierre Tchoreloff
Journal:  Pharm Res       Date:  2010-08-10       Impact factor: 4.200

4.  Pore direction in relation to anisotropy of mechanical strength in a cubic starch compact.

Authors:  Yu San Wu; Lucas J van Vliet; Henderik W Frijlink; Ietse Stokroos; Kees van der Voort Maarschalk
Journal:  AAPS PharmSciTech       Date:  2008-04-09       Impact factor: 3.246

  4 in total

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