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Brittle fracture during tableting – a problem for the pharmaceutical industry Professor RS Okor
Professor
of Pharmaceutics & Pharmaceutical Technology, Faculty of Pharmacy,
University of Benin, Benin City, Nigeria
Tropical Journal of Pharmaceutical Research 2005; 4(2): 381-382 ISSN: 1596-5996
Editorial Brittle
fracture refers to capping and lamination of tablets, which occurs at the point
of ejection of the tablets from the machine dies.
The problem is attributable primarily to the presence of entrapped air
(voids) or low density regions in the tablets.
The latter (low density region) is in turn associated with an uneven
consolidation of the tablet during compaction.
The voids or low-density regions constitute weak points in the tablet
from which cracks emanate and propagate when the tablet is subjected to
diametral stress (e.g. die wall pressure). Brittle fracture is thus a result of
stress concentration at the edge of the void or low-density region. Sudden
elastic recovery following tablet ejection from the die has been implicated as a
possible cause of brittle fracture, supported by the evidence of direct
correlation between the plasto-elasticity of materials and the brittle fracture
index (BF1) of resulting tablets1-3. This means that predominantly
elastic materials are more prone to brittle fracture than plastic materials.
Nevertheless the theory of stress concentration at the edge of a void and the
subsequent crack propagation from it is more acceptable. Plastic materials
ameliorate brittle fracture because they deform readily under stress to relieve
the stress that would have concentrated at the edge of the void4-5. Hiestand
et al4 applied crack theory to develop a quantitative
expression for the measurement of the brittle fracture tendency. Thus, the
brittle fracture index (BFI) of a tablet is give by; BFI
= 0.5 (T/To – 1) where
To and T are the tensile strengths of tablets with and without a centre hole,
respectively. The centre hole (£0.6mm)
is a built-in model defect to simulate actual void formed in the tablet during
compression. For
brittle fracture to occur, the ratio T/To=3. By subtracting 1 and
multiplying by 0.5 the maximal BFI value is 1 (unity).
The BFI value thus has a range of 0 (no fracture tendency) to 1 (maximal
fracture tendency).
Tablet samples with BFI values (³0.5)
displayed a high fracture incidence during actual tableting4. Brittle
fracture during tableting is considered a problem for the pharmaceutical
industry because it is associated with formulation factors such as insufficient
binder, a high plasto-elasticity of the tableting base, and process factors such
excessive compression pressures and over-drying of granules/ powders.
Very often tableting is halted as soon as brittle fracture is observed;
the batch is either rejected or reprocessed, which is un-economical. It
is therefore recommended that the Hiestand mathematical expression for BFI could
be used to test and select tablet formulations and tableting conditions that
will give low fracture tendency.
Such tests are to be carried out on small tablet samples during product
development which will provide a basis for the rational selection of optimal
conditions of formulation and processing for large scale production of tablets. References
1.
Itiola AO and Pipel N. Tableting characteristics of metronidazole
formulations. Int J Pharm. 1986; 31: 99-105. 2.
Okor RS, Eichie FE and Ngwa CN. Correlation between tablet mechanical
strength and brittle fracture tendency. J Pharm. Pharmacol. 1998; 4: 511-513. 3.
Uhumwangho MU and Okor RS. Anomalous effect of compression pressure on
the brittle fracture tendency of a-cellulose
tablets. Int J Pharm 2004; 284: 69-74. 4. Heistand EN Wells JE, Poet CB and Ochs JF. Physical process of tableting .J. Pharm Sci. 1977; 66: 510-519. 5. Roberts JR and Rowe RC. Brittle fracture propensity measurements on tablet-sized cylindrical compacts. Pharm Pharmacol. 1986; 38: 526-528.
Key words: Brittle fracture, plasto-elasticity, tableting.
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