Screening of several excipients for direct compression of tablets: A new perspective based on functional properties

ABSTRACT: Excipients are widely used to formulate solid drug forms by direct compression. However, the powder-forming and tableting properties of these excipients are affected by the presence of lubricants and active ingredients. In this study, a screening methodology was employed to test the perfor...

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Autores:
Rojas Camargo, John Jairo
Aristizábal, Julián
Henao, Manuel
Tipo de recurso:
Article of investigation
Fecha de publicación:
2013
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38192
Acceso en línea:
https://hdl.handle.net/10495/38192
https://rcfba.fcfar.unesp.br/index.php/ojs/article/view/230
Palabra clave:
Lubricantes
Lubricants
Tamizaje Masivo
Mass Screening
Comprimidos
Tablets
Dilución
Dilution
https://id.nlm.nih.gov/mesh/D054327
https://id.nlm.nih.gov/mesh/D008403
https://id.nlm.nih.gov/mesh/D013607
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABSTRACT: Excipients are widely used to formulate solid drug forms by direct compression. However, the powder-forming and tableting properties of these excipients are affected by the presence of lubricants and active ingredients. In this study, a screening methodology was employed to test the performance of an excipient for direct compression. The effects of three lubricants (magnesium stearate, stearic acid and talc) on the compressibility and compaction of these excipients were assessed by the compressibility index and lubricant sensitivity ratio, respectively. Likewise, the dilution potential in blends with a poorly compactible drug such as acetaminophen was also assessed. Finally, the elastic recovery of tablets was evaluated five days after production. All lubricants increased the compressibility of these excipients and improved their flowability. However, hydrophobic lubricants such as magnesium stearate had a marked negative effect on compactibility, especially in plastic-deforming and more regularly-shaped materials with a smooth surface such as Starch 1500. Alginic acid, rice and cassava starches had the largest elastic recovery (>5%), indicating a tendency to cap. Moreover, highly plastic deforming materials such as sorbitol and polyvinylpyrrolidone (PVP-K30) exhibited the best dilution potential (~10%), whereas alginic acid showed a very high value (~70%). In terms of performance, sorbitol, PVP-K30, Avicel PH-101, sodium alginate and pregelatinized starch were the most appropriate excipients for the direct compression of drugs.