<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml">A 23 factorial experimental design has been used to quantitatively study individual and interaction effects of the nature of binder (N), binder concentration (<italic>c</italic>) and relative density of tablet (<italic>d</italic>) on the disintegration time (<italic>DT</italic>) and dissolution times, <italic>t</italic>1, <italic>t</italic>50 and <italic>t</italic>90, of paracetamol tablet formulations. The factorial design was also used to study the quantitative effects of pregelatinization of starch binders on these parameters, <italic>i.e.</italic>, N, <italic>c</italic> and <italic>d.</italic> In general, the most common ranking of the individual effects on <italic>DT</italic>, <italic>t</italic>1, <italic>t</italic>50 and <italic>t</italic>90 for native/native, pregelatinized/pregelatinized and native/pregelatinized starch binder formulations was <italic>c</italic> > <italic>d</italic> > N. For interaction effects, the most common ranking was N-<italic>c</italic> > <italic>c-d</italic> > N-<italic>d</italic> for all formulations. The results generally showed that <italic>c</italic> can considerably affect <italic>DT, t</italic>1, <italic>t</italic>50 and <italic>t</italic>90 of the tablets.</abstract>

A 23 factorial experimental design has been used to quantitatively study individual and interaction effects of the nature of binder (N), binder concentration (c) and relative density of tablet (d) on the disintegration time (DT) and dissolution times, t1, t50 and t90, of paracetamol tablet formulations. The factorial design was also used to study the quantitative effects of pregelatinization of starch binders on these parameters, i.e., N, c and d. In general, the most common ranking of the individual effects on DT, t1, t50 and t90 for native/native, pregelatinized/pregelatinized and native/pregelatinized starch binder formulations was c > d > N. For interaction effects, the most common ranking was N-c > c-d > N-d for all formulations. The results generally showed that c can considerably affect DT, t1, t50 and t90 of the tablets.

Influence of process variables on release properties of paracetamol tablets

Department of Pharmaceutics Faculty of Pharmacy, Obafemi Awolowo University, Ile-Ife, Nigeria

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria

Acta Pharmaceutica

{"article-title":"Influence of process variables on release properties of paracetamol tablets"}

A 23 factorial experimental design has been used to quantitatively study individual and interaction effects of the nature of binder (N), binder concentration...

Influence of process variables on release properties of paracetamol tablets

Pubblicato online: 28 feb 2007

Pagine: 73 - 86

DOI: https://doi.org/10.2478/v10007-007-0006-8

Parole chiave
pregelatinization, starch, sorghum, plantain, disintegration, dissolution

This content is open access.

Influence of process variables on release properties of paracetamol tablets

Pubblicato online: 28 feb 2007

Pagine: 73 - 86

DOI: https://doi.org/10.2478/v10007-007-0006-8

Parole chiavepregelatinization, starch, sorghum, plantain, disintegration, dissolution

This content is open access.

Parole chiave
pregelatinization, starch, sorghum, plantain, disintegration, dissolution