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Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form

The aim of this investigation was to develop a novel multifunctional co-processed diluent consisting of microcrystalline cellulose (Avicel PH 102), crospovidone (Polyplasdone XL) and polyethylene glycol 4000. Colloidal silicon dioxide and talc were also incorporated as minor components in the diluen...

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Autores principales: Gohel, M. C., Patel, T. M., Parikh, R. K., Parejiya, P. B., Barot, B. S., Ramkishan, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660863/
https://www.ncbi.nlm.nih.gov/pubmed/23716865
http://dx.doi.org/10.4103/0250-474X.108412
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author Gohel, M. C.
Patel, T. M.
Parikh, R. K.
Parejiya, P. B.
Barot, B. S.
Ramkishan, A.
author_facet Gohel, M. C.
Patel, T. M.
Parikh, R. K.
Parejiya, P. B.
Barot, B. S.
Ramkishan, A.
author_sort Gohel, M. C.
collection PubMed
description The aim of this investigation was to develop a novel multifunctional co-processed diluent consisting of microcrystalline cellulose (Avicel PH 102), crospovidone (Polyplasdone XL) and polyethylene glycol 4000. Colloidal silicon dioxide and talc were also incorporated as minor components in the diluent to improve tableting properties. Melt granulation was adopted for preparation of co-processed diluent. Percentage of Avicel PH 102, Polyplasdone XL and polyethylene glycol 4000 were selected as independent variables and disintegration time was chosen as a dependent variable in simplex lattice design. The co-processed diluent was characterised for angle of repose, bulk density, tapped density, Carr's index, percentage of fines and dilution potential study. Acetaminophen and metformin were used as poorly compressible model drugs for preparation of tablets. The blend of granules of drug and extra-granular co-processed diluent exhibited better flow as compared to the blend of drug granules and physical mixture of diluents blend. The diluent exhibited satisfactory tableting properties. The tablets exhibited fairly rapid drug release. In conclusion, melt granulation is proposed as a method of preparing co-processed diluent. The concept can be used to bypass patents on excipient manufacturing.
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spelling pubmed-36608632013-05-28 Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form Gohel, M. C. Patel, T. M. Parikh, R. K. Parejiya, P. B. Barot, B. S. Ramkishan, A. Indian J Pharm Sci Research Paper The aim of this investigation was to develop a novel multifunctional co-processed diluent consisting of microcrystalline cellulose (Avicel PH 102), crospovidone (Polyplasdone XL) and polyethylene glycol 4000. Colloidal silicon dioxide and talc were also incorporated as minor components in the diluent to improve tableting properties. Melt granulation was adopted for preparation of co-processed diluent. Percentage of Avicel PH 102, Polyplasdone XL and polyethylene glycol 4000 were selected as independent variables and disintegration time was chosen as a dependent variable in simplex lattice design. The co-processed diluent was characterised for angle of repose, bulk density, tapped density, Carr's index, percentage of fines and dilution potential study. Acetaminophen and metformin were used as poorly compressible model drugs for preparation of tablets. The blend of granules of drug and extra-granular co-processed diluent exhibited better flow as compared to the blend of drug granules and physical mixture of diluents blend. The diluent exhibited satisfactory tableting properties. The tablets exhibited fairly rapid drug release. In conclusion, melt granulation is proposed as a method of preparing co-processed diluent. The concept can be used to bypass patents on excipient manufacturing. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3660863/ /pubmed/23716865 http://dx.doi.org/10.4103/0250-474X.108412 Text en Copyright: © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Gohel, M. C.
Patel, T. M.
Parikh, R. K.
Parejiya, P. B.
Barot, B. S.
Ramkishan, A.
Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title_full Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title_fullStr Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title_full_unstemmed Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title_short Exploration of Novel Co-processed Multifunctional Diluent for the Development of Tablet Dosage Form
title_sort exploration of novel co-processed multifunctional diluent for the development of tablet dosage form
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660863/
https://www.ncbi.nlm.nih.gov/pubmed/23716865
http://dx.doi.org/10.4103/0250-474X.108412
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