Development of Coprocessed Chitin-Calcium Carbonate as Multifunctional Tablet Excipient for Direct Compression, Part 2: Tableting Properties.


Journal

Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R

Informations de publication

Date de publication:
10 2019
Historique:
received: 17 02 2019
revised: 06 05 2019
accepted: 21 05 2019
pubmed: 31 5 2019
medline: 20 8 2020
entrez: 31 5 2019
Statut: ppublish

Résumé

The use of multifunctional excipients is gaining interest as it simplifies formulations by replacing the need of multiple monofunctional excipients. In previous work, coprocessed chitin-calcium carbonate (CC) showed to have good potential as a multifunctional excipient for fast disintegrating tablets produced by direct compression. It allowed for good tablet strength, enhanced powder flowability, and higher true and bulk densities with fast disintegrating properties. The objective of this work is to gain insight on CC tableting properties under different tablet manufacturing conditions (different lubrication levels, compression speeds, and dwell times) and in formulations with drug models: ibuprofen and paracetamol. Results showed that CC exhibited good tabletability, compressibility, and compactibility profiles. CC does not require the addition of lubricant and can be used at high compression speeds and different dwell times. When included in formulations with ibuprofen and paracetamol at different percentages, CC enhanced tablets strength and promoted fast disintegration and drug dissolution. In conclusion, this study shows that CC can be used as a multifunctional excipient (filler-disintegrant-binder) for fast disintegrating tablets produced by direct compression.

Identifiants

pubmed: 31145923
pii: S0022-3549(19)30323-5
doi: 10.1016/j.xphs.2019.05.021
pii:
doi:

Substances chimiques

Excipients 0
Powders 0
Tablets 0
Chitin 1398-61-4
Acetaminophen 362O9ITL9D
Calcium Carbonate H0G9379FGK
Ibuprofen WK2XYI10QM

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3319-3328

Informations de copyright

Copyright © 2019 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

Auteurs

Mohammad Chaheen (M)

Sciences Pharmaceutiques, Ecole Doctorale des Sciences et Technologie (EDST), Laboratoire de Valorisation des Ressources Naturelles et Produits de Santé (VRNPS), Université Libanaise, Beyrouth, Lebanon; Laboratoire de Pharmacie Galénique et Génie Pharmaceutique, Institut Charles Gerhardt, UMR 5253, Equipe MACS, UFR Sciences Pharmaceutiques et Biologiques, Université de Montpellier, France. Electronic address: mohammadchaheen@hotmail.com.

Bernard Bataille (B)

Laboratoire de Pharmacie Galénique et Génie Pharmaceutique, Institut Charles Gerhardt, UMR 5253, Equipe MACS, UFR Sciences Pharmaceutiques et Biologiques, Université de Montpellier, France.

Ahmad Yassine (A)

Sciences Pharmaceutiques, Ecole Doctorale des Sciences et Technologie (EDST), Laboratoire de Valorisation des Ressources Naturelles et Produits de Santé (VRNPS), Université Libanaise, Beyrouth, Lebanon.

Emmanuel Belamie (E)

Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM), Institut Charles Gerhardt, UMR 5253, EPHE, PSL, Equipe MACS, Ecole Nationale Supérieure de Chimie, Université de Montpellier, Montpellier, France.

Tahmer Sharkawi (T)

Laboratoire de Pharmacie Galénique et Génie Pharmaceutique, Institut Charles Gerhardt, UMR 5253, Equipe MACS, UFR Sciences Pharmaceutiques et Biologiques, Université de Montpellier, France. Electronic address: tahmer.sharkawi@umontpellier.fr.

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Classifications MeSH