Effects of thermal binders on chemical stabilities and tabletability of gabapentin granules prepared by twin-screw melt granulation.


Journal

International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127

Informations de publication

Date de publication:
25 Mar 2019
Historique:
received: 16 11 2018
revised: 21 12 2018
accepted: 11 01 2019
pubmed: 21 1 2019
medline: 14 6 2019
entrez: 21 1 2019
Statut: ppublish

Résumé

The effect of thermal binders on the physicochemical properties of gabapentin, a thermally labile drug, in granules prepared using twin-screw melt granulation was investigated in this study. Hydroxypropyl cellulose (HPC), a thermoplastic high molecular-weight binder, was compared against conventional low molecular-weight semi-crystalline thermal binders PEG 8000 and Compritol. Both the chemical degradation and polymorph form change of gabapentin were analyzed. The effects of particle size and molecular weight of HPC on the properties of granules were also studied. To overcome the high melt viscosity of HPC, higher barrel temperatures and higher specific mechanical energy were required to attain suitable granules. As a result, higher levels of gabapentin degradant were observed in HPC-based formulations. However, gabapentin form change was not observed in all formulations. Smaller particle size and lower molecular weight of HPC led to faster granule growth. The tabletability of granules was insensitive to the variations in particle size and molecular weight of HPC. Gabapentin crystal size reduction, HPC size reduction, and HPC enrichment on granule surface were observed for HPC-based granules.

Identifiants

pubmed: 30660749
pii: S0378-5173(19)30048-1
doi: 10.1016/j.ijpharm.2019.01.014
pii:
doi:

Substances chimiques

Excipients 0
Powders 0
Tablets 0
Gabapentin 6CW7F3G59X
Cellulose 9004-34-6
hydroxypropylcellulose 9XZ8H6N6OH

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

37-47

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Nada Kittikunakorn (N)

Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, 2409 University Avenue, A1920, Austin, TX 78712, USA.

J Joseph Koleng (JJ)

Division of Chemical Engineering, School of Engineering, the University of Texas at Austin, 200 E Dean Keeton St, Austin, TX 78712, USA.

Tony Listro (T)

Foster Delivery Sciences, 45 Ridge Road, Putnam, CT 06260, USA.

Changquan Calvin Sun (C)

Department of Pharmaceutics, University of Minnesota, 308 SE Harvard St, Minneapolis, MN 55455, USA.

Feng Zhang (F)

Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, 2409 University Avenue, A1920, Austin, TX 78712, USA. Electronic address: feng.zhang@austin.utexas.edu.

Articles similaires

Animals Dietary Fiber Dextran Sulfate Mice Disease Models, Animal
Nitriles Tensile Strength Materials Testing Gloves, Protective Product Packaging
Calcium Carbonate Sand Powders Construction Materials Materials Testing
Animals Rumen Methane Fermentation Cannabis

Classifications MeSH