Impact of alternative lubricants on process and tablet quality for direct compression.

Compaction simulator Direct compression Internal lubrication Lubrication Magnesium stearate Tablet properties Tableting

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 Aug 2022
Historique:
received: 11 05 2022
revised: 05 07 2022
accepted: 08 07 2022
pubmed: 16 7 2022
medline: 17 8 2022
entrez: 15 7 2022
Statut: ppublish

Résumé

Internal lubrication with magnesium stearate (MgSt) is associated with a reduced tensile strength and prolonged disintegration and dissolution times. In the current study, alternative lubricants to MgSt were compared with regard to lubrication efficacy and their impact on tablet properties. The lubricants were combined in different concentrations (0.5-5% w/w) with three fillers (lactose, mannitol and microcrystalline cellulose (MCC)). The high lubrication efficiency of MgSt was associated with the highest reduction of tensile strength. The micronized stearic acid (SA) grades proved good alternatives as they showed a good lubrication efficiency in combination with a limited negative effect on tensile strength. The hydrophobic lubricants (e.g., MgSt and SA) did not prolong disintegration. In contrast, delayed disintegration was observed for sucrose monopalmitate combined with all three fillers and for several other hydrophilic lubricants (sodium lauryl sulfate, poloxamers 188 and P407) combined with MCC. These unexpected findings were explained by the competition-for-water hypothesis. The potential of alternative lubricants to MgSt was demonstrated in this study. Nevertheless, the impact of lubricant addition on process and tablet quality depended on lubricant (type and concentration) and formulation (lubrication need, deformation mechanism and disintegration behavior) properties. Therefore, lubricant selection should be carefully considered in formulation development.

Identifiants

pubmed: 35839984
pii: S0378-5173(22)00567-1
doi: 10.1016/j.ijpharm.2022.122012
pii:
doi:

Substances chimiques

Excipients 0
Lubricants 0
Stearic Acids 0
Tablets 0
Lactose J2B2A4N98G

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122012

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Cedrine de Backere (C)

Laboratory of Pharmaceutical Technology, Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Julian Quodbach (J)

Institute of Pharmaceutics and Biopharmaceutics, Heinrich-Heine-University, Universitätsstraße 1, 40225 Duesseldorf, Germany; Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

Thomas De Beer (T)

Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Chris Vervaet (C)

Laboratory of Pharmaceutical Technology, Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.

Valérie Vanhoorne (V)

Laboratory of Pharmaceutical Technology, Department of Pharmaceutics, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium. Electronic address: Valerie.Vanhoorne@ugent.be.

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Classifications MeSH