Lipid‐Based Formulations Solidified Via Adsorption onto the Mesoporous Carrier Neusilin® US2: Effect of Drug Type and Formulation Composition on In Vitro Pharmaceutical Performance. Issue 6 (16th April 2014)
- Record Type:
- Journal Article
- Title:
- Lipid‐Based Formulations Solidified Via Adsorption onto the Mesoporous Carrier Neusilin® US2: Effect of Drug Type and Formulation Composition on In Vitro Pharmaceutical Performance. Issue 6 (16th April 2014)
- Main Title:
- Lipid‐Based Formulations Solidified Via Adsorption onto the Mesoporous Carrier Neusilin® US2: Effect of Drug Type and Formulation Composition on In Vitro Pharmaceutical Performance
- Authors:
- Williams, Hywel D.
Van Speybroeck, Michiel
Augustijns, Patrick
Porter, Christopher J. H. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The current study determined the extent to which the desorption of lipid‐based formulations (LBFs) from a mesoporous magnesium aluminometasilicate (Neusilin®‐US2) carrier is governed by drug properties, LBF composition, and LBF‐to‐adsorbent ratio. A secondary objective was to evaluate the impact of testing parameters (medium composition, pH, dilution, and agitation) on <italic>in vitro</italic> LBF performance. Two self‐emulsifying LBFs, with high/low lipid–surfactant ratios were studied in detail using danazol, fenofibrate, cinnarizine, and mefenamic acid as model drugs. A wider range of 38 different danazol‐containing LBF were also evaluated, where desorption was evaluated immediately after preparation and after 1 month of storage. The results revealed that incomplete desorption from Neusilin® was a feature of all drugs and LBFs tested. Desorption was insensitive to agitation but increased under conditions where ionizable drugs were charged. In addition, formulations containing a higher proportion (&gt;30%) of hydrophilic surfactant consistently exhibited higher desorption, and were least susceptible to decreased desorption on storage. In summary, although Neusilin® is an effective vehicle for LBF solidification, its use is accompanied by a risk of incomplete desorption of the vehicle from the carrier, irrespective of the drug. Lipid Formulation Classification System<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The current study determined the extent to which the desorption of lipid‐based formulations (LBFs) from a mesoporous magnesium aluminometasilicate (Neusilin®‐US2) carrier is governed by drug properties, LBF composition, and LBF‐to‐adsorbent ratio. A secondary objective was to evaluate the impact of testing parameters (medium composition, pH, dilution, and agitation) on <italic>in vitro</italic> LBF performance. Two self‐emulsifying LBFs, with high/low lipid–surfactant ratios were studied in detail using danazol, fenofibrate, cinnarizine, and mefenamic acid as model drugs. A wider range of 38 different danazol‐containing LBF were also evaluated, where desorption was evaluated immediately after preparation and after 1 month of storage. The results revealed that incomplete desorption from Neusilin® was a feature of all drugs and LBFs tested. Desorption was insensitive to agitation but increased under conditions where ionizable drugs were charged. In addition, formulations containing a higher proportion (&gt;30%) of hydrophilic surfactant consistently exhibited higher desorption, and were least susceptible to decreased desorption on storage. In summary, although Neusilin® is an effective vehicle for LBF solidification, its use is accompanied by a risk of incomplete desorption of the vehicle from the carrier, irrespective of the drug. Lipid Formulation Classification System (LFCS)Type IIIB LBFs comprising higher quantities of hydrophilic surfactants appear to desorb most from Neusilin®. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci</p> </abstract> … (more)
- Is Part Of:
- Journal of pharmaceutical sciences. Volume 103:Issue 6(2014:Jun.)
- Journal:
- Journal of pharmaceutical sciences
- Issue:
- Volume 103:Issue 6(2014:Jun.)
- Issue Display:
- Volume 103, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 103
- Issue:
- 6
- Issue Sort Value:
- 2014-0103-0006-0000
- Page Start:
- 1734
- Page End:
- 1746
- Publication Date:
- 2014-04-16
- Subjects:
- Pharmacy -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-6017 ↗
http://www.jpharmsci.org/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jps.23970 ↗
- Languages:
- English
- ISSNs:
- 0022-3549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5031.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4055.xml