Investigation of the interactions of enteric and hydrophilic polymers to enhance dissolution of griseofulvin following hot melt extrusion processing. (3rd February 2015)
- Record Type:
- Journal Article
- Title:
- Investigation of the interactions of enteric and hydrophilic polymers to enhance dissolution of griseofulvin following hot melt extrusion processing. (3rd February 2015)
- Main Title:
- Investigation of the interactions of enteric and hydrophilic polymers to enhance dissolution of griseofulvin following hot melt extrusion processing
- Authors:
- Bennett, Ryan C.
Keen, Justin M.
Bi, Yunxia (Vivian)
Porter, Stuart
Dürig, Thomas
McGinity, James W. - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jphp12388-sec-0001" sec-type="section"> <title>Objectives</title> <p>This study focuses on the application of hot melt extrusion (HME) to produce solid dispersions containing griseofulvin (GF) and investigates the in‐vitro dissolution performance of HME powders and resulting tablet compositions containing HME‐processed dispersions.</p> </sec> <sec id="jphp12388-sec-0002" sec-type="section"> <title>Methods</title> <p>Binary, ternary and quaternary dispersions containing GF, enteric polymer (Eudragit L100‐55 or AQOAT‐LF) and/or vinyl pyrrolidone‐based polymer (Plasdone K‐12 povidone or S‐630 copovidone) were processed by HME. Two plasticizers, triethyl citrate (TEC) and acetyl tributyl citrate (ATBC), were incorporated to aid in melt processing and to modify release of GF in neutral media following a pH‐change in dissolution. Products were characterized for GF recovery, degrees of compositional amorphous character, intermolecular interactions and non‐sink dissolution performance.</p> </sec> <sec id="jphp12388-sec-0003" sec-type="section"> <title>Key findings</title> <p>Binary dispersions exhibited lower maximum observed concentration values and magnitudes of supersaturated GF in neutral media dissolution in comparison with the ternary dispersions. The quaternary HME products, 1 : 2 : 1 : 0.6 GF : L100‐55 : S‐630 : ATBC and GF : AQOAT‐LF : K‐12 : ATBC, were determined as the most optimal concentration‐enhancing<abstract abstract-type="main"> <title>Abstract</title> <sec id="jphp12388-sec-0001" sec-type="section"> <title>Objectives</title> <p>This study focuses on the application of hot melt extrusion (HME) to produce solid dispersions containing griseofulvin (GF) and investigates the in‐vitro dissolution performance of HME powders and resulting tablet compositions containing HME‐processed dispersions.</p> </sec> <sec id="jphp12388-sec-0002" sec-type="section"> <title>Methods</title> <p>Binary, ternary and quaternary dispersions containing GF, enteric polymer (Eudragit L100‐55 or AQOAT‐LF) and/or vinyl pyrrolidone‐based polymer (Plasdone K‐12 povidone or S‐630 copovidone) were processed by HME. Two plasticizers, triethyl citrate (TEC) and acetyl tributyl citrate (ATBC), were incorporated to aid in melt processing and to modify release of GF in neutral media following a pH‐change in dissolution. Products were characterized for GF recovery, degrees of compositional amorphous character, intermolecular interactions and non‐sink dissolution performance.</p> </sec> <sec id="jphp12388-sec-0003" sec-type="section"> <title>Key findings</title> <p>Binary dispersions exhibited lower maximum observed concentration values and magnitudes of supersaturated GF in neutral media dissolution in comparison with the ternary dispersions. The quaternary HME products, 1 : 2 : 1 : 0.6 GF : L100‐55 : S‐630 : ATBC and GF : AQOAT‐LF : K‐12 : ATBC, were determined as the most optimal concentration‐enhancing compositions due to increased hydrogen bonding of enteric functional groups with carbonyl/acetate groups of vinyl pyrrolidone‐based polymers, reduced compositional crystallinity and presence of incorporated hydrophobic plasticizer.</p> </sec> <sec id="jphp12388-sec-0004" sec-type="section"> <title>Conclusions</title> <p>HME products containing combinations of concentration‐enhancing polymers can supersaturate and sustain GF dissolution to greater magnitudes in neutral media following the pH‐transition and be compressed into immediate‐release tablets exhibiting similar dissolution profiles.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of pharmacy and pharmacology. Volume 67:Number 7(2015:Jul.)
- Journal:
- Journal of pharmacy and pharmacology
- Issue:
- Volume 67:Number 7(2015:Jul.)
- Issue Display:
- Volume 67, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 67
- Issue:
- 7
- Issue Sort Value:
- 2015-0067-0007-0000
- Page Start:
- 918
- Page End:
- 938
- Publication Date:
- 2015-02-03
- Subjects:
- Pharmacy -- Periodicals
Pharmacology -- Periodicals
615.1 - Journal URLs:
- https://academic.oup.com/jpp ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)2042-7158 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.ingentaconnect.com/content/rpsgb/jpp ↗ - DOI:
- 10.1111/jphp.12388 ↗
- Languages:
- English
- ISSNs:
- 0022-3573
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5034.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3867.xml