Anti‐plasticizing Effect of Amorphous Indomethacin Induced by Specific Intermolecular Interactions with PVA Copolymer. Issue 9 (2nd June 2014)
- Record Type:
- Journal Article
- Title:
- Anti‐plasticizing Effect of Amorphous Indomethacin Induced by Specific Intermolecular Interactions with PVA Copolymer. Issue 9 (2nd June 2014)
- Main Title:
- Anti‐plasticizing Effect of Amorphous Indomethacin Induced by Specific Intermolecular Interactions with PVA Copolymer
- Authors:
- Ueda, Hiroshi
Aikawa, Shohei
Kashima, Yousuke
Kikuchi, Junko
Ida, Yasuo
Tanino, Tadatsugu
Kadota, Kazunori
Tozuka, Yuichi - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The mechanism of how poly(vinyl alcohol‐co‐acrylic acid‐co‐methyl methacrylate) (PVA copolymer) stabilizes an amorphous drug was investigated. Solid dispersions of PVA copolymer, poly(vinyl pyrrolidone) (PVP), and poly(vinyl pyrrolidone‐co‐vinyl acetate) (PVPVA) with indomethacin (IMC) were prepared. The glass transition temperature (<italic>T</italic><sub>g</sub>)‐proportion profiles were evaluated by differential scanning calorimetry (DSC). General <italic>T</italic><sub>g</sub> profiles decreasing with the IMC ratio were observed for IMC–PVP and IMC–PVPVA samples. An interesting antiplasticizing effect of IMC on PVA copolymer was observed; <italic>T</italic><sub>g</sub> increased up to 20% IMC ratio. Further addition of IMC caused moderate reduction with positive deviation from theoretical values. Specific hydrophilic and hydrophobic interactions between IMC and PVA copolymer were revealed by infrared spectra. The indole amide of IMC played an important role in hydrogen bonding with PVA copolymer, but not with PVP and PVPVA. X‐ray diffraction findings and the endotherm on DSC profiles suggested that PVA copolymer could form a semicrystalline structure and a possibility of correlation of the crystallographic nature with its low hygroscopicity was suggested. PVA copolymer was able to prevent crystallization of amorphous IMC through both low hygroscopicity and the formation<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The mechanism of how poly(vinyl alcohol‐co‐acrylic acid‐co‐methyl methacrylate) (PVA copolymer) stabilizes an amorphous drug was investigated. Solid dispersions of PVA copolymer, poly(vinyl pyrrolidone) (PVP), and poly(vinyl pyrrolidone‐co‐vinyl acetate) (PVPVA) with indomethacin (IMC) were prepared. The glass transition temperature (<italic>T</italic><sub>g</sub>)‐proportion profiles were evaluated by differential scanning calorimetry (DSC). General <italic>T</italic><sub>g</sub> profiles decreasing with the IMC ratio were observed for IMC–PVP and IMC–PVPVA samples. An interesting antiplasticizing effect of IMC on PVA copolymer was observed; <italic>T</italic><sub>g</sub> increased up to 20% IMC ratio. Further addition of IMC caused moderate reduction with positive deviation from theoretical values. Specific hydrophilic and hydrophobic interactions between IMC and PVA copolymer were revealed by infrared spectra. The indole amide of IMC played an important role in hydrogen bonding with PVA copolymer, but not with PVP and PVPVA. X‐ray diffraction findings and the endotherm on DSC profiles suggested that PVA copolymer could form a semicrystalline structure and a possibility of correlation of the crystallographic nature with its low hygroscopicity was suggested. PVA copolymer was able to prevent crystallization of amorphous IMC through both low hygroscopicity and the formation of a specific intermolecular interaction compared with that with PVP and PVPVA. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:2829–2838, 2014</p> </abstract> … (more)
- Is Part Of:
- Journal of pharmaceutical sciences. Volume 103:Issue 9(2014:Sep.)
- Journal:
- Journal of pharmaceutical sciences
- Issue:
- Volume 103:Issue 9(2014:Sep.)
- Issue Display:
- Volume 103, Issue 9 (2014)
- Year:
- 2014
- Volume:
- 103
- Issue:
- 9
- Issue Sort Value:
- 2014-0103-0009-0000
- Page Start:
- 2829
- Page End:
- 2838
- Publication Date:
- 2014-06-02
- 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.24023 ↗
- 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:
- 3610.xml