Authors:
B. Pose-Vilarnovo Universidad de Santiago de Compostela Campus Sur. Departamento de Farmacia e Tecnoloxía Farmacéutica, Facultad de Farmacia 15706 Santiago de Compostela Spain

Search for other papers by B. Pose-Vilarnovo in
Current site
Google Scholar
PubMed
Close
,
C. Rodríguez-Tenreiro Sánchez Universidad de Santiago de Compostela Campus Sur. Departamento de Farmacia e Tecnoloxía Farmacéutica, Facultad de Farmacia 15706 Santiago de Compostela Spain

Search for other papers by C. Rodríguez-Tenreiro Sánchez in
Current site
Google Scholar
PubMed
Close
,
N. Diéguez Moure Universidad de Santiago de Compostela Campus Sur. Departamento de Farmacia e Tecnoloxía Farmacéutica, Facultad de Farmacia 15706 Santiago de Compostela Spain

Search for other papers by N. Diéguez Moure in
Current site
Google Scholar
PubMed
Close
,
J. Vila-Jato Universidad de Santiago de Compostela Campus Sur. Departamento de Farmacia e Tecnoloxía Farmacéutica, Facultad de Farmacia 15706 Santiago de Compostela Spain

Search for other papers by J. Vila-Jato in
Current site
Google Scholar
PubMed
Close
, and
J. Torres-Labandeira Universidad de Santiago de Compostela Campus Sur. Departamento de Farmacia e Tecnoloxía Farmacéutica, Facultad de Farmacia 15706 Santiago de Compostela Spain

Search for other papers by J. Torres-Labandeira in
Current site
Google Scholar
PubMed
Close
Restricted access

Abstract  

The effect of a hydrophilic polymer, hydroxypropylmethyl cellulose K4M, on the complexation of diclofenac sodium with b- and hydroxypropyl-b-cyclodextrins has been studied. Multicomponent systems were prepared with the drug, both cyclodextrin and the polymer. Phase solubility diagrams revealed the positive effect of the polymer on the complexation of the drug but this effect was found after autoclaving the solutions. Solid inclusion complexes were prepared by freeze-drying and characterized by thermal analysis (DSC) and X-ray diffractometry. In solid state, binary inclusion complexes enhance the dissolution behaviour of diclofenac but, from the b-cyclodextrin multicomponent complex, the polymer controls the release of the drug. In the case of hydroxy- propyl-b-cyclodextrin multicomponent system, the solubility of the drugs increases significantly compared with the binary complex.

  • Collapse
  • Expand

Journal of Thermal Analysis and Calorimetry
Language English
Size A4
Year of
Foundation
1969
Volumes
per Year
1
Issues
per Year
24
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Publisher Akadémiai Kiadó
Springer Nature Switzerland AG
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
CH-6330 Cham, Switzerland Gewerbestrasse 11.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 1388-6150 (Print)
ISSN 1588-2926 (Online)

Monthly Content Usage

Abstract Views Full Text Views PDF Downloads
Jan 2025 7 0 0
Feb 2025 14 0 0
Mar 2025 15 0 0
Apr 2025 4 0 0
May 2025 8 0 0
Jun 2025 13 0 0
Jul 2025 0 0 0