Solubility enhancement of desloratadine by solid dispersion in poloxamers

International Journal of Pharmaceutics

Volumn 436, Issue 1-2, 2012, Pages 161-170

  Kolašinac, Nemanja ^a   Kachrimanis, Kyriakos ^c   Homšek, Irena ^a   Grujić, Branka ^a   Urić, Zorica ^b   Ibrić, Svetlana ^b  

^a Galenika Ad   (Serbia)

^b UNIVERSITY OF BELGRADE   (Serbia)

^c School of Pharmacy   (Greece)

Author keywords

Amorphous state; Desloratadine; Drug release; Poloxamer; Solid dispersion

Indexed keywords

DESLORATADINE; POLOXAMER; SURFACTANT;

ARTICLE; DIFFERENTIAL SCANNING CALORIMETRY; DRUG RELEASE; DRUG SOLUBILITY; FACTORIAL DESIGN; INFRARED SPECTROSCOPY; LOW TEMPERATURE; MELTING POINT; MOISTURE; PARTICLE SIZE; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SPECTROSCOPY; TABLET COMPRESSION; TABLET FORMULATION; TABLET POROSITY;

CALORIMETRY, DIFFERENTIAL SCANNING; HISTAMINE H1 ANTAGONISTS, NON-SEDATING; LORATADINE; PARTICLE SIZE; POLOXAMER; SOLUBILITY; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; SURFACE-ACTIVE AGENTS; TABLETS;

EID: 84865292964     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2012.06.060     Document Type: Article

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