Triamcinolone solubilization by (2-hydroxypropyl)-β-cyclodextrin: A spectroscopic and computational approach

Carbohydrate Polymers

Volumn 90, Issue 3, 2012, Pages 1288-1298

  Miro, Agnese ^a   Ungaro, Francesca ^a   Balzano, Federica ^b   Masi, Sofia ^b   Musto, Pellegrino ^c   La Manna, Pietro ^c   Uccello Barretta, Gloria ^b   Quaglia, Fabiana ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b UNIVERSITY OF PISA   (Italy)

^c CNR   (Italy)

Author keywords

Cyclodextrin; Diffusion; NMR; Raman; Solubility diagram; Triamcinolone acetonide

Indexed keywords

AQUEOUS SOLUBILITY; ASSOCIATION CONSTANT; COMPUTATIONAL APPROACH; HOMOGENEOUS SYSTEM; MOLAR RATIO; PHARMACEUTICAL FORMULATION; PHASE SOLUBILITY; RAMAN; RAMAN IMAGING; SOLUBILITY DIAGRAM; TRIAMCINOLONE; TRIAMCINOLONE ACETONIDE; UV- AND;

ACETONE; COMPUTATIONAL METHODS; CYCLODEXTRINS; DIFFUSION; DRUG PRODUCTS; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RAMAN SPECTROSCOPY;

SOLUBILITY;

2 HYDROXYPROPYL BETA CYCLODEXTRIN; 2-HYDROXYPROPYL-BETA-CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; TRIAMCINOLONE ACETONIDE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SOLUBILITY; ULTRAVIOLET SPECTROPHOTOMETRY;

BETA-CYCLODEXTRINS; CARBOHYDRATE CONFORMATION; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; SOLUBILITY; SPECTROPHOTOMETRY, ULTRAVIOLET; TRIAMCINOLONE ACETONIDE;

EID: 84865616353     PISSN: 01448617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carbpol.2012.06.075     Document Type: Article

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