The bioavailability difference between genuine cyclodextrin inclusion complexes and free-dried or ground drug cyclodextrin samples may be due to supersaturation differences

Drug Development and Industrial Pharmacy

Volumn 23, Issue 3, 1997, Pages 331-335

  Pedersen, Morten ^a  

^a PEDCY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLODEXTRIN DERIVATIVE;

ARTICLE; BIOAVAILABILITY; COMPLEX FORMATION; DISSOLUTION; DRUG SOLUBILITY; ENCAPSULATION; FREEZE DRYING;

EID: 0031003916     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.3109/03639049709149812     Document Type: Article

References (5)

1. J. Szejtli, Cyclodextrin Technology, Topics in Inclusion Science, Kluwer Academic Publishers, Dordrecht, 1988.
2. J. Szejtli, Cyclodextrin symposium, Pharmacia, Helsingborg, 1991.
3. M. Pedersen, submitted for publication.
4. K. H. Frömming and J. Szejtli, Cyclodextrins in Pharmacy, Topics in Inclusion Science, Kluwer Academic Publishers, Dordrecht, 1994.
5. T. Higuchi and K. A. Connors, Phase-solubility techniques, Adv. Anal. Chem. Instrum., 4, 117 (1965).