| Literature DB >> 11536201 |
E Redenti1, L Szente, J Szejtli.
Abstract
The objective of this mini-review is to summarize the findings concerning the physicochemical properties and the pharmaceutical applications of acidic drugs whose performances have been modified by simultaneous complexation with cyclodextrins and salt formation. Particular attention is paid to the approaches undertaken for increasing the solubility of the drugs by proper choice of the type of counterion analogously to what has been reported for complexes of basic drugs in the presence of hydroxy acids. Copyright 2001 Wiley-Liss, Inc.Entities:
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Year: 2001 PMID: 11536201 DOI: 10.1002/jps.1050
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534