Autor: Kaneto Uekama, Tetsumi Irie, Josef Pitha, Diane J. Lamb, Larry M. Mallis
Rok vydání: 1991
Předmět:
Zdroj: Pharmaceutical Research. :1151-1154
ISSN: 0724-8741
DOI: 10.1023/a:1015854402122
Popis: Alpha- and beta-cyclodextrins and their hydroxypropyl derivatives were converted by the reaction with chlorosulfonic acid in pyridine to the corresponding sulfates. Cyclodextrin sulfates were shown by fast-atom bombardment mass spectrometry (negative ion mode, tri-ethanolamine matrix) to be mixtures with nearly symmetrical distributions of degree of substitution by sulfate groups and by powder X-ray diffraction to be amorphous. Thus, in these aspects, cyclodextrin sulfates are similar to the potent drug solubilizers hydroxypropylcyclodextrins.
Databáze: OpenAIRE