| Literature DB >> 1788160 |
J Pitha1, L M Mallis, D J Lamb, T Irie, K Uekama.
Abstract
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, triethanolamine 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.Entities:
Mesh:
Substances:
Year: 1991 PMID: 1788160 DOI: 10.1023/a:1015854402122
Source DB: PubMed Journal: Pharm Res ISSN: 0724-8741 Impact factor: 4.200