By Juan JosГ© Torres Labandeira, JosГ© Luis Vila-Jato
This quantity comprises the complaints of the 9th foreign Symposium on Cyclodextrins, held in Santiago de Compostela, Spain, might 31 - June three, 1998. The papers gathered characterize a precis of the final years' achievements within the software of cyclodextrins in such varied fields as prescribed drugs, biotechnology, textiles, chromatography and environmental sciences.
Highlights: Chiral collection of chemical compounds, nuclear waste administration, cyclodextrins in nasal drug supply, cyclodextrins in pulmonary drug supply, cyclodextrins as pharmaceutical excipients, pharmacokinetics, stabilization of gear by way of cyclodextrins, structural characterization of cyclodextrin complexes by means of nuclear magnetic resonance and molecular modeling, synthetic receptors, huge cyclodextrins, cyclodextrins as enzyme types, new cyclodextrin derivatives and potentials.
Audience: This ebook may be of curiosity to researchers whose paintings contains biotechnology, prescription drugs, nutrition and chemical substances and chromatographic equipment, in addition to primary cyclodextrin learn.
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Extra resources for Proceedings of the Ninth International Symposium on Cyclodextrins
Example text
We also show that 2,6 DiMe and 15 OCH3 are the major products in most of the commercial samples (DM-(3-CDs B, C, D and E). 21). min"1, detection ELSD. min"1, detection ELSD. DM-(3-CD E seemed to be the purest sample : only one major peak corresponding to 2,6 DiMe and two minor peaks are obtained in the two chromatographic systems. It is in. good agreement with the manufacturer's claim that the amount of 2,6 DiMe in this sample was greater than 80 %. We also confirmed that DM-J3-CD D from the same manufacturer was less purified than batch E.
The right graphics display the corresponding side-views in closed and bisected form each; the 2-OH and 3-OH groups are directed upwards, whereas the 6-OH point downwards. References [1] 'Molecular Modeling of Saccharides1, Part 18. E. (1998). Molecular geometries of furanoid p(l->3)- and P(l-»6)-linked cyclogalactins, in Torres Labandeira, JJ. ), Proceedings 9th Internat. Symp. on Cyclodextrins, Kluwer Acad. , Dordrecht, NL. , and Immel, S. (1996). On the hydrophobic characteristics of cyclodextrins: computer-aided visualization of molecular lipophilicity patterns.
Supramole. Chem. 1996,8, 5. ; D'Souza, V. T. J. Org. Chem. 1994,59,7492. Parazak, D. ; Khan, A. ; D'Souza, V. ; Stine, K. J. Langmuir 1996,12,4046. CYCLODEXTRIN DERIVATIVES WITH ENHANCED SOLUBILIZING POWER AND LOWER TOXICITY JOSEF PITHA, 417 Anglesea Street, Baltimore, MD 21224. USA 1. Introduction Mixtures of partially substituted cyclodextrins (CDs) contain potentially millions of compounds, each with its own individuality. , partial methyl ethers of cyclodextrin) contain groups of compounds with little overlap.