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A solvent-free method for isotopically or radioactively labeling cyclodextrins and cyclodextrin-containing polymers.

Authors:
Ryan K Zeidan Stacey A Kalovidouris Thomas Schluep Robert Fazio Robert Andresini Mark E Davis

Bioconjug Chem 2006 Nov-Dec;17(6):1624-6

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena California 91125, USA.

A method for installing a distinguishable label onto cyclodextrins or cyclodextrin-containing polymers is reported. Cyclodextrins (CD) and cyclodextrin-containing polymers are exposed to labeled (2H or 14C) ethylene oxide (EO) vapor and the alcohol groups on the CD ring open the EO to give ether-linked labeled methylenes and a terminal alcohol. This method provides for the incorporation of an easily tracked and quantified label without the use of solvents or purification steps. The method can be generalized for use with materials that contain nucleophiles other than alcohols, e.g., amines.

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http://dx.doi.org/10.1021/bc060211eDOI Listing
January 2007

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Voltammetric/UV-Vis study of temozolomide inclusion complexes with cyclodextrin derivatives.

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University of Warsaw Faculty of Chemistry, Pasteura 1, 02-093 Warsaw, Poland; Faculty of Chemistry, Biological and Chemical Research Centre, University of Warsaw, Żwirki i Wigury 101, 02-089 Warsaw, Poland. Electronic address:

Temozolomide (TMZ) - a chemotherapeutic agent possessing cytotoxic activity is used in single or combined therapies of human glioma. Difficulties in these applications, connected with low solubility and stability of temozolomide lead us to study the inclusion complexes between TMZ, and three cyclodextrins: β-cyclodextrin (βCD), monodeoxy-6-monoamino-β-cyclodextrin hydrochloride (βCDamine), and β-cyclodextrin containing galactosamine and triazole ring in the side group (βCDgal). The voltammetric and spectroscopy studies showed the improvement of the drug solubility and formation of stable complexes. Read More

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