Syntheses and doxorubicin-inclusion abilities of beta-cyclodextrin derivatives with a hydroquinone alpha-glycoside residue attached at the primary side.

Abstract:

:This paper describes syntheses and doxorubicin-inclusion abilities of beta-cyclodextrin (CyD) derivatives with a hydroquinone alpha-glycoside residue attached at the primary side. The hydroquinone glycoside having an alpha-D-glucosidic or 2-acetamido-2-deoxy-alpha-D-glucosidic linkage became a useful component for providing an alpha-D-glucose- or 2-acetamido-2-deoxy-alpha-D-glucose-beta-CyD conjugate. The surface plasmon resonance analyses of these beta-CyD derivatives for the anticancer agent, doxorubicin, indicated that they had excellent inclusion associations on the order of 10(5 m)-1 for the immobilized doxorubicin.

authors

Oda Y,Miura M,Hattori K,Yamanoi T

doi

10.1248/cpb.57.74

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

74-8

issue

1

eissn

0009-2363

issn

1347-5223

pii

JST.JSTAGE/cpb/57.74

journal_volume

57

pub_type

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