2009
DOI: 10.1016/j.ccr.2008.08.011
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Inclusion complexation, encapsulation interaction and inclusion number in cyclodextrin chemistry

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Cited by 171 publications
(98 citation statements)
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“…Cyclodextrins (CD) are a series of naturally occurring macrocyclic oligosaccharides formed from ␣-1,4-linked-D -glucopyranose units [5][6][7]. The primary and secondary hydroxyl groups on the exterior of the cyclodextrin are polar, while the hydrogens inside of the cyclodextrin are apolar.…”
Section: Introductionmentioning
confidence: 99%
“…Cyclodextrins (CD) are a series of naturally occurring macrocyclic oligosaccharides formed from ␣-1,4-linked-D -glucopyranose units [5][6][7]. The primary and secondary hydroxyl groups on the exterior of the cyclodextrin are polar, while the hydrogens inside of the cyclodextrin are apolar.…”
Section: Introductionmentioning
confidence: 99%
“…The three most common CDs are their α, β, and γ forms consisting of six, seven, and eight glucose units, respectively (5)(6)(7). In our study, we assumed that the hydrophilic peripheral of CDs possess association potential to bind with certain inorganic ions, especially heavy metals, by the alcoholic hydroxyl groups.…”
Section: Introductionmentioning
confidence: 99%
“…Due to their hydrophobic cavity and hydrophilic outer surface, they are able to form inclusion (host-guest) complexes with a variety of organic and inorganic molecules, thus changing the chemical and physical properties of the guest molecules (Del Valle, 2004;Singh et al, 2002). Inclusion complex formation makes CDs attractive for the use in wide industrial applications including food, pharmacy, agriculture, cosmetics, analytical chemistry (Brewster and Loftsson, 2007;Del Valle, 2004;Loftsson and Duchene, 2007;Song et al, 2009;Szente and Szejtli, 2004).…”
Section: Introductionmentioning
confidence: 99%