Cyclodextrins in Pharmaceutics, Cosmetics, and Biomedicine 2011
DOI: 10.1002/9780470926819.ch17
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Cyclodextrin Nanosponges and their Applications

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Cited by 71 publications
(61 citation statements)
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“…The final properties of a CD-NS are strongly influenced by the nature of the cross-linker, the degree of cross-linking and the conditions of the synthesis reaction [21]. Several studies on the formulation and use of CD-NSs as nanocarriers have been conducted, showing that CD-NSs are a suitable delivery system for drugs, macromolecules and gases [22][23][24][25][26][27][28][29].…”
Section: L-dopa [(S)-2-amino-3-(34-dihydroxyphenyl)mentioning
confidence: 99%
“…The final properties of a CD-NS are strongly influenced by the nature of the cross-linker, the degree of cross-linking and the conditions of the synthesis reaction [21]. Several studies on the formulation and use of CD-NSs as nanocarriers have been conducted, showing that CD-NSs are a suitable delivery system for drugs, macromolecules and gases [22][23][24][25][26][27][28][29].…”
Section: L-dopa [(S)-2-amino-3-(34-dihydroxyphenyl)mentioning
confidence: 99%
“…It was not until the work performed by Trotta and co-workers [13] and the syntheses of new kinds of cyclodextrin nanosponges that they revealed their full potential in other fields, particularly as drug carriers.…”
Section: Reviewmentioning
confidence: 99%
“…FTIR and NMR analyses before and after sterilisation show their stability and the absence of degradation [13]. In addition, they do not act as surfactants and can be easily dispersed in water.…”
Section: Reviewmentioning
confidence: 99%
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“…These materials are constituted by hyper-reticulated polymers obtained joining supramolecular host units, as the monomers, by means of a suitable reticulating agent. Up to date, the examples by far most studied are constituted by cyclodextrin-based nanosponges ( Cy NSs) [45], which can be synthesized by reacting native β-cyclodextrin with double electrophiles such as epichlorohydrin [6], organic carbonates [79] or bis-isocyanates [10], in variable ratios depending on the required degree of reticulation. The process, of course, exploits the nucleophilic reactivity of the hydroxy groups of the macrocycle oligosaccharide unit.…”
Section: Introductionmentioning
confidence: 99%