2011
DOI: 10.1002/anie.201006193
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Photoregulated Release of Noncovalent Guests from Dendritic Amphiphilic Nanocontainers

Abstract: Supramolecular disassembly: Phototriggered release of noncovalently sequestered lipophilic guest molecules from dendritic supramolecular assemblies has been demonstrated. Facially amphiphilic dendrimers have been shown to provide a unique opportunity to fine‐tune the release kinetics of the guest molecules in response to light (see picture).

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Cited by 102 publications
(84 citation statements)
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“…Then we will discuss how the introduction of specific functional groups on these dendrimers renders them responsive to stimuli such as temperature, 32,33 light, 34 pH, 35 or biological stimuli such as proteins 36 and enzymes. 37 …”
Section: Introductionmentioning
confidence: 99%
“…Then we will discuss how the introduction of specific functional groups on these dendrimers renders them responsive to stimuli such as temperature, 32,33 light, 34 pH, 35 or biological stimuli such as proteins 36 and enzymes. 37 …”
Section: Introductionmentioning
confidence: 99%
“…Thayumanavan et al synthesized light-sensitive facially amphiphilic dendrimers, which could form selfassembled aggregates in water, using a photolabile 2-nitrobenzylesters as the liphophilic units and oligoethylene glycol as the hydrophilic units. Further, they demonstrated light-induced disassembly of the dendrimers using Nile red as the liphophilic guest molecule (Yesilyurt et al 2011). Although a number of lightresponsive carrier systems using O-nitrobenzyl group have been developed, most of them are activated by UV light that may cause skin damage.…”
Section: Light-responsive Nanoparticles Using Irreversible Photo-cleamentioning
confidence: 99%
“…Hydrophilic block copolymers that contain coumarin, which dimerizes when exposed to UV light, have been used to form micelles, which were then photochemically cross-linked 51 . Light-sensitive chemistry has also been used to formulate dendrimer nanocarriers that, with light exposure, release encapsulated drug 52 . These techniques are exportable to nanogel formulations, and are especially valuable since the cross-linking activity can be incorporated in such a way that it can be used to exert control over drug release by suppressing enzymatic degradation of substrate with light stimulation at one wavelength or by enhancing enzymatic degradation of substrate as a result of increased decrosslinking with light exposure at another wavelength 53 .…”
Section: Stimulus Responsive Nanogelsmentioning
confidence: 99%