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- W4205609375 abstract "β-1,4-Glucosidic bonds link six to eight glucose units to construct the oligosaccharides cyclodextrins (CDs). These cyclic compounds are soluble in water with variable solubility because of their external hydrophilic surface and the hydroxyl groups on the two rims of the truncated buckets. The interior of these molecular toroids is relatively much hydrophobic that infest them with the ability to encapsulate hydrophobic drugs. The hydroxyl groups at the rims of the CDs can form intermolecular hydrogen bonds in solution to produce CD nanotubes. This process is reinforced by the molecular guests sheltered inside the CD cavities. The nanotube formation through intermolecular hydrogen bonding can be exploited to construct CD suprastructures based on the structural nature of the guest compound or nanomaterials. The side chains of the guest molecules and the functionalities on the nanoparticle surfaces can be used to form the CD suprastructures that modulate the fluorescence properties of the fluorophoric guests." @default.
- W4205609375 created "2022-01-25" @default.
- W4205609375 creator A5078986739 @default.
- W4205609375 date "2022-01-01" @default.
- W4205609375 modified "2023-10-16" @default.
- W4205609375 title "Modulation of fluorescence of fluorophores by cyclodextrins forming supported suprastructures to nanoparticles" @default.
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- W4205609375 doi "https://doi.org/10.1016/b978-0-12-822351-2.00005-x" @default.
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