2021
DOI: 10.1007/s11356-021-16871-2
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Cyclodextrin applications in pharmacy, biology, medicine, and environment

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Cited by 9 publications
(2 citation statements)
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“…The driving force behind the formation of complexes involving CDs primarily comes from hydrophobic forces and van der Waals interactions between guest molecules and the hydrophobic cavity within CDs. The dimensions of these molecular cavities are approximately 0.53, 0.65, and 0.83 nm in diameter for α-, β-, and γCDs, respectively 22 The size of molecules that can be accommodated within a particular CD is closely related to the size of the cavity. For instance, αCDs can host alkyl chains of various lengths, while larger molecules like benzene are typically too bulky.…”
Section: ■ Introductionmentioning
confidence: 99%
“…The driving force behind the formation of complexes involving CDs primarily comes from hydrophobic forces and van der Waals interactions between guest molecules and the hydrophobic cavity within CDs. The dimensions of these molecular cavities are approximately 0.53, 0.65, and 0.83 nm in diameter for α-, β-, and γCDs, respectively 22 The size of molecules that can be accommodated within a particular CD is closely related to the size of the cavity. For instance, αCDs can host alkyl chains of various lengths, while larger molecules like benzene are typically too bulky.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Cyclodextrin (CD) has received focus in research due to its potential application as a drug delivery agent and bioactive compound capsule [1,2]. It is commonly synthesized from starch, catalyzed by the CD glucanotransferase enzyme (CGTase).…”
Section: Introductionmentioning
confidence: 99%