2018
DOI: 10.1007/978-3-319-76090-2_9
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Cyclodextrin Nanosponges in Drug Delivery and Nanotherapeutics

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Cited by 17 publications
(16 citation statements)
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“…Cyclodextrins (hereinafter referred to as CDs) are cyclic oligosaccharides composed of α- d -glucopyranose units combined with α-(1→4)-glycosidic bonds. Native CDs are a product of the enzymatic degradation of starch, in which cyclodextrin glycosyltransferases produce cyclic oligomers consisting of six (α-CD), seven (β-CD, Figure 2 a), or eight (γ-CD) glucose units [ 21 , 22 , 23 , 24 ]. Due to restricted rotation of glycosidic bonds and the chair conformation of each glucose unit, CDs possess the specific shape of a truncated cone with a hollow cavity ( Figure 2 b) [ 23 , 24 , 25 , 26 , 27 ].…”
Section: Cyclodextrin-based Drug Delivery Systems—a Short Summarymentioning
confidence: 99%
See 1 more Smart Citation
“…Cyclodextrins (hereinafter referred to as CDs) are cyclic oligosaccharides composed of α- d -glucopyranose units combined with α-(1→4)-glycosidic bonds. Native CDs are a product of the enzymatic degradation of starch, in which cyclodextrin glycosyltransferases produce cyclic oligomers consisting of six (α-CD), seven (β-CD, Figure 2 a), or eight (γ-CD) glucose units [ 21 , 22 , 23 , 24 ]. Due to restricted rotation of glycosidic bonds and the chair conformation of each glucose unit, CDs possess the specific shape of a truncated cone with a hollow cavity ( Figure 2 b) [ 23 , 24 , 25 , 26 , 27 ].…”
Section: Cyclodextrin-based Drug Delivery Systems—a Short Summarymentioning
confidence: 99%
“…On the other hand, the hydrophilic outer surface is responsible for increasing drug solubility through interactions with aqueous media via hydroxyl groups. Thus, CDs are great candidates for drug transport systems [ 21 , 23 , 24 , 25 , 26 , 30 , 31 , 35 ].…”
Section: Cyclodextrin-based Drug Delivery Systems—a Short Summarymentioning
confidence: 99%
“…To be properly entrapped within nanocavities, drug molecules are required to comply with specific properties such as simple to trap molecules, molecular mass between 100 and 400 Da, and fewer than five condensed rings. Additionally, the molecules should possess a melting point of around or less than 250 °C with solubility in water of not more than 10 mg/mL (Osmani et al, 2018a). Higher melting points of pharmaceuticals make it difficult to develop stable complexes between medicines and niacin due to the need to maintain higher stability constant values after loading in the NS.…”
Section: Type Of Drugs and Medium Used For Crosslinkingmentioning
confidence: 99%
“…This inner phase is added to PVA solution and stirred. The product is filtered out and dried [59]. Salunke et al [60] prepared budesonide-loaded nanosponges by quasi-emulsion solvent diffusion method.…”
Section: Quasi-emulsion Solvent Diffusionmentioning
confidence: 99%