2020
DOI: 10.1007/s10847-020-01029-3
|View full text |Cite
|
Sign up to set email alerts
|

Pharmaceutical applications of cyclodextrins and their derivatives

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
25
0
1

Year Published

2021
2021
2024
2024

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 50 publications
(26 citation statements)
references
References 150 publications
0
25
0
1
Order By: Relevance
“…As excipients, the most relevant use of CDs is as a complexing agent to improve drug solubility and bioavailability; the CD complexation can also be exploited to ameliorate the stability of drugs, in terms of reduction of the evaporation of volatile substances or protection of drugs from light and/or oxygen-induced degradation, as well as to cover bad flavors or scents or transform liquid substances into powders and, in general, to prevent incompatibility reactions between substances in the formulation [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…As excipients, the most relevant use of CDs is as a complexing agent to improve drug solubility and bioavailability; the CD complexation can also be exploited to ameliorate the stability of drugs, in terms of reduction of the evaporation of volatile substances or protection of drugs from light and/or oxygen-induced degradation, as well as to cover bad flavors or scents or transform liquid substances into powders and, in general, to prevent incompatibility reactions between substances in the formulation [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…CDs can be divided into two main classes: natural CDs, namely α, β and γ-CD ( Figure 2 ), and semisynthetic CDs obtained through the derivatization of the hydroxyl residues using various groups. Depending on the groups grafted to the CDs surface, the obtained derivatives possess several advantages such as increased inclusion capacity for certain compounds, superior water solubility (HP-β-CD) or lipophilicity (Methyl-β-CD) [ 62 ].…”
Section: Cyclodextrins—classification and Physicochemical Propertiesmentioning
confidence: 99%
“…The hydrophobic central cavity of a CD molecule can encapsulate various lipophilic molecules by inclusion complex formation. Besides various low molecular-weight drugs that are the most common guests [30,31], inclusion complexation can also occur with different lipids, including free fatty acids, their mono-, di-, and triglycerides, and phospholipids [29,[32][33][34]. Such interactions are dependent on the structure Fig.…”
Section: Interaction Of Cyclodextrins With Lipidsmentioning
confidence: 99%