Rational formulation engineering of fraxinellone utilizing 6-O-α-D-maltosyl-β-cyclodextrin for enhanced oral bioavailability and hepatic fibrosis therapy.
Animals
Animals, Outbred Strains
Benzofurans
/ administration & dosage
Caco-2 Cells
Cell Survival
/ drug effects
Chemistry, Pharmaceutical
Cyclodextrins
/ chemistry
Disease Models, Animal
Dose-Response Relationship, Drug
Drug Compounding
/ methods
Drug Liberation
Drug Stability
Humans
Liver Cirrhosis
/ drug therapy
Male
Maltose
/ analogs & derivatives
Mice
Rats
Rats, Wistar
Solubility
Fraxinellone
cyclodextrin derivatives
hepatic fibrosis
oral bioavailability
solubility
Journal
Drug delivery
ISSN: 1521-0464
Titre abrégé: Drug Deliv
Pays: England
ID NLM: 9417471
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
entrez:
14
9
2021
pubmed:
15
9
2021
medline:
15
1
2022
Statut:
ppublish
Résumé
Although Fraxinellone (Frax) isolated from
Identifiants
pubmed: 34519225
doi: 10.1080/10717544.2021.1976310
pmc: PMC8451604
doi:
Substances chimiques
Benzofurans
0
Cyclodextrins
0
maltosyl-cyclodextrin
0
fraxinellone
28808-62-0
Maltose
69-79-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1890-1902Références
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