2024
DOI: 10.3390/nano14080672
|View full text |Cite
|
Sign up to set email alerts
|

Advances in Nanocarrier Systems for Overcoming Formulation Challenges of Curcumin: Current Insights

Shery Jacob,
Fathima Kather,
Mohamed Morsy
et al.

Abstract: Curcumin, an organic phenolic molecule that is extracted from the rhizomes of Curcuma longa Linn, has undergone extensive evaluation for its diverse biological activities in both animals and humans. Despite its favorable characteristics, curcumin encounters various formulation challenges and stability issues that can be effectively addressed through the application of nanotechnology. Nano-based techniques specifically focused on enhancing solubility, bioavailability, and therapeutic efficacy while mitigating t… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 194 publications
0
0
0
Order By: Relevance
“…However, curcumin has limited bioavailability and is metabolized in the liver by aldo–keto reductase, in addition to having low water solubility (0.4 μg/mL at normal gastric pH 1.5–4.0) and limited BBB permeability. To solve these problems, various systems have been developed, including nanocarrier preparations for curcumin delivery, such as liposomes, micelles, solid lipid nanoparticles (SLNs), liquid crystalline nanoparticles (LCNs), polymeric nanoparticles, cell membrane nanocarriers, and cyclodestrin [ 27 , 28 , 29 ]. To determine the pharmacokinetics and pharmacodynamics of curcumin, Ravindranath and Chandrasekhara (1981, 1982) [ 30 , 31 ] administered 3 H-curcumin to rats, showing that curcumin undergoes several metabolic biochemical transformations.…”
Section: Curcumin: Bioavailability and Metabolismmentioning
confidence: 99%
“…However, curcumin has limited bioavailability and is metabolized in the liver by aldo–keto reductase, in addition to having low water solubility (0.4 μg/mL at normal gastric pH 1.5–4.0) and limited BBB permeability. To solve these problems, various systems have been developed, including nanocarrier preparations for curcumin delivery, such as liposomes, micelles, solid lipid nanoparticles (SLNs), liquid crystalline nanoparticles (LCNs), polymeric nanoparticles, cell membrane nanocarriers, and cyclodestrin [ 27 , 28 , 29 ]. To determine the pharmacokinetics and pharmacodynamics of curcumin, Ravindranath and Chandrasekhara (1981, 1982) [ 30 , 31 ] administered 3 H-curcumin to rats, showing that curcumin undergoes several metabolic biochemical transformations.…”
Section: Curcumin: Bioavailability and Metabolismmentioning
confidence: 99%