2024
DOI: 10.3390/antiox13030331
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Enhancing the Bioavailability and Bioactivity of Curcumin for Disease Prevention and Treatment

Caroline Bertoncini-Silva,
Adelina Vlad,
Roberta Ricciarelli
et al.

Abstract: Curcumin, a natural polyphenolic component from Curcuma longa roots, is the main bioactive component of turmeric spice and has gained increasing interest due to its proposed anti-cancer, anti-obesity, anti-inflammatory, antioxidant, and lipid-lowering effects, in addition to its thermogenic capacity. While intake from dietary sources such as curry may be sufficient to affect the intestinal microbiome and thus may act indirectly, intact curcumin in the body may be too low (<1 microM) and not sufficient to af… Show more

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Cited by 6 publications
(1 citation statement)
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“…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%