Compares antioxidant activity and solubility of curcumin solid dispersions, suggesting enhanced safety and effectiveness.
Objective To compare three different curcumin-loaded solid dispersions, assess their solubility, and conduct antioxidant and biological safety assays. Methods Three different curcumin-loaded solid dispersions were prepared using the solvent, solvent melting, and melting methods, and characterized using a scanning electron microscope, differential scanning calorimeter, and X-ray diffractometer. Additionally, the drug content, equilibrium solubility, dissolution, 1,1-diphenyl-2-picrylhydrazyl, 2,2ʹ-Azinobis-(3-ethylbenzthiazoline-6-sulphonate) scavenging ability, and biological safety were investigated. Results X-ray diffractometer and differential scanning calorimetry analyses confirmed that curcumin existed in an amorphous state in the solid dispersion, while Fourier-transform infrared spectroscopy suggested intermolecular interactions between curcumin and polyvinylpyrrolidone K29/32, and scanning electron microscope showed the disappearance of crystalline morphology and formation of a homogeneous matrix. The optimized solid dispersion significantly improved the aqueous solubility of curcumin. Rapid drug release was observed, with more than 70% of curcumin released within 20 min, whereas free curcumin exhibited very limited dissolution. The solubility of the solid dispersion was potential of hydrogen-dependent, with higher solubility under weakly acidic to near-neutral conditions and a marked decrease under alkaline conditions. In antioxidant assays, the solid dispersion exhibited stronger free radical scavenging activity than curcumin alone in a concentration-dependent manner. In addition, the solid dispersion showed reduced cytotoxicity, with improved cell viability compared with free curcumin at higher concentrations. Conclusion Solid dispersions supported by polyvinylpyrrolidone K29/32 showed significantly increased solubility of curcumin, and had higher antioxidant activity and biological safety than those of curcumin alone.
No takes yet. Share an insight, caveat, or question.
Tan et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: