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The present study reports the preparation and evaluation of a water soluble octenyl succinylated cassava starch‐curcumin nanoformulation with enhanced bioavailability and anticancer potential. The major drawback of curcumin as a bioactive compound is its poor aqueous solubility and the resultant low bioavailability. In this study, curcumin has been incorporated in octenyl succinate cassava starch by a wet grinding method and the product is characterized by Fourier transform infra red spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), atomic force microscopy (AFM), and X‐ray diffraction (XRD) analyses. The OSA starch loaded nanocurcumin is found to be non‐toxic to L929 cells, but shows anti‐cancer potential to HeLa cells. A significant enhancement in cellular uptake also can be achieved for the OSA starch loaded nanocurcumin as revealed by fluorescence microscopy. The in vitro release of curcumin from the nanostarch matrix is more controlled at simulated intestinal pH than that at gastric pH. Pharmacokinetic study shows that bioavailability of nanocurcumin is increased by about 71.27%. [ABSTRACT FROM AUTHOR]

Curcumin, a natural yellow pigment with a wide spectrum of bioactivities, was incorporated in nanocomposite films of cassava starch with poly(vinyl alcohol) (PVA) for achieving sustained release properties which improves its potential for use in cancer treatment. The ultra structure of the films was studied by scanning electron microscopy (SEM) and the formation of nanoparticles was confirmed by transmission electron microscopic (TEM) analysis. The curcumin incorporation in the films was confirmed by Fourier transform infra red spectroscopy (FTIR). The swelling capacity and erosion of the films were also recorded. It was observed that pH of the medium and storage conditions greatly affected the release of curcumin from the polymer matrices. The release behaviour of curcumin from starch-PVA matrices was studied and the kinetics behind the curcumin release was fitted to Higuchi model. The mechanism obtained from Korsemeyer-Peppas equation was a combination of diffusion and erosion controlled. Cytotoxicity study of the incorporated curcumin was carried out with normal as well as cancer cells and the results showed that it was non-toxic to normal cells and it also showed anticancer potential. The cell viability (%) in the case of cancer cells was lower for nanocomposite incorporated curcumin than pure curcumin which indicates higher anti cancer potential of the former. The size of curcumin was reduced in the nanocomposites as evidenced from TEM and SEM analysis results, which might have resulted in its greater cell availability and resultant higher anticancer activity. [ABSTRACT FROM AUTHOR]