| dc.description.abstract | Today, attempt to the preparation of stable drug with high drug delivery efficiency is inevitable. Curcumin (diferuloylmethane), with hydrophobic structure obtained from the herb of Curcuma longa, have various applications in cancer therapy. But, its low water solubility and bioavailability is possible for poor drug delivery of curcumin. In this study, we prepared beta-cyclodextrin-curcumin complex to determine the inhibitory effect of this drug on telomerase gene expression. Curcumin was encapsulated into cyclodextrin and the rate of curcumin loading was estimated. Cytotoxic effects of beta-cyclodextrin curcumin were investigated by colorimetric cell viability (MTT) assay. Then inhibition of telomerase gene expression was determined by real-time polymerase chain reaction (PCR). MTT assay demonstrated that beta-cyclodextrin have no cytotoxic effect on its own. Also, it showed dose-dependency and time-dependency for beta-cyclodextrin -curcumin on T47D cell line. Expression of telomerase gene in cells effectively was reduced as the concentration of beta-cyclodextrin -curcumin complex was increased. The results show that beta-cyclodextrin -curcumin complex have cytotoxic effect on T47D cell line through down regulation of telomerase expression and induction apoptosis by enhancing curcumin uptake by cells. So, beta-cyclodextrin could be good carrier for these kinds of hydrophobic agents. | |
