Manju and Sreenivasan103 demonstrated the fabrication of water soluble CUR conjugated gold NPs to try various cancer cell lines. CUR conjugated to hyaluronic prickly (HA) to profit a water soluble conjugate (HA-CUR) Gold nanoparticles (AuNPs) were prepared by reducing chloroauric acid using HA-CUR, which played the dual role of a reducing and stabilizing agent and later anchored folate conjugated PEG. Their relationships following cancer cell lines, such as HeLa cells, glyoma cells and Caco2 was followed by flow cytometry and confocal microscopy and the results showed significant cellular uptake and internalization of the particles by cells. HA-CUR@AuNPs exhibited more cytotoxicity comparing to doable CUR back enhanced targeting and better efficacy. Starch based microspheres modified by grafting vinyl groups from glycidyl methacrylate (GMA) were prepared by emulsion method to be applied as a device for controlled reprieve of CUR. The microspheres showed to be a enormously promising devise for the controlled straightforward of CUR, especially for the treatment of colon cancer, which in general decreases the pH of the colon. At simulated gastric formless the fraction released of CUR was 100% and in a controlled freshen, due to the sustained diffusion of CUR to the media and moreover due to the degradation of the polymer matrix. The CUR-loaded microspheres presented much highly developed fight adjoining Caco-2 and HCT-116 tumor cell lines than forgive CUR.104 Hasan et al105 reported an pretension in of encapsulation a CUR by nanoliposome to agree an bigger bioavailability of a ill absorbed hydrophobic mix and with demonstrated that liposomal preparations to concentrate on CUR tallying its bioavailability. Liposomes composed of salmon’s lecithin improved curcumin bioavailability compared to the amalgamated type of fatty acids in swap proportions of rapeseed and soya lecithins. A definite-period label-easy to lead to cell analysis system based more or less definite-epoch cell impedance monitoring was used to study the in vitro cytotoxicity of liposomal preparations. Liposomal encapsulation of CUR can mass cellular effect of the drug. Polyelectrolyte undistinguished nanoparticles (PENPs) based on hyaluronic choking/chitosan (HA/CS) as carrier were successfullyprepared for water-insoluble curcuminoids and explored in vitro doing closely brain glioma cells. Encapsulation of CUR into the PENPs was achieved gone high encapsulation efficiency and drug loading talent. CUR-PENPs showed stronger dose dependent cytotoxicity also to C6 glioma cells and to the lead-thinking take effect in uptake efficiency in C6 cells. Cellular uptake of CUR-PENPs was found to be governed by multi-mechanism in C6 cells, involving swift endocytosis, macropinocytosis, clathrin, caveolae and CD44- mediated endocytosis. CUR-PENPs could be a promising carrier for therapy of brain gliomas.