The aim of the work is to improve the release properties of curcumin onto human breast cancer cell lines using coated halloysite nanotubes (HNTs) with chitosan as a polycation. A loading efficiency of 70.2% (w/w) was attained for loading 4.9 mg of the drug into 0.204 g bed volume of HNTs using the vacuum suction method. Results acquired from Brunauer-Emmett-Teller (BET), Fourier-transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron spectroscopy (SEM), zeta potential, and thermogravimetric analysis (TGA) indicated the presence of the drug and the biopolymer in and around the nanotubes. The release properties of drug-loaded HNTs (DLHNTs) and chitosan-coated drug-loaded HNTs (DLHNTs-CH) were evaluated. The release percentages of DLHNTs and DLHNTs-CH after 6 h were 50.7 and 37%, respectively. Based on the correlation coefficients obtained by fitting the release nature of curcumin from the two samples, the Korsmeyer-Peppas model was found to be the best-fitted model. In vitro cell viability studies were carried out on the human breast cancer cell line MCF-7, using the MTT and trypan blue exclusion assays. Prior to the Trypan blue assay, the IC50 of curcumin was determined to be ~30 µM. After 24 h of incubation, the recorded cell viability values were 94, 68, 57, and 51% for HNTs, DLHNTs-CH, DLHNTs, and curcumin, respectively. In comparison to the release studies, it could be deducted that sustained lethal doses of curcumin were released from the DLHNTs-CH within the same time. It is concluded from this work that the “burst release” of naked drugs could be slowly administered using chitosan-coated HNTs as potential drug carriers.

In this study, a clay sample recovered from an archaeological excavation from the Krobo Mountains in Ghana was examined for its potential to decolorize and adsorb cationic methylene blue. The raw and calcined clay samples were characterized with XRD, SEM, FTIR and EDX. The supernatant obtained by washing the raw clay with 70% ethanol solution decolorized methylene blue. The decolorization of methylene blue was independent of calcination temperature up to 300°C. The clay material subjected to calcination temperature at 600°C showed strong adsorption towards cationic methylene blue. The equilibrium adsorption data fitted well with the Freundlich isotherm indicating adsorption unto heterogeneous surface with the interaction between the adsorbed molecules which is not restricted to the formation of a monolayer. The data also fitted well with the Weber and Morris model which described the rate-controlling steps. The intra-particle diffusion was controlled by pore and surface diffusion. In addition, the adsorption data followed a pseudo-second-order kinetic model, indicating a chemisorption process. The results highlight a unique property of the clay material as an effective decolorizing and adsorption agent for the removal of water-soluble dyes from contaminated water bodies.