“…Another strategy to enhance the solubility and long-term stability of curcumin is to conjugate the reactive phenol groups to the side chains of polyethylene glycol, , hyaluronic acid, − sodium alginate, or xylan . The diketone group in curcumin can also be functionalized by interacting with polymers bearing boronic acids , or complexation with metal ions. , Because the carrier polymers in drug-polymer conjugates are usually pharmaceutically inactive and only serve as a scaffold, drug loading is limited. , Higher drug loading can be achieved by directly incorporating curcumin into the polymer’s chemical structure, where such poly(pro-drugs) act both as the carrier matrix material and a depot of the drug itself . Curcumin-containing polyacetals, , polyoxalates, polycarbonates, , polyurethane, and polyesters , have been reported, and the release of curcumin from these materials were either rapid (<30 h) or sustained (2–80 days), ,,, depending on the stability of the linker chemistry used to enchain the drug molecules.…”