Common systemic chemotherapy often leads to adverse effects on healthy cells. Localized chemotherapy can reduce the adverse effects while providing a sustained release of chemotherapeutics at the target tumor. Therefore, injectable biodegradable hydrogels as targeted drug delivery systems for chemotherapeutics have shown great potential for treating cancer. This project aims to develop a series of smart injectable gels for localized drug delivery using soy protein isolate (SPI) and oxidized carboxymethyl cellulose (OCMC) loaded with doxorubicin
(DOX) as a model anticancer drug. Dynamic (reversible) imine (Schiff base) bonds, which are pressure and pH sensitive, will be formed between the three components and thus lead to the production of gels. The gels will be injectable because the imine bonds break under injection pressure and thus the gels become fluid-like; the gel state will be restored (i.e., self-healing) in the human body immediately after the injection, securing the anticancer drug inside the gels. The drug is released from the gels in a sustained manner only in a cancerous environment (pH = ~6) while the release is minimal within healthy tissues (pH = ~7.4). The formulation and processing parameters of the gels will be varied, and the drug-release properties of the produced gels will be investigated. Optimum formulations/parameters that are suitable for commercialization will be determined.