Synergistic Amplification of Oxidative Stress-Mediated Antitumor Activity via Liposomal Dichloroacetic Acid and MOF-Fe2

Abstract

Cancer cells are susceptible to oxidative stress; therefore, selective elevation of intracellular reactive oxygen species (ROS) is considered as an effective antitumor treatment. Here, a liposomal formulation of dichloroacetic acid (DCA) and metal-organic framework (MOF)-Fe²⁺ (MD@Lip) has been developed, which can efficiently stimulate ROS-mediated cancer cell apoptosis in vitro and in vivo. MD@Lip can not only improve aqueous solubility of octahedral MOF-Fe²⁺ , but also generate an acidic microenvironment to activate a MOF-Fe²⁺ -based Fenton reaction. Importantly, MD@Lip promotes DCA-mediated mitochondrial aerobic oxidation to increase intracellular hydrogen peroxide (H₂ O₂ ), which can be consequently converted to highly cytotoxic hydroxyl radicals (•OH) via MOF-Fe²⁺ , leading to amplification of cancer cell apoptosis. Particularly, MD@Lip can selectively accumulate in tumors, and efficiently inhibit tumor growth with minimal systemic adverse effects. Therefore, liposome-based combination therapy of DCA and MOF-Fe²⁺ provides a promising oxidative stress-associated antitumor strategy for the management of malignant tumors.

Keywords: MOF-Fe2+; antitumor treatment; dichloroacetic acid; liposomes; oxidative stress.