Developing Nanoceria‐Based pH‐Dependent Cancer‐Directed Drug Delivery System for Retinoblastoma. (12th November 2018) - Gao, Ruijuan
Abstract: Development of a single combinatorial nanoplatform technology to target cancer cells has been an unprecedented reality in boosting synergistic antitumor activities and in reducing off‐target effects. An antitumor delivery system is designed using a chemotherapy drug and a tumor target molecule covalently linked to cerium oxide nanoparticles (nanoceria). Nanoceria have a unique redox activity in that they possess antioxidant activity at physiological pH but have an intrinsic oxidase activity at acidic pH. The system is integrated with 1) extracellular pH responsive functionality, 2) tumor cell targetable (CXC chemokine receptor 4, CXCR4 receptor specific) antagonist, 3) reactive oxygen species (ROS) inducible nanoceria, and 4) chemotherapeutic doxorubicin (DOX). These combinatorial nanoparticles (AMD–GCCNPs–DOX) are not only sensitive to the extracellular acidic pH conditions and targeted tumor cells but can also instantaneously induce ROS and release DOX intracellularly to enhance the chemotherapeutic activity in retinoblastoma cells (WERI‐Rb‐1 and Y79) and in xenograft (Y79/GFP‐luc grafted) and genetic p107s (Rb Lox/lox, p107 +/−, p130 −/− ) orthotopic mice models. A lucidly engineered combinatorial nanoconstruct is introduced that offers a viable and simple strategy for delivering a cocktail of therapeutics into tumor cells under acidosis, exhibiting a promising new future for clinical therapeutic opportunities. Abstract : Exploiting the pH differential of the tumor microenvironment versus the pH of nonmalignant tissue is potentially useful for cancer treatment. This study focuses on the treatment of retinoblastoma using the nanoceria as a base‐component due to its antioxidant activity at physiological pH but intrinsic oxidase activity at acidic pH. The development of a pH‐responsive nanoplatform is shown that can effectively deliver a combination of therapeutics to target tumor cells.