Mesoporous calcium peroxide-ignited NO generation for amplifying photothermal immunotherapy of breast cancer.

• LA-CaO 2 @PDA are synthesized to achieve pH-responsive NO release. • The generated NO can aggravate intracellular Ca2+ overload and oxidative stress. • LA-CaO 2 @PDA provokes strong immunogenic cell death and antitumor immune response. • Significant inhibition on primary and distant tumor growth has been demonstrated. L-arginine (LA) as a semiessential amino acid within human body has shown great promise in cancer therapy since it can continuously generate nitric oxide (NO) in the presence of inducible NO synthase (iNOS) or reactive oxygen species (ROS). However, NO production efficiency in tumor tissue is severely restricted by the hypoxic and H 2 O 2 -deficient tumor microenvironment (TME). Herein, mesoporous calcium peroxide (CaO 2) with the ability of supplying O 2 /H 2 O 2 has been prepared to encapsulate and oxidize LA to achieve controllable local release of NO in the acidic TME. Interestingly, the generated NO can aggravate the abnormal retention of Ca2+ in cells, thus resulting in amplified oxidative stress and immunogenic cell death. To improve the stability of CaO 2 in the body fluid, polydopamine (PDA) is further introduced to coat on the surface of LA-CaO 2 and its high photothermal conversion property will reinforce the immunogenic dying of tumor cells. Such a NO-enhanced phototherapeutic nanoplatform, LA-CaO 2 @PDA, exhibit the most effective treatment in inhibiting primary and distant tumor growth and suppressing lung metastasis of 4T1 tumor by provoking a strong antitumor immune response. [ABSTRACT FROM AUTHOR]