Intracellular Criegee's mechanism-based synergistic ozone therapy mediated by oleogels for cancer treatment

机制(生物学) 细胞内 化学 药理学 癌症研究 医学 生物化学 哲学 认识论
作者
Jingsong Lu,Rong Zheng,Ziao Shi,Xiaohan Gao,Ying Li,Abdul Fahad,Neema Ufurahi-Pambe,Zeping Jin,Sumei Chen,Wensheng Xie,Zhenhu Guo,Jing Yu,Shenglei Che,Guifeng Zhang,Benhua Xu,Yen Wei,Lingyun Zhao
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:370: 879-890 被引量:6
标识
DOI:10.1016/j.jconrel.2024.05.039
摘要

Broad cellular components-initiated efficient chemical reactions that occur in malignant cells may contribute to exploring emerging strategies for cancer treatment. Herein, an ozonated oleogel (OG(O)) was developed to achieve cancer ozone therapy (O3-T) based on intracellular Criegee's reaction. By integrating the chemo-drug, the ozone-loaded oleogel (Dox@OG(O)) was prepared as a chemotherapeutic agent for local O3-T, associated with chemotherapy (CT)/radiotherapy (RT)/immunotherapy and wound healing. The in vitro results showed that, Dox@OG(O) could achieve high ozone loading efficiency and ensure its stability. This Oleogel-mediated O3-T could directly destroy tumor cells via intracellular Criegee's reaction occurred on cell membranes, as well as the effects of tumor microenvironment (TME) regulation by the generation of oxygen/reactive oxygen species (ROS) and depletion of glutathione (GSH). Meanwhile, under the stimulation of X-ray, an accelerated free radical's production was observed, further combined with the radio-sensitivity after TME regulation, an effective anti-tumor effect would be achieved. Further on, in vivo results demonstrated that the locally implanted Dox@OG(O) could effectively inhibit the growth of both primary and secondary tumors. Considering these results above, it will serve as inspiration for future studies investigating of O3-T, especially for postoperative skin diseases.

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