Near-infrared light-triggered nano-prodrug for cancer gas therapy.
Runcong LiuYongjun PengLigong LuShaojun PengTianfeng ChenMeixiao ZhanPublished in: Journal of nanobiotechnology (2021)
Gas therapy (GT) has attracted increasing attention in recent years as a new cancer treatment method with favorable therapeutic efficacy and reduced side effects. Several gas molecules, such as nitric oxide (NO), carbon monoxide (CO), hydrogen (H 2 ), hydrogen sulfide (H 2 S) and sulfur dioxide (SO 2 ), have been employed to treat cancers by directly killing tumor cells, enhancing drug accumulation in tumors or sensitizing tumor cells to chemotherapy, photodynamic therapy or radiotherapy. Despite the great progress of gas therapy, most gas molecules are prone to nonspecific distribution when administered systemically, resulting in strong toxicity to normal tissues. Therefore, how to deliver and release gas molecules to targeted tissues on demand is the main issue to be considered before clinical applications of gas therapy. As a specific and noninvasive stimulus with deep penetration, near-infrared (NIR) light has been widely used to trigger the cleavage and release of gas from nano-prodrugs via photothermal or photodynamic effects, achieving the on-demand release of gas molecules with high controllability. In this review, we will summarize the recent progress in cancer gas therapy triggered by NIR light. Furthermore, the prospects and challenges in this field are presented, with the hope for ongoing development.
Keyphrases
- room temperature
- photodynamic therapy
- nitric oxide
- carbon dioxide
- cancer therapy
- gene expression
- radiation therapy
- stem cells
- emergency department
- drug delivery
- early stage
- squamous cell carcinoma
- mesenchymal stem cells
- oxidative stress
- young adults
- fluorescence imaging
- working memory
- cell therapy
- squamous cell
- replacement therapy