Synergistic Gas Therapy and Targeted Interventional Ablation With Size‐Controllable Arsenic Sulfide (As 2 S 3 ) Nanoparticles for Effective Elimination of Localized Cancer Pain

作者：Yu Tang, Jiyun Zhang, Yuan Yuan, Kele Shen, Zhiyuan Luo, Luyu Jia, Xiaofeng Long, Peng Chi, Tian Xie, Xiaoyuan Chen, Pengfei Zhang · 发表于：Small · 年份：2024 · DOI：10.1002/smll.202407197 · 被引用次数：10 · 研究领域：Sulfur Compounds in Biology、Nanoplatforms for cancer theranostics、Bone health and treatments

Abstract The elimination of localized cancer pain remains a globally neglected challenge. A potential solution lies in combining gas therapy with targeted interventional ablation therapy. In this study, HA‐As 2 S 3 nanoparticles with controlled sizes are synthesized using different molecular weights of sodium hyaluronate (HA) as a supramolecular scaffold. Initially, HA co‐assembles with arsenic ions (As 3+ ) via coordinate bonds, forming HA‐As 3+ scaffold intermediates. These intermediates, varying in size, then react with sulfur ions to produce size‐controlled HA‐As 2 S 3 particles. This approach demonstrates that different molecular weights of HA enable precise control over the particle size of arsenic sulfide, offering a straightforward and environmentally friendly method for synthesizing metal sulfide particles. In an acidic environment, HA‐As 2 S 3 nanoparticles release hydrogen sulfide(H 2 S) gas and As 3+ . The released As 3+ directly damage tumor mitochondria, leading to substantial reactive oxygen species (ROS) production from mitochondria. Concurrently, the H 2 S gas inhibits the activity of catalase (CAT) and complex IV, preventing the beneficial decomposition of ROS and disrupting electron transfer in the mitochondrial respiratory chain. Consequently, it is found that H 2 S gas significantly enhances the mitochondrial damage induced by arsenic nanodrugs, effectively killing local tumors and ultimately eliminating cancer pain in mice.