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Sulfur Vacancy-Rich Bi2S3-x-Pt Heterojunction with Multi-enzymatic Activities for Enhanced Sonodynamic Therapy
Wanying Sun1, Xiaoxiao Yan1, Yingshu Li1
1Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Guangxi Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, P. R. China.
Abstract:
Although bismuth sulfide (Bi2S3) possesses a narrow bandgap, advantageous for sonodynamic therapy (SDT), a substantial portion of ultrasound (US)-excited electrons is lost due to rapid electron-hole pair recombination, hindering their surface participation in redox reactions. In this study, a sulfur vacancy engineering strategy was implemented to yield Bi2S3-x with in situ-generated abundant sulfur vacancies, which significantly enhanced electron-hole pair separation for reactive oxygen species (ROS) production under US irradiation. Subsequently, platinum (Pt) nanoparticles were in situ grown on the Bi2S3-x surface, forming a Bi2S3-x-Pt Schottky heterojunction and optimizing catalytic activity. These Pt nanoparticles functioned as electron traps, inducing upward energy band bending and establishing a Schottky barrier, thereby bolstering electron-hole pair separation under US stimulation. Furthermore, the catalase (CAT)- and peroxidase (POD)-like activities of the Pt nanoparticles mitigated tumor hypoxia to augment SDT-induced singlet oxygen generation and triggered oxidative stress, respectively. Sono-excited holes were capable of depleting excessive intratumoral glutathione (GSH) and decomposing hydrogen peroxide into O2, thus alleviating tumor hypoxia and consequently remodeling the tumor microenvironment. To further enhance tumor targeting and dispersity, Bi2S3-x-Pt was modified with hyaluronic acid (HA), which specifically binds to CD44 receptors overexpressed on tumor cells. Bi2S3-x-Pt@HA, exhibiting these combined functionalities, significantly suppressed tumor proliferation. This study outlines a methodology for enhancing the ROS generation efficiency of inorganic sonosensitizers characterized by narrow bandgaps.
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