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Exploring highly efficient ultrasound-triggered catalysts is pivotal for various areas. Herein, we presented that Ba doped brookite TiO nanorod (TiO: Ba) with polarization-induced charge separation is a candidate. The replacement of Ba for Ti not only induced significant lattice distortion to induce polarization but also created oxygen vacancy defects for facilitating the charge separation, leading to high-efficiency reactive oxygen species (ROS) evolution in the piezo-catalytic processes. Furthermore, the piezocatalytic ability to degrade dye wastewater demonstrates a rate constant of 0.172 min and achieves a 100 % antibacterial rate at a low dose for eliminating E. coli. This study advances that doping can induce piezoelectricity and reveals that lattice distortion-induced polarization and vacancy defects engineering can improve ROS production, which might impact applications such as water disinfection and sonodynamic therapy.
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http://dx.doi.org/10.1016/j.jcis.2024.05.148 | DOI Listing |
ACS Nano
September 2025
Departments of Ultrasound Medicine Beijing Chaoyang Hospital, Capital Medical University, North Road 8, Gongti, Chaoyang, Beijing 100020, China.
Although immune checkpoint inhibitor-based immunotherapy has shown clinical efficacy in various cancer types, its efficacy in pancreatic cancer remains limited. This limitation is primarily attributed to the dense stromal tumor microenvironment (TME) and highly immunosuppressive TME of pancreatic cancer. The dense stromal TME forms a physical barrier that severely hinders the penetration and accumulation of therapeutic agents and immune cells.
View Article and Find Full Text PDFMacromol Biosci
August 2025
Tianjin Key Laboratory for Modern Drug Delivery & High Efficiency, School of Pharmaceutical Science & Technology, Faculty of Medicine, Tianjin University, Tianjin, 300072, China.
Ultrasound-responsive drug delivery systems have emerged as a promising approach in cancer therapy, offering enhanced targeting precision, controlled drug release, and reduced systemic toxicity. These systems utilize the mechanical and thermal effects of ultrasound to enable the spatiotemporally triggered release of therapeutic payloads in tumor sites. This review provides an overview of the key mechanisms underlying ultrasound-responsive drug delivery, including the activation of sonosensitizers and prodrugs, as well as the role of ultrasound-responsive nanocarriers such as liposomes, micelles, nanobubbles, and metal-organic frameworks.
View Article and Find Full Text PDFEffective treatment of chronic pain remains hindered by the lack of drug delivery systems that simultaneously achieve long-term stability, high spatial precision, and non-invasiveness . Here, we utilize a programmable, ultrasound-responsive drug delivery platform based on hydrogen-bonded organic framework (HOF) nanoparticles, enabling on-demand anesthetic release with long-term and durable analgesic efficacy. A machine learning (ML)-guided screening pipeline was developed to evaluate about 250 FDA-approved drugs, spanning both hydrophilic and lipophilic agents, and identified bupivacaine (lipophilic) and lidocaine hydrochloride (hydrophilic) as optimal candidates.
View Article and Find Full Text PDFUltrasonics
December 2025
The BioRobotics Institute, Scuola Superiore Sant'Anna, Piazza Martiri della Libertà 33, 56127 Pisa, Italy; Department of Excellence in Robotics & AI, Scuola Superiore Sant'Anna, Piazza Martiri della Libertà 33, 56127 Pisa, Italy.
Perfluorocarbon droplets represent a promising platform for ultrasound-triggered drug delivery. Their liquid core can vaporize upon the application of a pressure wave such as ultrasound, resulting in the controlled and targeted release of their drug cargo. These carriers are highly tunable, exhibit a sharp on-off behavior and have longer lifetimes compared to ultrasound-responsive microbubbles.
View Article and Find Full Text PDFJ Nanobiotechnology
July 2025
Department of General Surgery, Academician (Expert) Workstation, Sichuan Digestive System Disease Clinical Medical Research Center, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, People's Republic of China.
Sonodynamic therapy (SDT) exhibits clinical potential for deep-tissue tumor treatment due to its deep tissue penetration and spatiotemporal controllability. Its core mechanism relies on ultrasound-activated sonosensitizers to generate reactive oxygen species (ROS), thereby inducing tumor cell apoptosis. However, conventional sonosensitizers face limitations in ROS yield and tumor-targeting efficiency.
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