Imaging Guided Endogenic H -Augmented Electrochemo-Sonodynamic Domino Co-therapy of Tumor in Vivo.

Adv Mater

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, China.

Published: March 2023

AI Article Synopsis

  • The research addresses the challenge of delivering hydrogen (H) directly to tumors for effective H-oncotherapy, highlighting its unknown effects on tumor microenvironments (TME).
  • A new treatment method called H-EC/SD co-therapy utilizes electrochemo-sonodynamic techniques to generate hydrogen at tumor sites, allowing rapid removal of tumors (up to 80 mm) within a day through combined mechanisms like vessel destruction and temperature elevation.
  • The treatment not only disrupts tumor cells' normal functions but also decreases the body's inflammatory response to cancer, potentially enhancing post-treatment immune recovery and offering a promising strategy for future clinical use.

Article Abstract

Precise and on-demand release of sufficient hydrogen (H ) to tumor sites remains a key challenge for emerging H -oncotherapy, and little is known about the physiological effects of "abundant" H on complex tumor microenvironments (TME). Here, a highly efficient and cost-effective imaging-guided/-assessed H -therapy of tumors based on a joint electrochemo-sonodynamic treatment (H -EC/SD co-therapy) with strong "domino effect" triggered by endogenous H generation at tumor sites is reported to speedily eliminate tumor tissue (≤80 mm ) within 1 day. Adequate H is controllably generated in tumor sites through mild electrochemistry in vivo due to acidic TME by using clinical acupuncture Fe needles as electrodes. Besides starvation damage due to gas blockage/destruction of vessels, nano-/micro-bubbles of H formed in situ can elevate the tumor's internal temperature and burst vessels to further destroy the tumor under ultrasound irradiation. Remarkably, vulnerable homeostasis of TME is disturbed as H also participates in the physiological activity of tumor cells, leading to tumor dysfunction. Last but not least, the body's inflammatory response to cancer is reduced after the treatment, which is beneficial for the body's immune system during post-treatment recovery. Based on all of these merits, the H -EC/SD co-therapy provides a potentially safe and viable therapeutic strategy for future clinical applications.

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Source
http://dx.doi.org/10.1002/adma.202208414DOI Listing

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