AI Article Synopsis

  • Photothermal therapy (PTT) shows promise for tumor treatment but faces challenges like uneven heat distribution and potential harm to healthy tissue from reactive oxygen species (ROS).
  • This research introduces a nanoplatform that combines imaging and thermal therapy, allowing for real-time tumor monitoring and more effective treatment.
  • The innovative design not only enhances photothermal therapy but also protects surrounding healthy cells, suggesting a safer approach for future clinical applications.

Article Abstract

Photothermal therapy (PTT) is a promising approach for treating tumors that offers multiple advantages. Nevertheless, its practical use in clinical settings faces several limitations, such as suboptimal delivery efficiency, uneven heat distribution, and challenges in predicting optimal treatment duration. In addition, the localized hyperthermia generated by the PTT method to induce cell apoptosis can result in the production of excessive reactive oxygen species (ROS) and the release of inflammatory cytokines, which can pose a threat to the healthy tissues surrounding the tumor. To address the above challenges, this work designs an integrated H delivery nanoplatform for multimodal imaging H thermal therapy. The combination of the second near-infrared window (NIR-II) fluorescence imaging (FL) agent (CQ4T) and the photothermal and photoacoustic (PA) properties of TiC (TC) enables real-time monitoring of the tumor area and guides photothermal treatment. Simultaneously, due to the acid-responsive H release characteristics of the nanoplatform, H can be utilized for synergistic photothermal therapy to eradicate tumor cells effectively. Significantly, acting as an antioxidant and anti-inflammatory agent, TiC-BSA-CQ4T-H (TCBCH) protects peritumoral normal cells from damage. The proposed technique utilizing H gas for combination therapies and multimodal imaging integration exhibits prospects for effective and secure treatment of tumors in future clinical applications.

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http://dx.doi.org/10.1002/adhm.202401060DOI Listing

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