Fabrication of NIR and ROS-responsive β-cyclodextrin/hyaluronic acid-based hybrid hydrogel for the treatment of HER2-positive gastric cancer cells.
The combined therapeutic approaches by unique biomaterial have great attention for gastric cancer therapy with peritoneal metastasis.
APA
Guo R, Wang J, et al. (2026). Fabrication of NIR and ROS-responsive β-cyclodextrin/hyaluronic acid-based hybrid hydrogel for the treatment of HER2-positive gastric cancer cells.. International journal of biological macromolecules, 355, 151472. https://doi.org/10.1016/j.ijbiomac.2026.151472
MLA
Guo R, et al.. "Fabrication of NIR and ROS-responsive β-cyclodextrin/hyaluronic acid-based hybrid hydrogel for the treatment of HER2-positive gastric cancer cells.." International journal of biological macromolecules, vol. 355, 2026, pp. 151472.
PMID
41861894
Abstract
The combined therapeutic approaches by unique biomaterial have great attention for gastric cancer therapy with peritoneal metastasis. In this research report, we designed NIR-responsive FeO@MIL-100(Fe)-Upconversion nanoparticles (FMUNPs) functionalized injectable β-cyclodextrin/hyaluronic acid macromolecular hydrogel-encapsulated with HER-2 targeting trastuzumab (TZB) molecules to induce ROS against gastric cancer cells. The developed FMUNPs could provide effective ROS generation ability by photo-Fenton rection with NIR irradiation for toxicity and cell death against gastric cancer cells (NCI-N87). The ROS generation-induced apoptotic efficiency of the treated groups was confirmed by expressions of pro-apoptotic and anti-apoptotic markers. The TZB/FMUNPs-hydrogel with NIR prominently produced cell death by apoptotic pathway, which was confirmed by flow cytometry method. In-vivo study demonstrated that the significant reduction on tumor volume and size when tumor-induced mice treated with developed formulation with NIR irradiation. This investigation outcome demonstrates this novel formulation could be a new avenue for the gastric cancer treatment.
MeSH Terms
Stomach Neoplasms; Hyaluronic Acid; Animals; beta-Cyclodextrins; Hydrogels; Humans; Cell Line, Tumor; Reactive Oxygen Species; Mice; Erb-b2 Receptor Tyrosine Kinases; Trastuzumab; Apoptosis; Infrared Rays; Nanoparticles; Xenograft Model Antitumor Assays
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