Acta Biomaterialia, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 1, 2024
Language: Английский
Acta Biomaterialia, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 1, 2024
Language: Английский
Acta Biomaterialia, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
2Biomaterials, Journal Year: 2024, Volume and Issue: 312, P. 122745 - 122745
Published: Aug. 3, 2024
Language: Английский
Citations
9Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 380, P. 85 - 107
Published: Feb. 5, 2025
Language: Английский
Citations
1Advanced NanoBiomed Research, Journal Year: 2024, Volume and Issue: 4(4)
Published: Jan. 26, 2024
This review is aiming to systematically elucidate the unique role of nanotechnology in optimizing therapeutic modalities for combinatorial cancer immunotherapy, which enables synergistic integration multiple treatment strategies. In particular, has enabled combination immunotherapy with physical therapies, chemotherapy, metal therapy, and nucleic acid therapy. each regimen, nanocarriers play multifaceted roles by achieving targeted codelivery different therapeutics individual modality. offers new paradigms guide precision medicine treatment. Immunotherapy alone unlikely achieve personalized cancer, are needed future. To overcome technical bottlenecks realize precise regulation tumor microenvironment treatment, it crucial develop novel nanosystems integrated sensing, targeting, functionalities.
Language: Английский
Citations
6Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 675, P. 1080 - 1090
Published: July 14, 2024
Language: Английский
Citations
6Polyoxometalates, Journal Year: 2025, Volume and Issue: 4(1), P. 9140074 - 9140074
Published: March 1, 2025
In recent years, polyoxometalates have been systematically studied in the treatment of diabetes, tumor, cancer, inflammation and other diseases vitro vivo, their main therapeutic mechanisms are related to generation reactive oxygen species causing oxidative stress. The site production is mitochondria, therefore, mechanism may be mitochondrial biosynthesis. This paper describes one diabetes mellitus, which involves increase species, resulting stress; at same time, preliminarily as antioxidants antitumor mellitus tumors, antioxidant properties provide an additional possibility for future a drug disease treatment; on basis study stress biomolecule due it, associating therapy actually closely through biosynthesis regulation relationship between mitochondria its impact three aspects order in-depth role drugs aspects.
Language: Английский
Citations
0Polymer, Journal Year: 2025, Volume and Issue: unknown, P. 128314 - 128314
Published: March 1, 2025
Language: Английский
Citations
0Nanoscale, Journal Year: 2024, Volume and Issue: 16(31), P. 14734 - 14747
Published: Jan. 1, 2024
A small-molecule nanomedicine with high drug loading, robust stability, responsive release and a synergistic photochemotherapeutic effect has been developed for cancer therapy. Image created Biorender.
Language: Английский
Citations
3ACS Applied Bio Materials, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 5, 2025
Despite its therapeutic potential, photodynamic therapy faces several key limitations in clinical applications, including poor drug delivery and insufficient tumor selectivity. We engineered RFYFYR-Ce6-RFYFYR (R-Ce6-R), a twin-tail peptide–photosensitizer conjugate that self-assembles into nanostructures for improved cancer treatment. By incorporating arginine-rich peptide sequences, this design not only enhances cellular internalization but also promotes peroxynitrite (ONOO–) formation, amplifying the effect. Our studies revealed R-Ce6-R achieves 33-fold higher potency than unmodified Ce6, with an IC50 of 0.18 μM. The demonstrated selective accumulation tissue, robust ROS generation, complete regression animal models while maintaining favorable safety profile. These results establish as innovative approach advancing
Language: Английский
Citations
0Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 16, 2025
Abstract The abnormal metabolism of tumor cells fulfills their high energy demands for rapid growth while simultaneously reshaping the microenvironment (TME), which suppresses immune cell function and facilitates evasion. Herein, a peptide‐based nanocomplex (DCK@siGLUT1) that synergizes with photodynamic therapy (PDT) to disrupt is developed. DCK@siGLUT1, utilizing mitochondria‐targeting peptide (dKLA) selectively accumulates in mitochondria, where it impairs mitochondrial membrane integrity, disrupts metabolism, induces apoptosis. Upon apoptosis, activated caspase‐3 (Casp3) cleaves releasing siGLUT1 silence glucose transporter 1 (GLUT1) expression, further inhibits uptake intensifies metabolic collapse, thereby amplifying apoptotic effects. Moreover, Ce6, conjugated dKLA, co‐delivered mitochondria and, upon light activation, exacerbates damage disruption. These combined mechanisms intensify oxidative stress activate Casp3, promote DCK@siGLUT1 cleavage, driving self‐amplifying tumoricidal cascade. Furthermore, effectively immunogenic death (ICD), triggers antitumor responses, both primary distant metastasis. This strategy offers novel approach targeting immunotherapy.
Language: Английский
Citations
0