Innovative applications of silicon dioxide nanoparticles for targeted liver cancer treatment
- PMID: 40421114
- PMCID: PMC12104587
- DOI: 10.3389/fbioe.2025.1595772
Innovative applications of silicon dioxide nanoparticles for targeted liver cancer treatment
Abstract
Liver cancer remains a major global health challenge, characterized by high mortality and limited treatment efficacy. Conventional therapies, including chemotherapy, immunotherapy, and viral vectors, are hindered by systemic toxicity, drug resistance, and high costs. Silica nanoparticles (SiO2NPs) have emerged as promising platforms for liver cancer therapy, offering precise drug delivery, stimuli-responsive release, and integrated diagnostic-therapeutic capabilities. This review critically examines the potential of SiO2NPs to overcome these therapeutic limitations. Notable advances include their high drug-loading capacity, customizable surface modifications, and dual-responsive systems (pH/redox/NIR-II) that enable >90% tumor-specific drug release. Preclinical studies have demonstrated synergistic efficacy in combination therapies. Additionally, theranostic SiO2NPs enable MRI-guided tumor delineation and real-time treatment monitoring. Despite promising results, challenges remain in long-term biosafety, scalable synthesis, and regulatory compliance. Early-phase clinical trials, including those using NIR-II-responsive platforms, highlight their translational potential but underscore the need for further validation of toxicity profiles and manufacturing standards. Future research should focus on optimizing combinatory treatment strategies, scaling up production, and aligning with evolving regulatory frameworks. By bridging nanomaterial innovation with clinical applications, SiO2NPs offer unparalleled potential for advancing precision oncology in hepatocellular carcinoma.
Keywords: liver cancer; nanomaterial; nanosystem; silicon dioxide; treatment.
Copyright © 2025 Fu, Duan, Sun, Ma, Wang, Wang, Tong and Wang.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Similar articles
-
Application of nanomaterials in precision treatment of lung cancer.iScience. 2024 Dec 26;28(1):111704. doi: 10.1016/j.isci.2024.111704. eCollection 2025 Jan 17. iScience. 2024. PMID: 39886464 Free PMC article. Review.
-
Smart Mesoporous Silica Nanoparticles in Cancer: Diagnosis, Treatment, Immunogenicity, and Clinical Translation.Small. 2025 Feb;21(7):e2408898. doi: 10.1002/smll.202408898. Epub 2025 Jan 22. Small. 2025. PMID: 39840493 Review.
-
Polyglutamic acid in cancer nanomedicine: Advances in multifunctional delivery platforms.Int J Pharm. 2025 May 15;676:125623. doi: 10.1016/j.ijpharm.2025.125623. Epub 2025 Apr 18. Int J Pharm. 2025. PMID: 40254191 Review.
-
Gelatin nanocarriers in oncology: A biocompatible strategy for targeted drug delivery.Int J Biol Macromol. 2025 May;310(Pt 1):143244. doi: 10.1016/j.ijbiomac.2025.143244. Epub 2025 Apr 17. Int J Biol Macromol. 2025. PMID: 40250682 Review.
-
Recent insights and applications of nanocarriers-based drug delivery systems for colonic drug delivery and cancer therapy: An updated review.Crit Rev Oncol Hematol. 2025 Apr;208:104646. doi: 10.1016/j.critrevonc.2025.104646. Epub 2025 Feb 4. Crit Rev Oncol Hematol. 2025. PMID: 39914570 Review.
References
-
- Akinyemiju T., Abera S., Ahmed M., Alam N., Alemayohu M. A., Allen C., et al. (2017). The burden of primary liver cancer and underlying etiologies from 1990 to 2015 at the global, regional, and national level: results from the global burden of disease study 2015. JAMA Oncol. 3 (12), 1683–1691. 10.1001/jamaoncol.2017.3055 - DOI - PMC - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Miscellaneous