Recent advances in targeted drug delivery for the treatment of glioblastoma
- PMID: 38606460
- DOI: 10.1039/d4nr01056f
Recent advances in targeted drug delivery for the treatment of glioblastoma
Abstract
Glioblastoma multiforme (GBM) is one of the highly malignant brain tumors characterized by significant morbidity and mortality. Despite the recent advancements in the treatment of GBM, major challenges persist in achieving controlled drug delivery to tumors. The management of GBM poses considerable difficulties primarily due to unresolved issues in the blood-brain barrier (BBB)/blood-brain tumor barrier (BBTB) and GBM microenvironment. These factors limit the uptake of anti-cancer drugs by the tumor, thus limiting the therapeutic options. Current breakthroughs in nanotechnology provide new prospects concerning unconventional drug delivery approaches for GBM treatment. Specifically, swimming nanorobots show great potential in active targeted delivery, owing to their autonomous propulsion and improved navigation capacities across biological barriers, which further facilitate the development of GBM-targeted strategies. This review presents an overview of technological progress in different drug administration methods for GBM. Additionally, the limitations in clinical translation and future research prospects in this field are also discussed. This review aims to provide a comprehensive guideline for researchers and offer perspectives on further development of new drug delivery therapies to combat GBM.
Similar articles
-
Targeted therapies for Glioblastoma multiforme (GBM): State-of-the-art and future prospects.Drug Dev Res. 2024 Nov;85(7):e22261. doi: 10.1002/ddr.22261. Drug Dev Res. 2024. PMID: 39485272 Review.
-
A comprehensive review in improving delivery of small-molecule chemotherapeutic agents overcoming the blood-brain/brain tumor barriers for glioblastoma treatment.Drug Deliv. 2019 Dec;26(1):551-565. doi: 10.1080/10717544.2019.1616235. Drug Deliv. 2019. PMID: 31928355 Free PMC article. Review.
-
Overcoming the blood-brain tumor barrier for effective glioblastoma treatment.Drug Resist Updat. 2015 Mar;19:1-12. doi: 10.1016/j.drup.2015.02.002. Epub 2015 Mar 6. Drug Resist Updat. 2015. PMID: 25791797 Review.
-
Contemporary strategies in glioblastoma therapy: Recent developments and innovations.Neuroscience. 2024 Nov 12;560:211-237. doi: 10.1016/j.neuroscience.2024.09.022. Epub 2024 Oct 3. Neuroscience. 2024. PMID: 39368608 Review.
-
Drug delivery approaches for the treatment of glioblastoma multiforme.Artif Cells Nanomed Biotechnol. 2016 Sep;44(6):1365-73. doi: 10.3109/21691401.2015.1052467. Epub 2015 Jun 5. Artif Cells Nanomed Biotechnol. 2016. PMID: 26046399 Review.
Cited by
-
The Importance of Biotinylation for the Suitability of Cationic and Neutral Fourth-Generation Polyamidoamine Dendrimers as Targeted Drug Carriers in the Therapy of Glioma and Liver Cancer.Molecules. 2024 Sep 10;29(18):4293. doi: 10.3390/molecules29184293. Molecules. 2024. PMID: 39339289 Free PMC article.
-
Recent advances in nanomaterial-based brain-targeted delivery systems for glioblastoma therapy.Nanomedicine (Lond). 2025 Jun;20(12):1495-1511. doi: 10.1080/17435889.2025.2503694. Epub 2025 May 12. Nanomedicine (Lond). 2025. PMID: 40353316 Review.
-
A self-directed Trojanbot-enzymatic nanobot in neutrobot for active target therapy of glioblastoma.Nat Commun. 2025 Jun 6;16(1):5263. doi: 10.1038/s41467-025-60422-z. Nat Commun. 2025. PMID: 40480985 Free PMC article.
-
Immunostimulatory Hydrogel with Synergistic Blockage of Glutamine Metabolism and Chemodynamic Therapy for Postoperative Management of Glioblastoma.Adv Sci (Weinh). 2025 Apr;12(15):e2412507. doi: 10.1002/advs.202412507. Epub 2025 Feb 20. Adv Sci (Weinh). 2025. PMID: 39976234 Free PMC article.
-
Progress in Drug Delivery Systems Based on Nanoparticles for Improved Glioblastoma Therapy: Addressing Challenges and Investigating Opportunities.Cancers (Basel). 2025 Feb 19;17(4):701. doi: 10.3390/cancers17040701. Cancers (Basel). 2025. PMID: 40002294 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical