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Review
. 2023 Aug 29;13(9):1328.
doi: 10.3390/jpm13091328.

Nanoparticle-Based Treatment in Glioblastoma

Affiliations
Review

Nanoparticle-Based Treatment in Glioblastoma

Diogo Roque et al. J Pers Med. .

Abstract

Glioblastoma (GB) is a malignant glioma associated with a mean overall survival of 12 to 18 months, even with optimal treatment, due to its high relapse rate and treatment resistance. The standardized first-line treatment consists of surgery, which allows for diagnosis and cytoreduction, followed by stereotactic fractionated radiotherapy and chemotherapy. Treatment failure can result from the poor passage of drugs through the blood-brain barrier (BBB). The development of novel and more effective therapeutic approaches is paramount to increasing the life expectancy of GB patients. Nanoparticle-based treatments include epitopes that are designed to interact with specialized transport systems, ultimately allowing the crossing of the BBB, increasing therapeutic efficacy, and reducing systemic toxicity and drug degradation. Polymeric nanoparticles have shown promising results in terms of precisely directing drugs to the brain with minimal systemic side effects. Various methods of drug delivery that pass through the BBB, such as the stereotactic injection of nanoparticles, are being actively tested in vitro and in vivo in animal models. A significant variety of pre-clinical studies with polymeric nanoparticles for the treatment of GB are being conducted, with only a few nanoparticle-based drug delivery systems to date having entered clinical trials. Pre-clinical studies are key to testing the safety and efficacy of these novel anticancer therapies and will hopefully facilitate the testing of the clinical validity of this promising treatment method. Here we review the recent literature concerning the most frequently reported types of nanoparticles for the treatment of GB.

Keywords: blood-brain barrier; glioblastoma; nanoparticles; therapy delivery.

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Conflict of interest statement

The authors declare no potential conflict of interest.

Figures

Figure 1
Figure 1
Schematic representation of nanoparticles in a spectrum of inorganic/organic molecules, macromolecules, and large molecular assemblies such as viruses and cells, measured in nanometers of different biological molecules (A). Distinct properties are shown as: size range (B); water affinity (C); and surface charge (D). Parts of the figure were drawn using pictures from Servier Medical Art. Servier Medical Art by Servier is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/, accessed on 17 March 2023).
Figure 2
Figure 2
Representation of the main types of nanoparticles being studied as potential candidates for the treatment of glioblastoma. Parts of the figure were drawn using pictures from Servier Medical Art. Servier Medical Art by Servier is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/, accessed on 17 March 2023).

References

    1. Alphandéry E. Nano-Therapies for Glioblastoma Treatment. Cancers. 2020;12:242. doi: 10.3390/cancers12010242. - DOI - PMC - PubMed
    1. Shergalis A., Bankhead A., Luesakul U., Muangsin N., Neamati N. Current challenges and opportunities in treating glioblastoma. Pharmacol. Rev. 2018;70:412–445. doi: 10.1124/pr.117.014944. - DOI - PMC - PubMed
    1. Zhao M., van Straten D., Broekman M.L., Préat V., Schiffelers R.M. Nanocarrier-based drug combination therapy for glioblastoma. Theranostics. 2020;10:1355–1372. doi: 10.7150/thno.38147. - DOI - PMC - PubMed
    1. Arifin D.Y., Lee K.Y.T., Wang C.-H., Smith K.A. Role of Convective Flow in Carmustine Delivery to a Brain Tumor. Pharm. Res. 2009;26:2289–2302. doi: 10.1007/s11095-009-9945-8. - DOI - PubMed
    1. Seystahl K., Wick W., Weller M. Therapeutic options in recurrent glioblastoma—An update. Crit. Rev. Oncol. 2016;99:389–408. doi: 10.1016/j.critrevonc.2016.01.018. - DOI - PubMed

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