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Review
. 2025 Jan 3:24:34-59.
doi: 10.17179/excli2024-7163. eCollection 2025.

A review on the role of nanoparticles for targeted brain drug delivery: synthesis, characterization, and applications

Affiliations
Review

A review on the role of nanoparticles for targeted brain drug delivery: synthesis, characterization, and applications

Payam Nawzad Mohammed et al. EXCLI J. .

Abstract

Unfortunately, nowadays, brain disorders, which include both neurological and mental disorders, are the main cause of years spent living with a disability worldwide. There are serious diseases with a high prevalence and a high mortality rate. However, the outmoded technical infrastructure makes their treatment difficult. The blood-brain barrier (BBB) serves as a protective mechanism for the central nervous system (CNS) and regulates its homeostatic processes. The brain is protected against injury and illness by an extremely complex system that precisely regulates the flow of ions, very few tiny molecules, and an even smaller number of macromolecules from the blood to the brain. Nevertheless, the BBB also considerably inhibits the delivery of medications to the brain, making it impossible to treat a variety of neurological diseases. Several strategies are now being studied to enhance the transport of drugs over the BBB. According to this research, nanoparticles are one of the most promising agents for brain disease treatment while many conventional drugs are also capable of crossing this barrier but there are amazing facts about nanoparticles in brain drug delivery. For example, 1. Precision Targeting: Through mechanisms such as receptor-mediated transport, ligand attachment, or the use of external stimuli (e.g., magnetic or thermal guidance), nanoparticles can deliver drugs specifically to diseased areas of the brain while minimizing exposure to healthy tissues. This targeted approach reduces side effects and enhances therapeutic outcomes. 2. Improved Drug Stability: Drugs can be encapsulated by nanoparticles, which keeps them stable and shields them from deterioration while being transported to the brain. 3. Therapeutic Payload: Nanoparticles possess a high surface-area-to-volume ratio, enabling them to encapsulate a substantial quantity of therapeutic agents relative to their size. This allows for enhanced drug delivery efficiency, maximizing therapeutic outcomes while potentially reducing the required dosage to achieve the desired effect. 4. Imaging Properties: Certain nanoparticles can also act as contrast agents for magnetic resonance imaging (MRI), allowing for the real-time visualization of drug distribution and administration in the brain. 5. Combination Therapy Possibility: Nanoparticles can be designed to co-deliver multiple medications or therapeutic agents, which could enhance synergistic effects. There have been in vivo studies where nanoparticles were successfully used for combination therapies, demonstrating potential for personalized treatments. One notable example is in cancer treatment, where nanoparticles have been designed to co-deliver multiple chemotherapeutic agents. In general, brain medication delivery by nanoparticles is a novel strategy that has the potential to revolutionize neurological disease therapy and enhance patient outcomes. The study furthermore includes a concise depiction of the structural and physiological characteristics of the BBB, and it also provides an overview of the nanoparticles that are most often used in medicine. A brief overview of the structural and physiochemical characteristics of the NPs, as well as the most popular nanoparticles used in medicine, is also included in the review.

Keywords: BBB; applications; brain disorders; methods; nanoparticles; synthesis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Table 1
Table 1. List of different types of nanoparticles with their properties
Figure 1
Figure 1. Blood-brain barrier anatomy
Figure 2
Figure 2. List of different types of nanoparticles with their properties
Figure 3
Figure 3. Schematic representation illustrating the various approaches used for synthesis of nanoparticles
Figure 4
Figure 4. Conventional methods of synthesis of nanoparticles
Figure 5
Figure 5. Schematic diagram of the mechanisms for crossing the BBB
Figure 6
Figure 6. Figure 6 shows the flow chart of research work.

References

    1. Abadeer NS, Murphy CJ. Recent progress in cancer thermal therapy using gold nanoparticles. J Phys Chem C. 2016;120:4691–4716. doi: 10.1021/acs.jpcc.5b11232. Available from: http://dx.doi.org/10.1021/acs.jpcc.5b11232. - DOI - DOI
    1. Al-Kassas R, Bansal M, Shaw J. Nanosizing techniques for improving bioavailability of drugs. J Controlled Release. 2017;260:202–212. doi: 10.1016/j.jconrel.2017.06.003. Available from: http://dx.doi.org/10.1016/j.jconrel.2017.06.003. - DOI - DOI - PubMed
    1. Anwar SH. A brief review on nanoparticles: types of platforms, biological synthesis and applications. Res Rev J Mater Sci. 2018;6:109–116. doi: 10.4172/2321-6212.1000222. Available from: http://dx.doi.org/10.4172/2321-6212.1000222. - DOI - DOI
    1. Baig N, Kammakakam I, Falath W. Nanomaterials: a review of synthesis methods, properties, recent progress, and challenges. Mater Adv. 2021;2:1821–1871. doi: 10.1039/D0MA00807A. Available from: http://dx.doi.org/10.1039/D0MA00807A. - DOI - DOI
    1. Baimanov D, Cai R, Chen C. Understanding the chemical nature of nanoparticle–protein interactions. Bioconjugate Chem. 2019;30:1923–1937. doi: 10.1021/acs.bioconjchem.9b00348. Available from: http://dx.doi.org/10.1021/acs.bioconjchem.9b00348. - DOI - DOI - PubMed

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