Keywords
liposomes, nanocarriers, brain, targeted drug delivery
Abstract
Due to their biocompatibility, non-toxicity, and surface-conjugation capabilities, liposomes are effective nanocarriers that can encapsulate chemotherapeutic drugs and facilitate targeted delivery across the blood–brain barrier (BBB). Additionally, strategies have been explored to synthesize liposomes that respond to internal and/or external stimuli to release their payload controllably. Although research into liposomes for brain cancer treatment is still in its infancy, these systems have great potential to fundamentally change the drug delivery landscape. This review paper attempts to consolidate relevant literature regarding the delivery to the brain using nanocarriers, particularly liposomes. The paper first briefly explains conventional treatment modalities for cancer, followed by describing the blood–brain barrier and ways, challenges, and techniques involved in transporting drugs across the BBB. Various nanocarrier systems are introduced, with attention to liposomes, due to their ability to circumvent the challenges imposed by the BBB. Relevant studies involving liposomal systems researched to treat brain tumors are reviewed in vitro, in vivo, and clinical studies. Finally, the challenges associated with the use of liposomes to treat brain tumors and how they can be addressed are presented.
Original Publication Citation
Raju, R., Abuwatfa, W. H., Pitt, W. G., & Husseini, G. A. (2023). Liposomes for the Treatment of Brain Cancer—A Review. Pharmaceuticals, 16(8), 1056. https://doi.org/10.3390/ph16081056
BYU ScholarsArchive Citation
    Raju, Richu; Abuwatfa, Wadd H.; Pitt, William G.; and Husseini, Ghaleb A., "Liposomes for the Treatment of Brain Cancer—A Review" (2023). Faculty Publications.  7766.
    
    
    
        https://scholarsarchive.byu.edu/facpub/7766
    
Document Type
Peer-Reviewed Article
Publication Date
2023-07-25
Publisher
MDPI
Language
English
College
Ira A. Fulton College of Engineering
Department
Chemical Engineering
Copyright Status
Copyright: © 2023 by the authors.
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