Red Blood Cell Inspired Strategies for Drug Delivery: Emerging Concepts and New Advances
- PMID: 35794397
- DOI: 10.1007/s11095-022-03328-5
Red Blood Cell Inspired Strategies for Drug Delivery: Emerging Concepts and New Advances
Abstract
In the past five decades, red blood cells (RBCs) have been extensively explored as drug delivery systems due to their distinguishing potential in modulating the pharmacokinetic, pharmacodynamics, and biological activity of carried payloads. The extensive interests in RBC-mediated drug delivery technologies are in part derived from RBCs' unique biological features such as long circulation time, wide access to many tissues in the body, and low immunogenicity. Owing to these outstanding properties, a large body of efforts have led to the development of various RBC-inspired strategies to enable precise drug delivery with enhanced therapeutic efficacy and reduced off-target toxicity. In this review, we discuss emerging concepts and new advances in such RBC-inspired strategies, including native RBCs, ghost RBCs, RBC-mimetic nanoparticles, and RBC-derived extracellular vesicles, for drug delivery.
Keywords: Drug delivery; Extracellular vesicle; Nanoparticle; RBC hitchhiking; Red blood cell.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
References
-
- Li W, Tang J, Lee D, Tice TR, Schwendeman SP, Prausnitz MR. Clinical translation of long-acting drug delivery formulations. Nature Reviews Materials. 2022.
-
- Furtado D, Björnmalm M, Ayton S, Bush AI, Kempe K, Caruso F. Overcoming the Blood-Brain Barrier: The Role of Nanomaterials in Treating Neurological Diseases. Adv Mater. 2018;30(46):1801362.
-
- Leandro K, Bicker J, Alves G, Falcão A, Fortuna A. ABC transporters in drug-resistant epilepsy: mechanisms of upregulation and therapeutic approaches. Pharmacol Res. 2019;144:357–76. - PubMed
-
- Vargason AM, Anselmo AC, Mitragotri S. The evolution of commercial drug delivery technologies. Nature Biomedical Engineering. 2021;5(9):951–67. - PubMed
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