Synergistic vesicle-vector systems for targeted delivery
Open accessAbstract
With the immense progress in drug delivery systems (DDS) and the rise of nanotechnology, challenges such as target specificity remain. The vesicle-vector system (VVS) is a delivery system that uses lipid-based vesicles as vectors for a targeted drug delivery. When modified with target-probing materials, these vesicles become powerful vectors for drug delivery with high target specificity. In this review, we discuss three general types of VVS based on different modification strategies: (1) vesicle-probes; (2) vesicle-vesicles; and (3) genetically engineered vesicles. The synthesis of each VVS type and their corresponding properties that are advantageous for targeted drug delivery, are also highlighted. The applications, challenges, and limitations of VVS are briefly examined. Finally, we share a number of insights and perspectives regarding the future of VVS as a targeted drug delivery system at the nanoscale. Graphical Abstract
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Even with nanotechnology, the efficiency of targeting disease or disordered area cells with EVs is quite low.
“To treat CNS disorders using EVs, EVs should only target the disease or disordered area cells, but even with nanotechnology, efficiency is quite low [333–336].”
From Extracellular vesicles as nanotheranostic platforms for targeted neurological disorder interventions (2024) · cites this paper as [334]
The Introduction (page not provided) says nanotechnology has improved drug delivery, but delivery to a targeted location remains challenging. Clinical Applications (page not provided) also notes concerns about the target specificity of mainly unmodified EVs. Neither passage establishes that targeting efficiency is quite low for nanotechnology-enhanced EVs treating CNS disorders specifically. (LLM, conf=0.84)
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Cited by
Sorted by citations
Extracellular vesicles as nanotheranostic platforms for targeted neurological disorder interventions
Choi, H. K., Chen, M., Goldston, L. L., & Lee, K.-B. (2024) · Nano Convergence · doi:10.1186/s40580-024-00426-5 · Cited by 26 · see citing works
- Authors
- Marquez, C. A., Oh, C.-I., Ahn, G., Shin, W.-R., Kim, Y.-H., & Ahn, J.-Y.
- Affiliations
- Chungbuk National University (KR)
- Corresponding author
- Kim, Yang-Hoon
- Ahn, Ji-Young
- Venue
- Journal of Nanobiotechnology
- Published
- 2024-01-03
- Volume
- 22
- Issue
- 1
- Pages
- 6-6
- ISSN
- 1477-3155 (ISSN-L)
- PMC
- PMC10763086
- OpenAlex
- W4390545796
- Cited by
- 37
- References
- 3
- Citations by year
- 2026: 14 · 2025: 14 · 2024: 9
- FWCI
- 1.05
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Journal of Nanobiotechnology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Research Foundation of Korea (2020R1A6A1A06046235)
- Commercializations Promotion Agency for R and D Outcomes (1711173792)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- targeted drug delivery, lipid vesicles, target specificity, nanomedicine
- MeSH terms
- Extracellular Vesicles, Drug Delivery Systems, Nanotechnology
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