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Review
. 2022 Aug 2;23(15):8579.
doi: 10.3390/ijms23158579.

Virus-like Particles: Fundamentals and Biomedical Applications

Affiliations
Review

Virus-like Particles: Fundamentals and Biomedical Applications

Jorge L Mejía-Méndez et al. Int J Mol Sci. .

Abstract

Nanotechnology is a fast-evolving field focused on fabricating nanoscale objects for industrial, cosmetic, and therapeutic applications. Virus-like particles (VLPs) are self-assembled nanoparticles whose intrinsic properties, such as heterogeneity, and highly ordered structural organization are exploited to prepare vaccines; imaging agents; construct nanobioreactors; cancer treatment approaches; or deliver drugs, genes, and enzymes. However, depending upon the intrinsic features of the native virus from which they are produced, the therapeutic performance of VLPs can vary. This review compiles the recent scientific literature about the fundamentals of VLPs with biomedical applications. We consulted different databases to present a general scenario about viruses and how VLPs are produced in eukaryotic and prokaryotic cell lines to entrap therapeutic cargo. Moreover, the structural classification, morphology, and methods to functionalize the surface of VLPs are discussed. Finally, different characterization techniques required to examine the size, charge, aggregation, and composition of VLPs are described.

Keywords: characterization; nanomedicine; nanotechnology; preparation; virus-like particles.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Different types of viral capsids: (A) helical, (B) icosahedral, (C) spherical, and (D) complex.
Figure 2
Figure 2
A schematic representation of the VLP production of virions as nanocarriers: (i) production, (ii) disassembling and nucleic acid removal, (iii) cargo encapsulation, and (iv) VLP functionalization.
Figure 3
Figure 3
General features of VLPs.
Figure 4
Figure 4
Several triangulations and diameters of viral entities. AAV, adeno-associated virus; CCMV, cowpea chlorotic mottle virus; HBV, hepatitis B virus; P22, bacteriophage; and PBCV, Paramecium bursaria Chlorella virus.
Figure 5
Figure 5
Factors influencing the design and production of VLPs.
Figure 6
Figure 6
Methods, classification, and possible ligands to functionalize VLPs.

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