Virus-like particles as drug delivery vectors

79Citations
Citations of this article
182Readers
Mendeley users who have this article in their library.

Abstract

Virus-like particles (VLPs) assemble spontaneously during the viral cycle or in heterologous systems during expression of viral structural protein. Depending on the complexity of the VLPs, they can be obtained by expression in prokaryotic or eukaryotic expression system from the suitable recombinant vectors, or formed in cell-free conditions. Moreover, they can be built from proteins of a single virus, or can present the proteins or peptides derived from a virus or cell on a platform derived from any other single virus, thus forming chimeric VLPs. VLPs are best known for their immunogenic properties, but the versatility of VLPs allows a wide variety of applications. They are lately in the centre of investigations in vaccinology, drug delivery and gene therapy. This review focuses on utilization of VLPs for drug delivery.

Author supplied keywords

Cite

CITATION STYLE

APA

Zdanowicz, M., & Chroboczek, J. (2016). Virus-like particles as drug delivery vectors. Acta Biochimica Polonica. Polskie Towarzystwo Biochemiczne. https://doi.org/10.18388/abp.2016_1275

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free