4.4 Article

The pharmacology of plant virus nanoparticles

期刊

VIROLOGY
卷 556, 期 -, 页码 39-61

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2021.01.012

关键词

Plant virus; Nanoparticle; Drug delivery; Imaging; Biodistribution; Toxicity; Biocompatibility; Nanomedicine

类别

资金

  1. National Institute of Health [U01-CA218292, R01CA253615, R01-CA224605, R01 HL137674]
  2. National Science Foundation [NSF RAPID CMMI-2027668]
  3. American Cancer Society [128319-RSG-15-144-01-CDD]

向作者/读者索取更多资源

The application of nanoparticles in medicine has greatly advanced, with plant virus-based nanoparticles being studied for drug delivery and imaging. While there are many reports on engineering and manufacturing aspects of VNPs, research on the nanotoxicity of this new platform nanotechnology is relatively scarce.
The application of nanoparticles for medical purposes has made enormous strides in providing new solutions to health problems. The observation that plant virus-based nanoparticles (VNPs) can be repurposed and engineered as smart bio-vehicles for targeted drug delivery and imaging has launched extensive research for improving the therapeutic and diagnostic management of various diseases. There is evidence that VNPs are promising high value nanocarriers with potential for translational development. This is mainly due to their unique features, encompassing structural uniformity, ease of manufacture and functionalization by means of expression, chemical biology and self-assembly. While the development pipeline is moving rapidly, with many reports focusing on engineering and manufacturing aspects to tailor the properties and efficacy of VNPs, fewer studies have focused on gaining insights into the nanotoxicity of this novel platform nanotechnology. Herein, we discuss the pharmacology of VNPs as a function of formulation and route of administration. VNPs are reviewed in the context of their application as therapeutic adjuvants or nanocarrier excipients to initiate, enhance, attenuate or impede the formulation's toxicity. The summary of the data however also underlines the need for meticulous VNP structurenanotoxicity studies to improve our understanding of their in vivo fates and pharmacological profiles to pave the way for translation of VNP-based formulations into the clinical setting.

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