4.8 Article

Effects of nanoparticle coatings on the activity of oncolytic adenovirus-magnetic nanoparticle complexes

期刊

BIOMATERIALS
卷 33, 期 1, 页码 256-269

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2011.09.028

关键词

Oncolytic adenovirus; Magnetic nanoparticles; Surface coating; Oncolytic activity; Multidrug-resistant cancer cells

资金

  1. Thailand Research Fund (TRF) [PHD/0002/2548]
  2. Faculty of Graduate Studies and Faculty of Pharmacy, Mahidol University
  3. German Research Foundation (DFG) [FOR917, PL 281/3-1]
  4. German Federal Ministry of Education and Research [ELA 10/002]

向作者/读者索取更多资源

Limitations to adenovirus infectivity can be overcome by association with magnetic nanoparticles and enforced infection by magnetic field influence. Here we examined three core-shell-type iron oxide magnetic nanoparticles differing in their surface coatings, particle sizes and magnetic properties for their ability to enhance the oncolytic potency of adenovirus Ad520 and to stabilize it against the inhibitory effects of serum or a neutralizing antibody. It was found that the physicochemical properties of magnetic nanoparticles are critical determinants of the properties which govern the oncolytic productivities of their complexes with Ad520. Although high serum concentration during infection or a neutralizing antibody had strong inhibitory influence on the uptake or oncolytic productivity of the naked virus, one particle type was identified which conferred high protection against both inhibitory factors while enhancing the oncolytic productivity of the internalized virus. This particle type equipped with a silica coating and adsorbed polyethylenimine, displaying a high magnetic moment and high saturation magnetization, mediated a 50% reduction of tumor growth rate versus control upon intratumoral injection of its complex with Ad520 and magnetic field influence, whereas Ad520 alone was inefficient. The correlations between physical properties of the magnetic particles or virus complexes and oncolytic potency are described herein. (C) 2011 Elsevier Ltd. All rights reserved.

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