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RESEARCH ARTICLE
Copyright © 2012 American Scientific Publishers
All rights reserved
Printed in the United States of America
Journal of
Bionanoscience
Vol. 6, 109–112, 2012
Physical Point of View for Antiviral Effect
Caused by the Interaction Between the
Viruses and Nanoparticles
V. Lozovski
1 2
, V. Lysenko
1
, V. Piatnytsia
2 ∗
, O. Scherbakov
3
,
N. Zholobak
3
, and M. Spivak
3
1
V. Lashkariov Institute of Semiconductor Physics NAS of Ukraine, Nauki Ave. 45, Kyiv, 03028, Ukraine
2
Institute of High Technologies, T. Shevchenko National University of Kyiv, 64 Volodymyrska Str.,
Kyiv, 01601, Ukraine
3
D. Zabolontyi Institute of Mikrobiology and Virology, NAS of Ukraine, 154 Zabolotnyi Str.,
Kyiv, 13143, Ukraine
The new mechanism of antiviral activity of nanoparticles based on the local-field interaction is
proposed. Several ways of realization of the mechanism are discussed. The experimental results
of antivirus therapy are presented for action of nanoparticles CeO
2
and Au on herpes simplex
virus (HSV) and the influenza virus A/FM/1/47 (H1N1). It was shown that the both nanoparticle
preparations have the strong antiviral activities.
Keywords: Nanoparticles, Viruses, Local-Field Enhancement, Antiviral Activity.
1. INTRODUCTION
A virus is a small “particle” which is infectious agent that
can replicate only inside the living cells of organisms.
1–2
Viruses infect all types of the organisms: bacteria, plants,
animals and human.
3
Viruses are the reason of a number
of human diseases, from simple chill to some kinds of
cancer.
4
The struggle against the viruses became at this
time of day the most important problem of the sciences
from medicine to physics. The characteristic dimensions of
the viruses are from 10 nm up to 500 nm. For example, the
dimensions of the adenoviruses are about 70–90 nm, the
dimension of AIDS virus is about 100 nm and dimensions
of the herpes viruses are about 170 nm. It means that the
viruses are the objects of nanophysics, specifically, near-
field physics.
5–7
Because from the physical point of view,
the viruses are the nanoparticles having the specific shape
and characterized by the rather essential linear and non-
linear polarizabilities, the interaction between the viruses
and solid nanoparticles can have the all features inherent
to the objects of near-field physics. For example, the virus-
nanoparticle interaction can be resonant. Namely, the so-
called configurational resonance
8
can be observed in the
system. The resonance obviously can lead to anomalously
effective absorption of the energy of external (relatively to
∗
Author to whom correspondence should be addressed.
the system) field. This field can be either the field of the
external radiation or the fluctuating field. From the other
hand, the local-field enhancement
9–10
can be observed in
the system “virus-nanoparticle” (see Fig. 1).
The all these effects can take place when the virus and
nanoparticle will be located closely from one to another.
The idea of the antiviral therapy of the nanoparticles was
discussed by authors in Ref. [11]. Moreover it would be in
preference when the virus and nanoparticle can form the
stable configuration. In this case the additional reason con-
nected with the geometrical characteristics of the system
strongly fall the infectious ability of the virus. In the previ-
ous work of the authors Ref. [11] the possibility of arising
of interaction potential between two nanoparticles, which
have as linear as nonlinear polarizabilities, characterized
as attractive as repulsive parts with rather deep minimum
was discussed. It means that as it is shown in Figure 2,
the stable configuration can be established in the system
‘virus-nanoparticle.’
Then, arising of the stable system ‘virus-nanoparticle’
can lead to the antiviral therapy effect at least by the sev-
eral types of the mechanisms:
It is clear that there is two definitely different mecha-
nisms of the viral activity inhibition. The total result of
the inhibition of the viral activity is consist of the two
processes.
J. Bionanosci. 2012, Vol. 6, No. 2 1557-7910/2012/6/109/004 doi:10.1166/jbns.2012.1084 109