Research Article
Comparative Study on the Synergistic Action of
Differentially Synthesized Silver Nanoparticles with
-Cephem Antibiotics and Chloramphenicol
Neethu Hari,
1
Tincy K. Thomas,
2
and A. Jayakumaran Nair
2
1
Centre for Nanoscience and Nanotechnology, University of Kerala, Kariavattom Campus, hiruvananthapuram, Kerala 695581, India
2
Department of Biotechnology, University of Kerala, Kariavattom Campus, hiruvananthapuram, Kerala 695581, India
Correspondence should be addressed to A. Jayakumaran Nair; ajayakumarannair@gmail.com
Received 31 July 2014; Revised 27 October 2014; Accepted 27 October 2014; Published 13 November 2014
Academic Editor: Mingwang Shao
Copyright © 2014 Neethu Hari et al. his is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Synergistic activity of cephem antibiotics with silver nanoparticles (Ag NPs) was investigated. Silver nanoparticles were synthesized
through biological and chemical method. he combined action of -lactam cephem antibiotics with both green and chemically
synthesized silver nanoparticles enhances the antibacterial activity against wide range of antibiotic resistant pathogens and making
them applicable to medical devices and microbial control systems. Synergistic activity of chloramphenicol with silver nanoparticles
was also studied.
1. Introduction
Beta-lactam antibiotics (penams and cephems) are the largest
group of antibiotics widely used in clinical medicine because
of their high antibacterial activity [1]. -Lactam groups
of compounds are the most successful example of natural
product application and chemotherapy [2]. All the natu-
ral and semisynthetic derivatives of -lactam have their
own properties and wide range of applications. Cephem
derivatives are one of the new groups of -lactam antibi-
otics with cephem ring and they show potent activity
against diferent types of bacteria. Cephem class includes
cephalosporins and cephamycins of which more than 22
antibiotics are now in clinical use and the eicacies of these
drugs depend on their antibacterial spectra, potencies, and
concentrations in tissues. But the empirical therapy and
extent use of these agents have caused the development of
bacterial resistance by diferent mechanisms like production
of diferent kinds of -lactamases (-lases), alteration of
the antibiotic target site, and prevention of access of the
antibiotic to the target by way of altered permeability or
forced elux and this may compromise the potential of -
lactam antibiotics. In this regard, considerable attention has
been given to silver nanoparticles (Ag NPs), which have
well-known antimicrobial properties and are used extensively
in various medical and general applications and also the
antibacterial, antifungal, and antiviral properties of silver
ions, silver compounds, and silver nanoparticles have been
extensively studied [3]. Moreover, high surface to volume
ratio of silver nanoparticles may contribute to their enhanced
antimicrobial properties by increasing the contact surface
of silver nanoparticles with the microorganisms. Several
studies also suggest that silver nanoparticles, which are well
known to have broad spectrum antimicrobial activity against
bacteria, virus, and eukaryotic microorganisms [4], interact
with the cell membrane and some of them will penetrate
the bacterial cell wall, thereby causing the death of bacteria
[5, 6] Synergistic action is now commonly used to describe an
interaction of two antimicrobial agents or occasionally more
than two [7], in which the efect produced by the drugs in
combination is greater than the sum of their individual efects
when the antibiotics are used alone [8]. In another study,
Vivekanandan et al. proposed that the silver nanoparticles
have the ability to destroy the stability of lipopolysacchrides
allowing increase in permeability of outer membrane and
Hindawi Publishing Corporation
Journal of Nanoscience
Volume 2014, Article ID 201482, 8 pages
http://dx.doi.org/10.1155/2014/201482