neighboring cells (Hemeg 2017; Neethirajan et al. 2014). The spread of bacterial
infection takes place when these gradually growing bacterial cells are detached
(Hemeg 2017). In lieu of this, a strategic solution has been provided by the NPs.
Lellouche et al. prepared crystalline yttrium fluoride (YF2) nanoparticles and
assessed their characteristic antibacterial and anti-biofilm property (Lellouche et al.
2012a). The study pointed to size-dependent toxicity of prepared nanosystems. It
was noted that smaller NPs exhibited more enhanced cytotoxicity in contrast to their
bigger counterparts. The outcomes of the study revealed that an infinitesimally low
concentration (mM) of NPs was able to produce a prominent cytotoxic effect in
bacteria, thus retarding the growth of bacterial biofilm (Lellouche et al. 2012a).
Several other research groups assessed the bactericidal effect of varied NPs (viz., Se,
TiO2, CdS, ZnO, Bi, and Ag) (Dakal et al. 2016; Dhanabalan and Gurunathan 2015;
Durán et al. 2016; Guisbiers et al. 2016; Hernandez-Delgadillo et al. 2012; Lee et al.
2014; Wong et al. 2015). The outcome of the study clearly corroborated the
abovementioned findings, and similar results highlighting the antibacterial targeting
propensity of NPs were reported.
11.4
Bactericidal Activity of Nanoparticles
In response to the harsh environmental milieu, cell wall and membrane are the two
most vital defensive parameters, which offer a protective niche to the bacteria. In
other words, it can be precisely said that the exact morphology of these pathogens
remains intact due to the protective coating offered by the bacterial cell wall (Wang
et al. 2017). Owing to a complex physicochemical composition of the cellular
membrane components, the intake of NPs generally takes place through diverse
adsorption pathways in both Gram-positive (+ve) and Gram-negative (ve) bacteria,
respectively (Lesniak et al. 2013; Wang et al. 2017). In case of Gram-negative
strains, the NPs are highly derived toward the bacterium, and a strong interaction
among them is established.
This can be explained on the basis that numerous LPS units are exposed on the
outer periphery of the cell wall, which imparts a significantly high negative charge.
This in turn offers direct communication between the NPs and the host based on
charge-charge interactions (Lesniak et al. 2013; Sarwar et al. 2015). On the other
hand, the presence of teichoic acid on the outer corona of Gram-positive bacteria
aided in widely distributing the NPs in accordance with the molecular phosphate
chains across the bacterial cell wall, thereby preventing the aggregation of functional
particles (Sarwar et al. 2015; Wang et al. 2017).
It became apparent from varied scientific studies that the NPs possess enhanced
bactericidal effect in case of Gram-positive bacteria while in their counterpart’s, viz.,
Gram-negative bacteria, showed comparatively lesser bacterial cell lysis/killing
(Wang et al. 2017). The presence of LPS, phospholipids, and proteins across the
cell wall of Gram-negative bacteria results in an altered cell morphology, thus
creating a shielding barrier across the bacteria. This penetration barrier allows only
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