Table 13.1 Diverse types of NPs used in the development of nanodrugs for treating kidney stones
Type
Composition
Properties
References
Organic NPs
PVP NPs
Polyvinylpyrrolidone (PVP),
poly[N-(2-hydroxypropyl)
methacrylamide] (pHPMA),
copolymers with PVP or
pHPMA as major components
Water and organic solvent
soluble, excellent
biocompatibility and
complexation capabilities
Due to their innate retention in
the kidneys and low level of
accumulation in other organs,
PVP NPs and their anionic
derivatives might prove
excellent drug carriers for
kidney stones.
Lee et al.
(2015)
Liposomal
NPs
Spherical lipid bilayer with an
aqueous core
Provides an effective route for
delivery of enzymatic drugs for
treatment of hyperoxaluria
Enhances enzymatic activity
and increases its stability,
reduces phagocytosis leading to
prolonged circulation half-life,
and reduces immunogenicity.
Kamaly
et al.
(2016)
Zhao et al.
(2017)
Dendrimer-
based NPs
Symmetrically branched
polymeric macromolecules
synthesized using polyamides
with a size <10 nm
Globular macromolecules with
three distinct domains, i.e., a
central core, a hyperbranched
mantle, and a corona with a
peripheral reactive functional
group.
Possess uniform size
distribution, solubility in water,
multivalency, high drug/gene-
loading ability, predictable
release profile and favorable
pharmacokinetics, which makes
them favorable for use in drug
delivery.
Lee et al.
(2015)
Longmire
et al.
(2014)
Kamaly
et al.
(2016)
Inorganic NPs
Gold NPs
Spherical-, rod-, or shell-based
colloids made from the
reduction of HAuCl4
Display a very short acting time
and reduced risk of adverse side
effects.
Kamaly
et al.
(2016)
Iron oxide
NP
Crystalline NPs of
Fe3O4/γ-Fe2O3
Superparamagnetic iron oxide
stabilized with dextran-induced
iron oxide NPs
Exhibit theranostic potential
due to a high surface to volume
ratio and surface stemmed
chemical residues that allow for
chemical drug loading.
Also possess intrinsic
superparamagnetic properties
that permit magnetic targeting.
Display no toxic effect on renal
and liver functions.
Kamaly
et al.
(2016)
Upadhyay
(2017)
Mulens-
Arias et al.
(2020)
(continued)
208
G. Shruti and K. S. Singh