This
review
paper
highlights
the
current
toxicological
aspects
of
magnetic
nanomaterials
in
field
medicine
and
environment,
conducted
through
a
comprehensive
literature
review.
The
main
goal
was
to
investigate
analyze
key
challenges
identified
that
impede
effective
utilization
these
systems,
particularly
focusing
on
iron
oxide
(Fe3O4)
nanoparticles.
We
aimed
factors
influence
their
intended
applications.
sought
understand
how
characteristics
produced
NPs
could
be
enhanced
improve
biocompatibility
compared
existing
samples
literature.
Additionally,
we
examined
morphological
directly
linked
physicochemical
potential
implications
for
toxicology
ecotoxicology.
Furthermore,
evaluated
regulatory
impact
nanostructured
materials.
Therefore,
initial
aspect
this
delved
into
historical
evolution
nanoparticles,
investigating
significant
milestones
have
influenced
exploration
technology.
discoveries,
influencing
choice
synthesis
methods,
most
prevalent
approaches
surface
functionalization
employed
by
scientists
materials
possessing
superparamagnetic
characteristics,
such
as
oxide.
second
focused
survey-based
global
regulation
progress
concerning
nanoparticles
throughout
years.
encountered
establishing
safety
criteria
diverse
applications
under
investigation.
encompassed
an
assessment
impacts
both
human
health
environment.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 17, 2024
Abstract
Iron-gold
(Fe0-Au)
nanoparticles
are
forefront
agents
in
biomedicine
because
of
their
magnetic
and
plasmonic
properties
prime
candidates
for
advanced
biomedical
applications
such
as
hyperthermia,
targeted
drug
delivery,
bioimaging.
Synthesizing
biocompatible,
stable
iron
phase,
minimal
borate-related
cytotoxicity,
Fe0-Au
hybrid
a
great
challenge,
This
study
presents
an
optimized,
two-step
synthetic
approach
to
produce
PEGylated
nanoparticles,
employing
NaBH4
reducing
agent
under
strictly
anaerobic
conditions.
UV-Vis
spectroscopy
confirmed
nanoparticle
formation,
with
absorbance
peaks
at
260
nm
Fe0
526
Au,
accompanied
by
discernible
color
shifts
the
colloidal
suspension,
indicative
successful
metal
reduction.
High
Transmission
electron
microscopy
(HRTEM)
revealed
uniform
spherical
morphology
average
diameter
50
nm,
while
X-ray
photoelectron
(XPS)
demonstrated
substantial
minimization
borate
byproducts,
these
potentially
cytotoxic
residues
14
atomic
percent.
Magnetization
assessments
showed
hysteresis-free
superparamagnetic
behavior
saturation
magnetization
75
Am²/kg
NPs,
validating
suitability
precision
hyperthermia
resonance
imaging.
These
findings
indicate
that
PEG
functionalization
enhances
stability
effectively
mitigates
toxicity
risks,
rendering
highly
viable
preclinical
translational
applications.
This
review
paper
highlights
the
current
toxicological
aspects
of
magnetic
nanomaterials
in
field
medicine
and
environment,
conducted
through
a
comprehensive
literature
review.
The
main
goal
was
to
investigate
analyze
key
challenges
identified
that
impede
effective
utilization
these
systems,
particularly
focusing
on
iron
oxide
(Fe3O4)
nanoparticles.
We
aimed
factors
influence
their
intended
applications.
sought
understand
how
characteristics
produced
NPs
could
be
enhanced
improve
biocompatibility
compared
existing
samples
literature.
Additionally,
we
examined
morphological
directly
linked
physicochemical
potential
implications
for
toxicology
ecotoxicology.
Furthermore,
evaluated
regulatory
impact
nanostructured
materials.
Therefore,
initial
aspect
this
delved
into
historical
evolution
nanoparticles,
investigating
significant
milestones
have
influenced
exploration
technology.
discoveries,
influencing
choice
synthesis
methods,
most
prevalent
approaches
surface
functionalization
employed
by
scientists
materials
possessing
superparamagnetic
characteristics,
such
as
oxide.
second
focused
survey-based
global
regulation
progress
concerning
nanoparticles
throughout
years.
encountered
establishing
safety
criteria
diverse
applications
under
investigation.
encompassed
an
assessment
impacts
both
human
health
environment.