Nanomedicines as disruptors or inhibitors of biofilms: Opportunities in addressing antimicrobial resistance
Journal of Controlled Release,
Journal Year:
2025,
Volume and Issue:
381, P. 113589 - 113589
Published: March 1, 2025
The
problem
of
antimicrobial
resistance
(AMR)
has
caused
global
concern
due
to
its
great
threat
human
health.
Evidences
are
emerging
for
a
critical
role
biofilms,
one
the
natural
protective
mechanisms
developed
by
bacteria
during
growth,
in
resisting
commonly
used
clinical
antibiotics.
Advances
nanomedicines
with
tunable
physicochemical
properties
and
unique
anti-biofilm
provide
opportunities
solving
AMR
risks
more
effectively.
In
this
review,
we
summarize
five
"A"
stages
(adhesion,
amplification,
alienation,
aging
allocation)
biofilm
formation
through
which
they
protect
internal
bacteria.
Aimed
at
characteristics
emphasize
design
"THAT"
principles
(targeting,
hacking,
adhering
transport)
their
interactions
biofilms
Furthermore,
recent
progresses
multimodal
antibacterial
nanomedicines,
including
disruption
bactericidal
activity,
types
currently
available
antibiofilm
contained
organic
inorganic
outlined
highlighted
potential
applications
development
preclinical
research.
Last
but
not
least,
offer
perspective
effectiveness
designed
address
challenges
associated
translation.
Language: Английский
Bimetallic Metal–Organic Framework Microneedle Array for Wound Healing through Targeted Reactive Oxygen Species Generation and Electron Transfer Disruption
Sirong Sun,
No information about this author
Xiangyu Liu,
No information about this author
Xiangdan Meng
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et al.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
The
development
of
reactive
oxygen
species
(ROS)-based
antibacterial
strategies
that
overcome
ROS's
ultrashort
diffusion
distance
and
disrupt
bacterial
electron
transfer
represents
a
promising
yet
underexplored
avenue
for
nonantibiotic
therapies.
In
this
study,
we
introduce
an
iron-copper
bimetallic
metal-organic
framework
(MOF)
with
peroxidase
(POD)-like
enzymatic
activity
engineered
to
integrate
dual
functionalities:
bactericidal
recognition
disruption
synergistically
enhance
efficacy.
Mechanistic
investigations
reveal
boronic-acid-cis-diol
interactions
enable
the
MOF
selectively
bind
membranes,
where
it
generates
localized
ROS,
effectively
killing
bacteria.
Concurrently,
alignment
energy
levels
redox
potential
facilitates
efficient
from
membrane
MOFs,
disrupting
integrity
inhibiting
critical
processes
such
as
transport
ATP
synthesis.
When
incorporated
into
biodegradable
microneedle
patches,
penetrates
biofilms
wound
exudates,
delivering
potent
effects
directly
infection
sites
while
simultaneously
promoting
tissue
repair.
This
strategic
combination
targeting,
disruption,
microneedle-mediated
delivery
highlights
approach
advance
Language: Английский
Ultrasmall platinum single-atom enzyme alleviates oxidative stress and macrophage polarization induced by acute kidney ischemia–reperfusion injury through inhibition of cell death storm
Keng Ye,
No information about this author
Kevin Lin,
No information about this author
Chengkun Wu
No information about this author
et al.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: April 27, 2025
Acute
kidney
injury
(AKI),
characterized
by
a
rapid
decline
in
renal
function,
is
associated
with
impaired
mitochondrial
function
and
excessive
reactive
oxygen
species
(ROS).
Therefore,
the
exploration
of
ROS
scavengers
provides
promising
new
opportunities
for
prevention
treatment
AKI
mitigating
oxidative
stress.
Here,
we
construct
an
ultrasmall
platinum
single-atom
enzyme
(Pt/SAE)
multiple
antioxidant
activities
to
protect
against
acute
ischemia-reperfusion
(I/R)
injury.
Pt/SAE
not
only
mimics
superoxide
dismutase
catalase
convert
anion
into
water
oxygen,
but
also
exhibits
impressive
hydroxyl
radical
scavenging
capacity,
thereby
reducing
pro-inflammatory
macrophage
levels
preventing
inflammation.
Furthermore,
reduces
accumulation
Z-form
DNA,
which
excessively
accumulates
following
I/R
damage,
thus
decreasing
its
interaction
Z-DNA
binding
protein
1,
consequently
progression
PANoptosis
Additionally,
downregulation
induced
suppresses
lipid
peroxidation,
return
ferroptosis
I/R.
Both
vitro
vivo
experiments
confirm
that
effectively
mitigates
inflammatory
cell
infiltration
promotes
shift
polarization
from
M1-like
M2-like
subtype.
This
study
information
development
novel
SAEs
as
viable
method
AKI.
Language: Английский