Cells,
Journal Year:
2024,
Volume and Issue:
13(21), P. 1778 - 1778
Published: Oct. 27, 2024
To
minimize
off-target
adverse
effects
and
improve
drug
efficacy,
various
tissue-specific
delivery
systems
have
been
developed.
However,
even
in
diseased
organs,
both
normal
stressed,
dying
cells
coexist,
a
targeted
system
specifically
for
has
yet
to
be
explored
mitigate
within
the
same
organ.
This
study
aimed
establish
such
system.
By
examining
surfaces
of
vitro,
we
identified
P-selectin
glycoprotein
ligand-1
(PSGL-1)
as
universal
marker
cells,
positioning
it
potential
target
selective
delivery.
We
demonstrated
that
liposomes
conjugated
with
PSGL-1
binding
protein
had
significantly
greater
efficiency
compared
control
proteins
E-selectin,
L-selectin,
galectin-1,
C-type
lectin-like
receptor
2.
Using
thioacetamide
(TAA)
induce
hepatitis
hepatocyte
damage
mice,
assessed
effectiveness
our
P-selectin-based
In
vivo,
P-selectin-conjugated
effectively
delivered
fluorescent
dye
apoptosis
inhibitor
z-DEVD
TAA-damaged
livers
wild-type
but
not
knockout
mice.
TAA-treated
unconjugated
required
100-fold
higher
dose
achieve
comparable,
albeit
less
effective,
therapeutic
outcome
lowering
plasma
alanine
transaminase
levels
alleviating
thrombocytopenia.
emphasizes
conjugation
enhances
by
approximately
These
results
suggest
could
promising
strategy
delivery,
enabling
diagnosis
treatment
delivering
cell-labeling
agents
rescue
via
P-selectin–PSGL-1
axis
at
individual
cell
level.
Nanoscale Advances,
Journal Year:
2024,
Volume and Issue:
6(9), P. 2270 - 2286
Published: Jan. 1, 2024
Breast
cancer
is
a
global
health
challenge
with
staggering
statistics
underscoring
its
pervasive
impact.
The
burden
of
this
disease
measured
in
terms
prevalence
and
the
challenges
it
poses
to
healthcare
systems,
necessitating
closer
look
at
epidemiology
Current
breast
treatments,
including
surgery,
chemotherapy,
radiation
therapy,
targeted
therapies,
have
made
significant
strides
improving
patient
outcomes.
However,
they
are
not
without
limitations,
often
leading
adverse
effects
development
drug
resistance.
This
comprehensive
review
delves
into
complex
landscape
cancer,
incidence,
current
treatment
modalities,
inherent
limitations
existing
therapeutic
approaches.
It
also
sheds
light
on
promising
role
nanotechnology,
encompassing
both
inorganic
organic
nanoparticles
equipped
ability
selectively
deliver
agents
tumor
sites,
battle
against
cancer.
addresses
emerging
their
associated
challenges,
future
prospects
delivery
management.
Applied Sciences,
Journal Year:
2024,
Volume and Issue:
14(19), P. 8948 - 8948
Published: Oct. 4, 2024
Using
nanostructured
drug
delivery
systems
has
attracted
increasing
interest
in
immunotherapeutic
approaches.
The
intrinsic
immunomodulatory
properties
and
versatility
of
nanoparticles
used
as
carriers
were
consistently
reported
to
augment
treatment
efficiency
nanoscaled
materials
increase
accumulation
at
the
desired
site,
enhance
cell
internalization,
improve
therapeutic
outcomes.
Thus,
numerous
studies
have
exploited
potential
use
vehicles
delivering
different
cargo
a
promising
alternative
for
treating
conditions
like
cancer,
autoimmune
diseases,
infectious
allergic
immune
disorders.
In
this
context,
paper
presents
solid
basis
innovations,
highlighting
their
advantages
improving
strategies,
reviewing
clinical
applications,
discussing
existing
challenges
ways
overcome
them.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
177, P. 117118 - 117118
Published: July 14, 2024
Hepatocellular
carcinoma
(HCC)
is
one
of
the
most
prevalent
malignant
tumors
in
contemporary
era,
representing
a
significant
global
health
concern.
Early
HCC
patients
have
mild
symptoms
or
are
asymptomatic,
which
promotes
onset
and
progression
disease.
Moreover,
advanced
insensitive
to
chemotherapy,
making
traditional
clinical
treatment
unable
block
cancer
development.
Sorafenib
(SFB)
first-line
targeted
drug
for
with
anti-angiogenesis
anti-tumor
cell
proliferation
effects.
However,
efficacy
SFB
constrained
by
its
off-target
distribution,
rapid
metabolism,
multi-drug
resistance.
In
recent
years,
nanoparticles
based
on
variety
materials
been
demonstrated
enhance
targeting
therapeutic
against
HCC.
Concurrently,
advent
joint
delivery
systems
has
furnished
crucial
empirical
evidence
reversing
This
review
will
summarize
application
nanotechnology
field
over
past
five
years.
It
focus
research
progress
combined
multiple
modalities
treatment.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 9, 2025
Despite
enormous
progress,
advanced
cancers
are
still
one
of
the
most
serious
medical
problems
in
current
society.
Although
various
agents
and
therapeutic
strategies
with
anticancer
activity
known
used,
they
often
fail
to
achieve
satisfactory
long-term
patient
outcomes
survival.
Recently,
immunotherapy
has
shown
success
patients
by
harnessing
important
interactions
between
immune
system
cancer.
However,
many
these
therapies
lead
frequent
side
effects
when
administered
systemically,
prompting
treatment
modifications
or
discontinuation
or,
severe
cases,
fatalities.
New
approaches
like
intratumoral
immunotherapy,
characterized
reduced
effects,
cost,
systemic
toxicity,
offer
promising
prospects
for
future
applications
clinical
oncology.
In
context
locally
metastatic
cancer,
combining
diverse
immunotherapeutic
other
targeting
multiple
cancer
hallmarks
appears
crucial.
Such
combination
hold
promise
improving
survival
promoting
a
sustained
response.
This
review
aims
provide
overview
approaches,
specifically
focusing
on
administration
drugs
cancers.
It
also
explores
integration
modalities
maximize
Additionally,
summarizes
recent
advances
discusses
novel
outlining
directions
field.
Chemistry - An Asian Journal,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 4, 2025
Abstract
We
synthesized
{[Cd
2
(dTMP)
(4,4'‐azpy)
(H
O)
]
⋅
3(O)}
n
a
novel
three‐dimensional
metal
nucleotide
coordination
polymer
(CP‐1).
An
assessment
of
the
CP‐1
binding
affinity
for
anticancer
drugs
was
conducted
using
molecular
dynamic
simulations.
The
virtual
screening
results
depict
that
has
lot
potential
encapsulating
anthracycline
drug
doxorubicin
(DOX).
It
hasn′t
yet
been
investigated
how
to
accomplish
high
loading
capacity,
efficiency,
and
controlled
release
DOX
in
dTMP‐based
3D
polymers.
Utilizing
as
model
our
system
drug‐loading
vehicle,
we
used
UV‐visible
circular
dichroism
titrations
examine
effects
its
encapsulation
release.
mechanism
through
pH‐responsive
behavior
by
adjusting
pH
value
8,
7,
6,
5.
indicate
robust
at
which
facilitates
on
porous
polymer.
However,
maximum
cumulative
87.11
%
observed
higher
correlation
coefficient
(R
)
obtained
5
with
Higuchi
equation.
indicated
released
primarily
diffusion
mechanism.
polymer‘s
ability
encapsulate
while
also
permitting
possible
controlled‐release
is
confirmed
combined
insights
from
experimental
findings,
energy
graphs,
RMSD
analysis,
radius
gyration
(Rg)
data
MD
Molecules,
Journal Year:
2025,
Volume and Issue:
30(3), P. 676 - 676
Published: Feb. 4, 2025
A
methodology
for
the
quantitative
estimation
of
drug
loading
iron
oxide-based
magnetic
nanoparticles
by
corroborating
magnetometry
and
Mössbauer
spectroscopy
investigations
is
reported.
The
proposed
exemplified
in
case
two
series
nanoparticles,
namely
Fe3O4
covered
with
citric
acid
molecules
further
functionalized
doxorubicin,
L-Cysteine
doxorubicin.
general
idea
to
probe
real
structure
core
via
low-temperature
correct
spontaneous
magnetization
core.
It
subsequently
uses
ratio
between
that
reliable
nondestructive
evaluation
nanoparticle
organic
molecules.
Although
magnetite-based
it
can
be
successfully
considered
a
large
class
medicine-loaded
Fe-containing
where
57Fe
applied.
Future Medicinal Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 15
Published: Feb. 20, 2025
The
advancement
of
targeted
drug
delivery
systems
has
opened
up
a
wide
array
opportunities
in
cancer
therapy,
leading
to
the
exploration
various
strategies.
Among
these,
use
prodrugs
stands
out
as
particularly
promising
approach
treatment,
aimed
at
enhancing
selectivity
and
effectiveness
cytotoxic
agents.
In
last
few
years,
there
been
considerable
progress
area
dimeric-based
therapy.
advantages
presented
by
have
significantly
improved
efficiency
delivering
anticancer
drugs,
characterized
high
loading
capacity,
advantageous
pharmacokinetics,
release
that
responds
tumor
stimuli.
With
respect
importance
dimerization
field
prodrug
development,
herein
we
review
latest
reports
covering
research
dimeric
prodrugs.
We
categorized
article
according
reported
also
spent
great
deal
attention
on
different
types
used
linkers
methods
dissociation
into
free
monomeric
drugs.
Readers
will
easily
be
able
compare
between
using
same
drugs
with
or
well
cell
lines
studies.
Technology in Cancer Research & Treatment,
Journal Year:
2025,
Volume and Issue:
24
Published: April 1, 2025
Immunotherapy
has
emerged
as
a
pivotal
advancement
in
oncological
therapeutics,
representing
paradigm
shift
from
conventional
treatment
modalities
including
surgery,
radiotherapy,
and
chemotherapy.
This
innovative
approach
demonstrates
considerable
clinical
potential
through
its
capacity
to
enhance
systemic
anti-tumor
responses
via
active
or
passive
immunomodulation.
Compared
traditional
therapies,
immunotherapy
offers
distinct
advantages
such
broad
applicability,
rapid
therapeutic
onset,
reduced
adverse
effects.
However,
critical
challenges
persist
implementation,
particularly
concerning
safety
efficacy
optimization.
Current
limitations,
drug
off-target
effects
biological
delivery
barriers,
frequently
result
suboptimal
outcomes
severe
complications
autoimmune
disorders
nonspecific
inflammation.
Recently
advancements
systems
(DDS)
present
transformative
solutions
these
challenges.
Sophisticated
DDS
platforms
enable
precise
spatiotemporal
of
tumor
antigens,
immunotherapeutic
agents,
immunostimulatory
molecules,
thereby
achieving
targeted
modulation
diverse
immune
cell
populations.
technological
innovation
not
only
enhances
but
also
significantly
mitigates
reactions,
while
facilitating
synergistic
combinations
with
cancer
treatments.
In
this
review,
we
outline
the
application
new
major
malignancies
(including
limited
melanoma,
non-small
lung
cancer,
hormone
receptor-positive
breast
hepatocellular
carcinoma).
We
further
propose
evidence-based
optimization
strategies
for
next-generation
platforms,
aiming
bridge
gap
between
preclinical
development
implementation
immunotherapy.
Materials Today Bio,
Journal Year:
2024,
Volume and Issue:
27, P. 101136 - 101136
Published: June 22, 2024
Tumor
mRNA
vaccines
present
a
personalized
approach
in
cancer
immunotherapy,
encoding
distinct
tumor
antigens
to
evoke
robust
immune
responses
and
offering
the
potential
against
emerging
variants.
Despite
this,
clinical
advancement
of
has
been
hampered
by
their
limited
delivery
capacity
inefficient
activation
antigen-presenting
cells
(APCs).
Herein,
we
employed
microfluidics
technology
engineer
mannose-modified
lipid-based
nanovaccines
for
specifically
targeting
APCs.
The
encapsulation
process
efficiently
entrapped
cyclic
guanosine
monophosphate-adenosine
monophosphate
(cGAMP)
agonist
along
with
antigens.
targeted
(TNVs)
exhibited
narrow
particle
size
distribution,
ensuring
consistent
efficient
delivery.
These
TNVs
significantly
enhanced
gene
expression
mRNA,
facilitating
antigen
presentation
activation.
When
compared
non-targeted
nanovaccines,
outperformed
terms
Furthermore,
combination
anti-PD-L1
antibodies
elicited
synergistic
anti-tumor
effect.
This
was
attributed
antibodies'
ability
overcome
suppression
cells.
Our
findings
suggest
that
treatment
most
memory
results
indicate
integrating
checkpoint
inhibitors
or
other
immunostimulatory
agents
may
be
crucial
enhancing
response.