Lipidic and Inorganic Nanoparticles for Targeted Glioblastoma Multiforme Therapy: Advances and Strategies
Micro,
Journal Year:
2025,
Volume and Issue:
5(1), P. 2 - 2
Published: Jan. 3, 2025
Due
to
their
biocompatibility,
nontoxicity,
and
surface
conjugation
properties,
nanomaterials
are
effective
nanocarriers
capable
of
encapsulating
chemotherapeutic
drugs
facilitating
targeted
delivery
across
the
blood–brain
barrier
(BBB).
Although
research
on
nanoparticles
for
brain
cancer
treatment
is
still
in
its
early
stages,
these
systems
hold
great
potential
revolutionize
drug
delivery.
Glioblastoma
multiforme
(GBM)
one
most
common
lethal
tumors,
heterogeneous
aggressive
nature
complicates
current
treatments,
which
primarily
rely
surgery.
One
significant
obstacles
poor
penetration
BBB.
Moreover,
GBM
often
referred
as
a
“cold”
tumor,
characterized
by
an
immunosuppressive
tumor
microenvironment
(TME)
minimal
immune
cell
infiltration,
limits
effectiveness
immunotherapies.
Therefore,
developing
novel,
more
treatments
critical
improving
survival
rate
patients.
Current
strategies
enhancing
outcomes
focus
controlled,
agents
cells
BBB
using
nanoparticles.
These
therapies
must
be
designed
engage
specialized
transport
systems,
allowing
efficient
penetration,
improved
therapeutic
efficacy,
reduced
systemic
toxicity
degradation.
Lipid
inorganic
can
enhance
while
minimizing
side
effects.
formulations
may
include
epitopes—small
antigen
fragments
that
bind
directly
free
antibodies,
B
receptors,
or
T
receptors—that
interact
with
enable
crossing,
thereby
boosting
efficacy.
Lipid-based
(LNPs),
such
liposomes,
niosomes,
solid
lipid
(SLNs),
nanostructured
carriers
(NLCs),
among
promising
due
unique
including
size,
modification
capabilities,
proven
biosafety.
Additionally,
gold
nanoparticles,
mesoporous
silica,
superparamagnetic
iron
oxide
dendrimers
offer
alternatives.
Inorganic
(INPs)
easily
engineered,
surfaces
modified
various
elements
biological
ligands
delivery,
biocompatibility.
Strategies
engineering
functionalization
have
been
employed
ensure
biocompatibility
reduce
cytotoxicity,
making
safer
clinical
applications.
The
use
INPs
has
shown
promise
efficacy
traditional
like
chemotherapy,
radiotherapy,
gene
therapy,
well
advancing
newer
strategies,
immunotherapy,
photothermal
photodynamic
therapies,
magnetic
hyperthermia.
This
article
reviews
latest
treating
GBM,
focusing
active
passive
targeting
approaches.
Language: Английский
Progress in Drug Delivery Systems Based on Nanoparticles for Improved Glioblastoma Therapy: Addressing Challenges and Investigating Opportunities
Cancers,
Journal Year:
2025,
Volume and Issue:
17(4), P. 701 - 701
Published: Feb. 19, 2025
Glioblastoma
multiforme
(GBM)
is
a
highly
malignant
brain
tumor
that
has
bleak
outlook
despite
existing
treatments
such
as
surgery,
radiation,
and
chemotherapy.
The
utilization
of
nanoparticles
for
drug
delivery
presents
promising
method
by
which
to
improve
the
effectiveness
treatment
while
reducing
harmful
effects
on
entire
body.
This
review
examines
application
in
GBM,
focusing
different
types
nanoparticles,
including
lipid-based,
polymeric,
metallic,
those
under
development.
Every
variety
analyzed
its
distinct
characteristics
therapeutic
capacity.
Lipid-based
liposomes
solid
lipid
enhance
transport
medicines
are
not
soluble
water
have
shown
considerable
potential
preclinical
investigations.
Polymeric
benefits
terms
controlled
release
targeted
distribution,
whereas
metallic
both
therapy
imaging.
In
current
we
would
like
emphasize
ways
medicine
delivery,
specifically
enhancing
penetration
blood-brain
barrier
(BBB),
targeting
tumors,
enabling
release.
Additionally,
also
discuss
clinical
discoveries,
highlighting
achievements
obstacles
process
converting
these
technologies
into
effective
GBM.
study
offers
thorough
examination
present
status
prospects
Language: Английский
INFLUENCE OF DRUG DELIVERY SYSTEMS ON THE SAFETY AND EFFECTIVENESS PROFILE OF RIBAVIRIN
International Journal of Applied Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
unknown, P. 65 - 77
Published: March 7, 2025
Ribavirin
is
an
antiviral
drug
with
a
wide
spectrum
of
pharmacological
activity.
The
development
delivery
systems
that
increase
the
safety
and
effectiveness
ribavirin
has
been
subject
scientific
research
for
decades.
aim
this
article
to
examine
published
information
on
topic,
evaluate
it
according
several
criteria,
outline
primary
perspectives
within
fields
pharmacy
pharmacology.
results
evaluation
indicate
that,
despite
extensive
ongoing
discourse
surrounding
potential
modifications
international
community,
majority
publications
adopt
illustrative
approach.
Many
relevant
promising
applied
studies
require
further
development,
comprehensive
biopharmaceutical
indicator
testing,
rigorous
clinical
efficacy
assessment,
thorough
patient
compliance.
Language: Английский
Development and In Vitro and In Vivo Efficacy Investigation of Multifunctional, Targeted, Theranostic Liposomes for Imaging and Photodynamic Therapy of Glioblastoma
Journal of Drug Delivery Science and Technology,
Journal Year:
2024,
Volume and Issue:
101, P. 106236 - 106236
Published: Oct. 5, 2024
Language: Английский
Trivalent Disulfide Unit-Masked System Efficiently Delivers Large Oligonucleotide
Lei Wang,
No information about this author
Xiao Liu,
No information about this author
Yiliang Wu
No information about this author
et al.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(17), P. 4223 - 4223
Published: Sept. 5, 2024
Oligonucleotide
drugs
are
shining
in
clinical
therapeutics,
but
efficient
and
safe
delivery
systems
severely
limit
their
widespread
use.
A
disulfide
unit
technology
platform
based
on
dynamic
thiol
exchange
chemistry
at
the
cell
membrane
has
potential
for
drug
delivery.
However,
alteration
of
CSSC
dihedral
angle
induced
by
different
substituents
directly
affects
effectiveness
this
its
stability.
Previously,
we
constructed
a
trivalent
low
that
can
effectively
promote
cellular
uptake
small
molecules.
Here,
novel
unit-masked
oligonucleotide
hybrid
unit,
motivated
prodrug
design.
Cellular
imaging
results
showed
such
system
exhibited
superior
efficiency
than
commercial
Lipo2000
without
cytotoxicity.
The
reagents
significantly
reduced
(57–74%),
which
proved
to
be
endocytosis-independent.
In
addition,
vivo
distribution
experiments
mice
rapidly
distributed
liver
tissues
with
duration
action
more
24
h,
representing
means
silencing
genes
involved
pathogenesis
liver-like
diseases.
conclusion,
deliver
large
drugs.
Language: Английский