Nanomedicine,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 15
Published: Dec. 16, 2024
Poly
(β-amino
Ester)
nanocarriers
show
promise
for
gene
therapy,
but
their
effectiveness
can
be
limited
by
the
environment
within
body.
This
study
aims
to
understand
how
common
cell
culture
media
components
affect
optimized
PBAE
nanocarrier
performance
in
delivery.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(20), P. 15352 - 15352
Published: Oct. 19, 2023
Ocular
diseases
profoundly
impact
patients’
vision
and
overall
quality
of
life
globally.
However,
effective
ocular
drug
delivery
presents
formidable
challenges
within
clinical
pharmacology
biomaterial
science,
primarily
due
to
the
intricate
anatomical
physiological
barriers
unique
eye.
In
this
comprehensive
review,
we
aim
shed
light
on
features
eye,
emphasizing
natural
it
administration.
Our
goal
is
provide
a
thorough
overview
various
characteristics
inherent
each
nano-based
system.
These
encompass
nanomicelles,
nanoparticles,
nanosuspensions,
nanoemulsions,
microemulsions,
nanofibers,
dendrimers,
liposomes,
niosomes,
nanowafers,
contact
lenses,
hydrogels,
microneedles,
innovative
gene
therapy
approaches
employing
techniques.
We
delve
into
biology
methodology
these
systems,
introducing
their
applications
over
past
decade.
Furthermore,
discuss
advantages
illuminated
by
recent
studies.
While
systems
for
ophthalmic
formulations
are
gaining
increasing
attention,
further
research
imperative
address
potential
safety
toxicity
concerns.
Polymers,
Journal Year:
2024,
Volume and Issue:
16(14), P. 2075 - 2075
Published: July 20, 2024
Starch
is
a
promising
polymer
for
creating
novel
microparticulate
systems
with
superior
biocompatibility
and
controlled
drug
delivery
capabilities.
In
this
study,
we
synthesized
polyethylene
glycol
(PEG)-modified
starch
microparticles
encapsulated
folic
acid
using
solvent-mediated
acid-base
precipitation
method
magnetic
stirring,
which
simple
effective
method.
To
evaluate
particle
degradation,
simulated
physiological
conditions
by
employing
an
enzymatic
degradation
approach.
Our
results
FTIR
SEM
confirmed
the
successful
synthesis
of
starch–PEG
encapsulating
acid.
The
average
size
was
4.97
μm
increased
to
6.01
upon
modification
PEG.
were
first
exposed
amylase
at
pH
6.7
pepsin
1.5
different
incubation
times
temperature
shaking.
Post-degradation
analysis
revealed
changes
in
morphology,
indicating
degradation.
spectroscopy
used
assess
chemical
composition
before
after
initial
spectra
displayed
characteristic
peaks
starch,
PEG,
acid,
showed
decreased
intensities
suggesting
alterations
composition.
These
findings
demonstrate
ongoing
development
other
biomedical
applications
provide
basis
further
exploration
PEG–starch
as
versatile
biomaterial
bioactive
compounds.
Nano Futures,
Journal Year:
2024,
Volume and Issue:
8(3), P. 032001 - 032001
Published: Sept. 1, 2024
Abstract
The
new
strategies
in
this
regard
of
nanotechnology
and
biotechnology
guarantee
new,
efficient
modalities
for
cancer
therapy.
In
study,
we
explore
nanobiohybrids,
the
bacterium-targeted
treatment
approach
that
presents
a
category
therapeutic
carriers
treating
cancer.
We
specifically
focus
on
bacteriomimetics,
where
bacteria
are
used
as
natural
agents.
These
possess
ability
pathotropism
localizing
themselves
around
tumor
tissues,
even
hypoxic
areas
generally
refractory
to
standard
therapies.
By
engineering
surface
these
bacteria,
enhance
how
they
target
cells
so
is
delivered
microenvironment
with
no
or
minimal
systemic
side
effects.
Furthermore,
synthetic
nanoparticles
inculcated
into
bacterial
systems
stabilize
drugs
also
provide
way
controlled
release,
which
important
maintain
effectiveness.
Our
results
established
such
nanobiohybrids
capable
delivery
chemotherapeutic
agents
conducting
local
real-time
response
from
perspective
personalized
treatment.
This
research
implies
huge
development
targeted
therapy
against
cancer,
further
work
has
focused
optimizing
biohybrid
clinical
applications.
Pharmaceuticals,
Journal Year:
2023,
Volume and Issue:
16(12), P. 1700 - 1700
Published: Dec. 8, 2023
Among
the
different
types
of
nanosystems
that
have
been
investigated
for
therapeutic
use,
lipid-based
ones
are
most
explored,
as
they
advantages
over
non-lipid
nanosystems,
especially
improving
transport
and
efficacy
drugs
through
routes
administration,
such
ocular,
cutaneous,
intranasal,
intravenous
[...].
Journal of Ocular Pharmacology and Therapeutics,
Journal Year:
2023,
Volume and Issue:
39(8), P. 572 - 582
Published: Oct. 1, 2023
The
dynamic
and
continuously
evolving
field
of
ophthalmology
necessitates
rigorous
regulatory
oversight
in
the
United
States.
This
review
outlines
multifaceted
Food
Drug
Administration's
(FDA)
approval
process
for
ophthalmic
products,
detailing
classifications,
pathways,
compliance
devices,
drugs,
biologics,
combination
products.
Particular
emphasis
is
placed
on
distinct
frameworks
Class
I,
II,
III
as
well
regulations
organizational
structure
FDA
detailed,
with
highlights
specific
Ophthalmology
divisions,
historical
evolution,
initiatives
such
Patient-Focused
Development.
An
in-depth
examination
journey,
ranging
from
initial
research
to
post-marketing
surveillance,
includes
practical
guidance
through
stages
Pre-Investigational
New
Drug/Pre-Submission
consultations,
clinical
trials,
new
drug
application/biologics
license
application/premarket
submissions,
advisory
committee
interactions.
article
underscores
importance
early
interactions
health
authorities,
interdisciplinary
team
collaboration,
adherence
current
standards,
anticipation
policy
changes
ensure
patient
safety.
It
concludes
an
analysis
4
key
FDA-approved
including
Eylea®,
Luxturna®,
Alphagan
P®,
Raindrop®
Near
Vision
Inlay,
their
contributions
care
offering
valuable
insights
into
respective
potential
implications.
These
case
studies
are
included
illustrate
both
successful
failed
product
launches,
thereby
highlighting
alignment
compliance.