Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(8), P. 4872 - 4931
Published: Jan. 1, 2021
This
review
comprehensively
summarises
stimulus-cleavable
linkers
from
various
research
areas
and
their
cleavage
mechanisms,
thus
provides
an
insightful
guideline
to
extend
potential
applications
controlled
drug
release
nanomaterials.
Journal of Nanobiotechnology,
Journal Year:
2018,
Volume and Issue:
16(1)
Published: Sept. 19, 2018
Nanomedicine
and
nano
delivery
systems
are
a
relatively
new
but
rapidly
developing
science
where
materials
in
the
nanoscale
range
employed
to
serve
as
means
of
diagnostic
tools
or
deliver
therapeutic
agents
specific
targeted
sites
controlled
manner.
Nanotechnology
offers
multiple
benefits
treating
chronic
human
diseases
by
site-specific,
target-oriented
precise
medicines.
Recently,
there
number
outstanding
applications
nanomedicine
(chemotherapeutic
agents,
biological
immunotherapeutic
etc.)
treatment
various
diseases.
The
current
review,
presents
an
updated
summary
recent
advances
field
nanomedicines
based
drug
through
comprehensive
scrutiny
discovery
application
nanomaterials
improving
both
efficacy
novel
old
drugs
(e.g.,
natural
products)
selective
diagnosis
disease
marker
molecules.
opportunities
challenges
from
synthetic/natural
sources
their
clinical
also
discussed.
In
addition,
we
have
included
information
regarding
trends
perspectives
area.
Journal of Controlled Release,
Journal Year:
2021,
Volume and Issue:
332, P. 312 - 336
Published: Feb. 27, 2021
Polymeric
micelles,
i.e.
aggregation
colloids
formed
in
solution
by
self-assembling
of
amphiphilic
polymers,
represent
an
innovative
tool
to
overcome
several
issues
related
drug
administration,
from
the
low
water-solubility
poor
permeability
across
biological
barriers.
With
respect
other
nanocarriers,
polymeric
micelles
generally
display
smaller
size,
easier
preparation
and
sterilization
processes,
good
solubilization
properties,
unfortunately
associated
with
a
lower
stability
fluids
more
complicated
characterization.
Particularly
challenging
is
study
their
interaction
environment,
essential
predict
real
vivo
behavior
after
administration.
In
this
review,
general
presentation
on
features
different
characterization
techniques
are
discussed,
ones
used
for
determination
basic
characteristics
(critical
micellar
concentration,
surface
charge,
morphology)
complex
approaches
figure
out
kinetic
stability,
release
presence
substrates
(fluids,
cells
tissues).
The
presented
(such
as
dynamic
light
scattering,
AFM,
cryo-TEM,
X-ray
FRET,
symmetrical
flow
field-flow
fractionation
(AF4)
density
ultracentrifugation),
each
one
own
advantages
limitations,
can
be
combined
achieve
deeper
comprehension
behavior.
set-up
validation
adequate
methods
description
starting
point
development
clinical
success.
Theranostics,
Journal Year:
2017,
Volume and Issue:
7(3), P. 538 - 558
Published: Jan. 1, 2017
The
development
of
traditional
tumor-targeted
drug
delivery
systems
based
on
EPR
effect
and
receptor-mediated
endocytosis
is
very
challenging
probably
because
the
biological
complexity
tumors
as
well
limitations
in
design
functional
nano-sized
systems.
Recently,
multistage
(Ms-DDS)
triggered
by
various
specific
tumor
microenvironment
stimuli
have
emerged
for
therapy
imaging.
In
response
to
differences
physiological
blood
circulation,
microenvironment,
intracellular
environment,
Ms-DDS
can
change
their
physicochemical
properties
(such
size,
hydrophobicity,
or
zeta
potential)
achieve
deeper
penetration,
enhanced
cellular
uptake,
timely
release,
effective
endosomal
escape.
Based
these
mechanisms,
could
deliver
maximum
quantity
drugs
therapeutic
targets
including
tissues,
cells,
subcellular
organelles
eventually
exhibit
highest
efficacy.
this
review,
we
expatiate
responsive
modes
stimuli,
introduce
recent
advances
nanoparticle
systems,
especially
multi-stimuli
discuss
functions,
effects,
prospects.
Chemical Society Reviews,
Journal Year:
2017,
Volume and Issue:
47(1), P. 28 - 52
Published: Oct. 23, 2017
Theranostic
systems
are
receiving
ever-increasing
attention
due
to
their
potential
therapeutic
utility,
imaging
enhancement
capability,
and
promise
for
advancing
the
field
of
personalized
medicine,
particularly
as
it
relates
diagnosis,
staging,
treatment
cancer.
In
this
Tutorial
Review,
we
provide
an
introduction
concepts
theranostic
drug
delivery
effected
via
use
conjugates
that
able
target
cancer
cells
selectively,
cytotoxic
chemotherapeutics,
produce
readily
monitored
signals
in
vitro
vivo.
The
underlying
design
concepts,
requiring
synthesis
composed
reporters,
masked
chemotherapeutic
drugs,
cleavable
linkers,
targeting
ligands,
discussed.
Particular
emphasis
is
placed
on
highlighting
benefits
fluorogenic
reaction-based
targeted
activated
both
therapy
by
cellular
entities,
e.g.,
thiols,
reactive
oxygen
species
enzymes,
which
present
at
relatively
elevated
levels
tumour
environments,
physiological
characteristics
cancer,
hypoxia
acidic
pH.
Also
discussed
external
stimulus,
such
light.
work
summarized
Review
will
help
define
role
reaction-based,
cancer-targeting
theranostics
may
have
discovery
efforts,
well
improving
our
understanding
uptake
release
mechanisms.
Advanced Science,
Journal Year:
2021,
Volume and Issue:
9(1)
Published: Nov. 19, 2021
Abstract
The
past
decades
have
witnessed
great
progress
in
cancer
immunotherapy,
which
has
profoundly
revolutionized
oncology,
whereas
low
patient
response
rates
and
potential
immune‐related
adverse
events
remain
major
clinical
challenges.
With
the
advantages
of
controlled
delivery
modular
flexibility,
nanomedicine
offered
opportunities
to
strengthen
antitumor
immune
responses
sensitize
tumor
immunotherapy.
Furthermore,
tumor‐microenvironment
(TME)‐responsive
been
demonstrated
achieve
specific
localized
amplification
tissue
a
safe
effective
manner,
increasing
immunotherapy
reducing
side
effects
simultaneously.
Here,
recent
TME‐responsive
for
is
summarized,
responds
signals
TME,
such
as
weak
acidity,
reductive
environment,
high‐level
reactive
oxygen
species,
hypoxia,
overexpressed
enzymes,
adenosine
triphosphate.
Moreover,
combine
nanomedicine‐based
therapy
immunotherapeutic
strategies
overcome
each
step
cancer‐immunity
cycle
enhance
discussed.
Finally,
existing
challenges
further
perspectives
this
rising
field
with
hope
improved
development
applications
are
Small,
Journal Year:
2019,
Volume and Issue:
15(45)
Published: Oct. 10, 2019
Abstract
Engineering
of
smart
photoactivated
nanomaterials
for
targeted
drug
delivery
systems
(DDS)
has
recently
attracted
considerable
research
interest
as
light
enables
precise
and
accurate
controlled
release
molecules
in
specific
diseased
cells
and/or
tissues
a
highly
spatial
temporal
manner.
In
general,
the
development
appropriate
light‐triggered
DDS
relies
on
processes
photolysis,
photoisomerization,
photo‐cross‐linking/un‐cross‐linking,
photoreduction,
which
are
normally
sensitive
to
ultraviolet
(UV)
or
visible
(Vis)
irradiation.
Considering
issues
poor
tissue
penetration
high
phototoxicity
these
high‐energy
photons
UV/Vis
light,
nanocarriers
have
been
developed
based
light‐response
low‐energy
photon
irradiation,
particular
wavelengths
located
near
infrared
(NIR)
range.
NIR
achieved
by
using
two‐photon
absorption
upconversion
processes.
Herein,
recent
advances
light‐responsive
nanoplatforms
reviewed,
covering
mechanism
responsive
small
polymers,
UV
Vis
nanocarriers,
nanocarriers.
NIR‐light
triggered
excitation
luminescence
strategies
is
also
included.
addition,
challenges
future
perspectives
highlighted.
Accounts of Chemical Research,
Journal Year:
2015,
Volume and Issue:
48(11), P. 2935 - 2946
Published: Oct. 29, 2015
Theranostics,
chemical
entities
designed
to
combine
therapeutic
effects
and
imaging
capability
within
one
molecular
system,
have
received
considerable
attention
in
recent
years.
Much
of
this
interest
reflects
the
promise
inherent
personalized
medicine,
including
disease-targeted
treatments
for
cancer
patients.
One
important
approach
realizing
latter
involves
development
so-called
theranostic
conjugates,
multicomponent
constructs
that
selectively
target
cells
deliver
cytotoxic
agents
while
producing
a
readily
detectable
signal
can
be
monitored
both
vitro
vivo.
This
requires
synthesis
relatively
complex
systems
comprising
reporters,
masked
chemotherapeutic
drugs,
cleavable
linkers,
targeting
ligands.
Ideally,
cleavage
process
should
take
place
or
near
activated
by
cellular
components
are
associated
with
states
specifically
expressed
at
higher
level
cells.
Among
linkers
currently
being
explored
construction
such
localizing
disulfide
bonds
particularly
attractive.
is
because
stable
most
blood
pools
but
efficiently
cleaved
thiols,
glutathione
(GSH)
thioredoxin
(Trx),
which
generally
found
elevated
levels
tumors.
When
linked
fluorophores,
changes
emission
intensity
shifts
maxima
typically
seen
upon
as
result
perturbations
internal
charge
transfer
(ICT)
processes.
In
well-designed
systems,
allows
facile
imaging.
Account,
we
summarize
our
studies
involving
disulfide-based
fluorescent
drug
delivery
preliminary
tests
their
biological
utility
To
date,
variety
agents,
doxorubicin,
gemcitabine,
camptothecin,
been
used
create
number
naphthalimide,
coumarin,
BODIPY,
rhodol,
Cy7.
The
resulting
core
(drug-disulfide-fluorophore)
further
any
several
site-localizing
entities,
galactose,
folate,
biotin,
RGD
(Arg-Gly-Asp)
peptide
sequence,
an
intrinsic
selectivity
over
normal
Site-specific
endogenous
thiols
serves
release
produce
easy-to-monitor
change
fluorescence
signature
cell.
On
basis
results
summarized
propose
cancer-targeting
theranostics
may
role
play
advancing
discovery
efforts,
well
improving
understanding
uptake
mechanisms.