ACS Nano,
Год журнала:
2020,
Номер
14(4), С. 5121 - 5134
Опубликована: Апрель 13, 2020
Supramolecular
nanomaterials
as
drug
carriers
have
recently
received
increasing
attention
due
to
their
intrinsic
merits
such
high
stability,
strong
inclusion
capability,
and
facile
modification
of
the
parental
structure;
however,
intelligent
ones
with
combined
capacities
long
blood
circulation,
highly
efficient
tumor
cell
uptake,
site-oriented
release
inside
cells
are
still
rather
limited.
Herein,
we
report
a
strategy
using
supramolecular
aggregation-induced
emission
(AIE)
nanodots
for
image-guided
delivery,
which
integrate
both
advantages
AIE
nanomaterials.
The
dots
prepared
by
host-guest
coassembly
matrix
metalloproteinase-2
(MMP-2)
sensitive
PEG-peptide
(PEG2000-RRRRRRRR
(R8)-PLGLAG-EKEKEKEKEKEK
(EK6))
functional
α-cyclodextrins
(α-CD)
derivatives
that
conjugated
anticancer
gemcitabine
(GEM)
far-red/near-infrared
fluorescent
rhodanine-3-acetic
acid-based
luminogen,
respectively.
realize
circulation
time
virtue
zwitterionic
stealth
peptide
EK6.
After
largely
accumulating
in
tissues
enhanced
permeability
retention
effect,
can
successively
respond
tumor-overexpressed
MMP-2
intracellular
reductive
microenvironment,
achieving
cancer
cellular
uptake
selective
GEM
within
cells,
thus
exhibit
excellent
inhibition
ability
subcutaneous
orthotopic
pancreatic
models.
Chemical Science,
Год журнала:
2024,
Номер
15(11), С. 4019 - 4030
Опубликована: Янв. 1, 2024
This
study
presents
a
new
type
of
boron
carrier
for
neutron
capture
therapy
that
integrates
imaging,
lung
cancer
targeting
drug
and
carborane,
showcases
an
impressive
therapeutic
efficacy
against
tumors
both
in
vitro
vivo
.
Accounts of Chemical Research,
Год журнала:
2019,
Номер
52(11), С. 3064 - 3074
Опубликована: Окт. 28, 2019
ConspectusFluorophore
probes
are
widely
used
for
bioimaging
in
cells,
tissues,
and
animals
as
well
monitoring
of
multiple
biological
processes
complex
environments.
Such
imaging
properties
allow
scientists
to
make
direct
visualizations
pathological
events
cellular
targets.
Conventional
fluorescent
molecules
have
been
developed
several
decades
achieved
great
successes,
but
their
emissions
often
weakened
or
quenched
at
high
concentrations
that
might
suffer
from
the
aggregation-caused
quenching
(ACQ)
effect,
which
reduces
efficiencies
applications.In
contrast
ACQ
aggregation-induced
emission
(AIE)
luminogens
(AIEgens)
display
much
higher
fluorescence
aggregated
states
possess
various
advantages
such
low
background,
long-term
tracking
ability,
strong
resistance
photobleaching.
Therefore,
AIEgens
employed
unique
building
blocks
biosensing
applications
fields
ions,
amino
acids,
carbohydrates,
DNAs/RNAs,
peptides/proteins,
organelles,
cancer
bacteria,
so
on.Quite
a
few
above
missions
accomplished
by
modular
peptide-modified
AIEgen
(MPAPs)
DNA-modified
(MDAPs)
because
capabilities
peptide
DNA
modules,
including
solubility,
biocompatibility,
recognition.
Meanwhile,
both
electrostatic
interactions
coupling
reactions
could
provide
efficient
methods
construct
different
MPAPs
MDAPs,
finally
resulting
large
variety
probes.
Those
exhibit
leading
features
detecting
nucleic
acids
proteins
mass
biomolecules.
For
example,
under
design,
modules
possessing
versatile
recognition
abilities
enable
detect
numerous
targets,
integrin
αvβ3,
aminopeptidase
N,
MMP-2,
MPO,
H2O2,
forth;
MDAP
mRNA
cells
tissue
chips,
suggesting
diagnostic
functions
clinical
samples.
Modular
design
offers
novel
strategy
generate
AIEgen-based
expedites
functional
biomacromolecules
research.
In
this
vein,
here
we
review
progress
on
MDAPs
most
recent
10
years
highlight
advanced
briefly
two
aspects:
(1)
detection
(2)
imaging.
By
use
MPAPs/MDAPs,
bioanalytes
can
be
efficiently
analyzed
directly
visualized
through
high-contrast
luminous
Compared
with
MPAPs,
quantities
limited
difficult
synthesis
long-length
strands.
future
work,
multifunctional
sequences
needed
explore
varieties
diverse
purposes.
At
end
Account,
some
deficiencies
challenges
mentioned
briging
more
attention
accelerate
development
Theranostics,
Год журнала:
2019,
Номер
9(11), С. 3223 - 3248
Опубликована: Янв. 1, 2019
Pathogenic
bacteria,
fungi
and
viruses
pose
serious
threats
to
the
human
health
under
appropriate
conditions.
There
are
many
rapid
sensitive
approaches
have
been
developed
for
identification
quantification
of
specific
pathogens,
but
challenges
still
exist.
Culture/colony
counting
polymerase
chain
reaction
classical
methods
used
pathogen
detection,
their
operations
time-consuming
laborious.
On
other
hand,
emergence
spread
multidrug-resistant
pathogens
is
another
global
threat.
It
thus
utmost
urgency
develop
new
therapeutic
agents
or
strategies.
Luminogens
with
aggregation-induced
emission
(AIEgens)
derived
supramolecular
systems
unique
optical
properties
as
fluorescent
probes
turn-on
sensing
high
sensitivity
specificity.
In
addition,
AIE-based
nanostructures
exhibit
excellent
photodynamic
inactivation
(PDI)
activity
in
aggregate,
offering
great
potential
not
only
light-up
diagnosis
pathogen,
also
image-guided
PDI
therapy
pathogenic
infection.
ACS Nano,
Год журнала:
2020,
Номер
14(4), С. 5121 - 5134
Опубликована: Апрель 13, 2020
Supramolecular
nanomaterials
as
drug
carriers
have
recently
received
increasing
attention
due
to
their
intrinsic
merits
such
high
stability,
strong
inclusion
capability,
and
facile
modification
of
the
parental
structure;
however,
intelligent
ones
with
combined
capacities
long
blood
circulation,
highly
efficient
tumor
cell
uptake,
site-oriented
release
inside
cells
are
still
rather
limited.
Herein,
we
report
a
strategy
using
supramolecular
aggregation-induced
emission
(AIE)
nanodots
for
image-guided
delivery,
which
integrate
both
advantages
AIE
nanomaterials.
The
dots
prepared
by
host-guest
coassembly
matrix
metalloproteinase-2
(MMP-2)
sensitive
PEG-peptide
(PEG2000-RRRRRRRR
(R8)-PLGLAG-EKEKEKEKEKEK
(EK6))
functional
α-cyclodextrins
(α-CD)
derivatives
that
conjugated
anticancer
gemcitabine
(GEM)
far-red/near-infrared
fluorescent
rhodanine-3-acetic
acid-based
luminogen,
respectively.
realize
circulation
time
virtue
zwitterionic
stealth
peptide
EK6.
After
largely
accumulating
in
tissues
enhanced
permeability
retention
effect,
can
successively
respond
tumor-overexpressed
MMP-2
intracellular
reductive
microenvironment,
achieving
cancer
cellular
uptake
selective
GEM
within
cells,
thus
exhibit
excellent
inhibition
ability
subcutaneous
orthotopic
pancreatic
models.