Nano Letters,
Journal Year:
2023,
Volume and Issue:
23(21), P. 9778 - 9787
Published: Oct. 25, 2023
The
development
of
precisely
engineered
vehicles
for
intracellular
delivery
and
the
controlled
release
payloads
remains
a
challenge.
DNA-based
nanomaterials
offer
promising
solution
based
on
A-T-G-C
alphabet-dictated
predictable
assembly
high
programmability.
Herein,
we
present
self-immolative
DNA
nanogel
vaccine,
which
can
be
tracelessly
released
in
compartments
activate
immune
response.
Three
building
blocks
with
cytosine-rich
overhang
domains
are
designed
to
self-assemble
into
framework
size.
Two
oligo
agonists
one
antigen
peptide
conjugated
via
an
acid-labile
chemical
linker.
Upon
internalization
acidic
endosomes,
formation
i-motif
configurations
leads
dissociation
vaccine.
linker
is
cleaved,
releasing
their
traceless
original
form
antigen-presenting
cells
This
study
presents
novel
strategy
constructing
platforms
intracellularly
stimuli-triggered
therapeutics.
ACS Nano,
Journal Year:
2022,
Volume and Issue:
16(12), P. 20975 - 20984
Published: Nov. 17, 2022
As
a
burgeoning
bioorthogonal
reaction,
the
fluoride-mediated
desilylation
is
capable
of
prodrug
activation.
However,
due
to
reactions
lack
cell
selectivity
and
unitary
therapy
modality,
this
strongly
impedes
their
biomedical
applications.
Herein,
we
construct
cancer
cell-selective
biomimetic
metal–organic
framework
(MOF)-F
platform
for
activation
enhanced
synergistic
chemodynamic
(CDT).
With
membranes
camouflage,
designed
nanocatalyst
displays
preferential
accumulation
homotypic
cells.
Then,
pH-responsive
releases
fluoride
ions
ferric
ions.
For
our
tert-butyldimethyl
silyl
(TBS)-hydroxycamptothecin
(TBSO-CPT),
can
desilylate
TBS
cleave
ether
linker
synthesize
OH-CPT
(10-hydroxycamptothecin)
drug
molecule,
which
effectively
kills
Intriguingly,
bioorthogonal-synthesized
upregulates
intracellular
H2O2
by
activating
nicotinamide
adenine
dinucleotide
phosphate
oxidase
(NOX),
amplifying
released
iron
induced
Fenton
reaction
CDT.
Both
in
vitro
vivo
studies
demonstrate
strategy
presents
versatile
fluoride-activated
catalyst
synthesis.
Our
work
may
accelerate
applications
chemistry.
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(7)
Published: Nov. 22, 2022
Abstract
Bioorthogonal
chemistry,
referring
to
the
rapid
and
selective
synthesis
of
imaging
and/or
therapeutic
molecules
in
live
animals
via
transition
metal‐mediated
non‐natural
chemical
transformation
without
disrupting
endogenous
reactions,
has
greatly
expanded
tools
techniques
for
biomedicine.
However,
owing
safety
concerns
associated
with
metal
toxicity,
selectivity,
sensitivity
stability,
efficient
bioorthogonal
reactions
that
can
be
reliably
executed
complex
biological
environments
remain
challenging.
In
this
study,
an
intelligent,
versatile
catalyst
based
on
ultrasmall
poly(acrylic
acid)‐modified
copper
nanocomplexes
(Cu@PAA
NCs)
achieve
high
spatiotemporal
catalytic
efficacy
is
established.
The
activity
Cu@PAA
NCs
reversibly
regulated
valence
state
interconversion
between
Cu(II)
Cu(I)
under
exogenous
ultrasound
irradiation,
promoting
off‐target
prodrug
activation
lesion
sites
through
Cu(I)‐catalyzed
azide–alkyne
cycloaddition
reaction.
Moreover,
ultrasound‐triggered
electron–hole
separation
endows
robust
sonosensitizing
ability
sonodynamic
therapy.
Furthermore,
exhibit
enhanced
contrast
magnetic
resonance
photoacoustic
imaging.
Notably,
renal‐clearable
intrinsically
benign
biocompatibility.
This
spatiotemporally
ultrasound‐mediated
catalysis
not
only
expands
repertoire
situ
agents
but
also
provides
a
new
avenue
disease
theranostics.
Nano Letters,
Journal Year:
2023,
Volume and Issue:
23(21), P. 9778 - 9787
Published: Oct. 25, 2023
The
development
of
precisely
engineered
vehicles
for
intracellular
delivery
and
the
controlled
release
payloads
remains
a
challenge.
DNA-based
nanomaterials
offer
promising
solution
based
on
A-T-G-C
alphabet-dictated
predictable
assembly
high
programmability.
Herein,
we
present
self-immolative
DNA
nanogel
vaccine,
which
can
be
tracelessly
released
in
compartments
activate
immune
response.
Three
building
blocks
with
cytosine-rich
overhang
domains
are
designed
to
self-assemble
into
framework
size.
Two
oligo
agonists
one
antigen
peptide
conjugated
via
an
acid-labile
chemical
linker.
Upon
internalization
acidic
endosomes,
formation
i-motif
configurations
leads
dissociation
vaccine.
linker
is
cleaved,
releasing
their
traceless
original
form
antigen-presenting
cells
This
study
presents
novel
strategy
constructing
platforms
intracellularly
stimuli-triggered
therapeutics.