Angewandte Chemie,
Год журнала:
2024,
Номер
136(31)
Опубликована: Май 20, 2024
Abstract
Dithioacetals
are
heavily
used
in
organic,
material
and
medical
chemistries,
exhibit
huge
potential
to
synthesize
degradable
or
recyclable
polymers.
However,
the
current
synthetic
approaches
of
dithioacetals
polydithioacetals
overwhelmingly
dependent
on
external
catalysts
organic
solvents.
Herein,
we
disclose
a
catalyst‐
solvent‐free
acetal‐thiol
click‐like
reaction
for
synthesizing
polydithioacetals.
High
conversion,
higher
than
acid
catalytic
reaction,
can
be
achieved.
universality
was
confirmed
by
monitoring
reactions
linear
cyclic
acetals
(including
renewable
bio‐sourced
furan‐acetal)
with
aliphatic
aromatic
thiols,
mechanism
monomolecular
nucleophilic
substitution
(S
N
1)
auto‐protonation
(activation)
thiol
clarified
combining
experiments
density
functional
theory
computation.
Subsequently,
utilize
this
readily
By
simple
heating
stirring,
w
~110
kDa
were
synthesized
from
acetal
dithiol,
depolymerization
into
macrocyclic
dithioacetal
repolymerization
polydithioacetal
achieved;
through
reactive
extrusion,
semi‐interpenetrating
polymer
dynamic
network
excellent
mechanical
properties
continuous
reprocessability
prepared
poly(vinyl
butyral)
pentaerythritol
tetrakis(3‐mercaptopropionate).
This
green
high‐efficient
synthesis
method
is
beneficial
sustainable
development
chemistry.
Advanced Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 7, 2025
Abstract
Colorectal
cancer
(CRC)
ranks
as
the
third
most
prevalent
worldwide.
It
is
associated
with
imbalanced
gut
microbiota.
Probiotics
can
help
restore
this
balance,
potentially
reducing
risk
of
CRC.
However,
hostile
environment
and
constant
changes
in
gastrointestinal
tract
pose
significant
challenges
to
efficient
delivery
probiotics
colon.
Traditional
methods
are
often
insufficient
due
their
low
viability
lack
targeting.
To
address
these
challenges,
researchers
increasingly
focusing
on
innovative
encapsulation
technologies.
One
such
approach
single‐cell
encapsulation,
which
involves
applying
nanocoatings
individual
probiotic
cells.
This
technique
improve
resistance
harsh
environment,
enhance
mucosal
adhesion,
facilitate
targeted
release,
thereby
increasing
effectiveness
delivery.
article
reviews
latest
developments
for
CRC
treatment,
emphasizing
potential
benefits
emerging
techniques.
also
analyzes
compares
advantages
disadvantages
current
Furthermore,
it
elucidates
underlying
mechanisms
through
prevent
treat
CRC,
evaluates
efficacy
safety
treatment
adjuvant
therapy,
discusses
future
directions
prevention.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 7, 2024
Probiotics
offer
promising
results
for
treating
inflammatory
bowel
disease,
yet
precision
therapy
remains
challenging,
particularly
in
manipulating
probiotics
spatially
and
temporally
shielding
them
from
oxidative
stress.
To
address
these
limitations,
herein
we
synthesized
bacteria-specific
DNA
nanopatches
to
modify
ultrasound-triggered
engineered
Proceedings of the National Academy of Sciences,
Год журнала:
2024,
Номер
121(52)
Опубликована: Дек. 16, 2024
Inflammatory
bowel
disease
(IBD)
is
often
associated
with
excessive
inflammatory
response
and
highly
dysregulated
gut
microbiota.
Traditional
treatments
utilize
drugs
to
manage
inflammation,
potentially
probiotic
therapy
as
an
adjuvant.
However,
current
standard
practices
suffer
from
detrimental
side
effects,
low
bioavailability,
unsatisfactory
therapeutic
outcomes.
Microbial
complexes
characterized
by
mutually
beneficial
symbiosis
hold
great
promise
for
IBD
therapy.
Here,
we
aggregated
Synechocystis
sp.
PCC6803
(Sp)
Bacillus
subtilis
(BS)
biomimetic
mineralization
form
cyanobacteria–probiotics
symbionts
(ASp@BS),
which
reshaped
a
healthy
immune
system
microbiota
in
murine
model
of
acute
colitis.
The
exhibited
excellent
tolerance
the
harsh
environment
gastrointestinal
tract.
Importantly,
probiotics
within
created
local
anaerobic
activate
[NiFe]-hydrogenase
enzyme
cyanobacteria,
facilitating
production
hydrogen
gas
(H
2
)
persistently
scavenge
elevated
reactive
oxygen
species
alleviate
factors.
resulting
reduced
inflammation
improves
viability
efficiently
regulate
reshape
intestinal
barrier
functions.
Our
research
elucidates
that
ASp@BS
leverages
synergistic
interaction
between
Sp
BS
create
platform
addresses
multiple
aspects
IBD,
offering
promising
comprehensive
solution
treatment.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(18), С. 9779 - 9779
Опубликована: Сен. 10, 2024
The
charge-reversal
nano-drug
delivery
system
(CRNDDS)
is
a
promising
for
delivering
chemotherapy
drugs
and
has
gained
widespread
application
in
cancer
treatment.
In
this
review,
we
summarize
the
recent
advancements
CRNDDSs
terms
of
We
also
delve
into
mechanism
CRNDDSs,
focusing
on
acid-responsive,
redox-responsive,
enzyme-responsive
mechanisms.
This
study
elucidates
how
these
systems
undergo
charge
transitions
response
to
specific
microenvironmental
stimuli
commonly
found
tumor
tissues.
Furthermore,
review
explores
pivotal
role
diagnosis
treatment,
their
potential
limitations.
By
leveraging
unique
physiological
characteristics
tumors,
such
as
acidic
pH,
redox
potential,
enzyme
activity,
demonstrate
enhanced
accumulation
penetration
at
sites,
resulting
improved
therapeutic
efficacy
diagnostic
accuracy.
implications
highlight
drug
novel
targeted
strategy
therapy
diagnosis.
The
potent
CRISPR-Cas9
technology
can
correct
genes
in
human
mutated
cells
to
achieve
the
treatment
of
multiple
diseases,
but
it
lacks
safe
and
effective
delivery
systems.
Herein,
we
proposed
an
oral
microto-nano
genome-editing
system
aiming
at
enteric
excessive
level
TNF-α
for
specific
gene
therapy
inflammatory
bowel
disease
(IBD).
This
editing
facilitated
assembly
Cas9/sgRNA
ribonucleoprotein
(RNP)
into
nanoclusters
(NCs)
through
bridging
disulfide
bonds.
RNP-NCs
were
subsequently
encapsulated
within
cell-targeted
lipopolysaccharide-deleted
outer
membrane
vesicles
(dOMVs)
sourced
from
Escherichia
coli
Nissle
1917,
which
further
shielded
by
layer
calcium
alginate
microspheres
(CAMs).
By
leveraging
protection
effect
CAMs,
administration
withstood
gastric
acid
degradation
upon
entry
stomach,
achieving
targeted
intestines
with
high
efficiency.
As
pH
gradually
rose,
microscale
CAMs
swelled
disintegrated,
releasing
nanoscale
dOMVs
intestines.
These
RNP-NCs@dOMVs
could
traverse
mucosal
barrier
target
macrophages
where
conditionally
activated
RNPs
effectively
perform
genomic
nucleus.
Such
systems
represent
a
promising
translational
platform
IBD.