Journal of Materials Chemistry B,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
Pharmacotherapy
is
a
treatment
for
rheumatoid
arthritis
with
limitations,
such
as
poor
drug
targeting,
low
effective
dosage
at
the
inflammatory
site,
and
high
systemic
toxicity.
The
combined
application
of
drug-loaded
nanobubbles
ultrasound
technology
provides
new
technique
treatment.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Окт. 9, 2023
Abstract
Skeletal
disorders
are
commonly
diagnosed
by
X-ray
imaging,
but
the
radiation
limits
its
use.
Optical
imaging
through
near-infrared-II
window
(NIR-II,
1000–1700
nm)
can
penetrate
deep
tissues
without
risk,
targeting
of
contrast
agent
is
non-specific.
Here,
we
report
that
lanthanide-doped
nanocrystals
passively
target
bone
marrow,
which
be
effective
for
over
two
months.
We
therefore
develop
high-resolution
NIR-II
method
disease
diagnosis,
including
3D
instrumentation
to
show
intravital
morphology.
demonstrate
monitoring
1
mm
defects
with
spatial
resolution
comparable
result.
Moreover,
reveal
early
onset
inflammation
as
synovitis
in
stage
rheumatoid
arthritis,
micro
computed
tomography
(μCT)
diagnosis
osteoarthritis,
symptoms
osteophyte
and
hyperostosis
knee
joint.
Molecules,
Год журнала:
2023,
Номер
28(16), С. 6125 - 6125
Опубликована: Авг. 18, 2023
Rheumatoid
arthritis
(RA)
is
an
autoimmune
disease
characterized
by
bone
and
joint
degeneration.
Existing
anti-inflammatory
chemotherapy
drugs
offer
temporary
relief
but
come
with
undesirable
side
effects.
Herbal
medications
have
shown
positive
effects
on
RA
symptoms
minimal
adverse
reactions.
In
this
study,
we
investigated
the
potential
of
Nyctanthes
arbor-tristis
(NAT)
through
in
vitro
silico
research.
Hydroethanolic
extracts
harsingar
were
prepared
using
reflux
method,
containing
alkaloids,
phenol,
saponin,
steroids,
proteins,
tannins,
terpenoids,
carbohydrates,
glycosides,
flavonoids,
which
exhibited
TPC
(98.56
±
0.46
mg
GAE/g)
TFC
(34.51
0.45
CE/g).
LC–MS/MS
analyzes
active
compounds
extract.
NAT
best
scavenging
capabilities
at
1
mg/mL
anti-oxidant
anti-arthritic
activity.
Maximum
splenocyte
proliferation
occurred
250
µg/mL.
cell
studies
revealed
downregulation
TNF-α
upregulation
IL-10.
Additionally,
study
demonstrated
that
bioactive
constituents
targets
bind
favorable
binding
affinity.
These
findings
demonstrate
exerting
effects,
as
supported
studies.
Further
mechanistic
research
necessary
to
validate
therapeutic
all
phytoconstituents
treatment.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Фев. 13, 2024
Background:
Rheumatoid
arthritis
(RA)
is
an
erosive-destructive
inflammation
of
the
joints,
and
chronic,
long-term
stiffness
deformation
induced
by
RA
are
some
symptoms
that
difficult
to
treat.
Dexamethasone
(DEX)
melittin
(MLT)
two
interesting
anti-inflammatory
substances,
both
which
possess
effects
exerted
through
suppression
immune
system.
The
purpose
this
study
was
explore
role
MLT
in
treatment
DEX
as
well
clarify
influence
on
efficacy
side
DEX.
Method:
rats
were
injected
with
Complete
Freund’s
Adjuvant
(CFA)
induce
arthritis,
followed
different
doses
and/or
MLT.
relevant
indexes
paw
determined,
appetite,
growth
status,
cytokine
levels,
organ
coefficient
evaluated.
In
addition,
paraffin
sections
joint
tissues
prepared
analyze
pathological
changes.
Result:
exhibited
effects,
notably
hindering
feed
intake
growth,
inducing
lesions
rats.
significantly
reduced
promoted
its
efficacy.
combination
demonstrated
a
synergistic
treatment,
showing
advantages
detumescence
reduction,
pro-inflammatory
inhibition,
internal
improvement.
Conclusion:
Thus,
adjuvant
rats,
offering
approach
reduce
use
dosage
Molecules,
Год журнала:
2023,
Номер
28(6), С. 2483 - 2483
Опубликована: Март 8, 2023
Rheumatoid
arthritis
(RA)
is
a
chronic
and
autoimmune
disease
characterized
by
inflammation,
dysfunction,
cartilage
bone
destruction.
In
this
review,
we
summarized
the
available
reports
on
protective
effects
of
Ganoderma
lucidum
polysaccharides
(GLP)
RA
in
terms
anti-inflammatory,
immunomodulatory,
anti-angiogenic
osteoprotective
effects.
Firstly,
GLP
inhibits
synovial
fibroblast
(RASF)
proliferation
migration,
modulates
pro-
anti-inflammatory
cytokines
reduces
inflammation.
Secondly,
regulates
differentiation
antigen-presenting
cells
such
as
dendritic
cells,
phagocytosis
mononuclear
macrophages
nature
killer
(NK)
ratio
M1,
M2
related
inflammatory
cytokines.
addition,
produced
activities
balancing
humoral
cellular
immunity,
regulating
immunoglobulin
production,
modulating
T
B
lymphocyte
proliferative
responses
cytokine
release,
exhibiting
immunomodulatory
Thirdly,
angiogenesis
through
direct
inhibition
vascular
endothelial
cell
induction
death
indirect
growth
factor
(VEGF)
production
cells.
Finally,
can
inhibit
matrix
metalloproteinases
promote
osteoblast
formation,
exerting
articular
cartilage.
It
suggested
that
may
be
promising
agent
for
treatment
RA.
Journal of Chromatography B,
Год журнала:
2023,
Номер
1230, С. 123917 - 123917
Опубликована: Окт. 29, 2023
Janus
kinase
inhibitors
(JAKi)
are
oral
small
molecules
used
in
the
treatment
of
a
broad
spectrum
autoimmune
and
myeloproliferative
diseases.
JAKi
exhibit
significant
intra-
inter-individual
pharmacokinetic
variabilities,
due
to
fluctuations
compliance
with
treatments
their
metabolism
essentially
driven
by
cytochrome
P450
enzymes.
Intrinsically,
have
dose-response
relationship
narrow
therapeutic
index:
drug
monitoring
(TDM)
is
expected
optimize
adapt
dosage
regimen
order
resolve
problems
efficacy
tolerance
linked
dose
safety.
A
sensitive
analytical
method
using
multiplex
high-performance
liquid-chromatography
coupled
tandem
mass
spectrometry
(HPLC-MS/MS)
was
developed
validated
for
simultaneous
quantification
plasma
6
major
currently
JAKi,
namely
abrocitinib,
baricitinib,
fedratinib,
ruxolitinib,
tofacitinib,
upadacitinib.
Plasma
samples
subjected
protein
precipitation
MeOH,
stable
isotopically
labelled
internal
standards.
The
separation
supernatants
diluted
1:1
ultrapure
H2O
performed
C18
column
Xselect
HSS
T3
2.5
µm,
2.1x150
mm
mobile
phase
composed
formic
acid
(FA)
0.2%
acetonitrile
(+FA
0.1%)
gradient
mode.
run
time
assay
7
min.
drugs
were
monitored
electrospray
ionization
positive
mode
followed
triple-stage
quadrupole
MS/MS
analysis.
according
SFSTP
ICH
guidelines
over
clinically
relevant
concentration
ranges
(0.5-200
ng/mL
baricitinib
upadacitinib;
1-400
tofacitinib;
0.5-400
10-800
fedratinib).
This
HPLC-MS/MS
achieved
good
performances
term
trueness
(91.1-113.5%),
repeatability
(3.0-9.9%),
intermediate
precision
(4.5-11.3%).
We
highly
upadacitinib
human
plasma.
will
be
applied
prospective
clinical
studies
determine
whether
TDM
programs
based
on
residual
concentrations
can
recommended
disease-specific
ranges.
Frontiers in Molecular Biosciences,
Год журнала:
2024,
Номер
11
Опубликована: Март 7, 2024
The
heterocycle
compounds,
with
their
diverse
functionalities,
are
particularly
effective
in
inhibiting
Janus
kinases
(JAKs).
Therefore,
it
is
crucial
to
identify
the
correlation
between
complex
structures
and
biological
activities
for
development
of
new
drugs
treatment
rheumatoid
arthritis
(RA)
cancer.
In
this
study,
a
set
28
heterocyclic
compounds
selective
JAK1
JAK3
was
employed
construct
quantitative
structure-activity
relationship
(QSAR)
models
using
multiple
linear
regression
(MLR).
Artificial
neural
network
(ANN)
were
QSAR
models.
robustness
stability
assessed
through
internal
external
methodologies,
including
domain
applicability
(DoA).
molecular
descriptors
incorporated
into
model
exhibited
satisfactory
receptor-ligand
JAKs
observed
X-ray
crystallography,
making
interpretable
predictive.
Furthermore,
pharmacophore
ADRRR
ADHRR
designed
each
JAK3,
proving
discriminating
active
decoys.
Both
demonstrated
good
performance
identifying
an
ROC
0.83
0.75
model.
Using
model,
most
promising
selected
based
on
strong
affinity
compared
studied
series
JAK3.
Notably,
pharmacokinetic,
physicochemical
properties,
(As
ZINC79189223
ZINC66252348)
found
be
consistent
therapeutic
effects
RA,
owing
non-toxic,
cholinergic
nature,
absence
P-glycoprotein,
high
gastrointestinal
absorption,
ability
penetrate
blood-brain
barrier.
ADMET
properties
assessed,
dynamics
MM/GBSA
analysis
revealed
these
molecules.
Biomedicine & Pharmacotherapy,
Год журнала:
2024,
Номер
178, С. 117219 - 117219
Опубликована: Июль 30, 2024
A
transdermal
delivery
system
offers
high
bioavailability
and
favorable
patient
adherence,
constituting
an
optimal
approach
for
localized
administration
in
rheumatoid
arthritis
(RA)
treatment.
However,
the
stratum
corneum
(SC)
impedes
efficiency
of
conventional
drug
systems.
Microneedles
(MNs)
can
temporarily
create
micropores
within
SC,
enabling
distribution
via
bypassing
this
barrier
enhancing
effectiveness.
Notably,
MNs
provide
a
painless
method
through
skin
may
directly
modulate
inflammation
immune
cells
by
delivering
drugs
lymphatic
during
administration.
MN
is
not
suitable
with
low
water
solubility
stability.
Additionally,
major
concerns
exist
regarding
safety
using
highly
cytotoxic
drugs,
given
that
it
could
result
local
concentration
at
site.
While
exhibit
some
degree
targeted
to
inflammatory
environment,
their
targeting
remains
suboptimal.
Nanoformulations
have
potential
significantly
address
limitations
RA
treatment
improving
targeting,
solubility,
stability,
biocompatibility.
Therefore,
review
provides
concise
overview
advantages,
disadvantages,
mechanisms
different
types
It
specifically
focuses
on
application
advantages
combining
nanoformulation
summarizes
current
trends
development
nanoformulations
combined
field
treatment,
offering
theoretical
support
future
advancements
clinical
applications.