Organoids-on-Chips Technology: Unveiling New Perspectives in Rare-Disease Research
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(9), P. 4367 - 4367
Published: May 4, 2025
The
scarcity
of
robust
models
and
therapeutic
options
for
rare
diseases
continues
to
hamper
their
preclinical
investigation.
Traditional
animal
two-dimensional
cell
cultures
are
limited
in
ability
replicate
human
heredity-associated
traits
complex
pathological
features.
Organoids-on-a-chip
approaches
open
up
new
frontiers
rare-disease
research
via
the
integration
organ
chips
organoid
technology.
This
integrative
strategy
offers
immense
opportunities
mimicry
disease-related
traits,
clarification
mechanisms
underlying
disease,
prediction
treatment
responses
a
highly
human-related
manner.
forward-looking
perspective
suggests
organoids
on
transformative
tools
parsing
pathogenesis,
accelerating
discovery,
bridging
gap
between
basic
precision
medicine.
Language: Английский
Coculture systems to study interactions between anaerobic bacteria and intestinal epithelium
Anaerobe,
Journal Year:
2025,
Volume and Issue:
unknown, P. 102949 - 102949
Published: Feb. 1, 2025
Language: Английский
Microfluidic organ-on-a-chip models for the gut–liver axis: from structural mimicry to functional insights
Weifeng Hu,
No information about this author
Yushen Wang,
No information about this author
Junlei Han
No information about this author
et al.
Biomaterials Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
review
discusses
advancements
in
organ-on-a-chip
models,
emphasizing
gut,
liver,
and
integrated
gut–liver
systems.
It
covers
their
applications
disease
modeling,
toxicity
testing,
drug
screening,
as
well
future
prospects.
Language: Английский
Innovative microfluidic model for investigating the intestinal mucus barrier: numerical and experimental perspectives
Drug Delivery and Translational Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 6, 2025
The
intestinal
mucus
layer
serves
as
a
critical
first
line
of
defense
against
external
agents,
functioning
barrier
to
the
absorption
drugs,
food,
and
pathogens.
While
numerous
in
vitro
studies
have
explored
role
preventing
particle
penetration,
effects
flowing
luminal
material,
dislodging
because
induced
shear
rate
by
lumen
material
interfacial
phenomena
remain
poorly
understood.
This
study
introduces
microfluidic
approach
simulate
interaction
between
layer.
successfully
measures
both
penetration
into
dislodgement
material.
A
biosimilar
model
(BSM)
Hank's
Balanced
Salt
Solution
(HBSS)
were
employed
mimics
human
fluid,
respectively.
To
investigate
effect
viscosity
on
pattern,
two
variants
used:
BSM-1,
representing
low-viscosity
model,
BSM-2,
high-viscosity
model.
velocity
fields
extracted
tracking
fluorescent
particles.
results
revealed
significant
differences
BSM-1
attributed
their
rheological
properties.
These
findings
further
confirmed
through
an
assessment
viscoelastic
properties
BSM
models.
utilized
COMSOL
Multiphysics
for
numerical
simulations,
predicting
experimental
outcomes
solving
fluid
flow
equations.
Physicochemical
characterizations
HBSS
performed
link
with
including
sweep
tests,
application
power-law
viscosity,
measurements
density
wettability.
proposes
platform
examining
low-
offer
valuable
insights
barrier's
response
stress.
validated
physicochemical
provide
foundation
future
rates
more
complex
geometries
diverse
conditions.
Language: Английский
Intelligent Manufacturing for Osteoarthritis Organoids
Xin Lyu,
No information about this author
Jian Wang,
No information about this author
Jiacan Su
No information about this author
et al.
Cell Proliferation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 26, 2025
ABSTRACT
Osteoarthritis
(OA)
is
the
most
prevalent
degenerative
joint
disease
worldwide,
imposing
a
substantial
global
burden.
However,
its
pathogenesis
remains
incompletely
understood,
and
effective
treatment
strategies
are
still
lacking.
Organoid
technology,
in
which
stem
cells
or
progenitor
self‐organise
into
miniature
tissue
structures
under
three‐dimensional
(3D)
culture
conditions,
provides
promising
vitro
platform
for
simulating
pathological
microenvironment
of
OA.
This
approach
can
be
employed
to
investigate
mechanisms,
carry
out
high‐throughput
drug
screening
facilitate
personalised
therapies.
review
summarises
structure,
OA
manifestations,
thereby
establishing
context
application
organoid
technology.
It
then
examines
components
arthrosis
system,
specifically
addressing
cartilage,
subchondral
bone,
synovium,
skeletal
muscle
ligament
organoids.
Furthermore,
it
details
various
constructing
organoids,
including
considerations
cell
selection,
classification
fabrication
techniques.
Notably,
this
introduces
concept
intelligent
manufacturing
organoids
by
incorporating
emerging
engineering
technologies
such
as
artificial
intelligence
(AI)
process,
forming
an
innovative
software
hardware
cluster.
Lastly,
discusses
challenges
currently
facing
highlights
future
directions
rapidly
evolving
field.
By
offering
comprehensive
overview
state‐of‐the‐art
methodologies
challenges,
anticipates
that
intelligent,
automated
will
expedite
fundamental
research,
discovery
translational
applications
orthopaedic
Language: Английский
Alginate-gelatin hydrogel scaffolds for establishing physiological barriers on a gut-brain-axis microchip
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 144084 - 144084
Published: May 1, 2025
Language: Английский
Ginsenoside Rb1 improves human nonalcoholic fatty liver disease with liver organoids-on-a-chip
Engineered Regeneration,
Journal Year:
2024,
Volume and Issue:
5(3), P. 283 - 294
Published: June 21, 2024
Non-alcoholic
fatty
liver
disease
(NAFLD),
a
type
of
for
which
no
treatment
is
currently
approved,
remains
major
concern
worldwide.
It
manifested
as
simple
hepatocyte
steatosis
and
can
develop
into
inflammation,
fibrosis,
cirrhosis
cancer
in
severe
cases.
However,
due
to
the
lack
appropriate
vitro
drug
testing
platforms,
an
in-depth
understanding
therapeutic
activity
ginsenoside
Rb1
NAFLD
challenging.
Here,
we
proposed
model
on
organoids
(LOs)-on-a-chip
platform
evaluate
effect
dynamic,
multi-condition
high-throughput
manner.
This
allowed
us
reshape
certain
features
such
multicellular
types
liver-specific
functions
physiology
human-relative
liver.
Free
acids
(FFAs)-induced
LOs
displayed
typical
pathological
characteristics
progression,
including
steatosis,
oxidative
stress,
lipid
peroxidation,
inflammation
fibrosis.
With
intervention,
these
be
significantly
improved,
may
provide
new
insights
potential
mechanisms
progression
suggest
clinical
implications
humans.
The
system
enables
formation,
differentiation,
function
serve
scalable,
sensitive
model,
potentially
expedite
discovery.
Language: Английский