Rapid Prototyping Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 25, 2024
Purpose
This
paper
aims
to
provide
a
full
introduction,
new
classification,
comparison
and
investigation
of
the
challenges
as
well
applications
layerless
3D
printing,
which
is
one
industry
4.0
pioneers.
Design/methodology/approach
Given
significance
novelty
uniform
more
than
250
publications
were
collected
reviewed
in
an
unbiased
clear
manner.
Findings
As
result,
majority
parts
printed
polymer
form
are
known
up
this
point.
In
novel
division
for
better
researchers’
comprehension,
printing
systems
classified
into
three
categories:
oxygen
inhibition
(OI),
liquid
lubrication
(LL)
photon
penetration
(PP),
each
was
thoroughly
investigated.
Furthermore,
these
approaches
evaluated
terms
speed,
precision
accuracy,
manufacturing
scale
cost.
Originality/value
The
parameters
approach
compared
independently,
then
practical
conducted
among
approaches.
Finally,
variety
technologies,
opportunities,
advantages
significant
method,
future
outlook
rapid
prototyping,
presented.
Advanced Healthcare Materials,
Journal Year:
2023,
Volume and Issue:
13(12)
Published: Oct. 23, 2023
Tissue
engineering
approaches
that
recapitulate
cartilage
biomechanical
properties
are
emerging
as
promising
methods
to
restore
the
function
of
injured
or
degenerated
tissue.
However,
despite
significant
progress
in
this
research
area,
generation
engineered
constructs
akin
native
counterparts
still
represents
an
unmet
challenge.
In
particular,
inability
accurately
reproduce
zonal
architecture
with
different
collagen
fibril
orientations
is
a
limitation.
The
arrangement
extracellular
matrix
(ECM)
plays
fundamental
role
determining
mechanical
and
biological
functions
study,
it
shown
novel
light-based
approach,
Filamented
Light
(FLight)
biofabrication,
can
be
used
generate
highly
porous,
3D
cell-instructive
anisotropic
lead
directional
deposition.
Using
photoclick-based
photoresin
optimized
for
tissue
engineering,
significantly
improved
maturation
cartilaginous
tissues
remarkable
native-like
demonstrated.
Tissue Engineering Part A,
Journal Year:
2024,
Volume and Issue:
30(13-14), P. 387 - 408
Published: Jan. 11, 2024
Bioprinting
describes
the
printing
of
biomaterials
and
cell-laden
or
cell-free
hydrogels
with
various
combinations
embedded
bioactive
molecules.
It
encompasses
precise
patterning
cells
to
create
scaffolds
for
different
biomedical
needs.
There
are
many
requirements
that
bioprinting
face,
it
is
ultimately
interplay
between
scaffold's
structure,
properties,
processing,
performance
will
lead
its
successful
translation.
Among
essential
properties
must
possess—adequate
appropriate
application-specific
chemical,
mechanical,
biological
performance—the
mechanical
behavior
hydrogel-based
bioprinted
key
their
stable
in
vivo
at
site
implantation.
Hydrogels
typically
constitute
main
scaffold
material
medium
biomolecules
very
soft,
often
lack
sufficient
stability,
which
reduces
printability
and,
therefore,
potential.
The
aim
this
review
article
highlight
reinforcement
strategies
used
approaches
achieve
enhanced
stability
bioinks
printed
scaffolds.
Enabling
robust
materials
processes
creation
truly
complex
remarkable
structures
could
accelerate
application
smart,
functional
settings.
a
powerful
tool
fabrication
3D
applications.
has
gained
tremendous
attention
recent
years,
bioink
library
expanding
include
more
combinations.
From
practical
perspective,
need
be
considered,
such
as
structure's
performances.
these,
constructs
critical
translation
into
clinic.
explore
stabilization
structures.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 21, 2025
Abstract
This
study
explores
the
application
of
photo-crosslinkable
gelatin
hydrogels
(constituting
GelSH
and
GelNB)
for
biofabrication
using
volumetric
additive
manufacturing
(VAM).
Three
variants
were
prepared,
yielding
degree
substitutions
(DS)
39%,
54%,
63%,
GelNB
with
a
DS
60%,
alongside
GelNB-GelSH
formulations
at
concentrations
5,
7.5,
10%
(w/v).
Physico-chemical
analyses
confirmed
that
these
variations
led
to
differences
in
mass
swelling
ratio
mechanical
properties.
VAM
enabled
fabrication
complex,
high-fidelity
3D
structures
from
optimized
formulations,
demonstrating
its
capacity
encapsulate
mesenchymal
stromal
cells
(MSCs)
within
biomimetic
matrix.
Compared
film
casted
constructs,
VAM-printed
scaffolds
exhibited
significantly
higher
ALP
activity
calcium
deposition,
confirming
effective
osteogenesis.
Conversely,
chondrogenic
adipogenic
differentiation
more
pronounced
groups
due
their
lower
crosslinking
density
compressive
elastic
modulus,
emphasizing
role
environment
guiding
cell
differentiation.
highlights
potential
produce
complex
functional
hydrogel
tissue
engineering,
lays
groundwork
future
work
on
finetuning
bioresin
enhance
across
multiple
lineages
various
engineering
applications,
including
softer
tissues.
Figure
investigates
(GelSH
(VAM)
biofabrication.
Different
influenced
produced
encapsulating
cells,
enhancing
osteogenesis
compared
film-cast
constructs.
The
findings
highlight
VAM’s
optimizing
bioresins
multi-lineage
differentiation,
Biofabrication,
Journal Year:
2025,
Volume and Issue:
17(2), P. 022008 - 022008
Published: Feb. 28, 2025
In
recent
years,
biofabrication
technologies
have
garnered
significant
attention
within
the
scientific
community
for
their
potential
to
create
advancedin
vitrocancer
models.
While
these
been
predominantly
applied
model
advanced
stages
of
cancer,
there
exists
a
pressing
need
develop
pertinent,
reproducible,
and
sensitive
3D
models
that
mimic
cancer
initiation
lesions
native
tissue
microenvironment.
Such
hold
profound
relevance
comprehending
intricacies
initiation,
devise
novel
strategies
early
intervention,
and/or
conduct
sophisticated
toxicology
assessments
putative
carcinogens.
Here,
we
will
explain
pivotal
factors
must
be
faithfully
recapitulated
when
constructing
models,
with
specific
focus
on
pancreatic
lesions.
By
synthesizing
current
state
research
in
this
field,
provide
insights
into
advances
breakthroughs.
Additionally,
delineate
key
technological
biological
challenges
necessitate
resolution
future
endeavors,
thereby
paving
way
more
accurate
insightfulin
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 18, 2025
Abstract
Vascularization
is
key
to
the
biofabrication
of
large‐scale
tissues.
Despite
progress,
there
remain
some
outstanding
challenges,
such
as
limited
vessel
density,
difficulty
in
fabricating
microvasculatures,
and
inhomogeneity
post‐seeding
cells.
Here,
a
new
form
bioink
called
microfiber‐templated
porogel
(µFTP)
introduced
engineer
vasculatures
down
filament
building
blocks
3D
bioprinted
hydrogels.
The
cell‐laden
sacrificial
microfibers
(diameter
ranges
from
50–150
µm)
are
embedded
template
tubular
voids
deliver
endothelial
cells
for
in‐situ
endothelialization.
inclusion
softening
hydrogel
retains
desirable
rheological
properties
extrusion‐based
bioprinting
well
inter‐contacted
extruded
filament.
Such
bioinks
can
be
printed
into
well‐defined
structure
with
tunable
porosities
up
55%.
Compared
conventional
bulk
counterpart,
µFTP
supports
significant
growth
spread
either
matrix
or
fibers,
free
post‐cell
seeding
procedure.
Furthermore,
scaffolds
based
on
seen
significantly
promote
in‐growth
blood
vessels
native
tissues
vivo.
approach
enables
engineering
bio‐interfaces
within
contributes
endothelialization
providing
versatile
tool
construction
customized
vascularized
tissue
models.
Trends in biotechnology,
Journal Year:
2024,
Volume and Issue:
42(6), P. 739 - 759
Published: Feb. 2, 2024
Organs-on-chips
(OoCs)
hold
promise
to
engineer
progressively
more
human-relevant
in
vitro
models
for
pharmaceutical
purposes.
Recent
developments
have
delivered
increasingly
sophisticated
designs,
yet
OoCs
still
lack
reproducing
the
inner
tissue
physiology
required
fully
resemble
native
human
body.
This
review
emphasizes
need
include
microarchitectural
and
microstructural
features,
discusses
promising
avenues
incorporate
well-defined
microarchitectures
down
single-cell
level.
We
highlight
how
their
integration
will
significantly
contribute
advancement
of
field
towards
highly
organized
structural
hierarchical
tissues-on-chip.
discuss
combination
state-of-the-art
micropatterning
technologies
achieve
resembling
human-intrinsic
complexity.
It
is
anticipated
that
these
innovations
yield
significant
advances
realization
next
generation
OoC
models.
Advanced Materials Technologies,
Journal Year:
2023,
Volume and Issue:
8(23)
Published: Oct. 6, 2023
Abstract
Tomographic
volumetric
additive
manufacturing
(VAM)
produces
arbitrary
3D
geometries
by
exposure
of
a
rotating
volume
photopolymer
resin
to
tomographically‐patterned
illumination.
This
enables
high
speed,
layer‐less
printing
parts
from
wide
range
photopolymers
not
amenable
layer‐by‐layer
processes.
Since
the
entire
geometry
is
produced
at
once
over
course
few
seconds
minutes,
molecular
diffusion
length
scales
become
significant
process.
Understanding
these
reaction
and
processes
imperative
for
advancing
VAM
usable
technology.
These
are
experimentally
very
difficult
monitor
measure.
Herein,
VirtualVAM
‐
simulation
framework
modeling
tomographic
process,
developed
validated.
simulates
reaction,
diffusion,
heat
generation
print
with
single‐voxel
resolution.
From
experimentally‐determined
input
parameters
set
images
projection,
able
generate
large
spatio‐temporal
data
any
given
print.
Using
VirtualVAM,
number
experimentally‐unattainable
aspects
process
investigated
such
as
conversion
profiles,
effect
oxygen,
stopping
time
determination.
also
optimization
patterns
further
improve
contrast
between
in‐part
out‐of‐part
delivered
dose.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 30, 2024
Abstract
Printing
human
tissue
constructs
replete
with
biomimetic
vascular
networks
is
of
growing
interest
for
and
organ
engineering.
While
it
now
possible
to
embed
perfusable
channels
within
acellular
densely
cellular
matrices,
they
lack
either
the
branching
or
multilayer
architecture
native
vessels.
Here,
we
report
a
generalizable
method
printing
hierarchical
soft
living
matrices.
We
vessels
into
granular
hydrogel
matrices
via
coaxial
embedded
(co-EMB3DP)
as
well
bulk
cardiac
tissues
sacrificial
writing
functional
(co-SWIFT).
Each
relies
on
an
extended
core-shell
printhead
that
promote
facile
interconnections
between
printed
Though
careful
optimization
multiple
inks
show
can
be
coaxially
printed,
which
possess
smooth
muscle
cell-laden
shell
surrounds
lumens.
Upon
seeding
these
confluent
layer
endothelial
cells,
exhibit
good
barrier
function.
As
final
demonstration,
construct
vascularized
composed
matrix
spheroids
derived
from
induced
pluripotent
stem
cells.
Importantly,
co-SWIFT
mature
under
perfusion,
beat
synchronously,
cardio-effective
drug
response
in
vitro.
This
advance
opens
new
avenues
scalable
biomanufacturing
organ-specific
testing,
disease
modeling,
therapeutic
use.