154 research outputs found
Fucoidan-based hydrogels particles as versatile carriers for diabetes treatment strategies
There is a current lack of fully efficient therapies for diabetes mel-litus, a chronic disease where the metabolism of blood glucose isseverely hindered by a deficit in insulin or cell resistance to thishormone. Therefore, it is crucial to develop new therapeutic strat-egies to treat this disease, including devices for the controlleddelivery of insulin or encapsulation of insulin-producing cells. Inthis work, fucoidan (Fu)â a marine sulfated polysaccharide exhib-iting relevant properties on reducing blood glucose and antioxi-dant and anti-inflammatory effectsâ was used for thedevelopment of versatile carriers envisaging diabetes advancedtherapies. Fu was functionalized by methacrylation (MFu) using8% and 12% (v/v) of methacrylic anhydride and further photo-crosslinked using visible light in the presence of triethanolamineand eosin-y to produce hydrogel particles. Degree of methacryla-tion varied between 2.78 and 6.50, as determined by1HNMR, andthe produced particles have an average diameter ranging from0.63 to 1.3mm (dry state). Insulin (5%) was added to MFu solutionto produce drug-loaded particles and the release profile wasassessed in phosphate buffer solution (PBS) and simulated intes-tinal fluid (SIF) for 24h. Insulin was released in a sustained man-ner during the initial 8 h, reaching then a plateau, higher in PBSthan in SIF, indicating that lower pH favors drug liberation.Moreover, the ability of MFu particles to serve as templates forthe culture of human pancreatic cells was assessed using 1.1B4cell line during up to 7 days. During the culture period studied,pancreatic beta cells were proliferating, with a global viabilityover 80% and tend to form pseudo-islets, thus suggesting thatthe proposed biomaterial could be a good candidate as versatilecarrier for diabetes treatment as they sustain the release of insulinand support pancreatic beta cells viability.We acknowledge ERDF for the financial support through POCTEP Project 0687_NOVOMAR_1_P, under the scope of INTERREG 2007-2013, and project 0302_CVMAR_I_1_P, under the scope of INTERREG Espana-Portugal 2014-2020, and Structured Projects NORTE-01-0145-FEDER-000021, NORTE-01-0145-FEDER-000023 and ATLANTIDA (ref. NORTE-01–0145-FEDER-000040), under the scope of Programa Operacional Regional do Norte (Norte 2020). Funding from the Portuguese Foundation for Science and Technology for doctoral grant (SFRH/BD/112139/2015) and post-doctoral grant (SFRH/BPD/85790/2012) is also acknowledge
Cartilage regeneration approach based on squid chitosan scaffolds : in-vitro assessment
During the past decades, marine organisms have been the focus of considerable attention as
potential source of valuable materials. For instance, chitosan is a biopolymer with high
potential in the biomedical field and can be produced from crustacean shells and squid pens
[1]. In this sense, we propose the use of chitosan to produce scaffolds for regenerative
medicine purposes. An alkaline solution was used to deproteinize squid pens and isolate β-
chitin (Chaussard 2004), which was further converted into chitosan through a deacetylation
reaction. Chitosan was then processed into porous structures by freeze-drying [3], where
chitosan solutions (4%) were submitted to different freezing temperature of -80ºC and -
196ºC. The produced structures were further submitted to neutralization methods with 4%
NaHO, including in some cases a pre-washing step using ethanol/water solutions (100:0;
90:10, 80:20; 70:30 and 50:50) [4]. The morphology of scaffolds produced using either squid
or commercial chitosan revealed a lamellar structure, independent of the source and/or
freezing temperature. All chitosan scaffolds produced exhibited no-cytotoxic behaviour over
L929 cells. To test the in vitro functionality of the scaffolds, cells from the mouse
chondrogenic cell line ATDC-5 were seeded in the scaffolds and cultured for different time
periods. Scaffolds made from squid chitosan were shown to promote better cell adhesion
than commercial chitosan scaffolds and comparable or better cell proliferation. This
demonstrates that squid chitosan is a valuable alternative to produce scaffolds for different
applications in regenerative medicine, namely the regeneration of cartilage
Valorization of chitosan from squid pens and further use on the development of scaffolds for biomedical applications
Objectives: The aim of the present work is the valorization of squid pens
through the production of chitosan that can be used for the development of biomedical
applications. The present work is focused on !-chitin extraction from
squid pens of the species Dosidicus gigas and its further conversion into chitosan.
The biomedical potential of the isolated squid chitosan was assessed by
processing this polymer as scaffolds for tissue engineering strategies.
Methods: Alkali solution was used to deproteinized squid pens and thus isolate
!-chitin, which was further converted into chitosan through a deacetylation reaction.
The chitosan scaffolds were developed using a freeze-drying process,
from 3% and 4% chitosan solutions in acetic acid and freezing at temperatures
of -80ºC and -196ºC. Chitosan scaffolds were neutralized using two different
methods: M1 – NaHO solution; and M2 – ethanol/water and NaHO solution.
Morphology, Mechanical properties, degradation, cytotoxicity (L929 cells) and
cellular adhesion (ATDC5 Chondrocytes like cells) of squid chitosan scaffolds
were assessed and compared with the properties of scaffolds produced with
commercial chitosan.
Results: The morphology of scaffolds revealed a lamellar structure for all produced
scaffolds, independent of the origin and concentration of chitosan. The
treatment with sodium hydroxide and ethanol caused the formation of larger
pores and loose of some lamellar features. Different freezing temperatures gave
different pore morphology and the lower temperature a smaller pore size. The
in vitro cell culture and cell adhesion studies showed that all chitosan scaffolds
exhibited a non-cytotoxic effect over the mouse fibroblast-like cell line, L929
cells.
Conclusions: The chitosan produced from the endoskeletons of giant squid
Dosidicus Gigas has proven to be a valuable alternative to the commercial one
when considering its use as biomaterial for different biomedical applications
Influence of freezing temperature and deacetylation degree on the performance of freeze-dried chitosan scaffolds towards cartilage tissue engineering
Chitosan-based porous structures have been significantly studied across the world as potential tissue engineering scaffolds. Despite the differences in chitosan produced from squid pens or crustacean shells, with the former being more reactive and easily available with a higher degree of deacetylation (DD), most of the studies report the use of crab or shrimp chitosan as they are readily available commercial sources. The aim of this work was to highlight the great potential of chitosan produced from squid pens for biomedical application. From freeze-dried scaffolds for soft tissue engineering, we investigated the influence of the DD of chitosan and the freezing temperature during processing on their performance. Chitosan was obtained by deacetylation of β-chitin previously isolated from endoskeleton of giant squid Dosidicus gigas (DD 91.2%) and compared with a commercially available batch obtained from crab shells (DD 76.6%). Chitosan solutions were frozen at â 80° C or â 196° C and further freeze-dried to obtain 3D porous structures (scaffolds). Scaffolds prepared at â 196° C have a compact structure with smaller pores, while those prepared at â 80° C showed a lamellar structure with larger pores. The compressive modulus varied from 0.7 up to 8.8 MPa. Both types of scaffolds were stable on PBS, including in the presence of lysozyme, up to 4 weeks. Furthermore, the squid chitosan scaffolds processed at â 80° C promoted ATDC5 chondrocyte-like cells adhesion and proliferation. The results suggest that the developed squid chitosan scaffolds might be further exploited for ap- plications in cartilage tissue engineering.This work was partially funded by ERDF through POCTEP Projects 0330_IBEROMARE_1_P and 0687_NOVOMAR_1_P, Atlantic
Area Project 2011-1/164 MARMED and by European Union through European Research Council – Project ComplexiTE (ERC-2012-ADG 20120216-321266). Portuguese Foundation for Science and Technology is gratefully acknowledged for post-doc grants of R.P.
Pirraco (SFRH/BPD/101886/2014) and S.S. Silva (SFRH/BPD/112140/2015) and PhD grant of Lara L. Reys (SFRH/BD/112139/2015). The authors would also like to acknowledge to Dr. Julio Maroto, from Fundación CETMAR (Spain) and Roi Vilela, from
PESCANOVA S.A. (Spain), for the kind offer of squid pens.info:eu-repo/semantics/publishedVersio
Development of marine-based nanocomposite scaffolds for biomedical applications
Despite
the
increasing
attention
that
marine
organisms
are
receiving,
many
of
those
are
not
efficiently
exploited
and
subproducts
with
valuable
compounds
are
being
discarded.
Two
examples
of
those
subproducts
are
the
endoskeleton
of
squid,
from
which
β-‐chitin
and
consecutively
chitosan
can
be
obtained;
and
fish-‐bones,
as
a
source
for
the
production
of
nano-‐
hydroxyapatite.
In
this
work,
inspired
in
the
nanocomposite
structure
of
human
bone,
marine-‐
based
nanocomposite
scaffolds
composed
by
chitosan
and
nano-‐hydroxyapatite
(nHA)
were
developed
using
particle
aggregation
methodology.
Chitosan
was
obtained
from
endoskeleton
of
giant
squid
Dosidicus
Gigas
while
fish
hydroxyapatite
nanoparticles
were
synthesized
from
fish-‐bones
by
pulsed
laser
in
deionized
water.
An
innovative
methodology
was
used
based
on
the
agglomeration
of
prefabricated
microspheres
of
chitosan/nHA,
generally
based
on
the
random
packing
of
microspheres
with
further
aggregation
by
physical
or
thermal
means
to
create
a
marine
nanocomposite
(CHA)
.The
morphological
analysis
of
the
developed
nanocomposites
revealed
a
low
porosity
structure,
but
with
high
interconnectivity,
for
all
produced
scaffolds.
Furthermore,
the
nanocomposite
scaffolds
were
characterized
in
terms
of
their
mechanical
properties,
bioactivity,
crystallinity
and
biological
behavior.
The
obtained
results
highlight
that
the
chitosan/nHA-‐based
marine
nanocomposite
can
be
a
good
candidate
for
biomedical
applications,
namely
on
bone
regeneration
Semiconductor gellan gum based composite hydrogels for tissue engineering applications
Publicado em "Journal of Tissue Engineering and Regenerative Medicine", vol. 7, supp. 1 (2013)Semiconductor hydrogels can be developed by combining the intrinsic
electrical properties of semiconductors with the specific characteristics
of hydrogels. These hydrogels have recently attracted much attention
for applications in tissue engineering, especially formulations incorporating
pyrrole and excellent biocompatibility. Several studies have
reported that electrical stimulation influences the migration, proliferation
and differentiation of stem cells and other cell lines [1]. The goal
of this work is to use in situ chemical polymerization of polypyrrole
(PPy) with gellan gum (GG) in order to obtain a new generation of
semiconductor composite hydrogels. For the synthesis of GG/PPy composites,
GG at 1.25% (w/v) final concentration was prepared in distilled
water at room temperature. The solution was then heated under
stirring at 90°C for 20 min. Temperature was decreased to 65°C and Py
was added under vigorous agitation. The crosslinker solution (CaCl2,
0.18%) was added at 50°C. After 2 h, GG/Py composite hydrogels
were obtained. In a further step, GG/Py samples were immersed in a
solution of oxidizing agent in PBS and the reaction was carried out for
18 h under agitation at room temperature. Finally, the samples were
frozen at -80°C for 48 h and lyophilized. The characterization of GG,
GG/PPy and PPy samples was performed by scanning electron microscopy
(SEM). The incorporation of PPy in the gellan gum was confirmed
by SEM analysis. The coating with PPy increases the thickness of each
sheet in 3 fold when compared with GG samples. Conductivity tests
were also performed. For cytotoxicity assay, the samples were rehydrated
with complete culture medium. MTS and DNA quantification assays
were performed to evaluate the metabolic activity and proliferation of
L929 fibroblast cells after 1, 3 and 7 days in culture with GG, GG/PPy
and PPy samples. MTS assays clearly indicate a proportional relation
between the cell viability and the PPy concentration: higher concentrations
of PPy resulted in lower cell viability. These results show that
lower concentration of PPy incorporated in the GG hydrogels can provide
an adequate electrical stimulus to improve cell behavior. In conclusion,
semiconductor hydrogels can be an excellent platform for tissue
engineering and electrochemical therapy application
Marine algae sulfated polysaccharides for tissue engineering and drug delivery approaches
Biomedical field is constantly requesting for new biomaterials, with innovative properties. Natural polymers appear as materials of election for this goal due to their biocompatibility and biodegradability. In particular, materials found in marine environment are of great interest since the chemical and biological diversity found in this environment is almost uncountable and continuously growing with the research in deeper waters. Moreover, there is also a slower risk of these materials to pose illnesses to humans.
In particular, sulfated polysaccharides can be found in marine environment, in different algae species. These polysaccharides don’t have equivalent in the terrestrial plants and resembles the chemical and biological properties of mammalian glycosaminoglycans. In this perspective, are receiving growing interest for application on health-related fields. On this review, we will focus on the biomedical applications of marine algae sulfated polymers, in particular on the development of innovative systems for tissue engineering and drug delivery approaches.European Regional Development Fund (ERDF)Fundação para a Ciência e a Tecnologia (FCT
The use of ionic liquids in the processing of chitosan/silk hydrogels for biomedical applications
Natural polymers are adequate renewable resources for the processability of well-defined architectures for
several applications. Combinations of polysaccharides and proteins may mimic the naturally occurring
environment of certain tissues. The main goal of this work renders the application of green chemistry
principles, namely the use of ionic liquids (ILs) and biorenewable sources, such as chitosan (CHT) and
silkfibroin (SF), to process new hydrogel-based constructs. Although the solubilization of both materials
in ILs has been studied individually, this work reports, for the first time, the role of ILs as solvent, for the
production of hydrogels from blends of chitosan and silkfibroin (CSF). These systems offer the
advantage of being homogeneous and presenting easy and short dissolution time of both
biomacromolecules. Moreover, the use of chitosan obtained fromα- andβ-chitin allowed the production
of blended hydrogels with distinct physical–chemical properties.In vitroassays demonstrated that these
hydrogels supported the adhesion and growth of primary human dermalfibroblasts. Taken these
properties together, the CSF hydrogels might be promising biomaterials to be explored for skin tissue
engineering approaches.Fundação para a Ciência e a Tecnologia FCT - SFRH/BPD/45307/2008, SFRH/BPD/
34704/2007, SFRH/BD/64601/2009, PTDC/QUI/68804/2006FEDER - POCTEP 0330_IBEROMARE_1_P
Materials of marine origin: a review on polymers and ceramics of biomedical interest
Marine organisms are constituted by materials with a vast range of properties and characteristics that may justify their potential application within the biomedical field. Moreover, assuring the sustainable exploitation of natural marine resources, the valorisation of residues from marine origin, like those obtained from food processing, constitutes a highly interesting platform for
development of novel biomaterials, with both economic and environmental benefits. In this perspective, an increasing number of different types of compounds are being isolated from aquatic organisms and transformed into profitable products for health applications, including controlled drug delivery and tissue engineering devices. This report reviews the work that is being developed on the isolation and characterisation of some polysaccharides, proteins, glycosaminoglycans and ceramics from marine raw materials. Emphasis is given to agar, alginates, carrageenans, chitin and chitosan, among other polysaccharides, collagen, glycosaminoglycans such as chondroitin sulphate, heparin and hyaluronic acid, calcium phosphorous compounds and biosilica. Finally, this report ends by reviewing the application of the previously mentioned materials on specific biomedical applications, in particular their participation on the development of controlled drug delivery systems and tissue engineering scaffolds.European Fund for Regional Development (EFRD)Fundação para a Ciência e a Tecnologia (FCT
Revealing the potential of squid chitosan-based structures for biomedical applications
In recent years, much attention has been given to different marine organisms, namely as potential sources of valuable materials with a vast range of properties and characteristics. In this work, β-chitin was isolated from the endoskeleton of the giant squid Dosidicus gigas and further deacetylated to produce chitosan. Then, the squid chitosan was processed into membranes and scaffolds using solvent casting and freeze-drying, respectively, to assess their potential biomedical application. The developed membranes have shown to be stiffer and less hydrophobic than those obtained with commercial chitosan. On the other hand, the morphological characterization of the developed scaffolds, by SEM and micro-computed tomography, revealed that the matrices were formed with a lamellar structure. The findings also indicated that the treatment with ethanol prior to neutralization with sodium hydroxide caused the formation of larger pores and loss of some lamellar features. The in vitro cell culture study has shown that all chitosan scaffolds exhibited a non-cytotoxic effect over the mouse fibroblast-like cell line, L929 cells. Thus, chitosan produced from the endoskeletons of the giant squid Dosidicus gigas has proven to be a valuable alternative to existing commercial materials when considering its use as biomaterial.This work was partially funded by FEDER through INTERREG III A Project Proteus and POCTEP Project IBEROMARE. The Portuguese Foundation for Science and Technology is gratefully acknowledged for post-doctoral grants of THS, JMO and SSS. The authors would also like to acknowledge to Dr Julio Maroto from the Fundacion CETMAR and Roi Vilela from PESCANOVA S.A, Spain, for the kind offer of squid pens and to Dr Ramon Novoa, Professor Ricardo Riguera and Professor Mariana Landin from the University of Santiago of Compostela for the SEC-MALLS measurements
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