Abstract:Neural tissue engineering is one of the most promising approaches for healing nerve damage, which bypasses the limits of contemporary conventional treatments. In a previous study, we developed a fibrous scaffold via electrospinning poly (glycerol dodecanedioate) (PGD) and gelatin that mimics the structure of a native extracellular matrix (ECM) for soft tissue engineering application. In this study, fumaric acid (FA) was incorporated into the PGD synthesis process, which produced a PGD derivative referred to as… Show more
“…The PGD was synthesized by a recipe modified from the previously reported one. ,− In details, dodecanedioic acid (DDA, 99%, Alfa Aesar) and glycerol (>99%, synthetic, ACROS Organics) were purchased from Thermo Fisher Scientific and used without further purification. They were weighed with a 1:1 molar ratio and put into a three-necked flask for reaction.…”
Thermotropic polymers
with the capability of thermally tuning transparency are widely applied
in smart windows and energy-saving windows, playing a critical role
in enhancing comfort level and energy efficiency of indoor spaces.
Usually, thermotropic polymer systems are constructed by physically
dispersing phase transition materials in transparent hosting materials.
However, bad interfaces universally exist in these systems, resulting
in poor mechanical properties, weak interfaces to substrates, or bad
long-term stability. Herein, we demonstrate a novel chemically interconnected
thermotropic polymer, which is obtained by reacting dodecanedioic
acid (DDA) with glycerol. In the system, some of DDA molecules were
cross-linked to form a polyester network, poly(glycerol-dodecanoate)
(PGD). Other grafted but non-cross-linked DDA molecules form semicrystalline
domains, which possess a solid–liquid phase transition within
the PGD matrix. The phase transition offers the resulting hybrid materials
with tunable optical transparency. The PGD–DDA system shows
stable performance after 100 heating–cooling cycles. In addition,
when applied for window coating, it results in tough interfacial bonding
to glass substrates with toughness of >6910 J m–2 below its transition temperature and >135 J m–2 above its transition temperature. It increases the impact resistance
of the window by multiple times.
“…The PGD was synthesized by a recipe modified from the previously reported one. ,− In details, dodecanedioic acid (DDA, 99%, Alfa Aesar) and glycerol (>99%, synthetic, ACROS Organics) were purchased from Thermo Fisher Scientific and used without further purification. They were weighed with a 1:1 molar ratio and put into a three-necked flask for reaction.…”
Thermotropic polymers
with the capability of thermally tuning transparency are widely applied
in smart windows and energy-saving windows, playing a critical role
in enhancing comfort level and energy efficiency of indoor spaces.
Usually, thermotropic polymer systems are constructed by physically
dispersing phase transition materials in transparent hosting materials.
However, bad interfaces universally exist in these systems, resulting
in poor mechanical properties, weak interfaces to substrates, or bad
long-term stability. Herein, we demonstrate a novel chemically interconnected
thermotropic polymer, which is obtained by reacting dodecanedioic
acid (DDA) with glycerol. In the system, some of DDA molecules were
cross-linked to form a polyester network, poly(glycerol-dodecanoate)
(PGD). Other grafted but non-cross-linked DDA molecules form semicrystalline
domains, which possess a solid–liquid phase transition within
the PGD matrix. The phase transition offers the resulting hybrid materials
with tunable optical transparency. The PGD–DDA system shows
stable performance after 100 heating–cooling cycles. In addition,
when applied for window coating, it results in tough interfacial bonding
to glass substrates with toughness of >6910 J m–2 below its transition temperature and >135 J m–2 above its transition temperature. It increases the impact resistance
of the window by multiple times.
“…Recently, the appearance of in vitro models incorporating NSC niche elements has facilitated studies of individual factors in NSC fate specification and possible NSC applications in regenerative medicine. 17,18 Representative engineering methods used to build in vitro NSC niches include bioactive polymers functionalized with multivalent ligands or peptides, 19,20 synthetically or biologically derived hydrogels, 21,22 3D substrates at the microscale or nanoscale with different stiffness or topographical properties, 23,24 and genetically engineered ECMs for artificial niches. 25 However, the absence of physiologically realistic NSC niche models with precise spatiotemporal control and effective methods for evaluation has hindered research of NSC fates.…”
Neural stem cell (NSC) transplantation has great therapeutic potential for neurodegenerative diseases and central nervous system injuries. Successful NSC replacement therapy requires precise control over the cellular behaviors. However, the regulation of NSC fate is largely unclear, which severely restricts the potential clinical applications. To develop an effective model, we designed an assembled microfluidic system to engineer NSC niches and assessed the effects of various culture conditions on NSC fate determination. Five types of NSC microenvironments, including two-dimensional (2D) cellular monolayer culture, 2D cellular monolayer culture on the extracellular matrix (ECM), dispersed cells in the ECM, three-dimensional (3D) spheroid aggregates, and 3D spheroids cultured in the ECM, were constructed within an integrated microfluidic chip simultaneously. In addition, we evaluated the influence of static and perfusion culture on NSCs. The efficiency of this approach was evaluated comprehensively by characterization of NSC viability, self-renewal, proliferation, and differentiation into neurons, astrocytes, or oligodendrocytes. Differences in the status and fate of NSCs governed by the culture modes and micro-niches were analyzed. NSCs in the microfluidic device demonstrated good viability, the 3D culture in the ECM facilitated NSC self-renewal and proliferation, and 2D culture in the static state and spheroid culture under perfusion conditions benefited NSC differentiation. Regulation of NSC self-renewal and differentiation on this microfluidic device could provide NSC-based medicinal products and references for distinct nerve disease therapy.
“…In addition to the original formulation of PGD previously reported, electrospun mats of PGD, PGD modified with fumaric acid (PGDF), or gelatin‐blended PGD have been explored for neural tissue engineering. It is presently unclear, however, if the mechanical properties of PGD can be altered to produce shape memory materials with a range of tangent stiffness values to accommodate use within multiple soft tissues.…”
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