PURPOSE: Porous Shape Memory Polymers (SMPs) are ideal candidates for the fabrication of defect fillers, able to support tissue regeneration via minimally invasive approaches. In this regard, control of pore size, shape and interconnection is required to achieve adequate nutrient transport and cell ingrowth. Here, we assessed the feasibility of the preparation of SMP porous structures and characterized their chemico-physical properties and in vitro cell response. METHODS: SMP scaffolds were obtained via solvent casting/particulate leaching of gelatin microspheres, prepared via oil/water emulsion. A solution of commercial polyether-urethane (MM-4520, Mitsubishi Heavy Industries) was cast on compacted microspheres and leached-off after polymer solvent evaporation. The obtained structures were characterized in terms of morphology (SEM and micro-CT), thermo-mechanical properties (DMTA), shape recovery behavior in compression mode, and in vitro cytocompatibility (MG63 Osteoblast-like cell line). RESULTS: The fabrication process enabled easy control of scaffold morphology, pore size, and pore shape by varying the gelatin microsphere morphology. Homogeneous spherical and interconnected pores have been achieved together with the preservation of shape memory ability, with recovery rate up to 90%. Regardless of pore dimensions, MG63 cells were observed adhering and spreading onto the inner surface of the scaffolds obtained for up to seven days of static in vitro tests. CONCLUSIONS: A new class of SMP porous structures has been obtained and tested in vitro: according to these preliminary results reported, SMP scaffolds can be further exploited in the design of a new class of implantable devices.
PURPOSE: Porous Shape Memory Polymers (SMPs) are ideal candidates for the fabrication of defect fillers, able to support tissue regeneration via minimally invasive approaches. In this regard, control of pore size, shape and interconnection is required to achieve adequate nutrient transport and cell ingrowth. Here, we assessed the feasibility of the preparation of SMP porous structures and characterized their chemico-physical properties and in vitro cell response. METHODS: SMP scaffolds were obtained via solvent casting/particulate leaching of gelatin microspheres, prepared via oil/water emulsion. A solution of commercial polyether-urethane (MM-4520, Mitsubishi Heavy Industries) was cast on compacted microspheres and leached-off after polymer solvent evaporation. The obtained structures were characterized in terms of morphology (SEM and micro-CT), thermo-mechanical properties (DMTA), shape recovery behavior in compression mode, and in vitro cytocompatibility (MG63 Osteoblast-like cell line). RESULTS: The fabrication process enabled easy control of scaffold morphology, pore size, and pore shape by varying the gelatin microsphere morphology. Homogeneous spherical and interconnected pores have been achieved together with the preservation of shape memory ability, with recovery rate up to 90%. Regardless of pore dimensions, MG63 cells were observed adhering and spreading onto the inner surface of the scaffolds obtained for up to seven days of static in vitro tests. CONCLUSIONS: A new class of SMP porous structures has been obtained and tested in vitro: according to these preliminary results reported, SMP scaffolds can be further exploited in the design of a new class of implantable devices.
Porous Shape Memory Polymers (SMPs) are ideal candidates for the fabrication of
defect fillers, able to support tissue regeneration via minimally invasive
approaches. In this regard, control of pore size, shape and interconnection is
required to achieve adequate nutrient transport and cell ingrowth. Here, we assessed
the feasibility of the preparation of SMP porous structures and characterized their
chemico-physical properties and in vitro cell response.
Methods
SMP scaffolds were obtained via solvent casting/particulate leaching of gelatin
microspheres, prepared via oil/water emulsion. A solution of commercial
polyether-urethane (MM-4520, Mitsubishi Heavy Industries) was cast on compacted
microspheres and leached-off after polymer solvent evaporation. The obtained
structures were characterized in terms of morphology (SEM and micro-CT),
thermo-mechanical properties (DMTA), shape recovery behavior in compression mode,
and in vitro cytocompatibility (MG63 Osteoblast-like cell line).
Results
The fabrication process enabled easy control of scaffold morphology, pore size, and
pore shape by varying the gelatin microsphere morphology. Homogeneous spherical and
interconnected pores have been achieved together with the preservation of shape
memory ability, with recovery rate up to 90%. Regardless of pore dimensions, MG63
cells were observed adhering and spreading onto the inner surface of the scaffolds
obtained for up to seven days of static in vitro tests.
Conclusions
A new class of SMP porous structures has been obtained and tested in vitro: according
to these preliminary results reported, SMP scaffolds can be further exploited in the
design of a new class of implantable devices.
Authors: Silvia Farè; Viviana Valtulina; Paola Petrini; Edoardo Alessandrini; Giampiero Pietrocola; M Cristina Tanzi; Pietro Speziale; Livia Visai Journal: J Biomed Mater Res A Date: 2005-04-01 Impact factor: 4.396
Authors: Carla M Haslauer; Matthew R Avery; Behnam Pourdeyhimi; Elizabeth G Loboa Journal: J Biomed Mater Res B Appl Biomater Date: 2014-09-17 Impact factor: 3.368
Authors: Piotr Rychter; Natalia Śmigiel-Gac; Elżbieta Pamuła; Anna Smola-Dmochowska; Henryk Janeczek; Wojciech Prochwicz; Piotr Dobrzyński Journal: Materials (Basel) Date: 2016-01-20 Impact factor: 3.623