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1.
Mater Sci Eng C Mater Biol Appl ; 62: 668-77, 2016 May.
Article in English | MEDLINE | ID: mdl-26952471

ABSTRACT

In the design of scaffolds for tissue engineering applications, morphological parameters such as pore size, shape, and interconnectivity, as well as transport properties, should always be tailored in view of their clinical application. In this work, we demonstrate that a regular and ordered porous texture is fundamental to achieve an even cell distribution within the scaffold under perfusion seeding. To prove our hypothesis, two sets of alginate scaffolds were fabricated using two different technological approaches of the same method: gas-in-liquid foam templating. In the first one, foam was obtained by insufflating argon in a solution of alginate and a surfactant under stirring. In the second one, foam was generated inside a flow-focusing microfluidic device under highly controlled and reproducible conditions. As a result, in the former case the derived scaffold (GF) was characterized by polydispersed pores and interconnects, while in the latter (µFL), the porous structure was highly regular both with respect to the spatial arrangement of pores and interconnects and their monodispersity. Cell seeding within perfusion bioreactors of the two scaffolds revealed that cell population inside µFL scaffolds was quantitatively higher than in GF. Furthermore, seeding efficiency data for µFL samples were characterized by a lower standard deviation, indicating higher reproducibility among replicates. Finally, these results were validated by simulation of local flow velocity (CFD) inside the scaffolds proving that µFL was around one order of magnitude more permeable than GF.


Subject(s)
Gases/chemistry , Microfluidic Analytical Techniques/methods , Tissue Scaffolds/chemistry , Alginates/chemistry , Bioreactors , Cell Line , Elastic Modulus , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Humans , Microfluidic Analytical Techniques/instrumentation , Microscopy, Electron, Scanning , Porosity , Spectroscopy, Fourier Transform Infrared , Surface-Active Agents/chemistry , X-Ray Microtomography
2.
ACS Appl Mater Interfaces ; 7(42): 23660-71, 2015 Oct 28.
Article in English | MEDLINE | ID: mdl-26436204

ABSTRACT

Ordered porous polymeric materials can be engineered to present highly ordered pore arrays and uniform and tunable pore size. These features prompted a number of applications in tissue engineering, generation of meta materials, and separation and purification of biomolecules and cells. Designing new and efficient vistas for the generation of ordered porous materials is an active area of research. Here we investigate the potential of microfluidic foaming within a flow-focusing (FF) geometry in producing 3D regular sponge-like polymeric matrices with tailored morphological and permeability properties. The challenge in using microfluidic systems for the generation of polymeric foams is in the high viscosity of the continuous phase. We demonstrate that as the viscosity of the aqueous solution increases, the accessible range of foam bubble fraction (Φb) and bubble diameter (Db) inside the microfluidic chip tend to narrow progressively. This effect limits the accessible range of geometric properties of the resulting materials. We further show that this problem can be rationally tackled by appropriate choice of the concentration of the polymer. We demonstrate that via such optimization, the microfluidic assisted synthesis of porous materials becomes a facile and versatile tool for generation of porous materials with a wide range of pore size and pore volume. Moreover, we demonstrate that the size of interconnects among pores-for a given value of the gas fraction-can be tailored through the variation of surfactant concentration. This, in turn, affects the permeability of the materials, a factor of key importance in flow-through applications and in tissue engineering.


Subject(s)
Biocompatible Materials/chemistry , Lab-On-A-Chip Devices , Surface-Active Agents/chemistry , Tissue Engineering , Permeability/drug effects , Polymers/chemistry , Tissue Scaffolds , Viscosity/drug effects
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