2009
DOI: 10.1088/0960-1317/19/7/074013
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A modular BioMEMS platform for new procedures and experiments in tissue engineering

Abstract: A modular BioMEMS platform for tissue engineering is presented. The smart combination of silicon, glass and polymers offers microenvironments with properties applicable to cultivation, observation and manipulation of cells. The implementation of the so-called ‘black silicon’ as a nanostructured surface allows easy mounting and assembly with standard polymer tubing and connectors only needing an extremely small additional volume as well as the smart integration of polymer scaffold structures. Parallelization of… Show more

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Cited by 7 publications
(7 citation statements)
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“…First, the results using MC3T3‐E1 cells seeded into the cultivation chamber by flushing in (Fig. 3A) show good viability, but spread uncontrollably all over the system's inner surfaces 6. In order to approach 3‐D cell cultivation, primary bovine chondrocytes were seeded on a scaffold (2 mm×2 mm 0.5 mm).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…First, the results using MC3T3‐E1 cells seeded into the cultivation chamber by flushing in (Fig. 3A) show good viability, but spread uncontrollably all over the system's inner surfaces 6. In order to approach 3‐D cell cultivation, primary bovine chondrocytes were seeded on a scaffold (2 mm×2 mm 0.5 mm).…”
Section: Resultsmentioning
confidence: 99%
“…Taking all these aspects into account, the general technology workflow has to be established long before the final design of the structures. Simple prototypes of our BioMEMS were fabricated, tested and published 6 in the past. A simplified, exemplary workflow for such cell‐cultivation BioMEMS is shown in Figure 1.…”
Section: Methodsmentioning
confidence: 99%
“…The overall dimensions (2 Â 2 Â 0.25 mm 3 , 1875 unit cells) of the cubic lattice scaffolds were adapted to the geometry of a flow-through chamber inside a microfluidic BioMEM, which was constructed for 4D analysis (x, y, z and time) of 3D cell cultures using TPLSM. [91,92] Even larger scaffolds with a volume of 8 Â 8 Â 2 mm 3 were produced by scaling up the unit cell dimensions to 500 mm (Fig. 6).…”
Section: Synthesis and Characterization Of Photopolymersmentioning
confidence: 99%
“…The front side of the substrate is covered with a glass wafer (Borofloat ® ) by anodic bonding to allow optical access and to close to the microfluidic chambers and channels. As said before, additional silicon components can be plugged into the microsystem from the backside via Velcro ® -like interface areas, see also [1]. They have got two functionalities.…”
Section: Biomemsmentioning
confidence: 99%