MICROBONE
"Multiscale poro-micromechanics of bone materials, with links to biology and medicine"
| Coordinatore | TECHNISCHE UNIVERSITAET WIEN
Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie. |
| Nazionalità Coordinatore | Austria [AT] |
| Totale costo | 1˙493˙399 € |
| EC contributo | 1˙493˙399 € |
| Programma | FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | ERC-2010-StG_20091028 |
| Funding Scheme | ERC-SG |
| Anno di inizio | 2010 |
| Periodo (anno-mese-giorno) | 2010-11-01 - 2015-10-31 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
TECHNISCHE UNIVERSITAET WIEN
Organization address
address: Karlsplatz 13 contact info |
AT (WIEN) | hostInstitution | 1˙493˙399.00 |
| 2 |
TECHNISCHE UNIVERSITAET WIEN
Organization address
address: Karlsplatz 13 contact info |
AT (WIEN) | hostInstitution | 1˙493˙399.00 |
Mappa
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Obiettivo del progetto (Objective)
'Modern computational engineering science allows for reliable design of the most breathtaking high-rise buildings, but it has hardly entered the fracture risk assessment of biological structures like bones. Is it only an engineering scientist's dream to decipher mathematically the origins and the evolution of the astonishingly varying mechanical properties of hierarchical biological materials? Not quite: By means of micromechanical theories, we could recently show in a quantitative fashion how 'universal' elementary building blocks (being independent of tissue type, species, age, or anatomical location) govern the elastic properties of bone materials across the entire vertebrate kingdom, from the super-molecular to the centimetre scale. Now is the time to drive forward these developments beyond elasticity, striving for scientific breakthroughs in multiscale bone strength. Through novel, experimentally validated micromechanical theories, we will aim at predicting tissue-specific inelastic properties of bone materials, from the 'universal' mechanical properties of the nanoscaled elementary components (hydroxyapatite, collagen, water), their tissue-specific dosages, and the 'universal' organizational patterns they build up. Moreover, we will extend cell population models of contemporary systems biology, towards biomineralization kinetics,in order to quantify evolutions of bone mass and composition in living organisms. When using these evolutions as input for the aforementioned micromechanics models, the latter will predict the mechanical implications of biological processes. This will open unprecedented avenues in bone disease therapies, including patient-specific bone fracture risk assessment relying on micromechanics-based Finite Element analyses.'