Difference between revisions of "Team:Pasteur Paris/Device"
ClaireDumont (Talk | contribs) |
|||
| Line 54: | Line 54: | ||
<div id="MainContent"> | <div id="MainContent"> | ||
<div class="block full"> | <div class="block full"> | ||
| − | <i><p>We designed a global | + | <i><p>We designed a global proposal, thinking of dimensions, materials, fabrication processes, always taking into consideration the industrial and medical feasibility and the user’s comfort. Our system includes an implantation stem featuring our engineered biofilm, an interface device to collect and process the signal from nerves, and also connect the future prosthesis. A charging station and an app are also part of our setup.</p></i> |
</div> | </div> | ||
<div class="block title" id="Implant"><h3 style="text-align: left;">Implanting a functional stem</h3></div> | <div class="block title" id="Implant"><h3 style="text-align: left;">Implanting a functional stem</h3></div> | ||
<div class="block full"> | <div class="block full"> | ||
| − | <p>To connect our device to the user’s stump, we designed | + | <p>To connect our device to the user’s stump, we designed a fully functional osseointegrated stem. |
</p> | </p> | ||
| − | <p>This internal device needs an extremely high precision for machining parts. Indeed, the biofilm and the membrane’s nanometric scales | + | <p>This internal device needs an extremely high precision for machining parts. Indeed, the biofilm and the membrane’s nanometric scales, coupled to necessity to extend a member, leads to constraining strength and precision’s placement. Directly in contact with bone, the sintered ceramic part links the bone and the titanium stem together (Figure1). Where the stem emerges from the bone, its diameter expands, increasing from 6 mm to 10 mm. The biofilm occupies the space in the few centimeters available between the bone and skin. It is contained by a nanoporous membrane. The latter, in PEDOT: PSS, is the surface upon which the nerves will come to fixate. This also allows the electric nerve current to be transformed into an electrical current on the membrane. This membrane is placed around the tube and will conduct the signal to the outside(Figure 2).</p> |
<p>The titanium implanted tube, which is biocompatible, has a resistance as measured by it Young’s modulo of 193 GPa, and a low density of 4510 Kg/M<sup>3</sup> compared to biocompatible stainless steel with 114 GPa and 800 Kg/M<sup>3</sup>. </p> | <p>The titanium implanted tube, which is biocompatible, has a resistance as measured by it Young’s modulo of 193 GPa, and a low density of 4510 Kg/M<sup>3</sup> compared to biocompatible stainless steel with 114 GPa and 800 Kg/M<sup>3</sup>. </p> | ||
</div> | </div> | ||
Revision as of 07:28, 14 October 2018
We designed a global proposal, thinking of dimensions, materials, fabrication processes, always taking into consideration the industrial and medical feasibility and the user’s comfort. Our system includes an implantation stem featuring our engineered biofilm, an interface device to collect and process the signal from nerves, and also connect the future prosthesis. A charging station and an app are also part of our setup.
Implanting a functional stem
To connect our device to the user’s stump, we designed a fully functional osseointegrated stem.
This internal device needs an extremely high precision for machining parts. Indeed, the biofilm and the membrane’s nanometric scales, coupled to necessity to extend a member, leads to constraining strength and precision’s placement. Directly in contact with bone, the sintered ceramic part links the bone and the titanium stem together (Figure1). Where the stem emerges from the bone, its diameter expands, increasing from 6 mm to 10 mm. The biofilm occupies the space in the few centimeters available between the bone and skin. It is contained by a nanoporous membrane. The latter, in PEDOT: PSS, is the surface upon which the nerves will come to fixate. This also allows the electric nerve current to be transformed into an electrical current on the membrane. This membrane is placed around the tube and will conduct the signal to the outside(Figure 2).
The titanium implanted tube, which is biocompatible, has a resistance as measured by it Young’s modulo of 193 GPa, and a low density of 4510 Kg/M3 compared to biocompatible stainless steel with 114 GPa and 800 Kg/M3.
Connecting the device to the stump
Once the nerves signal is conducted by the electrical wires, it has to be treated and amplified. This is done into an interface device placed between the stump and the bionic prosthesis.
As for the NeuronArch interface device, we chose ABS (Acrylonitrile-Butadiene-Styrene) as the main material. We wanted an injection moldable plastic to reduce the cost of machining as well as it offered the most interesting properties for our project, among all the available materials.
Charging and synchronizing the interface device
In order to recharge the NeuronArch device, we designed an induction charging box, that includes a power outlet connectable USB-C plug. The compatible loading station is made of ABS and is used for patient data synchronization. It also features a small elevation on the housing that allows the NeuronArch interface device to be perfectly engaged and stable while charging and synchronizing. For storing cables during transportation we anticipated an elastic strip on the back of the station.
Consulting and monitoring data
