Team:Groningen/Template/MODULE/project/MBD/specifications&equations
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+ | Specifications | ||
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- | + | Most of the requirements were found by placing ourselves in the minds of end-users and derived from interviews with people working at the Martini hospital. | |
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+ | 1. Start-up: breaking of the water pockets and hydrating gel/activating L. lactis.<br> | ||
+ | 2. Operation: growth of L. lactis, detecting quorum molecules and secreting Nisin, AiiA, DspB.<br> | ||
+ | 3. Shut-down: nutrient depletion, cell destruction.<br> | ||
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+ | <th>Requirement</th><th>Value</th><th>Note</th> | ||
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+ | <td>Activation time</td><td>3 h</td><td>Time required for the gel to hydrate after water pockets have been broken to be fully hydrated.</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Therapeutic action time</td><td>4h</td><td>After being applied to the wound. Amount of time for reaching the inhibitory concentrations of nisin, DspB and AiiA to pass the bottom membrane and into the wound. </td> | ||
+ | </tr> | ||
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+ | <td>Inhibitory nisin concentration</td><td>2-16 ng/µL</td><td>This concentration can be used for both MRSA and VRE. Source: Nisin, alone and combined with peptidoglycan-modulating antibiotics: activity ……. Brumfitt, Salton, Hamilton-Miller.</td> | ||
+ | </tr> | ||
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+ | <td>Inhibitory AiiA concentration</td><td>15 ng/µL</td><td>How much is needed to inhibit growth of PA/SA?</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Inhibitory DspB concentration</td><td>15 ng/µL</td><td>How much is needed to inhibit growth of PA/SA?</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Operating temperature</td><td>20-40 °C</td><td></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Lifetime</td><td>3 days</td><td></td> | ||
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Latest revision as of 03:48, 18 October 2014
Bandage specifications & requirements
Specifications
1. Top layer: Transparent polymethylpentene membrane permeable to gases, flexible.
2. Middle layer: Polyacrylamide hydrogel containing the chemically defined media.
3. Bottom layer: This layer acts as barrier between the wound and the ''L. lactis'' cells. They are inactive since the gel is normally in dehydrated form. This layer consists of a cellulose nitrate membrane of pore size 0.2 micrometers, permeable to protein, being hydrophilic and flexible.
2. Middle layer: Polyacrylamide hydrogel containing the chemically defined media.
3. Bottom layer: This layer acts as barrier between the wound and the ''L. lactis'' cells. They are inactive since the gel is normally in dehydrated form. This layer consists of a cellulose nitrate membrane of pore size 0.2 micrometers, permeable to protein, being hydrophilic and flexible.
Requirements
Most of the requirements were found by placing ourselves in the minds of end-users and derived from interviews with people working at the Martini hospital.
1. Start-up: breaking of the water pockets and hydrating gel/activating L. lactis.
2. Operation: growth of L. lactis, detecting quorum molecules and secreting Nisin, AiiA, DspB.
3. Shut-down: nutrient depletion, cell destruction.
2. Operation: growth of L. lactis, detecting quorum molecules and secreting Nisin, AiiA, DspB.
3. Shut-down: nutrient depletion, cell destruction.
Requirement | Value | Note |
---|---|---|
Activation time | 3 h | Time required for the gel to hydrate after water pockets have been broken to be fully hydrated. |
Therapeutic action time | 4h | After being applied to the wound. Amount of time for reaching the inhibitory concentrations of nisin, DspB and AiiA to pass the bottom membrane and into the wound. |
Inhibitory nisin concentration | 2-16 ng/µL | This concentration can be used for both MRSA and VRE. Source: Nisin, alone and combined with peptidoglycan-modulating antibiotics: activity ……. Brumfitt, Salton, Hamilton-Miller. |
Inhibitory AiiA concentration | 15 ng/µL | How much is needed to inhibit growth of PA/SA? |
Inhibitory DspB concentration | 15 ng/µL | How much is needed to inhibit growth of PA/SA? |
Operating temperature | 20-40 °C | |
Lifetime | 3 days |
Equations