Difference between revisions of "Team:Warwick"

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      <h1>Blueprint 361</h1>
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      <p style="color:#99b3e6">Revolutionising Implants</p>
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                    <li class="active" role="presentation"><a href="#">Project </a></li>
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        <h1 class="text-center" style="color:rgb(247,247,247);height:94px;font-size:88px;">Blueprint 361</h1>
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        <p class="text-center" style="color:rgb(255,252,252);font-size:27px;"><em>Lighting the future of 3D Bioprinting.</em></p>
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                        <h2 style="color:rgb(201,214,228);font-size:40px;width:660px;">Our Fundamental Application</h2>
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                        <p style="color:rgb(215,222,227);font-size:26px;width:661px;">Using Synthetic Biology, we aim to improve the Biomedical Engineering industry by creating surface coatings for current and future implants.</p>
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                        <h1 style="font-size:45px;">What is our problem?</h1>
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                        <p style="font-size:26px;font-family:Raleway, sans-serif;color:rgba(255,255,255,0.9);">Medical implants, such as knee and hip replacements, require membranes to coat them in order to characterise them as biocompatible.</p>
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                        <p style="font-size:26px;font-family:Raleway, sans-serif;color:rgba(255,255,255,0.9);">However, current methods to create sufficient membranes (for growing stem cells on) require expensive equipment and have a longer printing time. </p>
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                        <h1 style="font-size:44px;">What are we studying?</h1>
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                        <p style="font-size:25px;font-family:Raleway, sans-serif;color:#ffffff;">We are studying the characteristics of Osseointegration. This refers to the direct structural and functional connection between the surface of a load bearing artifical implant, and the bone in the living body. </p>
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                        <h1 style="font-size:45px;">Where does Synthetic Biology play its part?</h1>
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                        <p style="font-size:25px;color:#ffffff;font-family:Raleway, sans-serif;">We had genetically modified E coli K 12- whereby, when light of a specific wavelength is shined upon it, cellulose is produced. This acts as our ink.</p>
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                        <h1 style="font-size:45px;">How are we tying this all together?</h1>
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                        <p style="font-size:25px;color:#ffffff;font-family:Raleway, sans-serif;">Using our defined E coli, we are able to manufacture a novel 3D printer that creates surface coatings for implants. Once the light shines upon selected areas of the cell plate, a new surface coating strip will be created.</p>
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            <p class="text-center" data-aos="fade-up" data-aos-duration="1000" style="font-size:76px;color:rgb(255,245,245);font-family:Raleway, sans-serif;">Thank You to All Our Sponsors:</p>
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    <div class="hwrap"><h2>The Project</h2></div>
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<p>By providing a well-defined, biocompatible surface coating, the risk of bone and dental implant failure will be greatly reduced. In order to produce such coatings, light will have control over the spatial production of extra-cellular cellulose and formation of biofilm. The modified E.coli builds on work from previous iGEM teams, utilising a transmembrane protein complex: upon exposure to red light Cph8 prevents the phosphorylation of a promoter and begins the synthesis cascade. Using this technology, the team will be able to build a 3D printer where living bacteria act as the 'bio-ink'. They will then be able to produce biocompatible structures, featuring micrometre pores, which mimic the surface of broken bone for implants. Micropore structures have been shown to induce the body to produce new bone, helping the implant fuse efficiently and thus reduce overall failure rates.</p>
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Revision as of 19:44, 1 November 2017

Blueprint 361

Revolutionising Implants

The Project

By providing a well-defined, biocompatible surface coating, the risk of bone and dental implant failure will be greatly reduced. In order to produce such coatings, light will have control over the spatial production of extra-cellular cellulose and formation of biofilm. The modified E.coli builds on work from previous iGEM teams, utilising a transmembrane protein complex: upon exposure to red light Cph8 prevents the phosphorylation of a promoter and begins the synthesis cascade. Using this technology, the team will be able to build a 3D printer where living bacteria act as the 'bio-ink'. They will then be able to produce biocompatible structures, featuring micrometre pores, which mimic the surface of broken bone for implants. Micropore structures have been shown to induce the body to produce new bone, helping the implant fuse efficiently and thus reduce overall failure rates.

We thank our sponsors without whom none of this would have been possible: