|
|
(147 intermediate revisions by 11 users not shown) |
Line 3: |
Line 3: |
| | | |
| <body> | | <body> |
| + | |
| <!-- Header --> | | <!-- Header --> |
| <section id="header"> | | <section id="header"> |
Line 11: |
Line 12: |
| height: 10em; | | height: 10em; |
| } | | } |
| + | |
| + | <link rel="icon" type="image/png" href="2017.igem.org/wiki/images/c/cb/T--TU_Darmstadt--favi1.png" /> |
| + | |
| </style> | | </style> |
− | <span class="image avatar"><img src="https://static.igem.org/mediawiki/2017/3/3d/LogoOWL.png" alt="" /></span> | + | |
| + | <span class="image avatar"><a href="https://2017.igem.org/Team:TU_Darmstadt"><img src="https://static.igem.org/mediawiki/2017/3/3d/LogoOWL.png" alt="home" /></a></span> |
| <h1 id="logo"><a href="https://2017.igem.org/Team:TU_Darmstadt">ChiTUcare</a></h1> | | <h1 id="logo"><a href="https://2017.igem.org/Team:TU_Darmstadt">ChiTUcare</a></h1> |
− | <!--<p>iGEM TU Darmstadt<br />
| + | |
− | 2017</p>-->
| + | |
| </header> | | </header> |
| <nav id="nav"> | | <nav id="nav"> |
Line 26: |
Line 31: |
| <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chitinase">Chitinase</a></li> | | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chitinase">Chitinase</a></li> |
| <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chitin_deacetylase">Chitin Deacetylase</a></li> | | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chitin_deacetylase">Chitin Deacetylase</a></li> |
− | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/regulation_system">Regulation System</a></li> | + | <!--<li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/regulation_system">Regulatory System</a></li>--> |
− | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/hydrogel" class="active">Hydrogel</a></li> | + | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/hydrogel" class="active">Hydrogels</a></li> |
| <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chemistry">Chemistry</a></li> | | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/chemistry">Chemistry</a></li> |
− | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/modeling">Modeling</a></li> | + | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project |
− | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project/parts">Parts</a></li>
| + | /parts">Parts</a></li> |
| + | <li><a href="https://2017.igem.org/Team:TU_Darmstadt/project |
| + | /notebook">Notebook</a></li> |
| </div> | | </div> |
| <div class="mainmenu"> | | <div class="mainmenu"> |
Line 63: |
Line 70: |
| </header> | | </header> |
| <div class="post-it"> | | <div class="post-it"> |
− | <p style="font-size:20px">
| + | <p> |
− | Hydrogels are three-dimensional systems with hydrophilic polymer chains with high water content. The advantages of hydrogels are the special characteristics such as biocompatibility, elasticity and modifiable chemical properties. There are two kinds of gels, natural and synthetic. The natural ones consists of natural polysaccharides which are harvested from renewable resources and are abundant, nontoxic, inexpensive and biodegradable materials. They receive an increasing attention in various fields, like medicinal research. | + | Hydrogels are three-dimensional networks made out of synthetic or natural polymers containing large quantities of water, therefore they receive an increasing attention in various fields. We were focused on not using any expensive or toxic linker in combination with chitosan to manufacture a hydrogel, which could be formed in any shape with a perfect alignment to the surrounding tissue. |
− | <br>We want to produce such a hydrogel and modify it to detect pathogenic bacteria visually in wounds. To evaluate an ideal hydrogel, various compositions were tested, like pure chitosan or chitosan in combination with agarose, agar or alginate. During this work various promising hydrogels could be produced.
| + | The aim was to produce such a hydrogel with basic laboratory equipment and modify it to detect pathogenic bacteria visually in wounds. To evaluate an ideal hydrogel various gelation substrates were tested. During this work various promising hydrogels were produced. |
| </p></div> | | </p></div> |
| </div> | | </div> |
Line 73: |
Line 80: |
| <h3>Introduction</h3> | | <h3>Introduction</h3> |
| | | |
| + | <p>Patients with burn wounds or other poorly healing wounds, like diabetes wounds, often suffer from various complications such as infections. Until now the common medical bandages have to be removed to monitor the wound healing progress. To examine if there is an infection, which implies the presence of pathogenic bacteria, samples of the wound have to be taken and studied in a specialized laboratory. This is a time-consuming and expensive process and we want to simplify and accelerate this procedure. |
| | | |
| + | <p><img src="https://static.igem.org/mediawiki/2017/1/19/T--TU_Darmstadt--gel_cut.png" alt="gel_cut" width=34% style="float:right; margin-left: 1px;" /> |
| + | |
| + | <br>The solution for this problem is a hydrogel, with the advantages of the special characteristics of hydrogels such as biocompatibility, elasticity, and modifiable chemical properties. Most hydrogels can swell in aqueous solutions; for our purpose, as a wound bandage, it can be used to absorb some of the wound fluid <a href="#[3]">[3]</a><a href="#[4]">[4]</a>. Furthermore it can be attached hermetically and the moisture provided by the hydrogel therefore leads to ideal wound healing conditions <a href="#[5]">[5]</a> |
| + | <br>An optimal polymer for such a hydrogel is the unique aminopolysaccharide chitosan. Beside beneficial properties like its biocompatibility, biodegradability, and film forming ability, chitosan has reactive amine side groups. This offers possibilities for modifications, like the linkage of a fluorophore to detect pathogenic bacteria (See |
| + | <a href="https://2017.igem.org/Team:TU_Darmstadt/project/chemistry">Chemistry</a>) <a href="#[2]">[2]</a>. |
| + | <br>The hemostatic chitosan is reported to have intrinsic antifungal, antibacterial, and antiviral properties <a href="#[6]">[6]</a>. Furthermore, it promotes scar free wound healing, has healing effects and acts antiallergic <a href="#[7]">[7]</a>. It is an ideal scaffold material to manufacture different types of hydrogels as salves, beads, sponges or solid bandages. <br> |
| | | |
− | <p>Patients with burn wounds or other poor-healing wounds, like diabetes wounds, often suffer from various complications such as infections. Until now the common medical bandages have to be removed to monitor the wound healing progress. To examine if there is an infection, which implies the presence of pathogenic bacteria, samples of the wound have to be taken and studied in a specialized laboratory. This is a long time and expensive process and we want to simplify and accelerate this procedure.
| |
− | The solution for the problem is a hydrogel, which is characterized by containing water, forming a solid three-dimensional network structures and being water insoluble. Most hydrogels could swell in aqueous solutions; for our purpose, as a wound bandage, it can be used to absorb some of the wound fluid. Furthermore it can be attached hermetically and the moisture provided by the hydrogel leads therefore to ideal wound healing conditions.
| |
− | An optimal polymer for such a hydrogel is chitosan (poly-1,4-β-D-glucopyranosamine). It has beneficial properties like biocompatibility, biodegradability. Furthermore, chitosan has reactive amine side groups, which offer possibilities for modifications, like the linkage of a fluorophore to detect the pathogenic bacteria. <a href="#[2]">[2]</a><br>
| |
− | The hemostatic chitosan is reported to have intrinsic antifungal, antibacterial, and antiviral properties. Furthermore it promotes scar free wound healing and has care effects, and is antiallergic <a href="#[3]">[3]</a>. In addition human epithelium could heal along the chitosan matrix, so no wound distance grid is necessary and it has skin cooling effects. <a href="#[1]">[1]</a>. It is an ideal scaffold material to manufacture different types of hydrogels, salves, pastes or solid bandages. Most chitosan hydrogel topical wound dressings are formed using an expensive or toxic crosslinking agent, which we want to avoid.
| |
− | <br>Due to that we can deliver an optimal wound healing and monitoring bandage for these affected patients without the need to disrupt the healing process. The hydrogel should help preventing or treat wound infections of any degree of burns.
| |
| <br> | | <br> |
| </p> | | </p> |
| </div> | | </div> |
| </section> | | </section> |
| + | |
| <section id="three"><div class="container"> | | <section id="three"><div class="container"> |
− |
| |
− |
| |
| | | |
| <h3>Production</h3> | | <h3>Production</h3> |
− | <p>To evaluate an ideal hydrogel, various compositions were tested, like pure chitosan or chitosan in combination with agarose, agar or alginate. During this work various promising hydrogels could be produced. | + | <p>To evaluate an ideal hydrogel, various compositions were tested, like pure chitosan or chitosan in combination with agarose, agar or alginate. The commercially available high-molecular weight chitosan was provided by Sigma-Aldrich (Munich, Germany). |
− | The kind of hydrogels we want to create are due to their compounds not toxic, biodegradable, biocompatible, while at the same time having low-cost and easy to manufacturing processes. They are easy to produce in different sizes and thicknesses. While being flexible they keep their stability, which makes it comfortable for patients to wear, aswell easy to manufacture, handle and apply on patients.
| + | Due to their compounds, the hydrogels we wanted to create are not toxic, biodegradable, biocompatible, while at the same time being low-cost and simple manufacturing processes. They are easy to produce in different shapes and thicknesses. While being flexible they will not dissolve or disintegrate, which makes it comfortable for patients to wear. In addition to that, it is easy to manufacture, handle and use on patients. |
− | The pH-level of our hydrogels are easy to regulate.
| + | We were focused on working with basic laboratory equipment. For the preparation of chitosan hydrogels, an acidic environment is usually required to dissolve chitosan. Thus, the pH-level of our hydrogels are easy to regulate. We manufactured our chitosan containing hydrogel in aqueous acetic acid. <br> |
− | We were focused to work with basic laboratory equipment. For the preparation of chitosan hydrogels, an acidic environment is usually required to dissolve chitosan. We manufactured our chitosan containing hydrogel in aqueous acetic acid. <br> | + | A long time of continuous mechanical stirring (6 h) is required to dissolve the chitosan in the acetic acid-deionized water solution. Under continuous pH measurement it needs mechanical stirring for 12 h. This solution needs to rest for at least 12 h for further processing.</p> |
− | A long time continuous mechanical stirring (6 hours) is required to dissolve the chitosan in the acetic acid-deionized water solution. Under continuous pH measurement it needs mechanically stirring for 12 hours. This solution needs to rest for at least 12 hours for further processing.</p> | + | <p><br> |
| + | <a href="#gel1">Chitosan Hydrogel solidified in Alginate-Quercetin solution</a> |
| <br> | | <br> |
− | <a href="#till">TEXT GEL </a> | + | <a href="#gel2">Chitosan Hydrogel with high pH-Level</a> |
− | <div class="features">
| + | <br> |
| + | <a href="#gel3">Chitosan-Agarose Hydrogel</a> |
| + | <br> |
| + | <a href="#gel4">Chitosan-Agar Hydrogel</a></p> |
| + | |
| + | |
| | | |
| | | |
| <article> | | <article> |
− | <h5 id="till">Chitosan Hydrogel solidified in Alginate-Quercetin solution</h4> | + | <p id="gel1"> |
| + | </p> |
| + | <br> |
| + | <h5>Chitosan Hydrogel solidified in Alginate-Quercetin solution</h5> |
| | | |
| | | |
Line 110: |
Line 127: |
| | | |
| <br> | | <br> |
− | <p> The alginate/quercetin solution was poured into a mold and then liquid-friezed. The 2% chitosan solution was then poured onto it and streaked out to the certain thickness, covered with the alginate/quercetin solution, placed into the 37° incubator for 24 hours.</p> | + | <p> The alginate/quercetin solution was poured into a mold and then liquid-frozen. The 2.2 % chitosan solution was then poured onto it and streaked out to the certain thickness, covered with the alginate/quercetin solution and placed into the 37 °C incubator for 24 h.</p> |
− | <br>
| + | |
− | <p> After the solidification process the arosed solid hydrogel was rinsed with ultrapure water. Placed into an aqueous solution it will swell massively after time.
| + | |
| <br> | | <br> |
| + | <p> After the solidification process the arisen solid hydrogel was rinsed with ultrapure water. <br> |
| + | Placed into an aqueous solution it will swell massively after time, but stays soft and pliable. |
| The swelling degree of the hydrogel was calculated by | | The swelling degree of the hydrogel was calculated by |
| <br> | | <br> |
Line 123: |
Line 140: |
| <mfrac> | | <mfrac> |
| <mi>Ww - Wd</mi> | | <mi>Ww - Wd</mi> |
− | <mi>Ww </mi> | + | <mi><mn>Ww</mn> </mi> |
| </mfrac> | | </mfrac> |
− | x100
| + | <mn> x 100</mn> |
| </mrow> | | </mrow> |
− | </math> | + | </math> |
| <br> | | <br> |
| + | <figcaption> DS: degree of swelling. Wd: dry weight. Ww: wet weight </figcaption> |
| + | </figure> |
| + | </center> |
| | | |
− | <figcaption> DS: degree of swelling. Wd: dry weight. Ww: wet weight </figcaption></center>
| |
− | </figure>
| |
| <br> | | <br> |
− | <p>The hydrogel were saturated with the liquid in which it was immersed. Our manufactured hydrogel has a degree of swelling of almost 600 %. | + | <p>The hydrogels were saturated with the liquid in which it was immersed. Our manufactured hydrogel has a degree of swelling of almost 600%. |
| </p> | | </p> |
| <br> | | <br> |
Line 140: |
Line 158: |
| <img src="https://static.igem.org/mediawiki/2017/7/77/T--TU_Darmstadt--QuerMess1.jpeg" style="float: left; width: 33%; margin-bottom: 0.5em;"> | | <img src="https://static.igem.org/mediawiki/2017/7/77/T--TU_Darmstadt--QuerMess1.jpeg" style="float: left; width: 33%; margin-bottom: 0.5em;"> |
| <p style="clear: both;"> | | <p style="clear: both;"> |
− | </div>
| + | |
| </article> | | </article> |
| <article> | | <article> |
− | <div class="container">
| + | |
− | <h5> Chitosan Hydrogel with high pH-level</h5>
| + | <p id="gel2"> |
| + | </p> |
| <br> | | <br> |
− | <video src="https://static.igem.org/mediawiki/2017/6/6e/T--TU_Darmstadt--Gel-vid1.mp4" alt="Chitosan-Alkaline production" style="width:100%;max-width:800px;" controls> | + | <h5>Chitosan Hydrogel with high pH-level</h5> |
− | </div> | + | <p>The pH-level of the hydrogels are easy to adjust. Depending on the solution in which the hydrogel is swelling, the gel has a high, neutral or low pH-level (Production see video). |
− | <div class="container">
| + | |
− | <p> Manufacturing process of our chitosan hydrogel with a high pH-level was performed by rinsing the 2% chitosan solution with a defined NaOH solution with the desired pH-level. </p> | + | |
| <br> | | <br> |
| + | <br> |
| + | <video src="https://static.igem.org/mediawiki/2017/6/6e/T--TU_Darmstadt--Gel-vid1.mp4" alt="Chitosan-Alkaline production" style="width:100%;" controls> |
| | | |
− | <img src="https://static.igem.org/mediawiki/2017/d/d7/T--TU_Darmstadt--Alkaline2_90.jpeg"style="float: left; height: 15em; width: 30%; margin-right: 1%; margin-bottom: 0.5em;"> | + | <br> |
− | <img src="https://static.igem.org/mediawiki/2017/1/17/T--TU_Darmstadt--Alkaline1.jpeg" style="float: left; height: 15em; width: 69%; margin-bottom: 0.5em;"> </center> | + | <p> Manufacturing process of our chitosan hydrogel with a high pH-level was performed by rinsing the 2% chitosan solution with a defined NaOH solution with the desired pH-level. </p> |
| + | <br> |
| + | <p> |
| + | <img src="https://static.igem.org/mediawiki/2017/3/33/T--TU_Darmstadt--Bild1_Sam.png" style="float: left; width: 100%; margin-bottom: 0.5em;"> </center> |
| <p style="clear: both;"> | | <p style="clear: both;"> |
− | <figure><center> | + | </p> |
− | <figcaption> Produced hydrogel rinsed with NaOH solution(pH 10) (left). Transparency shown (right) </figcaption></center> | + | <p>The Produced hydrogel was rinsed with NaOH solution (pH 10) (left). The transparency is shown by placing the hydrogel on a nitrile glove (right)</p> |
− | </figure> | + | <br> |
| | | |
− | </div>
| |
| </article> | | </article> |
| <article> | | <article> |
− | <h5>Chitosan-Agarose</h5> | + | <p id="gel3"> |
| + | </p> |
| + | <br> |
| + | <h5>Chitosan-Agarose Hydrogel</h5> |
| <br> | | <br> |
| | | |
Line 169: |
Line 193: |
| <p>A hydrogel composed of chitosan and agarose fulfils most of the required criteria for an “ideal” wound dressing. | | <p>A hydrogel composed of chitosan and agarose fulfils most of the required criteria for an “ideal” wound dressing. |
| Agarose is a biocompatible, linear polysaccharide which is extracted from marine algae. It consists of 1,4-linked 3,6-anhydro-α-L-galactose and 1,3-linked β-D-galactose derivatives. | | Agarose is a biocompatible, linear polysaccharide which is extracted from marine algae. It consists of 1,4-linked 3,6-anhydro-α-L-galactose and 1,3-linked β-D-galactose derivatives. |
− | <br>When the agarose is dissolved in water, it forms a gel with a three-dimensional scaffold and a porous structure providing a good environment for cell adhesion, spreading and proliferation. It is capable of gelling within the desired site because of the polymer interaction. By varying the concentration of agarose in the hydrogel, the mechanical properties, which are similar to those of tissues, can easily be adjusted <a href="#[4]">[4]</a>. | + | <br>When the agarose is dissolved in water, it forms a gel with a three-dimensional scaffold and a porous structure providing a good environment for cell adhesion, spreading and proliferation. It is capable of gelling within the desired site because of the polymer interaction. By varying the concentration of agarose in the hydrogel, the mechanical properties, which are similar to those of tissues, can easily be adjusted <a href="#[8]">[8]</a>. The simplicity of preparing the hydrogel and its multifunctionality allows many future applications of agarose-based hydrogels |
− | <br>The preparation of such a hydrogel is quite simple. The desired amount of agarose is dissolved in water. 1 % acetic acid and the desired amount of chitosan are dissolved in water, simultaneously. Both solution are mixed and heated while stirring until the solution is clear. We transferred this mixture in a petri dish with the desired thickness.
| + | <a href="#[9]">[9]</a>. |
− | We examined gels with concentrations of 1 -3 % agarose and 1 – 3 % chitosan. The most promising variation is the hydrogel with 1 % agarose and 1 % chitosan. It forms a stable, elastic gel which allows easy handling.
| + | |
− | The simplicity of preparing the hydrogel and its multifunctionality allows many future applications of agarose-based hydrogels <a href="#[5]">[5]</a>. | + | |
| </p> | | </p> |
| <p> | | <p> |
− | <br><figure><center> | + | <br> |
− | <img src="https://static.igem.org/mediawiki/2017/3/3d/T--TU_Darmstadt--AgaroseH.jpeg", alt="Chitosan-Agarose-Hydrogel", width=36%,> | + | |
− | <figcaption>Chitosan-Agarose-Hydrogel</figcaption></center>
| + | <img src="https://static.igem.org/mediawiki/2017/5/5d/T--TU_Darmstadt--Bild2_Sam.png" style="float: left; width: 100%; margin-bottom: 0.5em;"> </center> |
− | </figure> | + | <p style="clear: both;"> |
| + | The shown hydrogel contains 1% chitosan, 1% acetic acid and 1% agarose. It is a very promising gel. It is a little bit adhesive to generate hermetically sealed, moist conditions for wound healing. |
| + | |
| </p> | | </p> |
| | | |
Line 185: |
Line 209: |
| </article> | | </article> |
| <article> | | <article> |
− | <h5>Chitosan-Agar</h5> | + | |
| + | <p id="gel4"> |
| + | </p> |
| + | <br> |
| + | <h5>Chitosan-Agar Hydrogel</h5> |
| <br> | | <br> |
| <p>The mixture of chitosan with agar forms hydrogels with enhanced swelling compared to pure chitosan ones. | | <p>The mixture of chitosan with agar forms hydrogels with enhanced swelling compared to pure chitosan ones. |
− | Agar is a hydrophilic cell-wall polysaccharide extracted from the family of seaweeds. It composes of alternating (1-4)-D-galactose and (1-3)-3,6-anhydro-L-galactose repeating units and forms reversible gels even with a low concentration because of the formation of hydrogen bonds<a href="#[2]">[2]</a><a href="#[6]">[6]</a>. It is soluble in hot water and forms a gel during cooling. The polymer is biodegradable, low-cost, environmentally friendly and easy to extract. It is already used in pharmaceutical industry as a gelling, stabilizing and encapsulating agent <a href="#[7]">[7]</a>. | + | Agar is a hydrophilic cell-wall polysaccharide extracted from the family of seaweeds. It composes of alternating (1-4)-D-galactose and (1-3)-3,6-anhydro-L-galactose repeating units and forms reversible gels even with a low concentration because of the formation of hydrogen bonds<a href="#[2]">[2]</a><a href="#[10]">[10]</a>. It is soluble in hot water and forms a gel during cooling. The polymer is biodegradable, low-cost, environmentally friendly and easy to extract. It is already used in pharmaceutical industry as a gelling, stabilizing and encapsulating agent <a href="#[11]">[11]</a>. It forms a stable, elastic gel which allows easy handling. |
− | The preparation is the same procedure as for agarose, just with agar instead of the agarose.
| + | |
− | The most promising variation was, as well as with agarose, the hydrogel with 1 % agar and 1 % chitosan. It forms a stable, elastic gel which allows easy handling.
| + | |
| </p> | | </p> |
| <br> | | <br> |
− | <img src="https://static.igem.org/mediawiki/2017/6/67/T--TU_Darmstadt--Agar-Hydrogel1.jpeg"style="float: left; height: 20em; width: 69%; margin-right: 1%; margin-bottom: 0.5em;"> | + | <img src="https://static.igem.org/mediawiki/2017/e/e1/T--TU_Darmstadt--Bild3_Sam.png" style="float: left; width: 100%; margin-bottom: 0.5em;"> </center> |
− | <img src="https://static.igem.org/mediawiki/2017/d/d9/T--TU_Darmstadt--Agar1.jpeg" style="float: left; height: 20em; width: 30%; margin-bottom: 0.5em;"> </center>
| + | |
| <p style="clear: both;"> | | <p style="clear: both;"> |
− | <figure><center>
| + | The shown hydrogel contains 1 % chitosan, 1 % acetic acid and 1 % agar. It is a very promising gel. It is a little bit adhesive to generate hermetically sealed, moist conditions for wound healing. Furthermore, it is more elastic than a gel with agarose. |
− | <figcaption> Produced chitosan-agar hydrogel </figcaption></center>
| + | |
− | </figure>
| + | |
| | | |
− | </figure>
| |
| </p> | | </p> |
| </div> | | </div> |
Line 207: |
Line 229: |
| <br> | | <br> |
| <br> | | <br> |
| + | <section id="four"><div class="container"> |
| + | <h3>Outlook</h3> |
| + | <p> |
| + | During the work with chitosan hydrogels various compositions were tested and promising hydrogels were produced. Hydrogels were manufactured with pure chitosan or chitosan in combination with agarose, agar or alginate. Depending on the concentration of chitosan and the respective gelling agent (agarose, agar, alginate), the gels were more or less solid. We manufactured stable and elastic gels which allow easy handling. According to the field of application a solid or smooth hydrogel is advisable. |
| + | <br>The pH-level of the hydrogels is easy to regulate by rinsing it with a solution with the properly defined pH-level or using a higher or lower acetic acid concentration to dissolve the chitosan in an aqueous solution. This is beneficial for an adjustment to the respective wound and its pH-level. |
| + | <br>Another advantage is the application for moist wound healing, as well as the factor that our hydrogels will seal the wounds airtightly. Here, the hydrogel prevents the formation of crusts and provides moisture. Both are important wound healing factors. The nutrient transport and release of signaling molecules is improved and scarring is massivly reduced with chitosan as wound toping layer. Our hydrogels can additionally deliver a monitoring bandage for affected patients without the need to disrupt the healing process and thus lighten the burden for the patients. The hydrogel should help to prevent or treat wound infections for example at any degree of burns. We thank the iGEM Team diagnost-X from Berlin for their provided expertise and informations regarding these medical problems. |
| + | <br>The chitosan in itself or in combination other natural polymers is an ideal scaffold material to manufacture different types of hydrogels as salves, micro-, macroparticles, solid bandages and so on. Due to its wound healing effects and in combination with the medical benefits of a hydrogel it means an optimal wound healing dressing. Our hydrogels should be easy to load and therefore an ideal local slow-release drug-delivery vehicle for various therapeutic agents, pharmaceuticals, antimircobials or growth factors readily incorporated <i>in situ</i> to a treated tissue. |
| + | |
| + | |
| + | </p> |
| + | </div> |
| + | </section> |
| + | |
| + | |
| + | |
| + | |
| + | <section id="five"><div class="container"> |
| + | <h3>Group Picture</h3> |
| + | |
| + | |
| + | <br><p> |
| + | <figure><center> |
| + | <img src="https://static.igem.org/mediawiki/2017/7/71/T--TU_Darmstadt--GrouppictureHydrogel.jpeg", alt="Best Group", width=70%,> |
| + | <figcaption> <b>Group Picture of the Hydrogel team.</b> <br>From left to right: Sophia Hein, Sven Storch, Bea Spiekermann, Till Zimmermann and Lisa-Marie Brenner </figcaption></center> |
| + | </figure></p> |
| + | |
| + | </div> |
| + | </section> |
| + | |
| + | |
| <br> | | <br> |
− | <section id="seven"><div class="container"> | + | <section id="six"><div class="container"> |
| <h3>References</h3> | | <h3>References</h3> |
− | <p>
| + | <table class="ref"> |
− | <table width="100%" border="0" cellpadding="0" cellspacing="2"> | + | |
| <tr> | | <tr> |
| <td id="[1]">[1]</td> | | <td id="[1]">[1]</td> |
Line 225: |
Line 276: |
| <tr> | | <tr> |
| <td id="[3]">[3]</td> | | <td id="[3]">[3]</td> |
− | <td>Ahsan, S. M., Thomas, M., Reddy, K. K., Sooraparaju, S. G., Asthana, A., and Bhatnagar, I. (2017) Chitosan as biomaterial in drug delivery and tissue engineering. <i>International Journal of Biological Macromolecules<i>/, In Press | + | <td>Chen, S.-C., Wu, Y.-C., Mi, F.-L., Lin, Y.-H., Yu, L.-C., and Sung, H.-W. (2004) A novel pH-sensitive hydrogel composed of <i>N,O</i>-carboxymethyl chitosan and alginate cross-linked by genipin for protein drug delivery. <i>Journal of Controlled Release</i>, 96, 285 – 300 |
− | <br>DOI: 10.1016/j.ijbiomac.2017.08.140 | + | <br>DOI: 10.1016/j.jconrel.2004.02.002 |
| </td> | | </td> |
| </tr> | | </tr> |
| <tr> | | <tr> |
| <td id="[4]">[4]</td> | | <td id="[4]">[4]</td> |
| + | <td>Kharkar, P., Kiick, K., and Kloxin, A. M. (2013) Desining degradable hydrogels for orthogonal control of cell microenviroments. <i>Chem Soc Rev</i>, 42, 7335 – 7372 |
| + | <br>DOI: 10.1039/c3cs60040h |
| + | </td> |
| + | </tr> |
| + | <tr> |
| + | <td id="[5]">[5]</td> |
| + | <td>Dissemond, J. (2006) Modern wound dressing for the therapy of chronic wounds. <i>Hautarzt</i>, 57, 881 – 887 |
| + | <br>DOI: 10.1007/s00105-005-1054-y |
| + | </td> |
| + | </tr> |
| + | <tr> |
| + | <td id="[6]">[6]</td> |
| + | <td>Kurita, K. (2006) Chitin and Chitosan: Functional Biopolymers from Marine Crustaceans. <i>Marine Biotechnology</i>, 8, 203 – 226 |
| + | <br>DOI: 10.1007/s10126-005-0097-5 |
| + | |
| + | </td> |
| + | </tr> |
| + | <tr> |
| + | <td id="[7]">[7]</td> |
| + | <td>Ahsan, S. M., Thomas, M., Reddy, K. K., Sooraparaju, S. G., Asthana, A., and Bhatnagar, I. (2017) Chitosan as biomaterial in drug delivery and tissue engineering. <i>International Journal of Biological Macromolecules</i>, In Press |
| + | <br>DOI: 10.1016/j.ijbiomac.2017.08.140 |
| + | </td> |
| + | </tr> |
| + | <tr> |
| + | <td id="[8]">[8]</td> |
| <td>Miguel, S. P., Ribeiro, M. P., Brancal, H., Coutinho, P., and Correia, I. J. (2014) Thermoresponsive chitosan-agarose hydrogel for skin regeneration. <i>Carbohydrate Polymers</i>, 111, 366 – 373 | | <td>Miguel, S. P., Ribeiro, M. P., Brancal, H., Coutinho, P., and Correia, I. J. (2014) Thermoresponsive chitosan-agarose hydrogel for skin regeneration. <i>Carbohydrate Polymers</i>, 111, 366 – 373 |
| <br>DOI: 10.1016/j.carbpol.2014.04.093 | | <br>DOI: 10.1016/j.carbpol.2014.04.093 |
Line 236: |
Line 312: |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td id="[5]">[5]</td> | + | <td id="[9]">[9]</td> |
| <td>Cao, Z., Gilbert, R. J., and He, W. (2009) Simple Agarose-Chitosan Gel Composite System for Enhanced Neuronal Growth in Three Dimensions. <i>Biomacromolecules</i>, 10, 2954 – 2959 | | <td>Cao, Z., Gilbert, R. J., and He, W. (2009) Simple Agarose-Chitosan Gel Composite System for Enhanced Neuronal Growth in Three Dimensions. <i>Biomacromolecules</i>, 10, 2954 – 2959 |
| <br>DOI: 10.1021/bm900670n | | <br>DOI: 10.1021/bm900670n |
Line 242: |
Line 318: |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td id="[6]">[6]</td> | + | <td id="[10]">[10]</td> |
| <td>El-Hefian, E. A., Nasef, M. M., and Yahaya, A. H. (2012) Preparation and Characterization of Chitosan/Agar Blended Films: Part 2. Thermal, Mechanical, and Surface Properties. <i>E-Journal of Chemistry</i>, 9, 510 – 516 | | <td>El-Hefian, E. A., Nasef, M. M., and Yahaya, A. H. (2012) Preparation and Characterization of Chitosan/Agar Blended Films: Part 2. Thermal, Mechanical, and Surface Properties. <i>E-Journal of Chemistry</i>, 9, 510 – 516 |
| <br>DOI: 10.1155/2012/285318 | | <br>DOI: 10.1155/2012/285318 |
Line 248: |
Line 324: |
| </tr> | | </tr> |
| <tr> | | <tr> |
− | <td id="[7]">[7]</td> | + | <td id="[11]">[11]</td> |
| <td>Sousa, A. M. M., Sereno, A. M., Hilliou, L., and Goncalves, M. P. (2010) Biodegradable Agar extracted from <i>Gracilaria Vermiculophylla</i>: Film Properties and Application to Edible Coating. <i>Materials Science Forum</i>, 636-637, 739 – 744 | | <td>Sousa, A. M. M., Sereno, A. M., Hilliou, L., and Goncalves, M. P. (2010) Biodegradable Agar extracted from <i>Gracilaria Vermiculophylla</i>: Film Properties and Application to Edible Coating. <i>Materials Science Forum</i>, 636-637, 739 – 744 |
| <br>DOI: 10.4028/www.scientific.net/MSF.636-637.739 | | <br>DOI: 10.4028/www.scientific.net/MSF.636-637.739 |
Line 259: |
Line 335: |
| | | |
| </section> | | </section> |
− |
| |
− |
| |
| | | |
| <!-- Footer --> | | <!-- Footer --> |
− | <section id="footer">
| + | </body> |
− | <div class="container">
| + | </html> |
− | <ul class="copyright">
| + | {{TU_Darmstadt/footerG}} |
− | <li>Design: <a href="http://html5up.net">HTML5 UP</a></li>
| + | <html> |
− | </ul>
| + | <body> |
− | </div>
| + | |
− | </section>
| + | |
− | | + | |
| </div> | | </div> |
| </body> | | </body> |
| </html> | | </html> |