Team:Peking/Project/3D/3D

From 2012.igem.org

(Difference between revisions)
m
 
(14 intermediate revisions not shown)
Line 1: Line 1:
<html></p></html>{{Template:Peking2012_Color_Prologue}}{{Template:Peking2012_Color_Project}}<html>
<html></p></html>{{Template:Peking2012_Color_Prologue}}{{Template:Peking2012_Color_Project}}<html>
-
 
<script type="text/javascript">
<script type="text/javascript">
sublists_Now = 3;
sublists_Now = 3;
Line 8: Line 7:
subsubitem.innerHTML=subsubitem.innerHTML+' >>>';
subsubitem.innerHTML=subsubitem.innerHTML+' >>>';
</script>
</script>
-
 
<div class="PKU_context floatR first">
<div class="PKU_context floatR first">
-
<h3 class="title1">3D Printing</h3>
+
<h3 id="title1">3D Printing</h3>
-
<p>
+
<p>
-
3D printing is a new technology that has been rising for many years. It is a form of additive manufacturing technology where a three dimensional object is created by laying down successive layers of material. The tools are effectively modified ink-jet printers that deposit successive layers of material until a three-dimensional object is built up. The methods for 3D printing in manufacturing are quite developed, but in synthetic biology, there have been only a few attempts made. We believe that 3D printing can be utilized in many applications in both medical and manufacturing, such as with the synthesis of artificial vessels, organs, or bone tissues, and the creation of high-order biomaterials based on the high spatial resolution of the light. With more precise control of the response threshold of the optic biosensor, we can obtain holographic images from a solid medium.<br/><br/>
+
3D printing is a promising technology that has been rising for many years. It is a form of additive manufacturing technology where a three dimensional object is created by laying down successive layers of material. The tools are effectively modified ink-jet printers that deposit successive layers of material until a three-dimensional object is built up. The methods for 3D printing in manufacturing are quite developed, but in synthetic biology, there have been only a few attempts made. We believe that 3D Bio-printing can be utilized in many applications in both medical and manufacturing, such as with the synthesis of artificial vessels, organs, or bone tissues, and the creation of high-order biomaterials based on the high spatial resolution of the light. With more precise control of the response threshold of the optic biosensor, we can obtain holographic images from a solid medium.
-
 
+
<br /><br />
-
Most modern 3D printers work by printing layer by layer. This is done by ‘cutting’ visual objects into 2D slides and printing each layer onto a surface. This process is both slow and these devices require precise programming . <br/><br/>
+
Most modern 3D printers work by printing layer by layer. This is done by ‘cutting’ visual objects into 2D slides and printing each layer onto a surface.
-
 
+
<br /><br />
-
The principal advantage of our system for 3D printing is the "graver"--light. Light is a cheap source with high spatial resolution, allowing for us to fabricate complex objects. The use of transparent LB or M9 medium allows light to be exposed to the entire culture. We’ve attempted 3D printing with our <i>Luminesensor</i>. <br/><br/>
+
The principal advantage of our system for 3D Bio-printing is the "graver"--light. Light is a cheap source with high spatial resolution, allowing for us to fabricate complex objects. The use of transparent LB or M9 medium allows light to be exposed to the entire culture. We’ve attempted 3D Bio-printing with our <i>Luminesensor</i>.
-
 
+
<br /><br />
-
We tried the current method--building up layer by layer. About more details, three identical masks were made and just as in 2D printing, after exposed to parallel light of 12hours, we obtain a series of luminous steps forming stairs by putting them layer by layer. Figure1 demonstrates the basic device for 3D printing. <br/><br/>
+
We tried the current method--building up layer by layer. About more details, many identical masks were made and just as in 2D Bio-printing, after exposed to parallel light of 12 hours, we obtain a series of luminous steps forming stairs by putting them layer by layer. Figure 1 demonstrates the basic device for 3D printing.
-
</p>
+
</p>
-
<p>
+
<div class="floatC">
-
<div class="floatC">
+
   <img src="/wiki/images/b/b1/Peking2012_3DprintingDNA3_b.png" style="width:400px;" />
   <img src="/wiki/images/b/b1/Peking2012_3DprintingDNA3_b.png" style="width:400px;" />
-
   <p class="description"style="text-align:center">
+
   <p class="description"style="text-align:center;">
-
  Figure 1a. the device used in the 3D printing.
+
Figure 1. the setup used in the 3D printing.
   </p>
   </p>
  </div>
  </div>
-
<p>Later, we tried a different approach. We inoculated a liquid culture of bacteria with LB medium and constructed a set-up that emits three orthogonal beams through the beaker. After incubation for 12 hours, we obtained a beaker culture with light (GFP) emitting bacteria with an orthonormal basis made of cultures without GFP expressed. Since the LB medium has a slight brightness under the light that can also excite GFP due to yeast extract being one of the ingredients in the LB medium, it is in some way an uncertain composition. We used a synthetic medium, M9 medium later because of its transparent property and chemical definition. </p>
+
<p>
-
<div class="floatC">
+
Consistent with our prediction, the layer-by-layer method works well with the <i>Luminesensor</i>. As a proof of concept, three layers of thin plate were printed using our 2D-Bioprinting method. After obtaineing the high-resolution 2D Bio-printing images on the plate, we build up all the three thin layers. As shown in Figure 2, a six-pointed star was build based on the three basic elements. The side view of the 3D Bio-printing product showed that there was indeed difference in the Z-dimension, which convinced us that the <i>Luminesensor</i> was very suitable for 3D Bio-printing.
-
   <img src="/wiki/images/a/ab/Peking2012_3D_Printing_Device.png" style="width:400px;" />
+
</p>
 +
<div class="floatC">
 +
   <img src="/wiki/images/1/1d/Peking2012_3D_Printing.png" style="width:400px;" />
   <p class="description"style="text-align:center">
   <p class="description"style="text-align:center">
-
   Figure 1b. the device used in the 3D printing.
+
   Figure 2. Result of 3D Bio-printing using the <i>Luminesensor</i>.
   </p>
   </p>
  </div>
  </div>
-
<p>Taking into consideration the most common application of 3D printing, the construction of a visual object, we also proposed to build a biobrick containing agarase, the enzyme that decompose agar and agarose, controlled by <i>Luminesensor</i>. As as a result, the light leads to the inhibition of the agarase expression, and the dark leads to the decomposition of the medium. This experiment will implement objects sculptured by light.
+
<p>
-
  </p>
+
We have realized that it may be the first 3D Bio-printing product controlled by light signal in Synthetic Biology. We proved that the general 3D printing principle, namely, layer-by-layer, was applicable in Bio-printing. Additionally, the high spatiotemporal specificity of light signal makes it possible to print more complex products with specific function, e.g. human issues or organs, a further step of what we have presented here.
 +
</p>
</div>
</div>
<div class="PKU_context floatR">
<div class="PKU_context floatR">
  <h3 id="title5">Reference</h3>
  <h3 id="title5">Reference</h3>
  <p></p>
  <p></p>
-
  <ul><li id="ref1">
+
  <ul class="refer"><li id="ref1">
1. Lam, C.X.F., Mo, X.M., Teoh, S.H., Hutmacher, D.W.(2002) Scaffold development using 3D printing with a starch-based polymer. <i>Mat. Sci. Eng. C.</i>, 20: 49: 56
1. Lam, C.X.F., Mo, X.M., Teoh, S.H., Hutmacher, D.W.(2002) Scaffold development using 3D printing with a starch-based polymer. <i>Mat. Sci. Eng. C.</i>, 20: 49: 56
-
   </li><li id = "ref2">
+
   </li><li id="ref2">
2. Nicola Jones(2012).Science in three dimensions: The print revolution. <i>Nature</i>, 487: 22: 23
2. Nicola Jones(2012).Science in three dimensions: The print revolution. <i>Nature</i>, 487: 22: 23
-
   </li><li id = "ref3">
+
   </li><li id="ref3">
3. Leukers, B., Gulkan, H., Irsen, S.H., Milz, S., Tille, C., Schieker, M., Seitz, H.(2005) Hydroxyapatite scaffolds for bone tissue engineering made by 3D printing. <i>J. Mater. Sci. Mater. Med.</i>, 16: 1121:1124
3. Leukers, B., Gulkan, H., Irsen, S.H., Milz, S., Tille, C., Schieker, M., Seitz, H.(2005) Hydroxyapatite scaffolds for bone tissue engineering made by 3D printing. <i>J. Mater. Sci. Mater. Med.</i>, 16: 1121:1124
-
   </li><li id = "ref4">
+
   </li><li id="ref4">
4. Erickson, B., Singh, R., Winters,  P.(2012) Synthetic Biology: Regulating Industry Uses of New Technologies. <i>Science</i>, 333:1254:1256
4. Erickson, B., Singh, R., Winters,  P.(2012) Synthetic Biology: Regulating Industry Uses of New Technologies. <i>Science</i>, 333:1254:1256
-
   </li><li id = "ref5">
+
   </li><li id="ref5">
-
5. Khalil, A.S., Collins, J.J.(2010)Synthetic biology: applications come of age. <i>Nat. Rev. Genet.</n>, 11:367: 379
+
5. Khalil, A.S., Collins, J.J.(2010)Synthetic biology: applications come of age. <i>Nat. Rev. Genet.</i>, 11:367: 379
  </li></ul>
  </li></ul>
</div>
</div>
</html>{{Template:Peking2012_Color_Epilogue}}
</html>{{Template:Peking2012_Color_Epilogue}}

Latest revision as of 05:14, 26 October 2012

3D Printing

3D printing is a promising technology that has been rising for many years. It is a form of additive manufacturing technology where a three dimensional object is created by laying down successive layers of material. The tools are effectively modified ink-jet printers that deposit successive layers of material until a three-dimensional object is built up. The methods for 3D printing in manufacturing are quite developed, but in synthetic biology, there have been only a few attempts made. We believe that 3D Bio-printing can be utilized in many applications in both medical and manufacturing, such as with the synthesis of artificial vessels, organs, or bone tissues, and the creation of high-order biomaterials based on the high spatial resolution of the light. With more precise control of the response threshold of the optic biosensor, we can obtain holographic images from a solid medium.

Most modern 3D printers work by printing layer by layer. This is done by ‘cutting’ visual objects into 2D slides and printing each layer onto a surface.

The principal advantage of our system for 3D Bio-printing is the "graver"--light. Light is a cheap source with high spatial resolution, allowing for us to fabricate complex objects. The use of transparent LB or M9 medium allows light to be exposed to the entire culture. We’ve attempted 3D Bio-printing with our Luminesensor.

We tried the current method--building up layer by layer. About more details, many identical masks were made and just as in 2D Bio-printing, after exposed to parallel light of 12 hours, we obtain a series of luminous steps forming stairs by putting them layer by layer. Figure 1 demonstrates the basic device for 3D printing.

Figure 1. the setup used in the 3D printing.

Consistent with our prediction, the layer-by-layer method works well with the Luminesensor. As a proof of concept, three layers of thin plate were printed using our 2D-Bioprinting method. After obtaineing the high-resolution 2D Bio-printing images on the plate, we build up all the three thin layers. As shown in Figure 2, a six-pointed star was build based on the three basic elements. The side view of the 3D Bio-printing product showed that there was indeed difference in the Z-dimension, which convinced us that the Luminesensor was very suitable for 3D Bio-printing.

Figure 2. Result of 3D Bio-printing using the Luminesensor.

We have realized that it may be the first 3D Bio-printing product controlled by light signal in Synthetic Biology. We proved that the general 3D printing principle, namely, layer-by-layer, was applicable in Bio-printing. Additionally, the high spatiotemporal specificity of light signal makes it possible to print more complex products with specific function, e.g. human issues or organs, a further step of what we have presented here.

Reference

  • 1. Lam, C.X.F., Mo, X.M., Teoh, S.H., Hutmacher, D.W.(2002) Scaffold development using 3D printing with a starch-based polymer. Mat. Sci. Eng. C., 20: 49: 56
  • 2. Nicola Jones(2012).Science in three dimensions: The print revolution. Nature, 487: 22: 23
  • 3. Leukers, B., Gulkan, H., Irsen, S.H., Milz, S., Tille, C., Schieker, M., Seitz, H.(2005) Hydroxyapatite scaffolds for bone tissue engineering made by 3D printing. J. Mater. Sci. Mater. Med., 16: 1121:1124
  • 4. Erickson, B., Singh, R., Winters, P.(2012) Synthetic Biology: Regulating Industry Uses of New Technologies. Science, 333:1254:1256
  • 5. Khalil, A.S., Collins, J.J.(2010)Synthetic biology: applications come of age. Nat. Rev. Genet., 11:367: 379
  • Totop Totop