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	<title>Semicrystalline &#187; biomaterials</title>
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		<title>Plastic Blood?</title>
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		<pubDate>Fri, 11 May 2007 18:53:36 +0000</pubDate>
		<dc:creator>vanillin</dc:creator>
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		<description><![CDATA[I’m a little behind on my ‘interesting papers’ at the moment, but when this story hit the headlines this morning I wanted to talk further about the concepts[1,2].  The RSC was ahead of the curve with their chemical science article last year[3].
The background is that Lance Twyman, (University of Sheffield) has developed a polymer-porphyrin system [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=semicrystalline.wordpress.com&blog=969298&post=8&subd=semicrystalline&ref=&feed=1" />]]></description>
			<content:encoded><![CDATA[<div class='snap_preview'><br /><p style="margin:0;" class="MsoNormal"><font face="Times New Roman">I’m a little behind on my ‘interesting papers’ at the moment, but when this story hit the headlines this morning I wanted to talk further about the concepts[1,2].<span>  </span>The RSC was ahead of the curve with their chemical science article last year[3].</font></p>
<p><font face="Times New Roman">The background is that Lance Twyman, (University of Sheffield) has developed a polymer-porphyrin system with potential for acting as synthetic hemoglobin[4,5]. Hemoglobin is the oxygen carrying protein in blood and has a porphyrin unit.<span>  </span>Porphyrin with Fe (II) can bind oxygen reversibly.<span>  </span>The protein structure of hemoglobin protects the oxygen at the active site, isolating the porphyrin and protecting against deactivation.<span>  </span>Synthetic molecules that mimic the properties of hemoglobin must have a mechanism to protect the oxygen species whilst retaining reversible binding.<span>  </span>Twyman uses a hyperbranced polymer based on 3,5-diacetoxybenzoic acid, starting with tetrakis(4-acetoxyphenyl)porphyrin as the core.<span>  </span>The advantage of this system over (for example) a dendritic system with similar structure is that the polymer can be made in one step, eliminating the growth-activation strategy that normally plagues dendrimer chemists.<span>  </span>There are several examples of dendritic hemoglobin mimics but none have as elegant a synthetic method as this one.</font></p>
<p style="margin:0;" class="MsoNormal"><img src="http://semicrystalline.files.wordpress.com/2007/05/branch.thumbnail.jpg" alt="branch.jpg" /><a href="http://semicrystalline.files.wordpress.com/2007/05/porphyrin.jpg" title="porphyrin.jpg"><img src="http://semicrystalline.files.wordpress.com/2007/05/porphyrin.thumbnail.jpg" alt="porphyrin.jpg" /></a></p>
<p><font face="Times New Roman">The polymer branch, and the porphyrin core. </font><font face="Times New Roman"></p>
<p style="margin:0;" class="MsoNormal">&nbsp;</p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">Blood is made of many different components, of which hemoglobin is just one. Artificial blood must perform a variety of functions including carrying oxygen around the body, but critically the viscosity of blood must also be maintained.<span>  </span>Ideally replacing lost blood should be done with a liquid of similar viscosity to maintain correct cardiac function.<span>   </span>One reason this polymeric porphyrin may be additionally useful is that the polymeric component may be sufficient to increase the viscosity of any solution.</font></p>
<p style="margin:0;" class="MsoNormal">&nbsp;</p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">The drawbacks of such a system are touched upon briefly by Twyman in the Guardian article [2].<span>  </span>Twyman believes that the polymer will be ignored by the body’s immune system but the experiments to date have been in vitro.<span>  </span>Any polymeric material for human use must meet stringent criteria.<span>  </span>The polymer and any potential breakdown materials must not be toxic.<span>  </span>The polymer can be biocompatible, bioinert, biodegradeable, but close attention must be paid to the ultimate fate of the polymer within the body.<span>  </span>Which organs would it accumulate in?<span>  </span>How and where and when will it breakdown?<span>  </span>These are all questions that must be answered before this system can be applied in medicine, but don’t detract in anyway from the potential life saving usefulness of this discovery.</font></p>
<p style="margin:0;" class="MsoNormal">&nbsp;</p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">My only concern regarding the articles I’ve seen to day is the use of the term ‘plastic blood’.<span>  </span>I appreciate that it is important to convey concepts to the public but do we really want people associating grocery bags and non-biodegradable landfill disasters with a blood substitute?<span>  </span>I think polymer is a better, although less understood term, in this application.<span>  </span>Plastic is a little too simplified.<span>  </span></font></p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">[1] </font><a href="http://news.bbc.co.uk/2/hi/uk_news/england/north_yorkshire/6645923.stm"><font color="#800080" face="Times New Roman">http://news.bbc.co.uk/2/hi/uk_news/england/north_yorkshire/6645923.stm</font></a></p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">[2] </font><a href="http://technology.guardian.co.uk/weekly/story/0,,2075544,00.html"><font color="#800080" face="Times New Roman">http://technology.guardian.co.uk/weekly/story/0,,2075544,00.html</font></a></p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">[3] </font><a href="http://www.rsc.org/Publishing/ChemScience/Volume/2006/05/artificial_blood.asp"><font color="#800080" face="Times New Roman">http://www.rsc.org/Publishing/ChemScience/Volume/2006/05/artificial_blood.asp</font></a></p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">[4] </font><a href="http://www.rsc.org/delivery/_ArticleLinking/DisplayArticleForFree.cfm?doi=b600831n&amp;JournalCode=CC"><font color="#800080" face="Times New Roman">http://www.rsc.org/delivery/_ArticleLinking/DisplayArticleForFree.cfm?doi=b600831n&amp;JournalCode=CC</font></a></p>
<p style="margin:0;" class="MsoNormal"><font face="Times New Roman">[5] </font><a href="http://www.shef.ac.uk/chemistry/staff/profiles/twyman.html"><font color="#800080" face="Times New Roman">http://www.shef.ac.uk/chemistry/staff/profiles/twyman.html</font></a></p>
<p align="center"><font face="Times New Roman"> </font><font face="Times New Roman"> </font><font face="Times New Roman"> <em>Vanillin</em></font></p>
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