<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>ChemCafé &#187; Miscellaneous</title>
	<atom:link href="http://www.chemcafe.net/category/uncategorized/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.chemcafe.net</link>
	<description>Chemistry and beyond</description>
	<lastBuildDate>Tue, 01 Nov 2011 04:21:40 +0000</lastBuildDate>
	<generator>http://wordpress.org/?v=2.8.2</generator>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
			<item>
		<title>Inject-and-solidify: new biomaterials for tissue restoration</title>
		<link>http://www.chemcafe.net/inject-and-solidify-new-biomaterials-for-tissue-restoration/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=inject-and-solidify-new-biomaterials-for-tissue-restoration</link>
		<comments>http://www.chemcafe.net/inject-and-solidify-new-biomaterials-for-tissue-restoration/#comments</comments>
		<pubDate>Mon, 26 Sep 2011 14:36:04 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=749</guid>
		<description><![CDATA[Biocompatible polymers are avidely sought for owing to their frequent use in reconstructive sugery and as prostheses. One of the challenges is to make implants that are easy to inserate, minimizing scarring and recovery time.
A team led by Prof. Jennifer Helisseeff at Johns Hopkins University recently presented a novel implant, that can be injected as [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Biocompatible polymers are avidely sought for owing to their frequent use in reconstructive sugery and as prostheses. One of the challenges is to make implants that are easy to inserate, minimizing scarring and recovery time.</p>
<p style="text-align: justify;">A team led by Prof. <a title="Jennifer Helisseeff" href="http://web1.johnshopkins.edu/JLAB/spip.php?article11#" target="_blank">Jennifer Helisseeff</a> at Johns Hopkins University recently presented a novel implant, that can be injected as a liquid under the skin, then modeled to appropriate shape, and solidified by exposure to light. The composite material is made by mixing polyethylene glycol (PEG), a widely used artificial polymer, with hyaluronic acid, a natural polysaccharide. The ratio of PEG and hyaluronic acid can be tuned, such as to modulate the properties of the final polymer: it can then be adapted to  the location where the injection takes place (fat, muscle, skin). After injection under the skin (tests were made on rodents and with human patients), the implants could be massaged into shape. Finally, exposure to visible light initiated a cross-linking reaction between the PEG molecules, transforming the implant into a solid, shape-persistent hydrogel with entrapped hyaluronic acid molecules.</p>
<p style="text-align: justify;">Although the newly-develped implants possess good longevity and stability, it was found that they cause more inflammation than currently used implants. However, the presented technique will probably find numerous application in reconstructive surgery, as soon as the last problems will have been sorted out.</p>
<div id="attachment_753" class="wp-caption aligncenter" style="width: 190px"><img class="size-full wp-image-753" title="news444-i1.0" src="http://www.chemcafe.net/wp-content/uploads/2011/09/news444-i1.0.jpg" alt="The liquid polymer is injected, and solidified by irradiation." width="180" height="402" /><p class="wp-caption-text">The liquid polymer is injected, and solidified by irradiation.</p></div>
<p>Reference: A. T. Hillel et al., <em>Sci. Trans. Med.</em> <strong>2011</strong>, <em>3</em>, 93ra67. DOI: <a title="Photoactivated Composite Biomaterial for Soft Tissue Restoration in Rodents and in Humans" href="http://stm.sciencemag.org/content/3/93/93ra67.abstract" target="_blank">10.1126/scitranslmed.3002331</a></p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/inject-and-solidify-new-biomaterials-for-tissue-restoration/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Neuroprotective Effects of Nicotine</title>
		<link>http://www.chemcafe.net/neuroprotective-effects-of-nicotine/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=neuroprotective-effects-of-nicotine</link>
		<comments>http://www.chemcafe.net/neuroprotective-effects-of-nicotine/#comments</comments>
		<pubDate>Tue, 02 Aug 2011 03:51:46 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=736</guid>
		<description><![CDATA[Sixteenth-century Swiss physician, botanist, alchemist, and astrologer Paracelsus* is widely known for his famous observation that &#8220;All things are poison, and nothing is without poison; only the dose permits something not to be poisonous&#8221;, generally summarized as &#8220;The dose makes the poison&#8221;.
No better illustration of the dual character of virtually any substance can be found [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Sixteenth-century Swiss physician, botanist, alchemist, and astrologer Paracelsus* is widely known for his famous observation that &#8220;All things are poison, and nothing is without poison; only the dose permits something not to be poisonous&#8221;, generally summarized as &#8220;The dose makes the poison&#8221;.</p>
<p style="text-align: justify;">No better illustration of the dual character of virtually any substance can be found than <a title="Neuroprotection of midbrain dopamine neurons by nicotine is gated by cytoplasmic Ca2+" href="http://www.fasebj.org/content/25/8/2563" target="_blank">this report</a> recently appeared in the <a title="FASEB journal" href="http://www.fasebj.org/" target="_blank">FASEB journal</a>. A team of researchers from Paris led by Patrick P. Michel investigated the beneficial effects of nicotine for neuroprotection. Their findings suggest potential development of novel therapies for diseases such as Parkinson&#8217;s, that target nicotine receptors: according to experiments performed on brain cells of mice, they found that nicotine seems to provide protective effect against some type of neuron loss, a symptom widely associated to Parkinson&#8217;s disease.</p>
<p style="text-align: justify;">Of course, as Gerald Weissmann, Editor-in-Chief of The FASEB Journal, comments on <a href="http://www.sciencedaily.com/releases/2011/08/110801111738.htm" target="_blank">ScienceDaily</a>: &#8220;If you&#8217;re a smoker, don&#8217;t get too excited. Even if smoking protects you from Parkinson&#8217;s, you might not live long enough to develop the disease because smoking greatly increases the risk for deadly cancers and cardiovascular diseases [...]&#8221; Still, this discovery is significant. Not only in terms of Parkinson&#8217;s diagnosis and treatment, but also because it shows that a usually ill-considered substance such as nicotine can have some positive effects &#8211; it might be a matter of dose after all! This is a lesson for scientists, who sometimes tend to neglect fields of research on the pretext they are not fashionable enough, and also for those who fund scientists: it is probably not the simplest task to raise money for studying such ill-reputed compound as nicotine.</p>
<p style="text-align: justify;">References:</p>
<p style="text-align: justify;">D. Toulorge, S. Guerreiro, A. Hild, U. Maskos, E. C. Hirsch, P. P. Michel., <em>The FASEB Journal</em> <strong>2011</strong>, <em>25</em> (8), 2563 DOI: <a title="http://www.fasebj.org/content/25/8/2563" href="http://www.fasebj.org/content/25/8/2563">10.1096/fj.11-182824<br />
</a><br />
ScienceDaily. Retrieved August 1, 2011, from  <a title="Nicotine Can Protect the Brain from Parkinson's Disease, Research Suggests" href=" http://www.sciencedaily.com­/releases/2011/08/110801111738.htm" target="_blank">http://www.sciencedaily.com­/releases/2011/08/110801111738.htm<br />
</a></p>
<p style="text-align: justify;">*born Philippus Aureolus Theophrastus Bombastus von Hohenheim&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/neuroprotective-effects-of-nicotine/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>DNA-based chemical computer calculates square roots</title>
		<link>http://www.chemcafe.net/dna-based-chemical-computer-calculates-square-roots/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=dna-based-chemical-computer-calculates-square-roots</link>
		<comments>http://www.chemcafe.net/dna-based-chemical-computer-calculates-square-roots/#comments</comments>
		<pubDate>Tue, 05 Jul 2011 19:47:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=728</guid>
		<description><![CDATA[DNA computing was first proposed in the mid-90s and uses chemical reactions to solve problems, using DNA strands as &#8216;bits&#8217;. The work recently published in Science by Lulu Qian and Erik Winfree from Caltech demonstrates the use of DNA for performing calculations (ie, finding the square roots of numbers up to 15). Made from 130 [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">DNA computing was first proposed in the mid-90s and uses chemical reactions to solve problems, using DNA strands as &#8216;bits&#8217;. The <a title="Scaling Up Digital Circuit Computation with DNA Strand Displacement Cascades" href="http://www.sciencemag.org/content/332/6034/1196.abstract?sid=34941e10-ee03-4446-8dc7-4de7d36ea10b">work</a> recently published in <a title="Science" href="http://www.sciencemag.org/" target="_blank&quot;">Science</a> by Lulu Qian and <a title="Winfree Lab" href="http://www.dna.caltech.edu/" target="_blank">Erik Winfree</a> from <a title="Caltech" href="http://www.caltech.edu/" target="_blank">Caltech</a> demonstrates the use of DNA for performing calculations (ie, finding the square roots of numbers up to 15). Made from 130 DNA strands, the systems uses logic gates (the OR, AND, etc. functions) that are made of carefully selected DNA sequences; the input and ouptut signals are also DNA strands.</p>
<p style="text-align: justify;">When input strands are added to a mixture containing the sophisticated DNA system, cascade reactions between the DNA strands are initiated, that sequencially zip and unzip from one another depending on the inputs. After the computation has been performed (<em>ie</em>, the cascade reactions stop), the response appears under the form of a given fluorescence colour. For each output, a specific colour indicates &#8216;0&#8242;, and another colour corresponds to &#8216;1&#8242; (like &#8216;real&#8217; computers, this one works in binary numbers). The researchers used the &#8217;square root solving problem&#8217; to demonstrate the capacities of their system. However, one of the remarkable points of the piece of work is its very systematic design: one can therefore imagine different function for such a system, like diagnosing illnesses: such a device could provide specific responses depending of what chemicals are present in a patient&#8217;s blood, for example.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/dna-based-chemical-computer-calculates-square-roots/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>PhDs in questions</title>
		<link>http://www.chemcafe.net/phds-in-questions/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=phds-in-questions</link>
		<comments>http://www.chemcafe.net/phds-in-questions/#comments</comments>
		<pubDate>Mon, 02 May 2011 02:13:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=711</guid>
		<description><![CDATA[George Whitesides from Harvard University and John Deutch from MIT initiated the debate in a Comment published in the first 2011 issue of the journal Nature. In an issue mostly dedicated to chemistry (remember, 2011 is International Year of Chemistry), they advocate several changes chemical research in universities should undergo in order to &#8220;solve big [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;"><a title="George M. Whitesides" href="http://gmwgroup.harvard.edu/people_biography.html" target="_blank">George Whitesides</a> from <a title="Harvard University" href="http://www.harvard.edu/" target="_blank">Harvard University</a> and <a title="John M. Deutch" href="http://mit.edu/chemistry/deutch/biography.html" target="_blank">John Deutch</a> from <a title="Massachusetts Institute of Technology" href="http://mit.edu/" target="_blank">MIT</a> initiated the debate in a <a title="Let's get practical" href="http://www.nature.com/nature/journal/v469/n7328/full/469021a.html" target="_blank">Comment</a> published in the <a title="Nature 469 7328 Celebrating Chemistry" href="http://www.nature.com/nature/journal/v469/n7328/index.html" target="_blank">first 2011 issue</a> of the journal <a href="http://www.nature.com/nature/index.html" target="_blank2 title=">Nature</a>. In an issue mostly dedicated to chemistry (remember, 2011 is International Year of Chemistry), they advocate several changes chemical research in universities should undergo in order to &#8220;solve big global problems and advance fundamental understanding&#8221;. Of particular interest for PhD students &#8211; and to a broader extent, for their supervisors &#8211; they outline the &#8216;ideal&#8217;, 21st-century doctoral candidate: He/she must be cross-disciplinary, educated not only in a narrow speciality but more globally in a whole domain (catalysis, materials, energy, etc.) and in non-scientific fields such as economics and corporate finance, in order to be more fit for post-graduation challenges. Here, it is necessary to mention that chemistry is somewhat particular in the sense that a large fraction of people engaging in doctoral studies do not plan to pursue academic careers &#8211; contrary to most scientific/technical fields. Chemistry-related industries are known not to be satisfied with only BSc&#8217;s or MSc&#8217;s but to require PhDs to populate their research labs.</p>
<p style="text-align: justify;">After this first charge against conservative academic research came the second strike, still in Nature, in the form of a whole issue (!) entitled <a title="The future of the PhD" href="http://www.nature.com/nature/journal/v472/n7343/index.html" target="_blank">&#8220;The future of the PhD&#8221;</a>. This time it is not about chemistry only, but about the PhD system as a whole. A series of articles (<a title="Education: the PhD factory" href="http://www.nature.com/news/2011/110420/full/472276a.html" target="_blank">&#8220;Education: the PhD factory&#8221;</a>, <a title="Education: rethinking PhDs" href="http://www.nature.com/news/2011/110420/full/472280a.html" target="_blank">&#8220;Education: rethinking PhDs&#8221;</a>) and opinions (<a title="Reform the PhD system or close it down" href="http://www.nature.com/news/2011/110420/full/472261a.html" target="_blank">&#8220;Reform the PhD system or close it down&#8221;</a>, <a title="What is a PhD really worth?" href="http://www.nature.com/nature/journal/v472/n7343/full/nj7343-381a.html" target="_blank">&#8220;What is a PhD really worth?&#8221;</a>, <a title="Fix the PhD" href="http://www.nature.com/nature/journal/v472/n7343/full/472259b.html" target="_blank">&#8220;Fix the PhD&#8221;</a>) highlight the qualities and defaults of PhDs &#8211; and raise numerous hot debates among readers. Essentially, there are more PhD students and more doctoral programmes than ever, and not enough academic positions for all these graduates &#8211; in most fields, the only jobs PhD students have ever been trained for. Consequently, hosts of PhDs will have to spend 5 or 10 tiresome years in ill-paid postdocs (waiting for an hypothetical academic position) or go to work in industry, but won&#8217;t be prepared for that: too specialized, not having the required &#8216;real-world&#8217; experience, too expensive, etc. None of these perspectives seems appealing, particularly when speaking of people who spent years and significant amounts of (taxpayers&#8217;) money to achieve the highest levels of education.</p>
<p style="text-align: justify;">There is probably no ready-made solution to these questions, but they must be of direct concern to the research world &#8211; particularly, to PhD students and recent graduates: they must be aware of the opportunities &#8211; or lack of them &#8211; that await them in the &#8216;post-doctorate&#8217; (in the literal sense) world, and of what it takes to be more attractive for a future career: broad field of knowledge, soft skills and profesionnal education.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/phds-in-questions/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Does technological progress mean less respect?</title>
		<link>http://www.chemcafe.net/does-technological-progress-mean-less-respect/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=does-technological-progress-mean-less-respect</link>
		<comments>http://www.chemcafe.net/does-technological-progress-mean-less-respect/#comments</comments>
		<pubDate>Mon, 30 Aug 2010 23:07:04 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[chemistry]]></category>
		<category><![CDATA[dye sensitized solar cell]]></category>
		<category><![CDATA[energy]]></category>
		<category><![CDATA[EuChEMS]]></category>
		<category><![CDATA[grätzel]]></category>
		<category><![CDATA[nanotechnology]]></category>
		<category><![CDATA[science]]></category>
		<category><![CDATA[solar cell]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=605</guid>
		<description><![CDATA[Still reporting from Nürnberg (where the EuCheMS meeting takes place this week), I had the opportunity this morning to observe and think on how people behave at a conference.
In my imagination, conferences in the past involved a passionate speaker (usually wearing a hat) who was disclosing his/her latest discoveries, vehemently speaking or writing on a [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Still reporting from Nürnberg (where the <a title="3 rd EuCheMS Chemistry Congress Nürnberg 2010" href="http://www.euchems-congress2010.org/" target="_blank">EuCheMS meeting</a> takes place this week), I had the opportunity this morning to observe and think on how people behave at a conference.</p>
<p style="text-align: justify;">In my imagination, conferences in the past involved a passionate speaker (usually wearing a hat) who was disclosing his/her latest discoveries, vehemently speaking or writing on a blackboard (sometimes performing live experiments) while the audience was listening in a profound, respectful silence.</p>
<p style="text-align: justify;">Today, what I saw was somewhat different &#8211; and I&#8217;m not talking of speakers not wearing hats. Actually, I was at a presentation seating next to a professor, <em>who was preparing the powerpoint he was going to present in the afternoon</em>. To do this, he had to ask his collaborator, seated next to him, about the meaning of some graphs he intended to include in the presentation. This took approximately one hour, and was quite disturbing to all the people around, since the discussion included mumblings and laughters.</p>
<p style="text-align: justify;">So, without even considering half of the members of the audience who checked their e-mails or the news on CNN every 5 minutes on their iPhone, I was wondering whether the speaker was noticing this lack of attention. The answer I guessed is probably no (because speakers are generally too busy and stressed to notice what happens behind the front row) but still, I&#8217;m wondering why people go to talks to prepare their own slides??</p>
<p style="text-align: justify;">Besides, I wanted to mention today&#8217;s plenary session, where Prof. <a title="Michael Grätzel" href="http://isic2.epfl.ch/page58671-en.html" target="_blank">Michael Grätzel</a> from <a href="http://www.epfl.ch/index.en.html">EPFL</a> (it&#8217;s always funny to go abroad to attend talks from our own faculty) presented the latest advances in dye sensitized solar cells (DSCs). I still hope to write a full post about Prof. Grätzel&#8217;s work sometimes  (like next October 6th), and here I just want to mention that there is now a <a title="Michael Grätzel Center" href="http://222.20.94.9:8083/article.php?catPath=0,1,1019&amp;catID=1035&amp;articleID=172" target="_blank">Michael Grätzel Center</a> in Wuhan (China) which, I think, is quite something. The optimism and enthusiasm of Prof. Grätzel are always extraordinarily communicative (especially when it comes to <a title="Dyesol" href="http://www.dyesol.com/page/Home" target="_blank">recent applications</a>), and I&#8217;m deeply convinced that the future is bright for dye-sensitized solar cells</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/does-technological-progress-mean-less-respect/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>WolframAlpha: A useful resource for chemistry basics</title>
		<link>http://www.chemcafe.net/a-useful-resource-for-chemistry-basics/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=a-useful-resource-for-chemistry-basics</link>
		<comments>http://www.chemcafe.net/a-useful-resource-for-chemistry-basics/#comments</comments>
		<pubDate>Tue, 29 Sep 2009 18:20:17 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[News]]></category>
		<category><![CDATA[chemical computation]]></category>
		<category><![CDATA[chemistry]]></category>
		<category><![CDATA[data base]]></category>
		<category><![CDATA[knowledge base]]></category>
		<category><![CDATA[research]]></category>
		<category><![CDATA[science]]></category>
		<category><![CDATA[teaching]]></category>
		<category><![CDATA[WolframAlpha]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=465</guid>
		<description><![CDATA[Among the loads of various &#8216;concentration calculators&#8217; and &#8216;grams-versus-moles converters&#8217; that are available online, I think the one provided by WolframAlpha can be quite useful and is nicely done. For example, if you need to know how many moles of iron are present in 5 grams, just query &#8216;how many moles are in 5 grams [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Among the loads of various &#8216;concentration calculators&#8217; and &#8216;grams-versus-moles converters&#8217; that are available online, I think the one provided by <a href="http://www.wolframalpha.com/" target="_blank" title="WolframAlpha">WolframAlpha</a> can be quite useful and is nicely done. For example, if you need to know how many moles of iron are present in 5 grams, just query &#8216;how many moles are in 5 grams of iron?&#8217; and the answer is computed and -in principle- given together with unit conversions. More generally, if you&#8217;d like to obtain information on, say, ruthenium, just type &#8216;ruthenium&#8217; in the query bar, and you&#8217;ll quickly get the element&#8217;s position in the periodic table, as well as its most important chemical and physical properties. Last but not least, this very practical tool for students: if you enter &#8216;5M NaCl&#8217;, you directly obtain the quantity of salt to dissolve in order to prepare your solution!</p>
<p><img class="aligncenter size-full wp-image-467" title="chemistry_1" src="http://www.chemcafe.net/wp-content/uploads/2009/09/chemistry_1.gif" alt="chemistry_1" width="500" height="351" /></p>
<p style="text-align: justify;">Now, to be complete, I must mention that WolframAlpha comes with some limitations &#8211; or should I say, it is still being developed &#8211; but may well become an interesting alternative to other search engines. Among the limitations, if for example you enter &#8216;taxol&#8217; in the query bar, you obtain a very approximate structure of the molecule, with no mention of stereochemistry, although it is of prime importance for this type of molecules. It also seems that the notion of &#8216;buffer&#8217; does not (yet) exist, even though a &#8216;buffer calculator&#8217; would be quite useful&#8230;</p>
<p style="text-align: justify;">So have a look at <a href="http://www.wolframalpha.com/" target="_blank" title="WolframAlpha">WolframAlpha</a> if you need simple information (on chemistry or whatever else btw) and also have a look at their <a href="http://blog.wolframalpha.com/" target="_blank" title="WolframAlpha Blog">blog</a>, reporting their latest innovations and ideas.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/a-useful-resource-for-chemistry-basics/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>There and Back Again: a Space Odyssey</title>
		<link>http://www.chemcafe.net/there-and-back-again-a-space-odyssey/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=there-and-back-again-a-space-odyssey</link>
		<comments>http://www.chemcafe.net/there-and-back-again-a-space-odyssey/#comments</comments>
		<pubDate>Fri, 19 Jun 2009 14:00:10 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[1969]]></category>
		<category><![CDATA[apollo 11]]></category>
		<category><![CDATA[moon]]></category>
		<category><![CDATA[nasa]]></category>
		<category><![CDATA[nature]]></category>
		<category><![CDATA[space]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=350</guid>
		<description><![CDATA[Well, this post is not really chemistry-related, but I think it should probably be of interest for a broad audience, especially for everyone who likes dreaming when looking at a cloudless night sky&#8230; Nature News reports on Twitter the Apollo 11 mission as it happened, exactly 40 years ago &#8211; wish I was alive then&#8230; [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Well, this post is not really chemistry-related, but I think it should probably be of interest for a broad audience, especially for everyone who likes dreaming when looking at a cloudless night sky&#8230; Nature News reports on Twitter the Apollo 11 mission as it happened, exactly 40 years ago &#8211; wish I was alive then&#8230; &#8211; following the mission&#8217;s crew travel to the moon and back, as well as technical and political challenges which came along with the space race. Here is the <a title="ApolloPlus40 on Twitter" href="http://twitter.com/ApolloPlus40" target="_blank">link</a>, and <a title="In the field: ApolloPlus40 archives" href="http://blogs.nature.com/news/blog/events/apolloplus40/" target="_blank&quot;">here</a> is an accompanying blog run by Nature reporters. Hope you&#8217;ll enjoy the links, and maybe one day I&#8217;ll post on the weird molecules that were detected in space &#8211; others than waste humans have been disseminating over the years of course!</p>
<p style="text-align: justify;">Chemically speaking, I&#8217;ll attend next week the <a title="ISMSC 2009 Maastricht" href="http://www.ismsc-2009.org/" target="_blank">International Symposium on Macrocyclic &amp; Supramolecular Chemistry</a> in Maastricht, the Netherlands, where I hope to find inspiration both for researching and for blogging!</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/there-and-back-again-a-space-odyssey/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Allergies and Chemistry</title>
		<link>http://www.chemcafe.net/allergies-and-chemistry/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=allergies-and-chemistry</link>
		<comments>http://www.chemcafe.net/allergies-and-chemistry/#comments</comments>
		<pubDate>Sun, 07 Jun 2009 21:23:07 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[Molecules & Reactions]]></category>
		<category><![CDATA[allergy]]></category>
		<category><![CDATA[anti histamine]]></category>
		<category><![CDATA[biochemistry]]></category>
		<category><![CDATA[biology]]></category>
		<category><![CDATA[cetirizin]]></category>
		<category><![CDATA[chemistry]]></category>
		<category><![CDATA[hay fever]]></category>
		<category><![CDATA[histamine]]></category>
		<category><![CDATA[pollen]]></category>
		<category><![CDATA[research]]></category>
		<category><![CDATA[zyrtec]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=322</guid>
		<description><![CDATA[Spring is usually associated with renewal, growth and mating. For some people (including myself) it also means hay fever. So last morning I was taking my daily pill against allergies, I looked at the label on the flask, where it is mentionned that the active ingredient is &#8216;cetirizine hydrochloride&#8216;, which serves as &#8216;antihistamine&#8216;. So, what [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">Spring is usually associated with renewal, growth and mating. For some people (including myself) it also means <strong>hay fever</strong>. So last morning I was taking my daily pill against allergies, I looked at the label on the flask, where it is mentionned that the active ingredient is &#8216;<strong>cetirizine hydrochloride</strong>&#8216;, which serves as &#8216;<strong>antihistamine</strong>&#8216;. So, what is that? What is histamine, a molecule apparently bad enough to have its associated &#8216;anti&#8217; compound?</p>
<p style="text-align: justify;">Histamine is a very simple molecule which is present is basically every single cell of our bodies. It is produced through enzymatic decarboxylation of amino acid histidine. Histamine&#8217;s many roles include neurotransmission  (particularly in the sleep regulation mechanism) and immunological response, explaining why it is involved in various immunological troubles, ranging from relatively mild allergies to severe autoimmune diseases.</p>
<div id="attachment_326" class="wp-caption aligncenter" style="width: 273px"><img class="size-full wp-image-326" title="histamine" src="http://www.chemcafe.net/wp-content/uploads/2009/06/histamine.png" alt="Histamine" width="263" height="92" /><p class="wp-caption-text">Histamine</p></div>
<p style="text-align: justify;">A high proportion of histamine is stored in cells called mastocytes, which are located mostly at &#8216;risky&#8217; places where the outside world can come into contact with our internal tissues: skin, lungs, mouth, nose&#8230; sounds like places where we can feel allergies right? When an allergy reaction takes place, the (harmless to non-allergic people) allergen interacts at the surface of the mastocyte, inducing the release of a massive amount of histamine in the surrounding environment. This results in well known consequences, such as mucuous secretions, itchiness, conjunctivitis. To produce these effects, histamine needs to interact with particular receptors, called, not so surprisingly, histamine receptors. The easy solution to overcome these effects is to prevent the histamine+receptor interaction: this is done thanks to antihistamine molecules which are also binding to histamine receptors, but without inducing allergic symptoms (pharmacologically speaking, antihistamine is an inverse agonist of histamine).</p>
<p style="text-align: justify;">Finally, what about the widely reported drowsiness side-effect? As stated before, histamine plays a role in the sleep regulation. Histamine metabolism is perturbated upon antihistamine injestion, and one of the side effects is a (slight) inhability to maintain vigilance. Recent drugs (including my relieving cetirizin) are supposed to possess attenuated side-effects, but in my experience it is still not perfect since I tend to feel an urge to sleep after each intake&#8230;</p>
<div id="attachment_328" class="wp-caption aligncenter" style="width: 299px"><img class="size-full wp-image-328" title="cetirizine" src="http://www.chemcafe.net/wp-content/uploads/2009/06/cetirizine.png" alt="Cetirizine, the active compound of many antihistamine drugs." width="289" height="135" /><p class="wp-caption-text">Cetirizine, the active compound of many antihistamine drugs.</p></div>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/allergies-and-chemistry/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Huge molecules and polygon nomenclature</title>
		<link>http://www.chemcafe.net/huge-molecules-and-polygon-nomenclature/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=huge-molecules-and-polygon-nomenclature</link>
		<comments>http://www.chemcafe.net/huge-molecules-and-polygon-nomenclature/#comments</comments>
		<pubDate>Wed, 22 Apr 2009 23:03:19 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[achim muller]]></category>
		<category><![CDATA[chemistry]]></category>
		<category><![CDATA[inorganic chemistry]]></category>
		<category><![CDATA[molybdenum]]></category>
		<category><![CDATA[nanocapsules]]></category>
		<category><![CDATA[nanospheres]]></category>
		<category><![CDATA[nanotechnology]]></category>
		<category><![CDATA[polygons]]></category>
		<category><![CDATA[research]]></category>
		<category><![CDATA[science]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=68</guid>
		<description><![CDATA[This afternoon came to EPFL Prof. Achim Müller from University of Bielefeld (Germany) to give a talk to our institute. Among a series of impressive giant molybdenum-based spheres (see figure below) he mentioned molecules belonging to either Archimedean or Platonic solids&#8230; Although the talk itself was quite fascinating, the question I was asking to myself [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: justify;">This afternoon came to <a title="Swiss Federal Institute of Technology" href="http://www.epfl.ch" target="_blank">EPFL</a> Prof. <a title="Achim Muller" href="http://www.uni-bielefeld.de/chemie/ac1/" target="_blank">Achim Müller</a> from <a title="Bielefeld University" href="http://www.uni-bielefeld.de" target="_blank">University of Bielefeld</a> (Germany) to give a talk to our institute. Among a series of impressive giant molybdenum-based spheres (see figure below) he mentioned molecules belonging to either Archimedean or Platonic solids&#8230; Although the talk itself was quite fascinating, the question I was asking to myself when leaving the auditorium was, what is the difference between these two types of polygons? Well, after a quick search, it turns out a Platonic solid is a regular polygon such as a tetrahedron, cube, octahedron, etc: they all have only one type of faces. On the other hand, an Archimedean solid is a semi-regular (or truncated) polygon. To this class belong truncated tetrahedrons, cuboctahedrons, or, probably more familiar to many readers, the famous buckyball (also known as football, or truncated icosahedron, or buckminsterfullerene), which possesses 12 pentagonal and 20 hexagonal faces.</p>
<p>And now, for people who would (should) be more interested in Prof. Müller&#8217;s work than in greek terminology, here are a couple of links to some of his most significant publications, mainly dealing with huge porous capsules, and therefore containing amazing pictures.</p>
<div id="attachment_75" class="wp-caption aligncenter" style="width: 298px"><img class="size-medium wp-image-75" title="guapo2" src="http://www.chemcafe.net/wp-content/uploads/2009/04/guapo2-288x300.png" alt="Spherical polyoxomolybdate based capsule. The 20 pores are occupied by guanidinium cations." width="288" height="300" /><p class="wp-caption-text">Spherical polyoxomolybdate based capsule. The 20 pores are occupied by guanidinium cations.</p></div>
<p><a title="Achim Muller Angewandte Chemie International Edition" href="http://www3.interscience.wiley.com/journal/109596850/abstract" target="_blank"><em><br />
Angew. Chem. Int. Ed.</em> <strong>2004</strong>, <em>43</em>, 4466-4470</a>;<br />
<a title="Achim Muller Angewandte Chemie International Edition" href="http://www3.interscience.wiley.com/journal/104531055/abstract" target="_blank"><em>Angew. Chem. Int. Ed.</em> <strong>2003</strong>, <em>42</em>, 2085-2090</a>;<br />
<a title="Achim Muller Angewandte Chemie International Edition" href="http://www3.interscience.wiley.com/journal/106556951/abstract" target="_blank"><em>Angew. Chem. Int. Ed.</em> <strong>2003</strong>, <em>42</em>, 5039-5044</a>;<br />
<a title="Achim Muller Angewandte Chemie International Edition" href="http://www3.interscience.wiley.com/journal/99016375/abstract" target="_blank"><em>Angew. Chem. Int. Ed.</em> <strong>2002</strong>, <em>41</em>, 3604-3609</a>;<br />
<a title="Achim Muller Angewandte Chemie International Edition" href="http://www3.interscience.wiley.com/journal/72500160/abstract" target="_blank"><em>Angew. Chem. Int. Ed. Engl.</em> <strong>2000</strong>, <em>39</em>, 1614-1616</a>;</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/huge-molecules-and-polygon-nomenclature/feed/</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Acetonitrile shortage</title>
		<link>http://www.chemcafe.net/acetonitrile-shortage/?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=acetonitrile-shortage</link>
		<comments>http://www.chemcafe.net/acetonitrile-shortage/#comments</comments>
		<pubDate>Sat, 18 Apr 2009 20:46:38 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Miscellaneous]]></category>
		<category><![CDATA[acetonitrile]]></category>
		<category><![CDATA[chemical synthesis]]></category>
		<category><![CDATA[chemistry]]></category>
		<category><![CDATA[research]]></category>
		<category><![CDATA[science]]></category>

		<guid isPermaLink="false">http://www.chemcafe.net/?p=49</guid>
		<description><![CDATA[I went yesterday to the chemical stores to get a new 2.5L bottle of acetonitrile, and I was stunned to see the price had moreless quadrupled since the last time I bought this solvent&#8230; I was aware of the world shortage of this compound, but had never so directly observed its consequences. The funny thing [...]]]></description>
			<content:encoded><![CDATA[<p>I went yesterday to the chemical stores to get a new 2.5L bottle of acetonitrile, and I was stunned to see the price had moreless quadrupled since the last time I bought this solvent&#8230; I was aware of the world shortage of this compound, but had never so directly observed its consequences. The funny thing is, though, that this shortage (and the price increase that goes with it) is a direct consequence of the current economic slowdown: acetonitrile is obtained industrially as a byproduct during the production of acrylonitrile. The latter is used in the production of acrylic fibers and resins (plastics). Since the beginning of the economic meltdown the use of such industrial compounds has substantially decreased, thus the production of acetonitrile has also decreased. To make bad things worse, production in China was shut down before and during the Olympics, and a factory in the US was damaged by the hurricane Ike.</p>
<p>The good news is that people from the chemical stores told me the situation should improve this summer, but the prices will never go as low as before &#8211; there is apparently lots of money to get if you&#8217;re an acetonitrile supplier&#8230;</p>
]]></content:encoded>
			<wfw:commentRss>http://www.chemcafe.net/acetonitrile-shortage/feed/</wfw:commentRss>
		<slash:comments>2</slash:comments>
		</item>
	</channel>
</rss>

