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	<title>Quantum Discovery Labs &#187; ADME</title>
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		<title>From Biological Spectra (multiple protein binding data) to pharmacological profiling!</title>
		<link>http://q-pharm.com/2008/09/from-biological-spectra-multiple-protein-binding-data-to-pharmacological-profiling/</link>
		<comments>http://q-pharm.com/2008/09/from-biological-spectra-multiple-protein-binding-data-to-pharmacological-profiling/#comments</comments>
		<pubDate>Thu, 25 Sep 2008 12:53:00 +0000</pubDate>
		<dc:creator>fedichev</dc:creator>
				<category><![CDATA[absorbtion]]></category>
		<category><![CDATA[active transport]]></category>
		<category><![CDATA[ADME]]></category>
		<category><![CDATA[bioavailability]]></category>
		<category><![CDATA[toxicity]]></category>

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		<description><![CDATA[An ideal drug cures a decease and does not kill a patient (or even lab animals in the course of preclinical testing). Usual drug discovery paradigm is based on studying...
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</ol>]]></description>
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		<slash:comments>0</slash:comments>
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		<title>From binding data to pharmacokinetics: a novel approach to active drug absorbtion prediction</title>
		<link>http://q-pharm.com/2008/09/from-binding-data-to-pharmacokinetics-a-novel-approach-to-active-drug-absorbtion-prediction/</link>
		<comments>http://q-pharm.com/2008/09/from-binding-data-to-pharmacokinetics-a-novel-approach-to-active-drug-absorbtion-prediction/#comments</comments>
		<pubDate>Thu, 25 Sep 2008 12:07:00 +0000</pubDate>
		<dc:creator>fedichev</dc:creator>
				<category><![CDATA[absorbtion]]></category>
		<category><![CDATA[active transport]]></category>
		<category><![CDATA[ADME]]></category>
		<category><![CDATA[bioavailability]]></category>
		<category><![CDATA[publications]]></category>

		<guid isPermaLink="false">http://q-pharm.com/?p=38</guid>
		<description><![CDATA[Oral administered drugs are mainly absorbed in the small intestine. Here, depending on drug composition and size, absorption can happen through a variety of processes . Through the epithelial cells...
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</ol>]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Model of Intestinal Passive Absorption</title>
		<link>http://q-pharm.com/2008/04/model-of-intestinal-passive-absorption/</link>
		<comments>http://q-pharm.com/2008/04/model-of-intestinal-passive-absorption/#comments</comments>
		<pubDate>Thu, 10 Apr 2008 06:10:00 +0000</pubDate>
		<dc:creator>fedichev</dc:creator>
				<category><![CDATA[absorbtion]]></category>
		<category><![CDATA[ADME]]></category>

		<guid isPermaLink="false">http://q-pharm.com/?p=26</guid>
		<description><![CDATA[Drug penetration from intestinum into blood can be divided into two processes: the drug diffusion to apical membrane of enterocytes and the drug diffusion through the membrane. Let C0, C1...
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>QUANTUM and HSA binding calculations: the role of protein flexibility</title>
		<link>http://q-pharm.com/2007/09/quantum-and-albumin-binding-calculations-the-role-of-protein-flexibility/</link>
		<comments>http://q-pharm.com/2007/09/quantum-and-albumin-binding-calculations-the-role-of-protein-flexibility/#comments</comments>
		<pubDate>Mon, 03 Sep 2007 08:52:00 +0000</pubDate>
		<dc:creator>fedichev</dc:creator>
				<category><![CDATA[ADME]]></category>
		<category><![CDATA[docking]]></category>
		<category><![CDATA[IC50]]></category>
		<category><![CDATA[Quantum Software]]></category>

		<guid isPermaLink="false">http://q-pharm.com/?p=13</guid>
		<description><![CDATA[Drug distribution within the body is determined mainly by free (unbound) concentration of drug in circulating plasma. The unbound fraction, in turn, depends on drug absorption by plasma proteins. Human...
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</ol>]]></description>
		<wfw:commentRss>http://q-pharm.com/2007/09/quantum-and-albumin-binding-calculations-the-role-of-protein-flexibility/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
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