<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>RSS for Quantification of thiopurine/UVA-induced singlet oxygen production</title><link>http://academic.research.microsoft.com/Rss.aspx?cata=9&amp;id=49497774</link><description>Search RSS feed for Microsoft Academic Search</description><generator>MSRA Libra RSS Burner</generator><copyright>(c)2008 Microsoft Corpration, All right reserved.</copyright><pubDate>Mon, 20 May 2013 09:23:59 GMT</pubDate><lastBuildDate>Mon, 20 May 2013 09:23:59 GMT</lastBuildDate><category /><item><title>Quantification of thiopurine/UVA-induced singlet oxygen production</title><link>http://academic.research.microsoft.com/Publication/49497774</link><pubDate>Mon, 20 May 2013 02:23:59 GMT</pubDate><guid isPermaLink="false">494977740</guid><description><![CDATA[<div><a href="http://academic.research.microsoft.com/Author/19886290">Yazhou Zhang</a>, <a href="http://academic.research.microsoft.com/Author/51010962">Ashley N. Barnes</a>, <a href="http://academic.research.microsoft.com/Author/53730738">Xianchun Zhu</a>, <a href="http://academic.research.microsoft.com/Author/53587926">Naomi F. Campbell</a>, <a href="http://academic.research.microsoft.com/Author/18152020">Ruomei Gao</a>:
            
            <span style="margin-left:20px" /><span style="margin-left:20px"><a href="http://www.sciencedirect.com/science/article/pii/S1010603011003704">view publication</a></span></div><div>Thiopurines were examined for their ability to produce <a href='http://academic.research.microsoft.com/Keyword/37922/singlet-oxygen'>singlet oxygen</a>  (1O2) with UVA light. The target compounds were three thiopurine prodrugs, azathioprine (Aza), 6-mercaptopurine (6-MP) and 6-thioguanine (6-TG), and their S-methylated derivatives of 6-methylmercaptopurine (me6-MP) and 6-methylthioguanine (me6-TG). Our results showed that these thiopurines were efficient 1O2 sensitizers under UVA irradiation but rapidly lost their photoactivities for 1O2 production over time by a self-sensitized photooxidation of sulfur atoms in the presence of oxygen and UVA light. The initial quantum yields of 1O2 production were determined to be in the range of 0.3–0.6 in aqueous solutions. Substitution of a <a href='http://academic.research.microsoft.com/Keyword/18809/hydrogen-atom'>hydrogen atom</a>  with a nitroimidazole or methyl group at S decreased the efficacy of photosensitized 1O2 production as found for Aza, me6-MP and me6-TG. 1O2-induced formation of 8-oxo-7,8-dihydro-2′-dexyguanosine (8-oxodGuo) was assessed by incubation of 6-methylthiopurine/UVA-treated <a href='http://academic.research.microsoft.com/Keyword/50903/calf-thymus'>calf thymus</a>  DNA with human repair <a href='http://academic.research.microsoft.com/Keyword/12659/enzyme'>enzyme</a>  8-oxodGuo DNA glycosylase (hOGG1), followed by apurinic (AP) site determination. Because more 8-oxodGuo was formed in Tris D2O than in Tris H2O, 1O2 is implicated as a key species in the reaction. These findings provided quantitative information on the photosensitization efficacy of thiopurines and to some extent revealed the correlations between photoactivity and phototoxicity.</div><div></div><div>Journal: <a href="http://academic.research.microsoft.com/Journal/2165">Journal of Photochemistry and Photobiology A-chemistry - J PHOTOCHEM PHOTOBIOL A-CHEM</a>, vol. 224, no. 1, pp. 16-24, 2011</div><div />]]></description></item></channel></rss>