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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>9</Volume><Issue>3-4</Issue></Journal><ArticleTitle>"Comparison of biodistribution of ¹¹¹In-Tropolone leukocytes and 125I-human nonspecific polyclonal IgG in normal and induced inflammation mice for detection of inflammation "</ArticleTitle><FirstPage>9</FirstPage><LastPage>17</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Shah Hosseini S</LastName></Author><Author><FirstName></FirstName><LastName>Hadizad T</LastName></Author><Author><FirstName></FirstName><LastName>Babaei MH</LastName></Author><Author><FirstName></FirstName><LastName>Najafi R</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Human nonspecific polyclonal IgG and granulocytes, which accumulate in inflammation foci, were radiolabeled with 125I and ¹¹¹In-Tropolone, respectively. Biodistribution of these two radiolabels was assessed in normal and inflammation-induced mice. 125I-IgG showed better localization to the inflammated areas. Blood levels with ¹¹¹In-Tropolone leukocytes were lower at all time points. In addition, the inflammatory thigh-to-blood ratios showed an improvement, whereas the ratios of inflammatory thigh-to-other normal tissues were higher for 125I-IgG than ¹¹¹In-Tropolone leukocytes. In conclusion, labeled IgG due to better localization in inflammated sites and higher target-to-background ratios is more suitable agent than labeled leukocytes for immunoscintigraphy of inflammation.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/122</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/122/122</pdf_url></Article></Articles>
