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        <full_title>The Open Dentistry Journal</full_title>
        <abbrev_title>TODENTJ</abbrev_title>
        <issn media_type="print">1874-2106</issn>
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        <publication_date media_type="print">
          <month>10</month>
          <day>16</day>
          <year>2009</year>
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        <journal_volume>
          <volume>3</volume>
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        <issue>1</issue>
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        <titles>
          <title>Effect of Short-Time Povidone-Iodine Application on Osteoblast Proliferation and Differentiation</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>P.R</given_name>
            <surname>Schmidlin</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>T</given_name>
            <surname>Imfeld</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>P</given_name>
            <surname>Sahrmann</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>A</given_name>
            <surname>Tchouboukov</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <given_name>F.E</given_name>
            <surname>Weber</surname>
          </person_name>
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        <jats:abstract>
             <jats:sec>
               <jats:title>Background and Objective:</jats:title>   
                 <jats:p>Povidone-iodine [polyvinylpyrrolidone-iodine complex (PVP-I)] is a broad-spectrum antimicrobial agent, frequently used in dentistry. In this study we investigated the short- and longterm effects on osteoblast number, viability, and function after short exposure to PVP-I with and without additional bone-morphogenetic protein-2 (BMP-2). </jats:p>
             </jats:sec>
             <jats:sec>
               <jats:title>Material and Methods:</jats:title>
                 <jats:p>Confluent osteoblast-like cell line (MC3T3-E1, subclone 24) cultures were exposed to pure PVP-I solution (7.7 mg/ml) and dilutions of 1:10, 1:100 and 1:1000 for 10 seconds and washed with phosphate buffer solution. Cell proliferation and viability was determined by MTT and differentiation status by alkaline phosphatase (ALP) activity 6 days after initial plating. In a separate experiment, long-term cell proliferation, viability and function were assessed 4 weeks after PVP-I treatment by MTT and deposited calcium using an Alizarin-red staining test.</jats:p>
             </jats:sec>
             <jats:sec>
               <jats:title>Results:</jats:title>   
                <jats:p>PVP-I decreased ALP activity substantially. Stimulation by BMP-2 recovered ALP activity to near control levels at 1:100 and 1:1000 dilutions of PVP-I. The MTT assay showed reduced proliferation of the preosteoblastic cells for all treatments, irrespective whether BMP-2 was used or not. Only at PVP-I dilutions of 1:1000 proliferation rate was back to normal levels (95.6±2.4 %). No adverse long-term effect of PVP-I on mineralization of the extracellular matrix (Alizarinred) for dilutions higher than 1:100 was observed. Interestingly, undiluted and 1:10 diluted PVP-I even showed a significant increase in mineral deposition, especially in the presence of BMP-2.</jats:p>
             </jats:sec>
             <jats:sec>
               <jats:title>Conclusion:</jats:title>
                <jats:p>Short-time application of PVP-I in concentrations of 1:10 and higher lead to decreased viability and impaired differentiation. However, surviving cells showed good recovery and mineralization potential.</jats:p>
             </jats:sec>            
            </jats:abstract>
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          <month>10</month>
          <day>16</day>
          <year>2009</year>
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          <first_page>208</first_page>
          <last_page>212</last_page>
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