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    <Identifier>25dkou300</Identifier>
    <IdentifierDoi>10.3205/25dkou300</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-25dkou3002</IdentifierUrn>
    <ArticleType>Meeting Abstract</ArticleType>
    <TitleGroup>
      <Title language="en">Evaluation of photoantimicrobials in the treatment of orthopaedic infections</Title>
    </TitleGroup>
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        <PersonNames>
          <Lastname>Youf</Lastname>
          <LastnameHeading>Youf</LastnameHeading>
          <Firstname>Raphaelle</Firstname>
          <Initials>R</Initials>
        </PersonNames>
        <Address>
          <Affiliation>University Hospital Regensburg, Regensburg, Deutschland</Affiliation>
        </Address>
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      <Creator>
        <PersonNames>
          <Lastname>Brasz</Lastname>
          <LastnameHeading>Brasz</LastnameHeading>
          <Firstname>Luc</Firstname>
          <Initials>L</Initials>
        </PersonNames>
        <Address>
          <Affiliation>University Hospital Regensburg, Regensburg, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Zhao</Lastname>
          <LastnameHeading>Zhao</LastnameHeading>
          <Firstname>You</Firstname>
          <Initials>Y</Initials>
        </PersonNames>
        <Address>
          <Affiliation>University Hospital Regensburg, Regensburg, Deutschland</Affiliation>
        </Address>
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      <Creator>
        <PersonNames>
          <Lastname>Alt</Lastname>
          <LastnameHeading>Alt</LastnameHeading>
          <Firstname>Volker</Firstname>
          <Initials>V</Initials>
        </PersonNames>
        <Address>
          <Affiliation>University Hospital Regensburg, Regensburg, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Riool</Lastname>
          <LastnameHeading>Riool</LastnameHeading>
          <Firstname>Martijn</Firstname>
          <Initials>M</Initials>
        </PersonNames>
        <Address>
          <Affiliation>University Hospital Regensburg, Regensburg, Deutschland</Affiliation>
        </Address>
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        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
    </SubjectGroup>
    <DatePublishedList>
      <DatePublished>20251031</DatePublished>
    </DatePublishedList>
    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
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      <Meeting>
        <MeetingId>M0634</MeetingId>
        <MeetingSequence>300</MeetingSequence>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Orthop&#228;die und Unfallchirurgie</MeetingCorporation>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Orthop&#228;die und Orthop&#228;dische Chirurgie</MeetingCorporation>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Unfallchirurgie</MeetingCorporation>
        <MeetingCorporation>Berufsverband f&#252;r Orthop&#228;die und Unfallchirurgie</MeetingCorporation>
        <MeetingName></MeetingName>
        <MeetingTitle>Deutscher Kongress f&#252;r Orthop&#228;die und Unfallchirurgie (DKOU 2025)</MeetingTitle>
        <MeetingSession>Grundlagenforschung &#124; Infekt &#38; Diagnostik 1</MeetingSession>
        <MeetingCity>Berlin</MeetingCity>
        <MeetingDate>
          <DateFrom>20251028</DateFrom>
          <DateTo>20251031</DateTo>
        </MeetingDate>
      </Meeting>
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    <ArticleNo>AB44-4676</ArticleNo>
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      <MainHeadline>Text</MainHeadline><Pgraph><Mark1>Objectives and questions: </Mark1>Despite the use of conventional local and systemic antibiotic therapies, biomaterial-associated infections (BAI) remain one of the most common complications in trauma patients. Alternative antimicrobial strategies are urgently needed. In trauma surgery, the use bioactive surfaces is a promising approach for decontamination and reducing bacterial attachment. This study aims to demonstrate the efficacy of phenothiazine-based photosensitizers (PS) against <Mark2>Staphylococcus aureus</Mark2> implant-related infections using two strategies: i) Evaluating photodynamic treatment (PDT) based on selected PS against bacteria attached to the surface of clinical metallic implants. ii) Synthesizing PS-loaded polymethylmethacrylate (PMMA)-based bone cements with varying PS concentrations to prevent bacterial attachment.</Pgraph><Pgraph><Mark1>Material and methods: </Mark1><Mark2>In vitro</Mark2> experiments were conducted to assess PDT efficiency by determining the minimal photo-bactericidal concentrations against clinical <Mark2>S. aureus</Mark2> strains in planktonic and biofilm condition. The DCFH-DA fluorescent probe was used to quantify reactive oxygen species (ROS) production. Based on these findings, PS-loaded PMMA formulations were prepared by using Palacos R bone cement. Eluates were collected at various time points to assess PS release (concentration and ROS production) and investigate their antibacterial and antibiofilm activity. <Mark2>In vivo</Mark2> experiments using <Mark2>Galleria mellonella</Mark2> infection models were conducted to examine PS and ROS biodistribution, as well as to evaluate PDT efficacy in preventing implant-related infections in larvae.</Pgraph><Pgraph><Mark1>Results: </Mark1>The combination of PS and light irradiation successfully photoinactivated clinical &#60;em&#62;S. aureus&#60;&#47;em&#62; strains. A complete bacterial eradication (8 logCFU&#47;mL) were achieved from 16 to 78 &#181;M, depending on the selected phenothiazine. Based on these results, a direct correlation was observed between the PS efficiency and its ability to produce ROS. Interestingly, PDT treatment significantly reduced bacterial counts after early to mature biofilm formation (4 to 48 h) on K-wire surfaces. When PS was incorporated into bone cement, an increase concentration release from the bone cement was observed over 5 days, regardless the PS-loaded concentration, <Mark2>i-e</Mark2> from 0.25 to 1&#37; (w&#47;w). However, a minimum concentration of 0.5&#37; PS-PMMA was required to release sufficient PS to achieve a significant reduction in bacterial load. <Mark2>in vivo</Mark2> biocompatibility studies demonstrated that PDT was well-tolerated in <Mark2>G. mellonella</Mark2>. </Pgraph><Pgraph><Mark1>Discussion and conclusions: </Mark1>Based on our strategies, PDT demonstrates encouraging results to prevent bacterial attachment on the surface of implant and could serve as a valuable addition to conventional antibiotic-based BAI prevention strategies. Further <Mark2>in vivo</Mark2> studies using this animal model are ongoing to evaluate the antibiofilm efficacy of this approach.</Pgraph></TextBlock>
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