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        <datestamp>2026-09-15T09:38:35Z</datestamp>
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          <dc:title>Enhanced antibacterial and antibiofilm activity of &lt;i&gt;Artemisia aucheri&lt;/i&gt; Boiss. extract-loaded niosomes against clinical MRSA isolates</dc:title>
          <dc:creator>Fatemeh Ashrafi (2626663)</dc:creator>
          <dc:creator>Mahtab Majdabadi (24923330)</dc:creator>
          <dc:creator>Pooria Moulavi (24923333)</dc:creator>
          <dc:creator>Sepideh Asadi (24923336)</dc:creator>
          <dc:creator>Sadegh Jozaie (24923339)</dc:creator>
          <dc:creator>Hojjatollah Shokri (24923342)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Artemisia aucheri</dc:subject>
          <dc:subject>antibacterial</dc:subject>
          <dc:subject>biofilm</dc:subject>
          <dc:subject>Staphylococcus aureus</dc:subject>
          <dc:subject>niosome</dc:subject>
          <dc:description>&lt;p&gt;To develop and characterize niosomes encapsulating ethanolic &lt;i&gt;Artemisia aucheri&lt;/i&gt; extract (Nio-Artemisia) and evaluate their antibacterial and antibiofilm activities against clinical methicillin-resistant &lt;i&gt;Staphylococcus aureus&lt;/i&gt; (MRSA) isolates.&lt;/p&gt; &lt;p&gt;Niosomes were prepared by thin-film hydration and optimized based on particle size, polydispersity index (PDI), and encapsulation efficiency (EE). Stability and &lt;i&gt;in vitro&lt;/i&gt; release were evaluated. Clinical &lt;i&gt;S. aureus&lt;/i&gt; isolates were identified using standard microbiological methods, and antibacterial activity was assessed by minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and growth kinetics. Antibiofilm activity and expression of &lt;i&gt;icaA&lt;/i&gt; and &lt;i&gt;icaB&lt;/i&gt; were evaluated using the crystal violet assay and quantitative real-time PCR, respectively.&lt;/p&gt; &lt;p&gt;The optimized formulation had a particle size of 230.2 ± 9.1 nm, PDI of 0.191 ± 0.020, and EE of 72.39 ± 1.45%. Release followed a biphasic pattern and fitted the Higuchi model. Of 30 clinical S. aureus isolates, 15 were MRSA. Niosomal encapsulation reduced MIC values 4- to 16-fold compared with free extract and significantly inhibited biofilm formation. icaA and icaB expression was significantly downregulated (&lt;i&gt;p&lt;/i&gt; &lt; 0.001).&lt;/p&gt; &lt;p&gt;Niosomal encapsulation enhanced the antibacterial and antibiofilm activities of &lt;i&gt;A. aucheri&lt;/i&gt; extract against clinical MRSA isolates.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T09:38:35Z</dc:date>
          <dc:type>Dataset</dc:type>
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          <dc:identifier>10.6084/m9.figshare.33782642.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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