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               <mods:identifier type="citation">Polymers (Basel). 2021;13(13):2141.</mods:identifier>
               <mods:identifier type="doi">10.3390/polym13132141</mods:identifier>
               <mods:identifier type="e-issn">2073-4360</mods:identifier>
               <mods:identifier type="journal">Polymers</mods:identifier>
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               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/13981</mods:identifier>
               <mods:abstract>The respiratory syncytial virus (RSV) causes respiratory infection and bronchiolitis, requiring hospitalization mainly in infants. The interaction between RSV, envelope glycoproteins G and F, and cell surface heparan sulfate proteoglycans (HSPG) is required for binding and entry into the host cells. A G2-S16 polyanionic carbosilane dendrimer was identified as a possible RSV inhibitor. We speculated that the G2-S16 dendrimer adheres to the host cell-surface HSPG, acts through binding to HS receptors, and prevents further RSV infection. The G2-S16 dendrimer was non-toxic when applied intranasally to Balb/c mice, and interestingly enough, this G2-S16 dendrimer inhibits 85% RSV. Therefore, our G2-S16 dendrimer could be a candidate for developing a new possible therapy against RSV infection.</mods:abstract>
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                  <mods:topic>G2-S16 dendrimer</mods:topic>
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                  <mods:title>Role of G2-S16 Polyanionic Carbosilane Dendrimer in the Prevention of Respiratory Syncytial Virus Infection In Vitro and In Vivo in Mice</mods:title>
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