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<oembed><version>1.0</version><provider_name>Novaptech</provider_name><provider_url>https://novaptech.com/en</provider_url><title>Aptamers as therapeutics - Novaptech</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="qTvy8aX2uM"&gt;&lt;a href="https://novaptech.com/en/portfolio_page/aptamers-as-therapeutics/"&gt;Aptamers as therapeutics&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://novaptech.com/en/portfolio_page/aptamers-as-therapeutics/embed/#?secret=qTvy8aX2uM" width="600" height="338" title="&#x201C;Aptamers as therapeutics&#x201D; &#x2014; Novaptech" data-secret="qTvy8aX2uM" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><description>Aptamers as therapeutics Aptamers have a huge potential as therapeutic agents. They can be addressed to intracellular targets, to membrane components or to circulating molecules. They can be used as drug-delivery agents to cells of interest. They can be employed as antagonists (preventing a specific receptor-ligand interaction), or as agonists (binding to a receptor and activating a signal). Aptamers can be easily modified for improving their properties (making them more resistant to nucleases or increasing their in vivo half-life). They induce a minimal immune response in vivo. Several clinical trials are on-going. Novaptech contributes to this field; see for instance :&#xA0; Millozzi, F., Mil&#xE1;n-Rois, P., Sett, A., Delli Carpini, G., De Bardi, M., Gisbert-Garzar&#xE1;n, M., Sandon&#xE0;, M., Rodr&#xED;guez-D&#xED;az, C., Mart&#xED;nez-Mingo, M., Pardo, I., Esposito, F., Viscomi, M. T., Bouch&#xE9;, M., Parolini, O., Saccone, V., Toulm&#xE9;, J.-J., Somoza, &#xC1;., &amp; Palacios, D. (2025). Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic muscles. Nature Communications, 16, Article 577.</description></oembed>
