<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Thauvin, Cédric</dc:creator>
  <dc:creator>Widmer, Jérôme</dc:creator>
  <dc:creator>Mottas, Inès</dc:creator>
  <dc:creator>Hocevar, Sandra</dc:creator>
  <dc:creator>Allémann, Eric</dc:creator>
  <dc:creator>Bourquin, Carole</dc:creator>
  <dc:creator>Delie, Florence</dc:creator>
  <dc:date>2019-06-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Resiquimod (R848), a member of the imidazoquinoline family, is a Toll-like receptor  7/8 agonist with high potency for cancer immunotherapy. However, tolerance induction  and adverse effects limit its development as a drug. Encapsulation in a polymer matrix  can circumvent these limitations, as shown in our formerly published approach where  R848 was loaded into polylactic acid (PLA)-based nanoparticles (NP). Although the  results were encouraging, low rates of encapsulation and rapid release of the drug  were observed. In this study, we present a new strategy using mixed NP from  modified linear PLA in order to improve the encapsulation and modulate the release  profile of R848. Modified PLA polymers were designed and synthesized by  microwave-assisted ring opening polymerization of d,l-lactide, using polyethylene  glycol as initiator to increase the hydrophilic properties of the polymer or linear  saturated aliphatic chains (C8 or C20) to increase the affinity with hydrophobic R848.  NP were prepared by solvent evaporation method, leading to particles of 205–288 nm  loaded with either R848 or DiO as a tracking agent. The release profile showed longer  retention of R848 at both neutral and acidic pH for NP from grafted polymers. Upon  exposure to phagocytic immune cells, NP were actively taken up by the cells and no  impact on cell viability was observed, independently of the constitutive polymer. All  R848-loaded NP activated macrophages to secrete interleukin-6, demonstrating that  the drug cargo was immunologically active. Importantly, macrophage activation by NP- delivered R848 was slower than with free R848, in accordance with the in vitro  release profiles. Thus, NP prepared from modified PLA polymers showed no signs of  toxicity to immune cells and efficiently delivered their immunoactive cargo in a delayed  manner. This delivery strategy may enhance the efficacy and safety of small-molecule  immunostimulants.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307995</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307995/files/mott_drl.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307995/files/mott_drl_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ejpb.2019.04.007</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>European Journal of Pharmaceutics and Biopharmaceutics. - 2019, vol. 139, p. 253–261</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Development of resiquimod-loaded modified PLA-based nanoparticles for cancer immunotherapy: A kinetic study</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
