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Characterization of Lipid-Based Hexosomes as Versatile Vaccine Carriers.
Rodrigues, Letícia; Kyriakos, Konstantinos; Schneider, Fabian; Dietz, Hendrik; Winter, Gerhard; Papadakis, Christine M; Hubert, Madlen.
Afiliación
  • Rodrigues L; Department of Pharmacy, Pharmaceutical Technology and Biopharmacy, Ludwig-Maximilians-Universität München , Butenandtstraße 5-13, DE-81377 Munich, Germany.
  • Kyriakos K; Physics Department, Soft Matter Physics Group, Technische Universität München , James-Franck-Straße 1, DE-85748 Garching, Germany.
  • Schneider F; Physics Department and Institute for Advanced Study, Walter Schottky Institute, Technische Universität München , Am Coulombwall 4a, DE-85748 Garching, Germany.
  • Dietz H; Physics Department and Institute for Advanced Study, Walter Schottky Institute, Technische Universität München , Am Coulombwall 4a, DE-85748 Garching, Germany.
  • Winter G; Department of Pharmacy, Pharmaceutical Technology and Biopharmacy, Ludwig-Maximilians-Universität München , Butenandtstraße 5-13, DE-81377 Munich, Germany.
  • Papadakis CM; Physics Department, Soft Matter Physics Group, Technische Universität München , James-Franck-Straße 1, DE-85748 Garching, Germany.
  • Hubert M; Department of Pharmacy, Pharmaceutical Technology and Biopharmacy, Ludwig-Maximilians-Universität München , Butenandtstraße 5-13, DE-81377 Munich, Germany.
Mol Pharm ; 13(11): 3945-3954, 2016 11 07.
Article en En | MEDLINE | ID: mdl-27607892
ABSTRACT
Subunit vaccines typically show insufficient immunogenicity. To address this issue, we developed a novel self-adjuvanting particulate carrier system based upon the lipids phytantriol (Phy) and mannide monooleate (MaMo). Phy is a lipid known to form nonlamellar phases in fully hydrated systems, whereas MaMo has been found to promote immune responses in emulsion form. A bulk phase composition of Phy/MaMo (14 wt %) showed hexagonal (HII) phase behavior over a practical temperature range (including room and body temperature), and was therefore used for particle development. Hexosomes stabilized with different concentrations of either poloxamer 407, Myrj 59, or Pluronic F108 were successfully prepared. To demonstrate the versatile nature of these systems, the particles were further modified with either positively or negatively charged lipids and loaded with model antigens, while maintaining the HII structure. These hexosomes are structurally robust and amenable to customization, rendering them suitable as antigen delivery carriers.
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Portadores de Fármacos / Vacunas Idioma: En Revista: Mol Pharm Asunto de la revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Alemania
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Portadores de Fármacos / Vacunas Idioma: En Revista: Mol Pharm Asunto de la revista: BIOLOGIA MOLECULAR / FARMACIA / FARMACOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Alemania