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End Group Dye-Labeled Polycarbonate Block Copolymers for Micellar (Immuno-)Drug Delivery.
Czysch, Christian; Medina-Montano, Carolina; Dal, Nils-Jørgen Knudsen; Dinh, Thi; Fröder, Yannick; Winterwerber, Pia; Maxeiner, Konrad; Räder, Hans-Joachim; Schuppan, Detlef; Schild, Hansjörg; Bros, Matthias; Biersack, Bernhard; Feranoli, Federico; Grabbe, Stephan; Nuhn, Lutz.
Afiliação
  • Czysch C; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Medina-Montano C; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 555131, Mainz, Germany.
  • Dal NK; Department of Bioscience, University of Oslo, Blindernveien 31, Oslo, 0371, Norway.
  • Dinh T; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Fröder Y; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Winterwerber P; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Maxeiner K; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Räder HJ; Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.
  • Schuppan D; Institute of Translational Immunology, University Medical Center Mainz, Obere Zahlbacherstraße 63, 55131, Mainz, Germany.
  • Schild H; Division of Gastroenterology, Beth Israel Deaconess Medical Center, Harvard Medical School Boston, 330 Brookline Ave, Boston, MA, 02215, USA.
  • Bros M; Institute for Immunology, University Medical Center Mainz, Langenbeckstraße 1, 55131, Mainz, Germany.
  • Biersack B; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 555131, Mainz, Germany.
  • Feranoli F; Organic Chemistry Laboratory, University of Bayreuth, Universitätsstraße 30, 95447, Bayreuth, Germany.
  • Grabbe S; Department of Bioscience, University of Oslo, Blindernveien 31, Oslo, 0371, Norway.
  • Nuhn L; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 555131, Mainz, Germany.
Macromol Rapid Commun ; 43(12): e2200095, 2022 Jun.
Article em En | MEDLINE | ID: mdl-35339115
Defined conjugation of functional molecules to block copolymer end groups is a powerful strategy to enhance the scope of micellar carriers for drug delivery. In this study, an approach to access well-defined polycarbonate-based block copolymers by labeling their end groups with single fluorescent dye molecules is established. Following controlled polymerization conditions, the block copolymers' primary hydroxy end group can be converted into activated pentafluorophenyl ester carbonates and subsequently aminolyzed with fluorescent dyes that are equipped with primary amines. During a solvent-evaporation process, the resulting end group dye-labeled block copolymers self-assemble into narrowly dispersed ∼25 nm-sized micelles and simultaneously encapsulate hydrophobic (immuno-)drugs. The covalently attached fluorescent tracer can be used to monitor both uptake into cells and stability under biologically relevant conditions, including incubation with blood plasma or during blood circulation in zebrafish embryos. By encapsulation of the toll-like receptor 7/8 (TLR7/8) agonist CL075, immune stimulatory polymeric micelles are generated that get internalized by various antigen-presenting dendritic cells and promote their maturation. Generally, such end group dye-labeled polycarbonate block copolymers display ideal features to permit targeted delivery of hydrophobic drugs to key immune cells for vaccination and cancer immunotherapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Micelas Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Micelas Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article