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End Group Dye-Labeled Polycarbonate Block Copolymers for Micellar (Immuno-)Drug Delivery.

Authors :
Czysch C
Medina-Montano C
Dal NK
Dinh T
Fröder Y
Winterwerber P
Maxeiner K
Räder HJ
Schuppan D
Schild H
Bros M
Biersack B
Feranoli F
Grabbe S
Nuhn L
Source :
Macromolecular rapid communications [Macromol Rapid Commun] 2022 Jun; Vol. 43 (12), pp. e2200095. Date of Electronic Publication: 2022 Apr 10.
Publication Year :
2022

Abstract

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.<br /> (© 2022 The Authors. Macromolecular Rapid Communications published by Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1521-3927
Volume :
43
Issue :
12
Database :
MEDLINE
Journal :
Macromolecular rapid communications
Publication Type :
Academic Journal
Accession number :
35339115
Full Text :
https://doi.org/10.1002/marc.202200095