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

被引:14
|
作者
Czysch, Christian [1 ]
Medina-Montano, Carolina [2 ]
Dal, Nils-Jorgen Knudsen [3 ]
Dinh, Thi [1 ]
Froeder, Yannick [1 ]
Winterwerber, Pia [1 ]
Maxeiner, Konrad [1 ]
Raeder, Hans-Joachim [1 ]
Schuppan, Detlef [4 ,5 ]
Schild, Hansjoerg [6 ]
Bros, Matthias [2 ]
Biersack, Bernhard [7 ]
Feranoli, Federico [3 ]
Grabbe, Stephan [2 ]
Nuhn, Lutz [1 ]
机构
[1] Max Planck Inst Polymer Res Mainz, Ackermannweg 10, D-55128 Mainz, Germany
[2] Univ Med Ctr Mainz, Dept Dermatol, Langenbeckstr 1, D-555131 Mainz, Germany
[3] Univ Oslo, Dept Biosci, Blindernveien 31, N-0371 Oslo, Norway
[4] Univ Med Ctr Mainz, Inst Translat Immunol, Obere Zahlbacherstr 63, D-55131 Mainz, Germany
[5] Harvard Med Sch, Div Gastroenterol, Beth Israel Deaconess Med Ctr, 330 Brookline Ave, Boston, MA 02215 USA
[6] Univ Med Ctr Mainz, Inst Immunol, Langenbeckstr 1, D-55131 Mainz, Germany
[7] Univ Bayreuth, Organ Chem Lab, Univ Str 30, D-95447 Bayreuth, Germany
关键词
aliphatic polycarbonates; block copolymers; immunodrug delivery; micelles; self-assembly; POLYMERIC MICELLES; DENDRITIC CELLS; TLR AGONISTS; ALIPHATIC POLYCARBONATES; IN-VIVO; NANOGELS;
D O I
10.1002/marc.202200095
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
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 similar to 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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页数:10
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