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用于胶束(免疫)药物递送的末端基团标记的聚碳酸酯嵌段共聚物。

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

机构信息

Max Planck Institute for Polymer Research Mainz, Ackermannweg 10, 55128, Mainz, Germany.

Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 555131, Mainz, Germany.

出版信息

Macromol Rapid Commun. 2022 Jun;43(12):e2200095. doi: 10.1002/marc.202200095. Epub 2022 Apr 10.

DOI:10.1002/marc.202200095
PMID:35339115
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.

摘要

将功能分子与嵌段共聚物端基进行定义性的键合是增强胶束载体用于药物输送范围的一种强大策略。在这项研究中,建立了一种通过用单个荧光染料分子标记其端基来获得结构明确的基于聚碳酸酯的嵌段共聚物的方法。在受控聚合条件下,嵌段共聚物的伯羟基端基可以转化为活化的五氟苯基碳酸酯酯,然后用带有伯胺的荧光染料进行氨解。在溶剂蒸发过程中,所得的端基染料标记的嵌段共聚物自组装成窄分散的约 25nm 大小的胶束,并同时包封疏水性(免疫)药物。共价连接的荧光示踪剂可用于监测细胞摄取和在包括与血浆孵育或在斑马鱼胚胎血液循环过程中的生物相关条件下的稳定性。通过封装 Toll 样受体 7/8(TLR7/8)激动剂 CL075,生成了具有免疫刺激性的聚合物胶束,各种抗原呈递树突细胞内化这些胶束并促进其成熟。通常,这种端基染料标记的聚碳酸酯嵌段共聚物具有理想的特性,可将疏水性药物靶向递送至疫苗接种和癌症免疫治疗的关键免疫细胞。

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