Universal NIR-II-Emitting Unimolecular Micelles with Tailorable Pharmacokinetic and Optical Properties for Adaptive Imaging

© 2025 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2025) vom: 23. Aug., Seite e09266
1. Verfasser: Hou, Shengxin (VerfasserIn)
Weitere Verfasser: Fan, GuiLing, Gu, Ying, Dong, Zhiyong, Wang, Mengying, Huang, Jia, Li, Heng, Han, Liang, Qian, Hujun, He, Feng, Qu, Songnan, Tian, Leilei
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2025
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article NIR‐II imaging pharmacokinetics polymer brushes unimolecular micelles π‐conjugated fluorophores
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520 |a π-Conjugated fluorophores show great potential for NIR-II bio-imaging owing to their superior brightness and photostability, yet their clinical translation has been hindered by suboptimal pharmacokinetics. To address this issue, a strategy is developed to tailor the in vivo behavior of π-conjugate fluorophores by breaking π-π stacking in polymer brush-engineered unimolecular micelles. This approach marks a significant shift from traditional methods of tuning micelles, which rely on varying the hydrophilic-to-hydrophobic ratios and are often ineffective for π-conjugated systems due to the dominance of π-π interactions. By disrupting π-π interactions in the unimolecular micelles, pharmacokinetics and photophysical properties can be precisely controlled by systematically varying the molecular weight and composition of the polymer brushes. Accordingly, the blood circulation half-life can be adjusted across a 60-fold range, and fluorescence emissions are improved by 47-fold, facilitating adaptive fluorophore applications from kidney dysfunction detection to tumor imaging. Additionally, the engineered unimolecular micelles exhibit reduced nonspecific uptake and improved tumor targeting efficiency, resulting in a 5-fold higher tumor-to-liver ratio than conventional π-π stacked nano-aggregates. These findings offer a solid solution to the pharmacokinetic optimization issues and provide a new design principle for π-conjugated phototheranostic materials 
650 4 |a Journal Article 
650 4 |a NIR‐II imaging 
650 4 |a pharmacokinetics 
650 4 |a polymer brushes 
650 4 |a unimolecular micelles 
650 4 |a π‐conjugated fluorophores 
700 1 |a Fan, GuiLing  |e verfasserin  |4 aut 
700 1 |a Gu, Ying  |e verfasserin  |4 aut 
700 1 |a Dong, Zhiyong  |e verfasserin  |4 aut 
700 1 |a Wang, Mengying  |e verfasserin  |4 aut 
700 1 |a Huang, Jia  |e verfasserin  |4 aut 
700 1 |a Li, Heng  |e verfasserin  |4 aut 
700 1 |a Han, Liang  |e verfasserin  |4 aut 
700 1 |a Qian, Hujun  |e verfasserin  |4 aut 
700 1 |a He, Feng  |e verfasserin  |4 aut 
700 1 |a Qu, Songnan  |e verfasserin  |4 aut 
700 1 |a Tian, Leilei  |e verfasserin  |4 aut 
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773 1 8 |g year:2025  |g day:23  |g month:08  |g pages:e09266 
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