A BODIPY-Based Donor/Donor-Acceptor System: Towards Highly Efficient Long-Wavelength-Excitable Near-IR Polymer Dots with Narrow and Strong Absorption Features

A BODIPY-Based Donor/Donor-Acceptor System: Towards Highly Efficient Long-Wavelength-Excitable Near-IR Polymer Dots with Narrow and Strong Absorption Features
复制标题

基于 BODIPY 的供体/供体-受体系统:实现具有窄而强吸收特性的高效长波长可激发近红外聚合物点

DOI:
10.1002/anie.201902077
复制
发表时间:
2019-05-20
影响因子:
16.6
通讯作者:
Chiu, Daniel T.
Chiu, Daniel T.
中科院分区:
化学1区
文献类型:
--
作者:
Chen, Lei;Chen, Dandan;Chiu, Daniel T.

文献摘要

被引文献

相似文献

明亮的长波长可激发半导体聚合物点(LWE-Pdot)是体内成像和多路复用体外生物测定非常需要的。通过将近红外(NIR)发射体并入聚合物主体的主链中以开发二元供体-受体(D-A)系统来获得LWE-Pdot。然而,它们通常遭受严重的浓度猝灭和荧光量子产率(Phi(f))和吸收截面(sigma)之间的权衡。本文中,我们描述了一种三元组分(D-1/D-2-A)策略,通过引入基于BODIPY的辅助聚合物供体作为D-1来实现具有窄带NIR发射的超亮、绿色激光可激发的Pdot。与相应的二进制D-2-A Pdot相比,D-1/D-2-A Pdot具有改进的Phi(f)和sigma。它们的Phi(f)高达40.2%,是报道的最有效的近红外Pdot之一。D-1/D-2-A Pdot在532 nm激光激发下显示出比Qdot 705亮83倍的单粒子亮度。当注射到小鼠中时,使用三元Pdot相对于二元D-A Pdot实现了更高对比度的体内肿瘤成像。
Bright long-wavelength-excitable semiconducting polymer dots (LWE-Pdots) are highly desirable for invivo imaging and multiplexed invitro bioassays. LWE-Pdots have been obtained by incorporating a near-infrared (NIR) emitter into the backbone of a polymer host to develop a binary donor-acceptor (D-A) system. However, they usually suffer from severe concentration quenching and a trade-off between fluorescence quantum yield (Phi(f)) and absorption cross-section (sigma). Herein, we describe a ternary component (D-1/D-2-A) strategy to achieve ultrabright, green laser-excitable Pdots with narrow-band NIR emission by introducing a BODIPY-based assistant polymer donor as D-1. The D-1/D-2-A Pdots possess improved Phi(f) and sigma compared to corresponding binary D-2-A Pdots. Their Phi(f) is as high as 40.2%, one of the most efficient NIR Pdots reported. The D-1/D-2-A Pdots show ultrahigh single-particle brightness, 83-fold brighter than Qdot 705 when excited by a 532nm laser. When injected into mice, higher contrast invivo tumor imaging was achieved using the ternary Pdots versus the binary D-A Pdots.