| Literature DB >> 30912228 |
Lei Chen1, Dandan Chen2, Yifei Jiang1, Jicheng Zhang1, Jiangbo Yu1, Christopher C DuFort3, Sunil R Hingorani3,4,5, Xuanjun Zhang6, Changfeng Wu2, Daniel T Chiu1.
Abstract
Bright long-wavelength-excitable semiconducting polymer dots (LWE-Pdots) are highly desirable for in vivo imaging and multiplexed in vitro 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 (Φf ) and absorption cross-section (σ). Herein, we describe a ternary component (D1 /D2 -A) strategy to achieve ultrabright, green laser-excitable Pdots with narrow-band NIR emission by introducing a BODIPY-based assistant polymer donor as D1 . The D1 /D2 -A Pdots possess improved Φf and σ compared to corresponding binary D2 -A Pdots. Their Φf is as high as 40.2 %, one of the most efficient NIR Pdots reported. The D1 /D2 -A Pdots show ultrahigh single-particle brightness, 83-fold brighter than Qdot 705 when excited by a 532 nm laser. When injected into mice, higher contrast in vivo tumor imaging was achieved using the ternary Pdots versus the binary D-A Pdots.Entities:
Keywords: BODIPY; in vivo imaging; narrow-band absorption; near-infrared emission; semiconducting polymer dots
Year: 2019 PMID: 30912228 PMCID: PMC6513679 DOI: 10.1002/anie.201902077
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336