Bright and Stable NIR‐II J‐Aggregated AIE Dibodipy‐Based Fluorescent Probe for Dynamic In Vivo Bioimaging. Issue 8 (23rd December 2020)

• Record Type: Journal Article
• Authors: Zhang, Qisong; Yu, Peng; Fan, Yong; Sun, Caixia; He, Haisheng; Liu, Xuan; Lu, Lingfei; Zhao, Mengyao; Zhang, Hongxin; Zhang, Fan
• Is Part Of: Angewandte Chemie international edition. Volume 60:Issue 8(2021)
• Page Start: 3967
• Page End: 3973
• Publication Date: 2020-12-23
• Subjects: aggregation-induced emission -- bioimaging -- dibodipy -- J-aggregation -- NIR-II fluorescence; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202012427
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Organic dyes emitting in the second near‐infrared (NIR‐II, 900–1700 nm) window, with high molar extinction coefficients (MEC) and quantum yields (QY) in aqueous, are essential for in vivo bioimaging and biosensing. In this work, we developed a dibodipy‐based aggregation‐induced emission (AIE) fluorescent probe, THPP, to meet this aim. THPP exhibits a high MEC and has intensified absorption and emission in J‐aggregated state, which significantly enhance the fluorescence intensity (≈55 folds) and extend the maximal absorption/emission wavelengths to 970/1010 nm in NIR‐II region. Based on the bright THPP, imaging with a high frame rate (34 frames per second) at a deep "valid penetration depth" up to 6 mm can be achieved. This enabled simultaneous and dynamic imaging of vasculatures and deep tissues. Besides, we succeeded in monitoring the respiratory rate of acute‐lung‐injury mice and tracing the collateral circulation process with a high frame rate. Abstract : A J‐aggregated AIE dibodipy‐based fluorescent probe, THPP, was synthesized. The probe exhibits enhanced fluorescence intensity in the NIR‐II window for dynamic in vivo imaging.