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Target-Activated Modulation of Dual-Color and Two-Photon Fluorescence of Graphene Quantum Dots for in Vivo Imaging of Hydrogen Peroxide

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posted on 2016-04-13, 00:00 authored by Wenjie Zhao, Yinhui Li, Sheng Yang, Yun Chen, Jing Zheng, Changhui Liu, Zhihe Qing, Jishan Li, Ronghua Yang
The development of nanoprobes suitable for two-photon microscopy techniques is highly desirable for mapping biological species in living systems. However, at the current stage, the nanoprobes are restricted to single-color fluorescence changes, making it unsuitable for quantitative detection. To circumvent this problem, we report here a rational design of a dual-emission and two-photon (TP) graphene quantum dot (GQD<sup>420</sup>) probe for imaging of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>). For specific recognition of H<sub>2</sub>O<sub>2</sub> and lighting the fluorescence of TPGQD<sup>420</sup>, a boronate ester-functionalized merocyanine (BMC) fluorophore was used as both target-activated trigger and the dual-emission fluorescence modulator. Upon two-photon excitation at 740 nm, TPGQD<sup>420</sup>–BMC displays a green-to-blue resolved emission band in response to H<sub>2</sub>O<sub>2</sub> with an emission shift of 110 nm, and the H<sub>2</sub>O<sub>2</sub> can be determined from 0.2 to 40 μM with a detection limit of 0.05 μM. Moreover, the fluorescence response of the TPGQD<sup>420</sup>–BMC toward H<sub>2</sub>O<sub>2</sub> is rapid and extremely specific. The feasibility of the proposed method is demonstrated by two-photon ratiometrically mapping the production of endogenous H<sub>2</sub>O<sub>2</sub> in living cells as well as in deep tissues of murine mode at 0–600 μm. To the best of our knowledge, this is the first paradigm to rationally design a dual-emission and two-photon nanoprobe via fluorescence modulation of GQDs with switchable molecules, which will extend new possibility to design powerful molecular tools for in vivo bioimaging applications.

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