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.