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With reduced background and high sensitivity, photoelectrochemistry (PEC) may be applied as an intracellular nanotool and open a new technological direction of single‐cell study. Nevertheless, the present palette of single‐cell tools lacks such a PEC‐oriented solution. Here a dual‐functional photocathodic single‐cell nanotool capable of direct electroosmotic intracellular drug delivery and evaluation of oxidative stress is devised by engineering a target‐specific organic molecule/NiO/Ni film at the tip of a nanopipette. Specifically, the organic molecule probe serves simultaneously as the biorecognition element and sensitizer to synergize with p‐type NiO. Upon intracellular delivery at picoliter level, the oxidative stress effect will cause structural change of the organic probe, switching its optical absorption and altering the cathodic response. This work has revealed the potential of PEC single‐cell nanotool and extended the boundary of current single‐cell electroanalysis. [ABSTRACT FROM AUTHOR]

Single nanoparticle collision (SNC) technology has attracted increasing attention to explore single nanoparticle electrochemistry. By improving the temporal resolution of electrochemical recording, several recent studies have uncovered the intermittent electron transfer processes during the SNC of single silver nanoparticles. The electrode current curve displayed multiple current peaks that were completely separated, instead of a single peak. In the present work, we employed surface plasmon resonance microscopy to monitor the collision and oxidation processes of single silver nanoparticles. Simultaneous optical and electrochemical recordings provided comprehensive capability to correlate the physical movement of nanoparticles (from optical signal) and the electron transfer activity (from electrochemical signal). While previous studies hypothesized the physical detachment of nanoparticles from the electrode due to electrostatic repulsion or Brownian motion, the optical imaging revealed that nanoparticles often remained in physical touch with the electrode even though no electron transfer was occurring. These results demonstrated that the electrical contact between nanoparticle and electrode, which could be rather stochastic due to thermal motion and micro‐convection, played critical roles in regulating the multi‐peak behavior of single silver nanoparticles. In touch: surface plasmon resonance microscopy is utilized to monitor collision and oxidation processes of single silver nanoparticles. Simultaneous optical and electrochemical recordings reveal that nanoparticles often remain in physical touch with the electrode even though no electron transfer is occurring. The electrical contact plays critical roles in regulating the multi‐peak behavior of single silver nanoparticles. [ABSTRACT FROM AUTHOR]

Abstract: Ionic current rectification (ICR) based nanopipettes allow accurate monitoring of cellular behavior in single living cells. Herein, we proposed a 30 nm nanopipette functionalized with G‐quadruplex DNAzyme as an efficient biomimetic recognizer for ROS generation at subcellular level via the changes of current–voltage relationship. Taking advantages of the ultra‐small tip, the nanopipette could penetrate into a single living cell repeatedly or keep measuring for a long time without compromising the cellular functions. Coupled with precision nanopositioning system, generation of ROS in mitochondria in response to cell inflammation was determined with high spatial resolution. Meanwhile, the changes of aerobic metabolism in different cell lines under drug‐induced oxidative stress were monitored continuously. We believe that the ICR‐nanopipette could be developed as a powerful approach for the study of cellular activities via electrochemical imaging in living cells. [ABSTRACT FROM AUTHOR]