The respiration activity of an individual living cell is an indicator of its metabolic vitality. Closely positioned microelectrodes have been suggested for determination of the respiration activity by monitoring the local oxygen concentration. Although first attempts for visualization of the oxygen consumption rate of single living cells by means of scanning electrochemical microscopy (SECM) were already described in 1998, evaluation of the respiratory activity of individual cells remains challenging and the complexity is often underestimated. In particular, the dimensions of the cell itself lead to limitations of conventionally used constant-height mode SECM investigations. Apart from convolution of the oxygen reduction current at the SECM tip with topographic effects, constant-height mode experiments require working distances comparable or below the height of the cell body, thus increasing the risk of tip crash. Attempts to overcome these restrictions include among others positioning of the tip to distances outside the feedback range, embedding of the cells into cavities, or efforts to subtract topographic contributions after cell death. Moreover, as living cells are irregular in dimension, the tip-to-cell distance varies with the tip position. Therefore, constant-distance mode (cd-mode) SECM techniques are inherently advantageous for this purpose. In particular, coupling SECM with scanning probe techniques, such as atomic force microscopy (AFM) and scanning ion conductance microscopy (SICM) as well as shearforce and impedance-based techniques, led to efficient strategies to control the tip-to-sample separation. Recently, we described a shearforce-based cd method (4D SF/ CD-SECM) that is able to work at various tip-to-sample separations. It can hence detect complete diffusion profiles in the surroundings of sources or sinks of redox-active species. Although SECM distance control systems are available, the detection of the respiration activity of single living cells remains challenging. Owing to the small rate of oxygen consumption by a single cell, only small current variations ontop of a high background current are measured. Even more importantly, a biological cell acts as an immiscible liquid– liquid interface in a SECM experiment. Lipophilic redox mediators are known to undergo transmembrane diffusion processes and can be utilized to investigate intracellular redox activity. However, concentration changes in the vicinity of the cellular membrane, for example by the tip reaction, may induce local concentration gradients and cause a diffusional exchange of redox species over the lipid bilayer in a socalled SECM-induced transfer (SECM-IT) mode. The high solubility of oxygen in lipids promotes this transmembrane diffusion and oxygen can easily cross the cell membrane. This diffusion process superimposes the detection of cell respiration. As a result, in most reports addressing detection of cell metabolism based on the detection of variations in the local oxygen concentration, the positioned microelectrode does not act as a passive observer but actively influences the oxygen concentration inside the gap between tip and cell, resulting in imaging artifacts that have not previously been addressed. Even though mentioned occasionally, this effect was neglected in SECM investigations of respiration activity at living cells. Herein, we address the influence of the oxygen reduction rate at the SECM tip on imaging the respiration activity at living cells. We provide strategies to avoid limitations resulting from a strong tip reaction using a potential pulse profile at the tip with a time dependent data acquisition in the shearforce-based cd-mode of SECM. Commonly, the detection of the local oxygen concentration in close proximity to the cell body is performed by means of a variation of the generator-collector mode of SECM with the tip being continuously polarized at oxygen reduction potential. The tip competes with the respiring living cell for the available oxygen inside the gap between SECM tip and cell surface. Crossing the cell body during a SECM line scan should therefore lead to a decrease of the tip current owing to a locally lowered oxygen concentration caused by cell [*] Dr. M. Nebel, S. Gr tzke, Prof. Dr. W. Schuhmann Lehrstuhl f r Analytische Chemie, Elektroanalytik & Sensorik and Center for Electrochemical Sciences, CES Ruhr-Universit t Bochum Universit tsstrasse 150, 44780 Bochum (Germany) E-mail: wolfgang.schuhmann@rub.de