Fast confocal imaging was achieved by combining remote focusing with differential spinning disk optical sectioning to rapidly acquire images of live samples at cellular resolution. Axial and lateral full width half maxima less than 5 um and 490 nm respectively are demonstrated over 130 um axial range with a 256 x 128 um field of view. A water-index calibration slide was used to achieve an alignment that minimises image volume distortion. Application to live biological samples was demonstrated by acquiring image volumes over a 24 um axial range at 1 volume/s, allowing for the detection of calcium-based neuronal activity in Platynereis dumerilii larvae.
@article{arxiv.2002.06576,
title = {Spinning Disk -- Remote Focusing Microscopy},
author = {Michele Gintoli and Sharika Mohanan and Patrick Salter and Elizabeth Williams and James D. Beard and Gaspar Jekely and Alexander D. Corbett},
journal= {arXiv preprint arXiv:2002.06576},
year = {2020}
}