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High speed multiphoton imaging

Research output: Chapter in Book/Report/Conference proceeding › Conference Paper › peer-review

1 Citation (Scopus)

Abstract

Intravital multiphoton microscopy has emerged as a powerful technique to visualize cellular processes in-vivo. Real time processes revealed through live imaging provided many opportunities to capture cellular activities in living animals. The typical parameters that determine the performance of multiphoton microscopy are speed, field of view, 3D imaging and imaging depth; many of these are important to achieving data from in-vivo. Here, we provide a full exposition of the flexible polygon mirror based high speed laser scanning multiphoton imaging system, PCI-6110 card (National Instruments) and high speed analog frame grabber card (Matrox Solios eA/XA), which allows for rapid adjustments between frame rates i.e. 5 Hz to 50 Hz with 512 × 512 pixels. Furthermore, a motion correction algorithm is also used to mitigate motion artifacts. A customized control software called Pscan 1.0 is developed for the system. This is then followed by calibration of the imaging performance of the system and a series of quantitative in-vitro and in-vivo imaging in neuronal tissues and mice.

Original languageEnglish
Title of host publicationSPIE BioPhotonics Australasia
EditorsEwa M. Goldys, Mark R. Hutchinson
PublisherSPIE
ISBN (Electronic)9781510604346
DOIs
Publication statusPublished - 2016
EventSPIE BioPhotonics Australasia - Adelaide, Australia
Duration: 17 Oct 2016 → 19 Oct 2016

Publication series

NameProceedings of SPIE - The International Society for Optical Engineering
Volume10013
ISSN (Print)0277-786X
ISSN (Electronic)1996-756X

Conference

ConferenceSPIE BioPhotonics Australasia
Country/TerritoryAustralia
CityAdelaide
Period17/10/16 → 19/10/16

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