Widefield multiphoton imaging at depth with temporal focusing

Philip Wijesinghe*, Kishan Dholakia

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Optical imaging has the potential to reveal high-resolution information with minimal photodamage. The recent renaissance of super-resolution, widefield, ultrafast, and computational imaging methods has broadened its horizons even further. However, a remaining grand challenge is imaging at depth over a widefield and with a high spatiotemporal resolution. This achievement would enable the observation of fast collective biological processes, particularly those underpinning neuroscience and developmental biology. Multiphoton imaging at depth, combining temporal focusing and single-pixel detection, is an emerging avenue to address this challenge. The novel physics and computational methods driving this approach offer great potential for future advances. This chapter articulates the theories of temporal focusing and single-pixel detection and details the specific approach of TempoRAl Focusing microscopy with single-pIXel detection (TRAFIX), with a particular focus on its current practical implementation and future prospects.
Original languageEnglish
Title of host publicationAll-optical methods to study neuronal function
EditorsEirini Papagiakoumou
Place of PublicationNew York, NY
PublisherHumana Press Inc.
Chapter9
Pages263-291
Number of pages29
ISBN (Electronic)9781071627648
ISBN (Print)9781071627631, 9781071627662
DOIs
Publication statusPublished - 21 Feb 2023

Publication series

NameNeuromethods
Volume191
ISSN (Print)0893-2336
ISSN (Electronic)1940-6045

Keywords

  • Compressive sensing
  • Imaging at depth
  • Multiphoton microscopy
  • Single-pixel imaging
  • Temporal focusing
  • Widefield imaging

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