Real-time pixelwise phasor analysis for video-rate two-photon fluorescence lifetime imaging microscopy
Abstract
Two-photon fluorescence lifetime imaging microscopy (FLIM) is a widely used technique in biomedical optical imaging. Presently, many two-photon time-domain FLIM setups are limited by long acquisition and postprocessing times that decrease data throughput and inhibit the ability to image fast sub-second processes. Here, we present a versatile two-photon FLIM setup capable of video-rate (up to 25 fps) imaging with graphics processing unit (GPU)-accelerated pixelwise phasor analysis displayed and saved simultaneously with acquisition. The system uses an analog output photomultiplier tube in conjunction with 12-bit digitization at 3.2 GHz to overcome the limited maximum acceptable photon rate associated with the photon counting electronics in many FLIM systems. This allows for higher throughput FLIM acquisition and analysis, and additionally enables the user to assess sample fluorescence lifetime in real-time. We further explore the capabilities of the system to examine the kinetics of Rhodamine B uptake by human breast cancer cells and characterize the effect of pixel dwell time on the reduced nicotinamide adenine dinucleotide and reduced nicotinamide adenine dinucleotide phosphate (NAD(P)H) autofluorescence lifetime estimation accuracy.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jun 11, 2021
- Source ID
- 10.1364/boe.424533
Entities
People
- Andrew J Bower
- Darold R Spillman
- Eric J. Chaney
- Haohua Tu
- Janet E. Sorrells
- Lingxiao Yang
- Rishyashring R Iyer
- Stephen A. Boppart
Organizations
- Air Force Office of Scientific Research
- National Institutes of Health
- National Science Foundation
- University of Illinois Urbana–Champaign