TY - GEN
T1 - VAMPIRE microscopy enables fast and simultaneous structural, metabolic, and chemical characterization of living tissues label-free
AU - Iyer, Rishyashring R.
AU - Sorrells, Janet E.
AU - Yang, Lingxiao
AU - Chaney, Eric J.
AU - Boppart, Stephen A.
N1 - Publisher Copyright:
© 2024 SPIE.
PY - 2024
Y1 - 2024
N2 - We present a completely label-free technology that captures eight complementary contrasts describing the metabolic, chemical, structural, and dynamic profiles of the tissue microenvironment with a single laser source, called VAMPIRE (Versatile Autofluorescence lifetime imaging, Multiharmonic generation, Polarization-sensitive Interferometry, and Raman scattering in Epi-detection) microscopy. VAMPIRE microscopy maximizes the spectral utility of light-matter interactions by creating four nonlinear (second harmonic generation, two-channel two-photon fluorescence, coherent Raman scattering) and two linear interactions (backscattering, birefringence) simultaneously with a single laser. Innovations in each modality improved the overall speed and sensitivity. Fast fluorescence lifetime imaging microscopy (FLIM) was accelerated with our computational photon counting algorithm called single-and-multi photon peak event detection (SPEED), capable of counting up to 250% photon rates. Dual-channel fast two-photon FLIM was achieved by compressed sensing of analog photocurrents on a field-programmable gate array on board the digitizer. We developed a new and faster method for hyperspectral coherent Raman microscopy using supercontinuum generation and custom pulse shapers, which facilitated rapid tuning to desired vibrational states. Polarization multiplexing in optical coherence imaging enabled compressed sensing of birefringence. Finally, computational approaches to maximize the information from these complementary contrasts yielded new insights into the processes within the tissue microenvironment. VAMPIRE microscopy is the nexus of label-free microscopy research, advances in optoelectronic technologies, and our innovations in computational and multimodal imaging for diverse applications.
AB - We present a completely label-free technology that captures eight complementary contrasts describing the metabolic, chemical, structural, and dynamic profiles of the tissue microenvironment with a single laser source, called VAMPIRE (Versatile Autofluorescence lifetime imaging, Multiharmonic generation, Polarization-sensitive Interferometry, and Raman scattering in Epi-detection) microscopy. VAMPIRE microscopy maximizes the spectral utility of light-matter interactions by creating four nonlinear (second harmonic generation, two-channel two-photon fluorescence, coherent Raman scattering) and two linear interactions (backscattering, birefringence) simultaneously with a single laser. Innovations in each modality improved the overall speed and sensitivity. Fast fluorescence lifetime imaging microscopy (FLIM) was accelerated with our computational photon counting algorithm called single-and-multi photon peak event detection (SPEED), capable of counting up to 250% photon rates. Dual-channel fast two-photon FLIM was achieved by compressed sensing of analog photocurrents on a field-programmable gate array on board the digitizer. We developed a new and faster method for hyperspectral coherent Raman microscopy using supercontinuum generation and custom pulse shapers, which facilitated rapid tuning to desired vibrational states. Polarization multiplexing in optical coherence imaging enabled compressed sensing of birefringence. Finally, computational approaches to maximize the information from these complementary contrasts yielded new insights into the processes within the tissue microenvironment. VAMPIRE microscopy is the nexus of label-free microscopy research, advances in optoelectronic technologies, and our innovations in computational and multimodal imaging for diverse applications.
KW - Computational imaging
KW - Fluorescence lifetime imaging microscopy
KW - Hyperspectral Coherent Raman scattering microscopy
KW - Multimodal imaging
KW - Multiphoton microscopy
KW - Optical coherence microscopy
KW - Polarization-sensitive imaging
UR - http://www.scopus.com/inward/record.url?scp=85194404175&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85194404175&partnerID=8YFLogxK
U2 - 10.1117/12.3000644
DO - 10.1117/12.3000644
M3 - Conference contribution
AN - SCOPUS:85194404175
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Multiphoton Microscopy in the Biomedical Sciences XXIV 2024
A2 - Periasamy, Ammasi
A2 - So, Peter T.
A2 - Konig, Karsten
PB - SPIE
T2 - Multiphoton Microscopy in the Biomedical Sciences XXIV 2024
Y2 - 28 January 2024 through 30 January 2024
ER -