TY - GEN
T1 - System model for laser-scanning photoacoustic microscopy
AU - La Rivière, Patrick J.
AU - Zhang, Hao F.
PY - 2009
Y1 - 2009
N2 - In this work we derive a system model for a laser-scanning, optical-resolution photoacoustic microscopy system.We use the model to derive a simple image reconstruction algorithm and then analyze the depth resolution achievable by this algorithm. There has recently been development of high-frequency photoacoustic microscopy (PAM) systems with the ability to image biological tissue at a microscopic scale. The imaging depths achievable (a few mm) are shallower than in photoacoustic tomography (which has lower spatial resolution), but deeper than conventional optical microscopy. PAM usually employs a focused single-element high-frequency ultrasonic transducer and a spatially overlapped optical illumination. These existing PAMs require mechanical scanning of the ultrasonic-optical assembly, which is relatively slow and also not compatible with other optical microscopic modalities such as confocal microscopy, two-photon microscopy, and optical coherence tomography. Recently one of us (H.Z.) has developed a laser-scanning OR-PAM (LSOR-PAM) to demonstrate the feasibility of employing optical scanning in PAM. In LSOR-PAM, the ultrasonic detector is kept stationary and only the laser light is raster-scanned within the FOV during data acquisition. Further improvements in image quality and the development of image quality metrics will benefit from the system model derived in this work.
AB - In this work we derive a system model for a laser-scanning, optical-resolution photoacoustic microscopy system.We use the model to derive a simple image reconstruction algorithm and then analyze the depth resolution achievable by this algorithm. There has recently been development of high-frequency photoacoustic microscopy (PAM) systems with the ability to image biological tissue at a microscopic scale. The imaging depths achievable (a few mm) are shallower than in photoacoustic tomography (which has lower spatial resolution), but deeper than conventional optical microscopy. PAM usually employs a focused single-element high-frequency ultrasonic transducer and a spatially overlapped optical illumination. These existing PAMs require mechanical scanning of the ultrasonic-optical assembly, which is relatively slow and also not compatible with other optical microscopic modalities such as confocal microscopy, two-photon microscopy, and optical coherence tomography. Recently one of us (H.Z.) has developed a laser-scanning OR-PAM (LSOR-PAM) to demonstrate the feasibility of employing optical scanning in PAM. In LSOR-PAM, the ultrasonic detector is kept stationary and only the laser light is raster-scanned within the FOV during data acquisition. Further improvements in image quality and the development of image quality metrics will benefit from the system model derived in this work.
UR - http://www.scopus.com/inward/record.url?scp=77951165934&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77951165934&partnerID=8YFLogxK
U2 - 10.1109/NSSMIC.2009.5401749
DO - 10.1109/NSSMIC.2009.5401749
M3 - Conference contribution
AN - SCOPUS:77951165934
SN - 9781424439621
T3 - IEEE Nuclear Science Symposium Conference Record
SP - 3333
EP - 3337
BT - 2009 IEEE Nuclear Science Symposium Conference Record, NSS/MIC 2009
T2 - 2009 IEEE Nuclear Science Symposium Conference Record, NSS/MIC 2009
Y2 - 25 October 2009 through 31 October 2009
ER -