TY - GEN
T1 - A low noise current readout architecture for fluorescence detection in living subjects
AU - Heitz, Roxana T.
AU - Barkin, David B.
AU - O'Sullivan, Thomas D.
AU - Parashurama, Natesh
AU - Gambhir, Sanjiv S.
AU - Wooley, Bruce A.
PY - 2011
Y1 - 2011
N2 - Optical molecular imaging is emerging as a powerful preclinical research tool for investigating and quantifying molecular events in living subjects, with applications including earlier detection of disease, therapeutic monitoring and understanding fundamental biology [1]. For example, imaging the fluorescent molecular probe RGD-Cy5.5, which specifically binds to molecules (αvβ3 integrin receptors) that regulate new blood vessel growth in tumors, can be used to quantify this growth [2]. Capturing the fluorescent signal in living subjects with an implanted biosensor would enable continuous monitoring of tumors in freely moving subjects. Continuous monitoring in the setting of cancer would give valuable information on tumor progression, both in assessing drug efficacy and detecting recurrent tumor growth after treatment. Presently, fluorescence imaging in living subjects is performed with bulky instrumentation that does not permit continuous monitoring of freely moving subjects over long time periods. In order to make a fluorescence-detection system implantable, and portable, a laser excitation source, a photodetector and a readout circuit for measuring and digitizing photocurrents are integrated in a single package, and continuous fluorescence detection is demonstrated in live animals.
AB - Optical molecular imaging is emerging as a powerful preclinical research tool for investigating and quantifying molecular events in living subjects, with applications including earlier detection of disease, therapeutic monitoring and understanding fundamental biology [1]. For example, imaging the fluorescent molecular probe RGD-Cy5.5, which specifically binds to molecules (αvβ3 integrin receptors) that regulate new blood vessel growth in tumors, can be used to quantify this growth [2]. Capturing the fluorescent signal in living subjects with an implanted biosensor would enable continuous monitoring of tumors in freely moving subjects. Continuous monitoring in the setting of cancer would give valuable information on tumor progression, both in assessing drug efficacy and detecting recurrent tumor growth after treatment. Presently, fluorescence imaging in living subjects is performed with bulky instrumentation that does not permit continuous monitoring of freely moving subjects over long time periods. In order to make a fluorescence-detection system implantable, and portable, a laser excitation source, a photodetector and a readout circuit for measuring and digitizing photocurrents are integrated in a single package, and continuous fluorescence detection is demonstrated in live animals.
UR - https://www.scopus.com/pages/publications/79955712461
U2 - 10.1109/ISSCC.2011.5746331
DO - 10.1109/ISSCC.2011.5746331
M3 - Conference contribution
AN - SCOPUS:79955712461
SN - 9781612843001
T3 - Digest of Technical Papers - IEEE International Solid-State Circuits Conference
SP - 308
EP - 309
BT - 2011 IEEE International Solid-State Circuits Conference - Digest of Technical Papers, ISSCC 2011
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2011 IEEE International Solid-State Circuits Conference, ISSCC 2011
Y2 - 20 February 2011 through 24 February 2011
ER -