TY - JOUR
T1 - High resolution phase-sensitive magnetomotive optical coherence microscopy for tracking magnetic microbeads and cellular mechanics
AU - Crecea, Vasilica
AU - Graf, Benedikt W.
AU - Kim, Taewoo
AU - Popescu, Gabriel
AU - Boppart, Stephen A.
PY - 2014/3
Y1 - 2014/3
N2 - We present a real-time multimodal near-infrared imaging technology that tracks externally-induced axial motion of magnetic microbeads in single cells in culture. The integrated multimodal imaging technique consists of phase-sensitive magnetomotive optical coherence microscopy (MM-OCM) and multiphoton microscopy (MPM). MPM is utilized for the visualization of multifunctional fluorescent and magnetic microbeads, while MM-OCM detects, with nanometer-scale sensitivity, periodic displacements of the microbeads induced by the modulation of an external magnetic field. Magnetomotive signals are measured from mouse macrophages, human breast primary ductal carcinoma cells, and human breast epithelial cells in culture, and validated with full-field phase-sensitive microscopy. This methodology demonstrates the capability for imaging controlled cell dynamics and has the potential for measuring cell biomechanical properties, which are important in assessing the health and pathological state of cells.
AB - We present a real-time multimodal near-infrared imaging technology that tracks externally-induced axial motion of magnetic microbeads in single cells in culture. The integrated multimodal imaging technique consists of phase-sensitive magnetomotive optical coherence microscopy (MM-OCM) and multiphoton microscopy (MPM). MPM is utilized for the visualization of multifunctional fluorescent and magnetic microbeads, while MM-OCM detects, with nanometer-scale sensitivity, periodic displacements of the microbeads induced by the modulation of an external magnetic field. Magnetomotive signals are measured from mouse macrophages, human breast primary ductal carcinoma cells, and human breast epithelial cells in culture, and validated with full-field phase-sensitive microscopy. This methodology demonstrates the capability for imaging controlled cell dynamics and has the potential for measuring cell biomechanical properties, which are important in assessing the health and pathological state of cells.
KW - Cellular biomechanics
KW - magnetic tweezers
KW - multimodal microscopy
KW - multiphoton microscopy (MPM)
KW - optical coherence tomography (OCT)
UR - http://www.scopus.com/inward/record.url?scp=84889256827&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84889256827&partnerID=8YFLogxK
U2 - 10.1109/JSTQE.2013.2280501
DO - 10.1109/JSTQE.2013.2280501
M3 - Article
C2 - 25400496
AN - SCOPUS:84889256827
SN - 1077-260X
VL - 20
JO - IEEE Journal on Selected Topics in Quantum Electronics
JF - IEEE Journal on Selected Topics in Quantum Electronics
IS - 2
M1 - 6657709
ER -