TY - JOUR
T1 - Low coherence interferometry of the cochlear partition
AU - Choudhury, Niloy
AU - Song, Guiju
AU - Chen, Fangyi
AU - Matthews, Scott
AU - Tschinkel, Tanja
AU - Zheng, Jiefu
AU - Jacques, Steven
AU - Nuttall, Alfred L.
N1 - Funding Information:
The authors thank Dr. Ernst Dalhoff for technical editorial comments on this report. This work was supported by the National Institutes of Health Grants, R01-DC06273, P30 DC005983 and R01-EB000224.
PY - 2006/10
Y1 - 2006/10
N2 - Interferometric measurement of the vibration of the organ of Corti in the isolated guinea pig cochlea was conducted using low-coherence light (1310 ± 47 nm wavelength) from a superluminescent diode. The short coherence length of the light source localized measurements along the axial direction to within a ∼10-μm window (in tissue), even when using a low numerical-aperture lens. The ability to accomplish this is important because measurement of the vibration of the basal-turn organ of Corti is generally done via a small hole in the bone of the cochlea, which effectively limits the numerical aperture. The axial localization, combined with the inherent sensitivity of the method, allowed distinct measurements of the basilar membrane (BM) and the putative reticular lamina (RL) vibration using only the native tissue reflectance, that is without requiring the use of reflective particles. The system was first operated in a scanning mode as an optical coherence tomography (OCT) system to yield an image of the organ of Corti. The reflectance of intensity from the BM and RL was 8 × 10-5 and 8 × 10-6, respectively. The internal structure between the BM and RL presented a variable reflectivity of about 10-7. A mirror would define a reflectance of 1.00. Then the instrument was operated as a homodyne interferometer to measure the displacement of either the BM or RL. Vibration at 16 kHz was induced by a piezoelectric actuator, causing whole movement of a dissected cochlea. After calibration of the system, we demonstrated clear measurement of mechanically driven vibration for both the BM and RL of 0.30 nm above a noise floor equivalent to 0.03 nm. OCT interferometry, when adapted for in vivo organ of Corti measurements, appears suitable to determine the micromechanical vibration of cells and tissue elements of the organ.
AB - Interferometric measurement of the vibration of the organ of Corti in the isolated guinea pig cochlea was conducted using low-coherence light (1310 ± 47 nm wavelength) from a superluminescent diode. The short coherence length of the light source localized measurements along the axial direction to within a ∼10-μm window (in tissue), even when using a low numerical-aperture lens. The ability to accomplish this is important because measurement of the vibration of the basal-turn organ of Corti is generally done via a small hole in the bone of the cochlea, which effectively limits the numerical aperture. The axial localization, combined with the inherent sensitivity of the method, allowed distinct measurements of the basilar membrane (BM) and the putative reticular lamina (RL) vibration using only the native tissue reflectance, that is without requiring the use of reflective particles. The system was first operated in a scanning mode as an optical coherence tomography (OCT) system to yield an image of the organ of Corti. The reflectance of intensity from the BM and RL was 8 × 10-5 and 8 × 10-6, respectively. The internal structure between the BM and RL presented a variable reflectivity of about 10-7. A mirror would define a reflectance of 1.00. Then the instrument was operated as a homodyne interferometer to measure the displacement of either the BM or RL. Vibration at 16 kHz was induced by a piezoelectric actuator, causing whole movement of a dissected cochlea. After calibration of the system, we demonstrated clear measurement of mechanically driven vibration for both the BM and RL of 0.30 nm above a noise floor equivalent to 0.03 nm. OCT interferometry, when adapted for in vivo organ of Corti measurements, appears suitable to determine the micromechanical vibration of cells and tissue elements of the organ.
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U2 - 10.1016/j.heares.2006.06.006
DO - 10.1016/j.heares.2006.06.006
M3 - Article
C2 - 16945496
AN - SCOPUS:33748304188
SN - 0378-5955
VL - 220
SP - 1
EP - 9
JO - Hearing Research
JF - Hearing Research
IS - 1-2
ER -