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1.
Opt Lett ; 39(2): 247-50, 2014 Jan 15.
Article in English | MEDLINE | ID: mdl-24562118

ABSTRACT

We report a novel linear-in-wavenumber (k-linear) swept laser source based on an acousto-optic deflector (AOD). The AOD-based optical filter includes an acousto-optic deflector and a reflection grating. The laser may tune k linearly in wavenumber over time due to its appropriate configuration and is favorable for fast imaging because it avoids data resampling and recalibration, as are required in conventional swept source optical coherence tomography (SS-OCT). We achieved k-linearity with Pearson's r correlation coefficients of 0.99995 without and 0.99997 with optimization. The laser has a tuning range of 50 nm, a 3 dB swept range of 42 nm (FWHM), output power of 2.56 mW, 6 dB sensitivity roll-off depth of 0.941 mm, and central wavelength of 1064 nm at a scanning rate of ∼20 kHz. Scanning rate as high as ∼400 kHz is also achieved for this laser with the tuning range 49 nm, swept linearity of 0.99990, output power of 2.30 mW, and a 6 dB sensitivity roll-off depth 0.550 mm. SS-OCT imaging with linear-in-wavenumber swept laser is also demonstrated.

2.
J Biomed Opt ; 18(8): 86011, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23955393

ABSTRACT

We present an endoscopic probe for optical coherence tomography (OCT) equipped with a miniaturized hollow ultrasonic motor that rotates the objective lens and provides an internal channel for the fiber to pass through, enabling 360 deg unobstructed circumferential scanning. This probe has an outer diameter of 1.5 mm, which is ultra-small for motorized probes with an unobstructed view in distal scanning endoscopic OCT. Instead of a mirror or prism, a customized aspheric right-angle lens is utilized, leading to an enlargement of the numerical aperture and thus high transverse resolution. Spectral-domain OCT imaging of bio-tissue and a phantom are demonstrated with resolution of 7.5 µm(axial)×6.6 µm(lateral) and sensitivity of 96 dB.


Subject(s)
Endoscopes , Image Enhancement/instrumentation , Lenses , Lighting/instrumentation , Micro-Electrical-Mechanical Systems/instrumentation , Tomography, Optical Coherence/instrumentation , Transducers , Equipment Design , Equipment Failure Analysis , High-Energy Shock Waves , Miniaturization , Motion , Phantoms, Imaging , Reproducibility of Results , Semiconductors , Sensitivity and Specificity
3.
J Biomed Opt ; 18(5): 50505, 2013 May.
Article in English | MEDLINE | ID: mdl-23698317

ABSTRACT

The spindle plays a crucial role in normal chromosome alignment and segregation during meiosis and mitosis. Studying spindles in living cells noninvasively is of great value in assisted reproduction technology (ART). Here, we present a novel spindle imaging methodology, full-field optical coherence tomography (FF-OCT). Without any dye labeling and fixation, we demonstrate the first successful application of FF-OCT to noninvasive three-dimensional (3-D) live imaging of the meiotic spindles within the mouse living oocytes at metaphase II as well as the mitotic spindles in the living zygotes at metaphase and telophase. By post-processing of the 3-D dataset obtained with FF-OCT, the important morphological and spatial parameters of the spindles, such as short and long axes, spatial localization, and the angle of meiotic spindle deviation from the first polar body in the oocyte were precisely measured with the spatial resolution of 0.7 µm. Our results reveal the potential of FF-OCT as an imaging tool capable of noninvasive 3-D live morphological analysis for spindles, which might be useful to ART related procedures and many other spindle related studies.


Subject(s)
Imaging, Three-Dimensional/methods , Meiosis/physiology , Mitosis/physiology , Spindle Apparatus/physiology , Spindle Apparatus/ultrastructure , Tomography, Optical Coherence/methods , Animals , Female , Male , Mice , Mice, Inbred ICR , Oocytes/cytology , Zygote/cytology
4.
J Biomed Opt ; 18(1): 10503, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23238420

ABSTRACT

The morphogenetic relationship between early patterning and polarity formation is of fundamental interest and remains a controversial issue in preimplantation embryonic development. We use a label-free three-dimensional (3-D) imaging technique of full-field optical coherence tomography (FF-OCT) successfully for the first time to study the dynamics of developmental processes in mouse preimplantation lives. Label-free 3-D subcellular time-lapse images are demonstrated to investigate 3-D spatial relationship between the second polar body (2PB) and the first cleavage plane. By using FF-OCT together with quantitative study, we show that only 25% of the predicted first cleavage planes, defined by the apposing plane of two pronuclei, pass through the 2PB. Also only 27% of the real cleavage planes pass through the 2PB. These results suggest that the 2PB is not a convincing spatial cue for the event of the first cleavage. Our studies demonstrate the feasibility of FF-OCT in providing new insights and potential breakthroughs to the controversial issues of early patterning and polarity in mammalian developmental biology.


Subject(s)
Blastocyst/cytology , Blastomeres/cytology , Embryonic Development/physiology , Tomography, Optical Coherence/methods , Animals , Embryo, Mammalian/chemistry , Embryo, Mammalian/physiology , Embryology/methods , Equipment Design , Female , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Male , Mice , Mice, Inbred ICR , Tomography, Optical Coherence/instrumentation
5.
Opt Lett ; 37(15): 3075-7, 2012 Aug 01.
Article in English | MEDLINE | ID: mdl-22859090

ABSTRACT

We propose a novel method called compressed sensing with linear-in-wavenumber sampling (k-linear CS) to retrieve an image for spectral-domain optical coherence tomography (SD-OCT). An array of points that is evenly spaced in wavenumber domain is sampled from an original interferogram by a preset k-linear mask. Then the compressed sensing based on l1 norm minimization is applied on these points to reconstruct an A-scan data. To get an OCT image, this method uses less than 20% of the total data as required in the typical process and gets rid of the spectral calibration with numerical interpolation in traditional CS-OCT. Therefore k-linear CS is favorable for high speed imaging. It is demonstrated that the k-linear CS has the same axial resolution performance with ~30 dB higher signal-to-noise ratio (SNR) as compared with the numerical interpolation. Imaging of bio-tissue by SD-OCT with k-linear CS is also demonstrated.


Subject(s)
Image Processing, Computer-Assisted/methods , Tomography, Optical Coherence/methods , Algorithms , Humans , Interferometry , Onions/cytology , Skin/cytology
6.
J Biomed Opt ; 17(7): 070503, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22894459

ABSTRACT

Early patterning and polarity is of fundamental interest in preimplantation embryonic development. Label-free subcellular 3D live imaging is very helpful to its related studies. We have developed a novel system of full-field optical coherence tomography (FF-OCT) for noninvasive 3D subcellular live imaging of preimplantation mouse embryos with no need of dye labeling. 3D digitized embryos can be obtained by image processing. Label-free 3D live imaging is demonstrated for the mouse embryos at various typical preimplantation stages with a spatial resolution of 0.7 [micro sign]m and imaging rate of 24 fps. Factors that relate to early patterning and polarity, such as pronuclei in zygote, shapes of zona pellucida, location of second polar body, cleavage planes, and the blastocyst axis, can be quantitatively measured. The angle between the two second cleavage planes is accurately measured to be 87 deg. It is shown that FF-OCT provides a potential breakthrough for early patterning, polarity formation, and many other preimplantation-related studies in mammalian developmental biology.


Subject(s)
Blastocyst/ultrastructure , Image Interpretation, Computer-Assisted/methods , Imaging, Three-Dimensional/methods , Subcellular Fractions/ultrastructure , Tomography, Optical Coherence/instrumentation , Animals , Equipment Design , Equipment Failure Analysis , Image Enhancement/methods , Mice , Mice, Inbred ICR , Reproducibility of Results , Sensitivity and Specificity , Staining and Labeling
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