We present what is to our knowledge the first in vivo tomograms of human retina obtained by Fourier domain optical coherence tomography. We would like to show that this technique might be as powerful as other optical coherence tomography techniques in the ophthalmologic imaging field. The method, experimental setup, data processing, and images are discussed.

We interfaced color Doppler Fourier domain optical coherence tomography (CD-FDOCT) with a commercial OCT system to perform in vivo studies of human retinal blood flow in real time. FDOCT does not need reference arm scanning and records one full depth and Doppler profile in parallel. The system operates with an equivalent A-scan rate of 25 kHz and allows real time imaging of the color encoded Doppler information together with the tissue morphology at a rate of 2-4 tomograms (40 x 512 pixel) per second. The recording time of a single tomogram (160 x 512 data points) is only 6,4ms. Despite the high detection speed we achieve a system sensitivity of 86dB using a beam power of 500microW at the cornea. The fundus camera allows simultaneous view for selection of the region of interest. We observe bi-directional blood flow and pulsatility of blood velocity in retinal vessels with a Doppler detection bandwidth of 12.5 kHz and a longitudinal velocity sensitivity in tissue of 200microm/s.

We present, for the first time, in vivo ultrahigh resolution (~2.5 microm in tissue), high speed (10000 A-scans/second equivalent acquisition rate sustained over 160 A-scans) retinal imaging obtained with Fourier domain (FD) OCT employing a commercially available, compact (500x260mm), broad bandwidth (120 nm at full-width-at-half-maximum centered at 800 nm) Titanium:sapphire laser (Femtosource Integral OCT, Femtolasers Produktions GmbH). Resolution and sampling requirements, dispersion compensation as well as dynamic range for ultrahigh resolution FD OCT are carefully analyzed. In vivo OCT sensitivity performance achieved by ultrahigh resolution FD OCT was similar to that of ultrahigh resolution time domain OCT, although employing only 2-3 times less optical power (~300 microW). Visualization of intra-retinal layers, especially the inner and outer segment of the photoreceptor layer, obtained by FDOCT was comparable to that, accomplished by ultrahigh resolution time domain OCT, despite an at least 40 times higher data acquisition speed of FD OCT.

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We propose a modified method of acquisition and analysis of Spectral Optical Coherence Tomography (SOCT) data to provide information about flow velocities. The idea behind this method is to acquire a set of SOCT spectral fringes dependent on time followed by a numerical analysis using two independent Fourier transformations performed in time and optical frequency domains. Therefore, we propose calling this method as joint Spectral and Time domain Optical Coherence Tomography (joint STdOCT). The flow velocities obtained by joint STdOCT are compared with the ones obtained by known, phase-resolved SOCT. We observe that STdOCT estimation is more robust for measurements with low signal to noise ratio (SNR) as well as in conditions of close-to-limit velocity measurements. We also demonstrate that velocity measurement performed with STdOCT method is more sensitive than the one obtained by the phase-resolved SOCT. The method is applied to biomedical imaging, in particular to in vivo measurements of retinal blood circulation. The applicability of STdOCT different measurement modes for in vivo examinations, including 1, 5 and 40 mus of CCD exposure time, is discussed.

An improved spectral optical coherence tomography technique is used to obtain cross-sectional ophthalmic images at an exposure time of 64 micros per A-scan. This method allows real-time images as well as static tomograms to be recorded in vivo.

Standard Fourier-domain optical coherence tomography (FDOCT) suffers from the presence of autocorrelation terms that obscure the object information and degrade the sensitivity and signal-to-noise ratio. By exploiting the phase information of the recorded interferograms, it is possible to remove those autocorrelation terms and to double the measurement range. However, standard phase-retrieval algorithms need three to five interferograms. We present a novel technique that shows all the features of complex FDOCT with only two recorded interferograms.

The possibility of measuring a full Doppler flow depth profile in parallel by use of frequency-domain optical coherence tomography is demonstrated. The method is based on a local phase analysis of the backscattered signal and allows for imaging of bidirectional Doppler flow. The Doppler frequency limit is 5 kHz for the presented measurements and is set by half of the frame rate of the CCD detector array. We measured the flow of 0.3-microm microspheres suspended in distilled water at controlled flow rates and in vitro human blood flow through a 200-microm capillary with a real-time color-encoded Doppler tomogram rate of 2-3/s.