Ruikang K. Wang

Theory, developments and applications of optical coherence tomography

In this paper, we review the developments in optical coherence tomography (OCT) for three-dimensional non-invasive imaging. A number of different OCT techniques are discussed in some detail including time-domain, frequency-domain, full-field, quantum and Doppler OCT. A theoretical treatment is given and some relevant comparisons made between various implementations. The current and potential applications of OCT are discussed, with close attention paid to biomedical imaging and its metrological issues.

Three dimensional optical angiography.

With existing optical imaging techniques three-dimensional (3-D) mapping of microvascular perfusion within tissue beds is severely limited by the efficient scattering and absorption of light by tissue. To overcome these limitations we have developed a method of optical angiography (OAG) that can generate 3-D angiograms within millimeter tissue depths by analyzing the endogenous optical scattering signal from an illuminated sample. The technique effectively separates the moving and static scattering elements within tissue to achieve high resolution images of blood flow, mapped into the 3-D optically sectioned tissue beds, at speeds that allow for perfusion assessment in vivo. Its development has its origin in Fourier domain optical coherence tomography. We used OAG to visualize the cerebral microcirculation, of adult living mice through the intact cranium, measurements which would be difficult, if not impossible, with other optical imaging techniques.

Ultrahigh sensitive optical microangiography for in vivo imaging of microcirculations within human skin tissue beds

In this paper, we demonstrate for the first time that the detailed cutaneous blood flow at capillary level within dermis of human skin can be imaged by optical micro-angiography (OMAG) technique. A novel scanning protocol, i.e. fast B scan mode is used to achieve the capillary flow imaging. We employ a 1310nm system to scan the skin tissue at an imaging rate of 300 frames per second, which requires only ~5 sec to complete one 3D imaging of capillary blood flow within skin. The technique is sensitive enough to image the very slow blood flows at ~4 microm/sec. The promising results show a great potential of OMAGs role in the diagnosis, treatment and management of human skin diseases.

Depth-resolved imaging of capillary networks in retina and choroid using ultrahigh sensitive optical microangiography

We demonstrate the depth-resolved and detailed ocular perfusion maps within retina and choroid can be obtained from an ultrahigh sensitive optical microangiography (OMAG). As opposed to the conventional OMAG, we apply the OMAG algorithm along the slow scanning axis to achieve the ultrahigh sensitive imaging to the slow flows within capillaries. We use an 840 nm system operating at an imaging rate of 400 frames/s that requires 3 s to complete one 3D scan of approximately 3 x 3 mm(2) area on retina. We show the superior imaging performance of OMAG to provide functional images of capillary level microcirculation at different land-marked depths within retina and choroid that correlate well with the standard retinal pathology.

In vivo volumetric imaging of vascular perfusion within human retina and choroids with optical micro-angiography

Optical micro-angiography (OMAG), based on Fourier domain optical coherence tomography (OCT), is a recently developed imaging modality that provides dynamic blood flow imaging within microcirculation tissue beds in vivo. This paper presents its first application in imaging the blood circulations in posterior chamber of human eye. To eliminate/minimize the motion artifacts in OMAG flow image caused by the inevitable subject movement, we describe a method to compensate the bulk tissue motion by use of phase changes in sequential OCT A scan signals. By use of a fast OMAG/OCT imaging system at ~840nm wavelength band, we show that OMAG is capable of providing volumetric vasculatural images in retina and choroids, down to capillary level imaging resolution, within approximately 10 s. The depth-resolved volumetric views of the separate retina and choroid vasculatures are also presented. In the end of this paper, we provide a comparison of the OMAG results with those from Doppler OCT and optical coherence angiography.

Random phase encoding for optical security

A new optical encoding method for security applications is proposed. The encoded image (encrypted into the security products) is merely a random phase image statistically and randomly generated by a random number generator using a computer, which contains no information from the reference pattern (stored for verification) or the frequency plane filter (a phase‐only function for decoding). The phase function in the frequency plane is obtained using a modified phase retrieval algorithm. The proposed method uses two phase‐only functions (images) at both the input and frequency planes of the optical processor leading to maximum optical efficiency. Computer simulation shows that the proposed method is robust for optical security applications.

Doppler optical micro-angiography for volumetric imaging of vascular perfusion in vivo

We propose a Doppler optical micro-angiography (DOMAG) method to image flow velocities of the blood flowing in functional vessels within microcirculatory tissue beds in vivo. The method takes the advantages of recently developed optical micro-angiography (OMAG) technology, in which the endogenous optical signals backscattered from the moving blood cells are isolated from those originated from the tissue background, i.e., the tissue microstructures. The phase difference between adjacent A scans of OMAG flow signals is used to evaluate the flow velocity, similar to phase-resolved Doppler optical coherence tomography (PRDOCT). To meet the requirement of correlation between adjacent A scans in using the phase resolved technique to evaluate flow velocity, an ideal tissue-sample background (i.e., optically homogeneous tissue sample) is digitally reconstructed to replace the signals that represent the heterogeneous features of the static sample that are rejected in the OMAG flow images. Because of the ideal optical-homogeneous sample, DOMAG is free from the characteristic texture pattern noise due to the heterogeneous property of sample, leading to dramatic improvement of the imaging performance. A series of phantom flow experiments are performed to evaluate quantitatively the improved imaging performance. We then conduct in vivo experiments on a mouse brain to demonstrate that DOMAG is capable of quantifying the flow velocities within cerebrovascular network, down to capillary level resolution. Finally, we compare the in vivo imaging performance of DOMAG with that of PRDOCT, and show that DOMAG delivers at least 15-fold increase over the PRDOCT method in terms of the lower limit of flow velocity that can be detected.

In vivo full range complex Fourier domain optical coherence tomography

The author presents a system and algorithm to achieve full range complex Fourier domain optical coherence tomography (OCT) capable of imaging biological tissues in vivo. The method utilizes the Hilbert transformation to obtain the analytic functions for spatial interference signals obtained from each single wavelength covered in the broadband OCT light source before performing the Fourier transformation to localize the scatters within a sample. A constant carrier frequency is introduced in the spatial OCT interference signal so that its Hilbert transformation is strictly equal to its quadrature representation. The method is experimentally validated for in vivo imaging.

Phase-sensitive optical coherence elastography for mapping tissue microstrains in real time

The authors present a phase-sensitive optical coherence elastography (PSOCE) approach to image instantaneous tissue deformations, strain rates, and strains of soft tissue in real time with sensitivity at the nanometer scale. This method exploits the phase information available in the complex optical coherence tomography images and measures the phase changes between the successive B scans to resolve the instantaneous tissue deformations. The PSOCE system described is capable of producing localized microstrain rate and strain maps of tissue subjected to a dynamic compression in real time. They show that this approach is capable of resolving deformations as small as 0.26nm.

Tissue Doppler optical coherence elastography for real time strain rate and strain mapping of soft tissue

The authors present a tissue Doppler optical coherence elastography (tDOCE) method to image tissue movements, strain rates, and strains of soft tissue in real time. The method exploits the Doppler effect in optical coherence interferograms induced by tissue motion and measures the phase changes between successive A scans to resolve the instantaneous tissue displacement. The tDOCE system is capable of displaying the strain rates and strain maps of tissue subjected to a dynamic compression in real time. The system is demonstrated by the use of a heterogeneous tissue phantom with known mechanical properties.