| Literature DB >> 31409819 |
Hendrik Spahr1,2, Clara Pfäffle1,2, Sazan Burhan1, Lisa Kutzner1,2, Felix Hilge1,2, Gereon Hüttmann1,2,3, Dierck Hillmann4,5.
Abstract
Phase-sensitive coherent imaging exploits changes in the phases of backscattered light to observe tiny alterations of scattering structures or variations of the refractive index. But moving scatterers or a fluctuating refractive index decorrelate the phases and speckle patterns in the images. It is generally believed that once the speckle pattern has changed, the phases are scrambled and any meaningful phase difference to the original pattern is removed. As a consequence, diffusion and tissue motion that cannot be resolved, prevent phase-sensitive imaging of biological specimens. Here, we show that a phase comparison between decorrelated speckle patterns is still possible by utilizing a series of images acquired during decorrelation. The resulting evaluation scheme is mathematically equivalent to methods for astronomic imaging through the turbulent sky by speckle interferometry. We thus adopt the idea of speckle interferometry to phase-sensitive imaging in biological tissues and demonstrate its efficacy for simulated data and imaging of photoreceptor activity with phase-sensitive optical coherence tomography. We believe the described methods can be applied to many imaging modalities that use phase values for interferometry.Entities:
Year: 2019 PMID: 31409819 PMCID: PMC6692410 DOI: 10.1038/s41598-019-47979-8
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
Figure 1(a) In average, each speckle (schematically represented by the blue ellipses) carries valid phase information only for the correlation time of the speckle pattern. Assuming that all speckle in the averaged area are subject to a common phase change in addition to random uncorrelated phase changes, one can use the phase of speckle A as long as it is valid and then continue with the phase of speckle B. Using multiple speckle, phase information for times significantly exceeding the correlation time can be extracted. (b,e) Exemplary cross-spectrum magnitude and phase assuming infinite correlation time. Total phase changes can either be computed directly (blue arrow) or using the Knox-Thompson path (green arrows). (c,f) Magnitude and phase of the cross-spectrum without averaging; neither method can extract the phase beyond the correlation time. (d,g) Magnitude and phase of ensemble averaged cross-spectrum. Direct phase differences (blue) cannot be used for phase extraction, but Knox-Thompson (green) method can be applied since phase values for small Δt are valid.
Figure 2Flowdiagram of the actual implementation of the extended Knox-Thompson algorithm.
Figure 3Phase images and speckle patterns obtained from the simulation. (a–d) Phase evaluated by phase differences for different σ and time steps. (e–h) Phase evaluated using the extended Knox-Thompson methods for the same σ and time steps as shown in (a–d). (i–k) Speckle patterns for σ = λ/32 after a different number of time steps. Scale bars are 500λ.
Figure 4Extracting a single phase curve from simulated images of point scatterers that move between successive measurements by subtracting the phase of the first image (a–d) and extended Knox-Thompson evaluation of phases (e–h) while random 3D motion of the simulated scatterers is increased from 0 to λ/16. (i–k) Autocorrelation of temporal changes of the wave field. Each curve was simulated 100×; the grey areas indicate the standard deviation of the obtained values.
Quantitative comparison of the simulated results (compare Fig. 4).
| Mean over all | Final | |||
|---|---|---|---|---|
| Phase differences | Extended Knox-Thompson | Phase differences | Extended Knox-Thompson | |
| 0.0 ± 0.0 | 0.0 ± 0.0 | 0.0 ± 0.0 | 0.0 ± 0.0 | |
| 0.17 ± 0.38 | 0.00038 ± 0.00042 | 2.8 ± 6.6 | 0.0010 ± 0.0012 | |
| 2.1 ± 1.3 | 0.00068 ± 0.00082 | 7.3 ± 8.1 | 0.0015 ± 0.0020 | |
| 3.7 ± 1.3 | 0.0024 ± 0.0031 | 6.8 ± 7.8 | 0.0054 ± 0.0073 | |
Values indicate the mean squared errors over the simulated datasets taken all values (mean over all t) or only the final values in a time series (final t) into account.
Figure 5Phase differences between the ends of the photoreceptor outer segment in the living human eye at different times compared to the initial phase at t = 0. The entire measurement ended at about t = 14.6 s after initiating a light stimulus. (a–g) Phase difference obtained by directly comparing to pre-stimulus phase with phase after different times. (h–n) Phase difference obtained from the cross-spectrum as described in the Methods section (by minimizing Eq. (14)). (o–u) Speckle pattern of one of the involved layers before the stimulus and at the respective times. It can clearly be seen, that that the speckle pattern changes with time. Scale bars are 200 μm.
Computational time required to evaluate single datasets of the data shown in Figs 3–5, for both simulated and experimental data.
| Simulated data | Experimental data | ||
|---|---|---|---|
| Image (Fig. | Curve (Fig. | Image (Fig. | |
| Standard | 0.34 ± 0.08s | 0.27 ± 0.06s | 2.33 ± 0.06s |
| Extended Knox-Thompson | 109 ± 6s | 40 ± 1s | 109 ± 2s |
Figure 6Full-field swept-source optical coherence tomography setup used for acquiring in vivo data.