| Literature DB >> 23082305 |
Gangjun Liu1, Alexander J Lin, Bruce J Tromberg, Zhongping Chen.
Abstract
We compare, in detail, the phase-resolved color Doppler (PRCD), phase-resolved Doppler variance (PRDV) and intensity-based Doppler variance (IBDV) methods. All the methods are able to quantify flow speed when the flow rate is within a certain range, which is dependent on the adjacent A-line time interval. While PRCD is most sensitive when the flow direction is along the probing beam, PRDV and IBDV can be used to measure the flow when the flow direction is near perpendicular to the probing beam. However, the values of PRDV and IBDV are Doppler angle-dependent when the Doppler angle is above a certain threshold. The sensitivity of all the methods can be improved by increasing the adjacent A-line time interval while still maintaining a high sampling density level. We also demonstrate for the first time, to the best of our knowledge, high resolution inter-frame PRDV method. In applications where mapping vascular network such as angiogram is more important than flow velocity quantification, IBDV and PRDV images show better contrast than PRCD images. The IBDV and PRDV show very similar characteristics and demonstrate comparable results for vasculature mapping. However, the IBDV is less sensitive to bulk motion and with less post-processing steps, which is preferred for fast data processing situations. In vivo imaging of mouse brain with intact skull and human skin with the three methods were demonstrated and the results were compared. The IBDV method was found to be able to obtain high resolution image with a relative simple processing procedure.Entities:
Keywords: (170.3890) Medical optics instrumentation; (170.4500) Optical coherence tomography
Year: 2012 PMID: 23082305 PMCID: PMC3469988 DOI: 10.1364/BOE.3.002669
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732
Fig. 1The dependence of IBDV and PRDV values on the flow rate.
Fig. 2The dependence of IBDV and PRDV values on the Doppler angle.
Fig. 3The dependence of IBDV and PRDV values on the time interval.
Fig. 4Beam scanning protocol for acquiring the 3D OCT data set.
Fig. 5In vivo OCT imaging of mouse brain with intact skull: (a) OCT image; (b) IF-PRDV image without bulk phase removal; (c) IF-PRCD image without bulk phase removal; (d) IF-IBDV image; (e) IF-PRDV image with bulk phase removal; (f) IF-PRCD image with bulk phase removal. Scale bar: 1mm.
Fig. 6En face maximum intensity projection (MIP) view image of mouse brain with intact skull. (a) MIP view IF-IBDV image for depth 0–360 μm. (b) MIP view IF-PRDV image for depth 150–360 μm. (c) MIP view IF-PRCD image for depth 150–360 μm. (d) MIP view IF-IBDV image for depth 150–540 μm. (e) MIP view IF-PRDV image for depth 150–540 μm. (f) MIP view IF-PRCD image for depth 150–540 μm. Scale bar, 1mm.
Fig. 7En face MIP view image of human palm skin. (a) Photography of the imaging area (in the white rectangle). (b) En face MIP view IF-IBDV image for depth of 120–360 μm. (c) En face MIP view IF-PRDV image for depth of 120–360 μm. (d) En face MIP view IF-PRCD image for depth of 120–360 μm. (e) En face MIP view IF-IBDV image for depth of 120–600 μm. (f) En face MIP view IF-PRDV image for depth of 120–600 μm. (g) En face MIP view IF-PRCD image for depth of 120–600 μm. (h) En face MIP view IF-IBDV image for depth of 120–640 μm. (i) En face MIP view IF-PRDV image for depth of 120–840 μm. (j) En face MIP view IF-PRCD image for depth of 120–840 μm. Scale bar, 1mm.