Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2001 Dec 1;40(34):6367-80.
doi: 10.1364/ao.40.006367.

Simultaneous near-infrared diffusive light and ultrasound imaging

Simultaneous near-infrared diffusive light and ultrasound imaging

N G Chen et al. Appl Opt. .

Abstract

We have constructed a near-real-time combined imager suitable for simultaneous ultrasound and near-infrared diffusive light imaging and coregistration. The imager consists of a combined hand-held probe and the associated electronics for data acquisition. A two-dimensional ultrasound array is deployed at the center of the combined probe, and 12 dual-wavelength laser source fibers (780 and 830 nm) and 8 optical detector fibers are deployed at the periphery. We have experimentally evaluated the effects of missing optical sources in the middle of the combined probe on the accuracy of the reconstructed optical absorption coefficient and assessed the improvements of a reconstructed absorption coefficient with the guidance of the coregistered ultrasound. The results have shown that, when the central ultrasound array area is in the neighborhood of 2 cm x 2 cm, which corresponds to the size of most commercial ultrasound transducers, the optical imaging is not affected. The results have also shown that the iterative inversion algorithm converges quickly with the guidance of a priori three-dimensional target distribution, and only one iteration is needed to reconstruct an accurate optical absorption coefficient.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Schematic arrangement of NIR source and detector fibers on the probe. Small solid circles are the source fibers and larger solid cycles are the detector fibers.
Fig. 2
Fig. 2
Picture of an experimental probe. An ultrasound array of 8 × 8 = 64 transducers occupies the central 3 cm × 3 cm area, and 12 dual-wavelength source fibers and 8 detector fibers are deployed at the periphery.
Fig. 3
Fig. 3
Schematic of the NIR frequency-domain imaging system. The modulation frequency is 140 MHz. The 12 dual-wavelength source channels are switched on sequentially by a PC, and 8 detector channels receive signals in parallel. BPF, bandpass filter; OSC, oscillator.
Fig. 4
Fig. 4
(a) Log(ραβ 2Aαβ) versus distancev ραβ after calibration. (b) Phase ϕαβ versus distance ραβ after calibration.
Fig. 5
Fig. 5
Schematic of our ultrasound scanner. We connected 64 ultrasound transducers to 64 parallel transmission and reception channels. The transmission part consists of 64 high-voltage pulsers, which can be controlled by computer-generated delay profiles. The reception part consists of 64 two-stage amplifiers and A/D converters. CH, channel.
Fig. 6
Fig. 6
Ultrasound subarray scanning configuration.
Fig. 7
Fig. 7
Picture of our combined system. NIR system (top) and ultrasound system (bottom) are mounted on a hospital cart.
Fig. 8
Fig. 8
Reconstructed NIR images of deeper targets (2.5 cm in depth, 1 cm in diameter, and the fitted background μa and μs′ are 0.015 and 5.36 cm−1, respectively). The left column corresponds to images of a high-contrast target (μa = 0.25 cm−1) obtained from different probe configurations, and the right column corresponds to images of a low-contrast target (μa = 0.1 cm−1). Each row is related to a specific hole size: (a) and (b) no hole, (c) and (d) 2 cm × 2 cm, (e) and (f) 3 cm × 3 cm.
Fig. 9
Fig. 9
Reconstructed NIR images for shallow targets (1.5 cm in depth, 1 cm in diameter, and the fitted background μa and μs′ are 0.015 and 5.36 cm−1, respectively). The left column corresponds to images of a high-contrast target (μa = 0.25 cm−1), and the right column corresponds to images of a low-contrast target (μa = 0.1 cm−1). Each row is related to a specific hole size: (a) and (b) no hole, (c) and (d) 2 cm × 2 cm, (e) and (f) 3 cm × 3 cm.
Fig. 10
Fig. 10
Deep target (2.5 cm in depth, 1 cm in diameter) of low optical contrast (μa = 0.10 cm−1 and fitted background μa and μs′ are 0.02 and 5.08 cm−1, respectively). (a) A-scan line of the reflected ultrasound pulse-echo signal indicating the target depth. (b) Absorption image of the low-contrast target obtained from optical-only reconstruction. (c) Ultrasound-guided reconstruction at target depth.
Fig. 11
Fig. 11
Simultaneously obtained ultrasound and NIR absorption images. The fitted background μa and μs′ are 0.017 and 4.90 cm−1, respectively. (a) Ultrasound and (b) NIR absorption image of two high-contrast targets (target μa = 0.25 cm−1). (c) Ultrasound and (d) NIR image of two low-contrast targets (target μa = 0.10 cm−1). In both high- and low-contrast cases, the two targets were located at 2.5 cm in depth.
Fig. 12
Fig. 12
(a) and (c) −6-dB contour plots of ultrasound images shown in Figs. 11(a) and 11(c). The outer contour is −6 dB from the peak, and the contour spacing is 1 dB. (b) and (d) Corresponding NIR absorption maps reconstructed in target regions specified by ultrasound.

References

    1. Stavros TA, Thickman D, Rapp C. Solid breast nodules: use of sonography to distinguish between benign and malignant lesions. Radiology. 1995;196:123–134. - PubMed
    1. Rahbar G, Sie AC, Hansen GC, Prince JS, Melany ML, Reynolds H, Jackson VP, Sayre JW, Bassett LW. Benign versus malignant solid breast masses: US differentiation. Radiology. 1999;213:889–894. - PubMed
    1. Jackson VP. The current role of ultrasonography in breast imaging. Radiol. Clin. North Am. 1995;33:1161–1170. - PubMed
    1. Tromberg B, Shah N, Lanning R, Cerussi A, Espinoza J, Pham T, Svaasand L, Butler J. Non-invasive in vivo characterization of breast tumors using photon migration spectroscopy. Neoplasia. 2000;2:26–40. - PMC - PubMed
    1. Fantini S, Walker S, Franceschini M, Kaschke M, Schlag P, Moesta K. Assessment of the size, position, and optical properties of breast tumors in vivo by noninvasive optical methods. Appl. Opt. 1998;37:1982–1989. - PubMed

LinkOut - more resources