Author Affiliations
1MOE Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, Guangdong, China2Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, Guangdong, Chinashow less
Fig. 1. Principle and main modes of PA imaging
[3]. (a) Principle of PA imaging; (b) schematic diagram of PAM; (c) schematic diagram of PACT; (d) schematic diagram of PAE
Fig. 2. Embodiments of different arrayed ultrasound transducers for PACT. (a) PACT system based on planar array ultrasound transducer for PA imaging of mouse brain
[6]; (b) PACT system based on cylindrical array ultrasound transducer for PA imaging of breast
[11]; (c) PACT system based on spherical array ultrasonic transducer for PA imaging of hand
[12] Fig. 3. Embodiment of PACT based on LED
[16]. (a) Schematic of probe with imaging plane and illumination source; (b) PA and US imaging of skin and vasculature
Fig. 4. Embodiment of deep learning for PA imaging
[34]. (a) Architecture of Y-NET; (b)
in-
vitro results of chicken breast phantom
Fig. 5. Embodiments of high/super-resolution PAM. (a) Schematic diagram of GR-PAM and GR-PAM imaging of red blood cells
[41]; (b) schematic diagram of ULM-PAM and ULM-PAM imaging of lipids and proteins
[42] Fig. 6. Embodiments of extended depth-of-field technology in PAM. (a) Diagram of virtual detector concept in SAFT and original and 2D SAFT PA imaging of leaf vein
[45]; (b) numerical simulation and experimental measurement of parameter of Bessel beam and PA imaging of zebrafish based on Gaussian beam and Bessel beam illumination
[47] Fig. 7. Embodiments of high-speed PAM. (a) High-speed PAM based on MEMS
[54]; (b) high-speed PAM based on GM
[56]; (c) high-speed PAM based on polygon-mirror scanner
[59]; (d) high-speed PAM based on microlens array
[60] Fig. 8. Embodiments of all-optical PAM. (a) Schematic diagram of BD-AO-PAM system and
in vivo PA imaging of microvasculature of mouse ear
[69]; (b) schematic diagram of PARS microscope system and
in vivo PA imaging of chorioallantoic membrane from a chicken embryo
[70] Fig. 9. Embodiments of PAE based on optical scanning. (a) Schematic diagram of PAE probe based on MEMS scanning and PA imaging of resected mouse colon tissue
[76]; (b) schematic diagram of all-optical forward-viewing PAE probe and PA imaging of mouse abdominal skin microvasculature
[77] Fig. 10. Embodiments of extended depth-of-field technology in PAE. (a) Schematic diagram of imaging probe of AF-PAE and PA imaging of rabbit rectum
[82]; (b) schematic diagram of imaging probe of large-depth-of-field OR-PAE and PA imaging of rabbit rectum
[74] Fig. 11. Embodiments of dual-modality PAE. (a) Schematic diagram of imaging probe of PA-US endoscope and PA-US imaging of rat rectum; (b) schematic diagram of all-optical PA-OCT intravascular probe and PA-OCT imaging of vascular phantom
[87]; (c) schematic diagram of imaging probe of PA-HSI endscope and PA-HSI imaging of rabbit rectum
in vivo[90]; (d) schematic diagram of imaging probe of PA-PE endscope and US-PA-PE imaging of aorta
[91] Fig. 12. PA molecular imaging in NIR region. (a) Absorption coefficient spectra of endogenous tissue chromophores at their typical concentrations in human body
[110]; (b) reduced scattering coefficients of different biological tissues and of intralipid scattering tissue phantom as function of wavelength in 400-1700 nm region, which covers visible, NIR-I, and NIR-II windows
[110]; (c) MPE as function of excitation wavelength
[110]; (d) PA imaging of mice tumor with 680 nm and 950 nm
[113]; (e) PA-US imaging of mice tumor with 1064 nm
[112]; (f) PA-US imaging of mice tumor with 1280 nm
[111] Fig. 13. Embodiment of contrast-enhanced PA molecular imaging
[116]. (a) Synthesis process of prepared AgBr@PLGA NCs and schematic illustration that tumor area is graphically fixed via redox reaction; (b) PA imaging of mice injected AgBr@PLGA+GSH and graphene
Fig. 14. Embodiment of ratiometric PA molecular imaging
[118]. (a) Design and synthesis of quantitative PA diagnosis of gastric and intestinal diseases; (b) US imaging and PA imaging at 790 nm, PA imaging at 1200 nm, and ratiometric PA molecular imaging of stomach
Fig. 15. Embodiment of highly specific activatable probes
[120]. (a) Schematic diagram of photoconversion process; (b) cartoon illustration of background-suppressed PA molecular imaging; (c) PA molecular imaging of chicken breast tissue
Fig. 16. Embodiment of probe for integration of diagnosis and treatment
[127]. (a) Schematic illustration of NIR-II fluorescence/PA dual-modality imaging guiding tumor targeted combination therapy; (b) FI of Hela-tumor-bearing mice; (c) PA imaging of Hela-tumor-bearing mice; (d) tumor growth profiles of different groups of mice
Scanner type | Scanning speed | Imaging range | Lateral resolution /μm | Portable | Ref. |
---|
Voice coil | 20 Hz/B-scan | 9 mm | 3.4 | No | [53] | MEMS scanner | 5 s/volumetric scan | 2 mm×2 mm | 3.8 | Yes | [55] | MEMS scanner | 35 Hz/B-scan | 2.8 mm | 12.0 | Yes | [54] | Galvanometer scanner | 140 Hz·mm-1/B-scan | 15 mm | 4.9 | No | [56] | Galvanometer scanner | 500 Hz/B-scan | 2.4 mm | 7.5 | Yes | [57] | Polygon-mirror scanner | 900 Hz/B-scan | 9 mm | 10.0 | No | [58] | Polygon-mirror scanner | 2 Hz/volumetric scan | 11 mm×7.5 mm×1.5 mm | 10.0 | No | [59] | Microlens array | 36 s/cross-sectional scan | 10 mm×10 mm | 29.4 | No | [60] | Microlens array | 10 s/volumetric scan | 10 mm×10 mm | 13.0 | No | [61] | MEMS+motor | 15 min/volumetric scan | 5 mm×5 mm | 1.0 | No | [62] |
|
Table 1. Performance of scanning systems for high-speed PAM