• Photonics Research
  • Vol. 8, Issue 12, 1875 (2020)
Jiangbo Chen1、†, Yachao Zhang1、†, Xiaozhen Li2、†, Jingyi Zhu1, Dengfeng Li1, Shengliang Li2, Chun-Sing Lee2、4、*, and Lidai Wang1、3、5、*
Author Affiliations
  • 1Department of Biomedical Engineering, City University of Hong Kong, 999077 Hong Kong SAR, China
  • 2Center of Super-Diamond and Advanced Films (COSDAF) and Department of Chemistry, City University of Hong Kong, 999077 Hong Kong SAR, China
  • 3City University of Hong Kong Shenzhen Research Institute, Shenzhen 518057, China
  • 4e-mail: apcslee@cityu.edu.hk
  • 5e-mail: lidawang@cityu.edu.hk
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    DOI: 10.1364/PRJ.409378 Cite this Article Set citation alerts
    Jiangbo Chen, Yachao Zhang, Xiaozhen Li, Jingyi Zhu, Dengfeng Li, Shengliang Li, Chun-Sing Lee, Lidai Wang. Confocal visible/NIR photoacoustic microscopy of tumors with structural, functional, and nanoprobe contrasts[J]. Photonics Research, 2020, 8(12): 1875 Copy Citation Text show less
    Schematic of the CVN-PAM. ACL, achromatic lens; AL, acoustic lens; CL, convex lens; BPF, bandpass filter; CP, coupler; DM, dichroic mirror; HWP, half-wave plate; MR, mirror; NDF, neutral density filter; PBS, polarization beam splitter; UT, ultrasonic transducer.
    Fig. 1. Schematic of the CVN-PAM. ACL, achromatic lens; AL, acoustic lens; CL, convex lens; BPF, bandpass filter; CP, coupler; DM, dichroic mirror; HWP, half-wave plate; MR, mirror; NDF, neutral density filter; PBS, polarization beam splitter; UT, ultrasonic transducer.
    (a) Measured and fitted edge spread function (ESF) and derived line spread function (LSF) at 532 nm, 558 nm, and 1064 nm; acoustic axial resolution. (b) Penetration depths, 0.95 mm for 532 nm and 1.45 mm for 1064 nm with a 6 dB SNR. (c) Depth-encoded vascular image of the mouse ear at 532 nm. (d) Depth-encoded vascular image of the mouse ear at 1064 nm. (e) sO2 image of the mouse ear computed from 532 nm and 558 nm wavelengths.
    Fig. 2. (a) Measured and fitted edge spread function (ESF) and derived line spread function (LSF) at 532 nm, 558 nm, and 1064 nm; acoustic axial resolution. (b) Penetration depths, 0.95 mm for 532 nm and 1.45 mm for 1064 nm with a 6 dB SNR. (c) Depth-encoded vascular image of the mouse ear at 532 nm. (d) Depth-encoded vascular image of the mouse ear at 1064 nm. (e) sO2 image of the mouse ear computed from 532 nm and 558 nm wavelengths.
    (a) PA image of SPNs at 532 nm. (b) PA image of SPNs at 1064 nm. (c) PA image of blood at 1064 nm. (d) PA image of water at 1064 nm. (e) PA image of blood at 532 nm. (f) Comparison of average PA amplitudes of these samples. Error bars are standard deviations.
    Fig. 3. (a) PA image of SPNs at 532 nm. (b) PA image of SPNs at 1064 nm. (c) PA image of blood at 1064 nm. (d) PA image of water at 1064 nm. (e) PA image of blood at 532 nm. (f) Comparison of average PA amplitudes of these samples. Error bars are standard deviations.
    (a) Mouse ear before injecting tumor cells (day 0). The black dotted box is the region of interest. (b) Microvasculature image of the mouse ear at 532 nm on day 0. (c) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 0. (d) The mouse ear on day 6 (before injecting SNPs). (e) Microvasculature image of the mouse ear at 532 nm on day 6. (f) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 6. (g) The mouse ear on day 7 (24 h after SPN injection). (h) Microvasculature image of the mouse ear at 532 nm on day 7. (i) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 7.
    Fig. 4. (a) Mouse ear before injecting tumor cells (day 0). The black dotted box is the region of interest. (b) Microvasculature image of the mouse ear at 532 nm on day 0. (c) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 0. (d) The mouse ear on day 6 (before injecting SNPs). (e) Microvasculature image of the mouse ear at 532 nm on day 6. (f) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 6. (g) The mouse ear on day 7 (24 h after SPN injection). (h) Microvasculature image of the mouse ear at 532 nm on day 7. (i) The color-coded depth microvasculature image of the mouse ear at 532 nm on day 7.
    (a) The sO2 of the mouse ear before injecting cancer cells (day 0). (b) The sO2 of the mouse ear on day 7. (c) Extracted sO2 of the tumor region. The feeding vessels and draining vessels are pointed out. (d) Imaging of the mouse ear at 1064 nm on day 0 and day 7. (e) The combined image of sO2 and 1064 nm image. (f) The sO2 pixels percentage in the mouse ear on day 0 and day 7. The vertical axis is the percentage ratio of the pixel number at an sO2 value to the total pixel number of the blood vessels in the image. The sO2 value interval on the x axis is 0.001. (g) The sO2 pixels percentage of R1 and R2 in the mouse ear on day 7. (h) The sO2 change of the feeding vessels and draining vessels. The OEFs of the tumor region are extracted from the sO2 values.
    Fig. 5. (a) The sO2 of the mouse ear before injecting cancer cells (day 0). (b) The sO2 of the mouse ear on day 7. (c) Extracted sO2 of the tumor region. The feeding vessels and draining vessels are pointed out. (d) Imaging of the mouse ear at 1064 nm on day 0 and day 7. (e) The combined image of sO2 and 1064 nm image. (f) The sO2 pixels percentage in the mouse ear on day 0 and day 7. The vertical axis is the percentage ratio of the pixel number at an sO2 value to the total pixel number of the blood vessels in the image. The sO2 value interval on the x axis is 0.001. (g) The sO2 pixels percentage of R1 and R2 in the mouse ear on day 7. (h) The sO2 change of the feeding vessels and draining vessels. The OEFs of the tumor region are extracted from the sO2 values.
    (a) Color-coded vessel tortuosity of the microstructure on day 0 and day 7. The extracted blood vessels are overlaid with the vessel centerlines. (b) Color-coded vessel diameter on day 0 and day 7. The extracted blood vessels are overlaid with the vessel centerlines. (c) Color-coded vessel density on day 0 and day 7. The image is divided into 40×34 subareas.
    Fig. 6. (a) Color-coded vessel tortuosity of the microstructure on day 0 and day 7. The extracted blood vessels are overlaid with the vessel centerlines. (b) Color-coded vessel diameter on day 0 and day 7. The extracted blood vessels are overlaid with the vessel centerlines. (c) Color-coded vessel density on day 0 and day 7. The image is divided into 40×34 subareas.
    RegionTimeVessel Tortuosity (a.u.)Vessel Diameter (μm)Vessel Density (a.u.)
    Tumor R3Day 01.06±0.0518.20±3.600.51±0.04
    Day 71.21±0.1128.40±5.100.81±0.13
    Non-tumor R4Day 01.08±0.0618.30±3.640.49±0.05
    Day 71.07±0.0810.56±4.250.55±0.08
    Table 1. Vessel Parameters in Tumor and Non-Tumor Regions
    Jiangbo Chen, Yachao Zhang, Xiaozhen Li, Jingyi Zhu, Dengfeng Li, Shengliang Li, Chun-Sing Lee, Lidai Wang. Confocal visible/NIR photoacoustic microscopy of tumors with structural, functional, and nanoprobe contrasts[J]. Photonics Research, 2020, 8(12): 1875
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