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Optical-resolution photoacoustic microscopy (OR-PAM) has been widely used for imaging blood vessel and oxygen saturation of hemoglobin (sO2), providing high-resolution functional images of living animals in vivo. However, most of them require one or multiple bulky and costly pulsed lasers, hindering their applicability in preclinical and clinical settings. In this paper, we demonstrate a reflection-mode low-cost high-resolution OR-PAM system by using two cost-effective and compact laser diodes (LDs), achieving microvasculature and sO2 imaging with a high lateral resolution of ∼6 µm. The cost of the excitation sources has dramatically reduced by ∼20–40 times compared to that of the pulsed lasers used in state-of-the-art OR-PAM systems. A blood phantom study was performed to show a determination coefficient R2 of 0.96 in linear regression analysis. Experimental results of in vivo mouse ear imaging show that the proposed dual-wavelength LD-based PAM system can provide high-resolution functional images at a low cost.

Histopathology based on formalin-fixed and paraffin-embedded tissues has long been the gold standard for surgical margin assessment (SMA). However, routine pathological practice is lengthy and laborious, failing to guide surgeons intraoperatively. In this report, we propose a practical and low-cost histological imaging method with wide-field optical-sectioning microscopy (i.e., High-and-Low-frequency (HiLo) microscopy). HiLo can achieve rapid and non-destructive imaging of freshly-excised tissues at an extremely high acquisition speed of 5 cm2/min with a spatial resolution of 1.3 µm (lateral) and 5.8 µm (axial), showing great potential as an SMA tool that can provide immediate feedback to surgeons and pathologists for intraoperative decision-making. We demonstrate that HiLo enables rapid extraction of diagnostic features for different subtypes of human lung adenocarcinoma and hepatocellular carcinoma, producing surface images of rough specimens with large field-of-views and cellular features that are comparable to the clinical standard. Our results show promising clinical translations of HiLo microscopy to improve the current standard of care.

We proposed a high-throughput label-free and slide-free imaging technique by ultraviolet-excited autofluorescence, assisted by speckle illumination and a deep learning algorithm, to generate subcellular-resolution histology-like images of unprocessed tissues, simplifying the workflow of standard-of-care histopathology.

By implementing microscopy with ultraviolet surface excitation using speckle illumination, we have improved the spatial resolution by 1.5 times and preserved the long depth of focus, achieving sharp imaging of thick and rough specimens.

Microscopy with ultraviolet surface excitation (MUSE) is a promising slide-free imaging technique to improve the time-consuming histopathology workflow. However, since the penetration depth of the excitation light is tissue dependent, the image contrast could be significantly degraded when the depth of field of the imaging system is shallower than the penetration depth. High-resolution cellular imaging normally comes with a shallow depth of field, which also restricts the tolerance of surface roughness in biological specimens. Here we propose the incorporation of MUSE with speckle illumination (termed MUSES), which can achieve sharp imaging on thick and rough specimens. Our experimental results demonstrate the potential of MUSES in providing histological images with ∼ 1 μm spatial resolution and improved contrast, within 10 minutes for a field of view of 1.7 mm × 1.2 mm . With the extended depth of field feature, MUSES also relieves the constraint of tissue flatness. Furthermore, with a color transformation assisted by deep learning, a virtually stained histological image can be generated without manual tuning, improving the applicability of MUSES in clinical settings.

Ultraviolet photoacoustic microscopy (UV-PAM) has recently been demonstrated as a potential imaging tool for surgical margin analysis (SMA). UV-PAM does not require staining or micrometer-thick slicing, which is inevitable in conventional histological imaging. To promote UV-PAM as a practical intraoperative diagnostic tool, the imaging speed should be improved while preserving the high-resolution imaging capability and simplistic system design. In this Letter, we developed a galvanometer mirror-based UV-PAM (GM-UV-PAM) system for high-speed histology-like imaging. By using a UV laser with a high repetition rate (55 kHz) and a one-dimensional galvanometer mirror, our GM-UV-PAM system can generate subcellular images in less than 15 min for a typical brain biopsy ( 5 m m × 5 m m ), with a lateral resolution of ∼ 1.0 µ m . The images of mouse brain slices obtained by our GM-UV-PAM system show that it can provide histological information for SMA.