Reflection-mode virtual histology using photoacoustic remote sensing microscopy

• Published in: Scientific reports Vol. 10; no. 1; p. 19121
• Main Authors: Bell, Kevan, Abbasi, Saad, Dinakaran, Deepak, Taher, Muba, Bigras, Gilbert, van Landeghem, Frank K. H., Mackey, John R., Haji Reza, Parsin
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 05-11-2020; Nature Publishing Group
• Subjects: 631/1647/245/2160; 631/1647/328; 639/624/1107/328; 639/624/1107/510; 692/4028/546; Animals; Basal cell carcinoma; Breast cancer; Epithelium; Humanities and Social Sciences; Humans; Kidney - pathology; Kidneys; Mice; Microscopy; Microscopy - methods; multidisciplinary; Neuroimaging; Paraffin; Photoacoustic Techniques; Remote sensing; Remote Sensing Technology; Science; Science (multidisciplinary); Skin - pathology; Staining and Labeling
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-76155-6

Histological visualizations are critical to clinical disease management and are fundamental to biological understanding. However, current approaches that rely on bright-field microscopy require extensive tissue preparation prior to imaging. These processes are both labor intensive and contribute to creating significant delays in clinical feedback for treatment decisions that can extend to 2–3 weeks for standard paraffin-embedded tissue preparation and interpretation, especially if ancillary testing is needed. Here, we present the first comprehensive study on the broad application of a novel label-free reflection-mode imaging modality known as photoacoustic remote sensing (PARS) for visualizing salient subcellular structures from various common histopathological tissue preparations and for use in unprocessed freshly resected tissues. The PARS modality permits non-contact visualizations of intrinsic endogenous optical absorption contrast to be extracted from thick and opaque biological targets with optical resolution. The technique was examined both as a rapid assessment tool that is capable of managing large samples (> 1 cm
2
) in under 10 min, and as a high contrast imaging modality capable of extracting specific biological contrast to simulate conventional histological stains such as hematoxylin and eosin (H&E). The capabilities of the proposed method are demonstrated in a variety of human tissue preparations including formalin-fixed paraffin-embedded tissue blocks and unstained slides sectioned from these blocks, including normal and neoplastic human brain, and breast epithelium involved with breast cancer. Similarly, PARS images of human skin prepared by frozen section clearly demonstrated basal cell carcinoma and normal human skin tissue. Finally, we imaged unprocessed murine kidney and achieved histologically relevant subcellular morphology in fresh tissue. This represents a vital step towards an effective real-time clinical microscope that overcomes the limitations of standard histopathologic tissue preparations and enables real-time pathology assessment.