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Global Translational Medicine                                      Rapid diagnostic imaging on biopsy needle



                        A






                        B                  C









            Figure 6. Microscopy with ultraviolet surface excitation imaging of a mouse tumor model obtained via a 14-gauge core needle biopsy gun. (A) Image of the
            mouse tumor, stitched using ImageJ. Scale bar: 500 µm; magnification: 10×, (B) Zoomed-in segment of the tumor from (A), stitched using ImageJ. Nuclei
            are stained with Hoechst with a Rhodamine B counterstain. Scale bar: 500 µm; magnification: 10×, (C) Color-adjusted image using ImageJ to improve
            visual comparison between pig breast biopsies and mouse tumor biopsies. Scale bar: 500 µm; magnification: 10×.

            applications (Figure 7A and B). These comparative images   A
            demonstrate the level of image clarity achievable with
            optimized sample handling and preparation, further
            supporting the notion that, with continued refinement, the
            CoreView ION platform holds strong promise for rapid,
            point-of-care diagnostic applications.

            3.3. Biopsy integrity under compression testing
            Understanding the effects of compression on biopsy   B
            samples is critical since the prototype requires a flat
            surface for planar microscopic imaging. When the biopsy
            is pressed against the imaging window, the specimen is
            flattened, allowing for a greater percentage of the tissue
            surface in full focus and direct contact with the quartz
            coverslip, improving image quality and resolution.
            However, CNBs are structurally fragile, and external
            stressors can lead to mechanical breakdown. Therefore,   Figure  7.  High-quality MUSE images  from core biopsies in
            confirming if compression leads to tissue damage that   non-needle-based applications. (A) Fresh normal prostate core biopsy
            could compromise downstream histopathological analysis   stained with alternative Rhodamine and Hoechst, imaged using MUSE
                                                               by the Levenson Lab, University of California, Davis. Scale bar: 500 µm;
            is essential.                                      magnification: 10×, (B) Fresh cancerous prostate core biopsy stained
              After conducting a study to assess the effects of   with alternative Rhodamine and Hoechst, also imaged using MUSE by
                                                                                                22
                                                               the Levenson Lab, University of California, Davis.  Scale bar: 500 µm;
            varying compression levels on biopsy integrity, the   magnification: 10×.
            pig breast samples were processed through a standard   Abbreviation: MUSE: Microscopy with ultraviolet surface excitation.
            histopathological  workflow  at  the UW  Histology and
            Imaging Core for H&E staining (Figure 8). The resulting   compression applied using  the  CoreView  ION  system—
            digital pathology slides were reviewed by a breast   the tissue maintained structural and molecular integrity.
            pathology specialist from the UW Medicine Department of   This preservation suggests that the samples  will remain
            Pathology. On evaluation, the pathologist remarked, “The   viable for downstream pathological assessment.
            tissue quality and staining are excellent… able to make a   It is important to note that while the compression
            diagnosis on tissue samples of this quality” (Dr. Suzanne   mechanism utilized in this study differs from that of
            Dintzis, MD, PhD, October 28, 2022). These findings,   CoreView ION, the employed test fixture allowed for more
            later confirmed by a board-certified pathologist from the   precise compression control, as well as improved specimen
            University of California, Davis, Department of Pathology,   accessibility and processing speed. One limitation of this study
            indicate that even under high compression—flattening the   is the absence of cancerous tissue in the test samples; while
            specimen to 30% of its original thickness, more than the   healthy tissue demonstrated no observable differences across


            Volume 4 Issue 3 (2025)                        112                          doi: 10.36922/GTM025170039
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