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International Journal of Bioprinting                                       PAI for 3D bioprinted constructs




            monitoring of functional cerebral dynamics in response   approaches remains challenging. A deeply seated placenta
            to  physiological  stimuli.  Demonstrative  mouse  brain   is normally inaccessible with conventional optical imaging
            images acquired using UFF-PAM revealed the complete   techniques. Biomedical tomography such as magnetic
            vascular network of the cortex, along with maps of the sO2   resonance imaging or X-ray computed tomography
            delineated by individual vessels (Figure 6a). A maximum   require contrast agent administration for angiographic
            rapid volumetric frame rate of 2 Hz allowed the capture   presentation but still lack sufficient spatial resolution
            of spreading depolarization (SD) wave propagation   and molecular sensitivity.  The advent of UFF-PAM via
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            in the gray matter and the associated hemodynamics   placental window overcomes these technical limitations, as
            induced by ischemic stroke (Figure 6b). This facilitated   being a high-resolution, high-speed, in-depth functional
            the measurement of a propagating speed of 2.56 mm/min,   microvessel imaging technique providing intrinsic optical
            alongside a precise determination of the origin location   contrast from hemoglobin. They longitudinally monitored
            for each SD wave. A continuous monitoring of the vessel   the daily changes in the mouse placenta during a healthy
            diameter (Figure 6c) and sO2 (Figure 6d) during the   pregnancy term, from 7 to 19 embryonic days. Moreover,
            propagation of SD waves revealed local vasoconstriction   the observed changes in each parameter displayed notable
            and hypoxia in response to spreading ischemia.     correlations with the specific trimesters of pregnancy. Rapid

               In a demonstration of the application of UFF-PAM,   microvessel development was evident in the first trimester,
            Zhu et al. achieved a longitudinal imaging of the placental   whereas the second trimester witnessed an increase in both
            vasculature of maternal mouse using an intravital window.    the quantity and size of placental vessels. Throughout the
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            The placental vasculature, which supplies nutrients and   third trimester, vascular development persisted along with
            oxygen crucial for embryo development and growth,   elevated vascular branching. Notably, sO  levels reflect the
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            plays a vital role in embryonic development and growth.   transition from indirect oxygen delivery via trophoblasts
            While microvascular alterations and placental pathologies   to direct delivery via fetal circulation.
            have been correlated from histological findings, 72,73    Rebling  et  al.  utilized  large-scale  optoacoustic
            investigation of hemodynamic functions and metabolic   microscopy (LSOM) to longitudinally image the
            changes in mouse placental vessels using in vivo imaging   revascularization process during wound healing, thereby




































            Figure 6. Ultrafast functional photoacoustic microscopy (UFF-PAM) presenting pathophysiological changes in vasculature. (a) A mouse brain image over
            the entire cortex and its corresponding topical oxygen saturation (sO2) map measured from 532/558 nm dual-wavelength excitation. (b) Propagation time
            map of spreading depolarization (SD) waves observed from a stroke-induced mouse model. (c) Monitoring of vessel diameter changes and (d) change in
            sO2 during SD wave propagation. The images are reproduced with permission from. 70


            Volume 10 Issue 4 (2024)                        8                                 doi: 10.36922/ijb.3448
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