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Journal of Clinical and
            Translational Research                                                        US-mediated drug delivery



            pressure varying between 0.4 MPa and 0.5 MPa. Parameters   the Région Centre-Val de Loire for the funding of PhD
            such as time, acoustic pressure, and frequency are tailored   students (K.E.).
            to each study. Pre-clinical protocols further differ across
            research laboratories, often due to the use of lab-made US   Conflict of interest
            devices. The number of sonication session also varies, with   The authors declare no conflict of interest.
            some studies employing a single treatment while others
            span 3 weeks with 2 sessions per week, for example. Despite   Author contributions
            these variations, all methods demonstrate success in BBB   Conceptualization: Karen Ea, Patrick Vourc’h, Jean- Michel
            opening, suggesting the need for standardized protocols.   Escoffre
            It  would  be  beneficial  to  establish  defined  parameters   Writing – original draft: Karen Ea, Patrick Vourc’h, Jean-
            tailored to specific species (e.g.,  mice, rats, non-human   Michel Escoffre
            primates, and humans) and target areas (e.g.,  striatum,   Writing – review & editing: Nicolas Taulier, Christiane
            motor cortex, hippocampus).                           Contino-Pépin,  Wladimir   Urbach,  Stéphane
              Regarding NDs, only one pre-clinical study has      Desgranges, Hélène Blasco, Yara Al-Ojaimi, Philippe
            employed them for BBB opening in neurodegenerative    Corcia
            diseases.  One reason for this limited use is the relative
                   62
            novelty of NDs, which are still being optimized despite the   Ethics approval and consent to participate
            known advantages of ADV since 1998.  In addition, no   Not applicable.
                                            44
            NDs are clinically approved, making their use in clinical
            settings impossible. The greater familiarity and clinical   Consent for publication
            approval of MBs make them a more accessible option.   Not applicable.
            Nonetheless, studies using NDs have validated BBB
            opening in wild-type animals, such as with dextran in   Availability of data
            mice  and Evan’s blue in rats.  Chen et al.  demonstrated   Not applicable.
                                              57
                                   108
                57
            that NDs are more effective than MBs in delivering drugs.
            While only one study has used NDs for neurodegenerative   References
            diseases (specifically AD ), other studies have focused on
                                62

            cancer therapy. These include in vivo studies on ovarian   1.   Maladies Neurologiques: Une Approche Intégrée. Available
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                                        145
            cancer,  hepatocellular carcinoma,  and glaucoma,  as   from:  https://www.elsevier.com/fr-fr/connect/les-maladies-
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                147
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            10. Conclusion                                        doi: 10.1038/nrn1824
            MB/ND-assisted US offers a promising approach for   3.   Abbott NJ, Patabendige AAK, Dolman DEM, Yusof SR,
            improving the i.c. delivery of therapeutic molecules   Begley DJ. Structure and function of the blood-brain barrier.
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            humans. While the studies reviewed here focus primarily      doi: 10.1016/j.nbd.2009.07.030
            on  neurodegenerative  diseases,  this  approach  could   4.   Pardridge WM. The blood-brain barrier: Bottleneck in brain
            also  be  applied  to  other  conditions  requiring  barrier-  drug development. NeuroRx. 2005;2(1):3-14.
            crossing treatments. This approach holds great promise
            for advancing patient care by providing less invasive      doi: 10.1602/neurorx.2.1.3
            alternatives in the future.                        5.   Hawkins BT, Davis TP. The blood-brain barrier/
                                                                  neurovascular unit in health and disease.  Pharmacol Rev.
            Acknowledgments                                       2005;57(2):173-185.

            None.                                                 doi: 10.1124/pr.57.2.4
                                                               6.   Löscher W, Potschka H. Blood-brain barrier active efflux
            Funding                                               transporters: ATP-binding cassette gene family.  NeuroRx.

            We would like to thank the Agence Nationale de la     2005;2(1):86-98.
            Recherche (ANR) for funding (ANR-22-CE19-0031) and      doi: 10.1602/neurorx.2.1.86


            Volume 11 Issue 2 (2025)                        20                            doi: 10.36922/jctr.24.00061
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