AI Article Synopsis

  • Systemic drugs can treat retinal issues, but the blood-retina barrier (BRB) limits their effectiveness, prompting research into sonication, which uses ultrasound to temporarily open the BRB.
  • In a study with C57/BL6J mice, sonication at 0.15 MPa proved best for safely increasing BRB permeability without harming retinal structure or function.
  • This method allows larger molecules (up to 150 kDa) to penetrate the BRB, enhancing drug delivery to the retina without significant side effects.

Article Abstract

Systemic drugs can treat various retinal pathologies such as retinal cancers; however, their ocular diffusion may be limited by the blood-retina barrier (BRB). Sonication corresponds to the use of ultrasound (US) to increase the permeability of cell barriers including in the BRB. The objective was to study the efficacy and safety of sonication using microbubble-assisted low-intensity pulsed US in inducing a transient opening of the BRB. The eyes of C57/BL6J mice were sonicated at different acoustic pressures (0.10 to 0.50 MPa). Efficacy analyses consisted of fluorescein angiography (FA) performed at different timepoints and the size of the leaked molecules was assessed using FITC-marked dextrans. Tolerance was assessed by fundus photographs, optical coherence tomography, immunohistochemistry, RT-qPCR, and electroretinograms. Sonication at 0.15 MPa was the most suitable pressure for transient BRB permeabilization without altering the morphology or function of the retina. It did not increase the expression of inflammation or apoptosis markers in the retina, retinal pigment epithelium, or choroid. The dextran assay suggested that drugs up to 150 kDa in size can cross the BRB. Microbubble-assisted sonication at an optimized acoustic pressure of 0.15 MPa provides a non-invasive method to transiently open the BRB, increasing the retinal diffusion of systemic drugs without inducing any noticeable side-effect.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384184PMC
http://dx.doi.org/10.3390/pharmaceutics15071896DOI Listing

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