AI Article Synopsis

  • Mannitol is used to reduce intracranial pressure and create osmotic blood-brain barrier openings, but a safer, non-invasive monitoring method for its dosing is needed.
  • The study developed a label-free MRI technique, utilizing Chemical Exchange Saturation Transfer (CEST), to measure mannitol levels in the brain after administration in rat models.
  • Results showed that CEST MRI effectively detected mannitol in the brain, with high doses leading to accumulation, and this method could help optimize mannitol usage for enhanced safety and effectiveness in clinical settings.

Article Abstract

Purpose: Mannitol is a hyperosmolar agent for reducing intracranial pressure and inducing osmotic blood-brain barrier opening (OBBBO). There is a great clinical need for a non-invasive method to optimize the safety of mannitol dosing. The aim of this study was to develop a label-free Chemical Exchange Saturation Transfer (CEST)-based MRI approach for detecting intracranial accumulation of mannitol following OBBBO.

Methods: In vitro MRI was conducted to measure the CEST properties of D-mannitol of different concentrations and pH. In vivo MRI and MRS measurements were conducted on Sprague-Dawley rats using a Biospec 11.7T horizontal MRI scanner. Rats were catheterized at the internal carotid artery (ICA) and randomly grouped to receive either 1 mL or 3 mL D-mannitol. CEST MR images were acquired before and at 20 min after the infusion.

Results: In vitro MRI showed that mannitol has a strong, broad CEST contrast at around 0.8 ppm with a mM CEST MRI detectability. In vivo studies showed that CEST MRI could effectively detect mannitol in the brain. The low dose mannitol treatment led to OBBBO but no significant mannitol accumulation, whereas the high dose regimen resulted in both OBBBO and mannitol accumulation. The CEST MRI findings were consistent with H-MRS and Gd-enhanced MRI assessments.

Conclusion: We demonstrated that CEST MRI can be used for non-invasive, label-free detection of mannitol accumulation in the brain following BBBO treatment. This method may be useful as a rapid imaging tool to optimize the dosing of mannitol-based OBBBO and improve its safety and efficacy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695341PMC
http://dx.doi.org/10.3390/pharmaceutics14112529DOI Listing

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