AI Article Synopsis

  • Recent studies suggest that non-steroidal anti-inflammatory drugs like ibuprofen could lower the risk of Alzheimer's disease, making drug-repurposing a promising avenue for treatment.
  • An innovative ibuprofen microemulsion was created for intranasal delivery, which allows for non-invasive access to the brain.
  • Tests in rats showed this microemulsion dramatically increased ibuprofen's brain uptake (4 times more than standard solutions) and demonstrated excellent stability under various storage conditions.

Article Abstract

Studies have shown the use of non-steroidal anti-inflammatory drugs, such as ibuprofen could reduce the risk of Alzheimer's disease. The drug-repurposing strategy offers a bright opportunity for these patients. Intranasal administration through the olfactory pathway provides noninvasive and direct drug delivery to the target brain. A novel ibuprofen microemulsion was prepared, characterized and assessed the brain uptake in rats. The solubility of ibuprofen in various oils, surfactants, co-surfactants, and different ratios of surfactant/co-surfactant mixtures was screened and the phase diagrams were constructed. The colloidal particle size was 166.3 ± 2.55 nm and the zeta potential was -22.7 mV. Conductivity and dilution test identified an O/W type microemulsion with pH 4.09 ± 0.08. The rheological study showed a Newtonian flow behavior with cP 10.633 ± 0.603 (mPa⋅s). A steady drug release and linear permeation profiles were observed and showed a 90% permeation rate from the released drug. Ibuprofen microemulsion showed excellent stability in 3-months accelerated storage conditions, heating-cooling and freeze-thaw cycles, accelerated centrifugation, and 6- and 12-months long-term storage conditions. studies in rats further demonstrated a 4-fold higher brain uptake of ibuprofen from the microemulsion compared to the reference solution and nearly 4-fold and 10-fold higher compared to the intravenous and oral administrations. This study provides an exciting repurposing strategy and new administration route for the treatment of Alzheimer's disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205090PMC
http://dx.doi.org/10.1080/10717544.2021.1937383DOI Listing

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