Ex vivo and in vivo analysis demonstrated enhanced brain delivery of carmustine using a nanogel composite, suggesting non-invasive strategies.
In this study, the efficacy of a Nanogel Composite was evaluated and compared to the conventional drug carmustine (BCNU) through ex vivo and in vivo studies using New Zealand White rabbits. The Nanogel Composite is a thermosensitive, electro-responsive, and mucoadhesive gel containing BCNU-loaded paramagnetic nanoparticles known as Nano-co-Plex (NCP). Following intranasal administration, electrical stimulation (ES) was applied to the rabbit's nasal cavity, initiating the release of BCNU-NCP. Subsequently, a magnetic headband placed on the rabbit's head rapidly attracted the released nanoparticles toward the brain. The in vivo results showed high amount of BCNU in cerebrospinal fluid (CSF) and the brain of the rabbit for Nanogel Composite compared to the conventional drug with BCNU concentration values in the CSF, brain and plasma being 0.2571µg/mL, 0.199µg/g and 0.0078µg/mL, respectively, after 30 minutes of administration with the application of ES and MF; and 0.0087µg/mL, 0.0076µg/g and 0.0078µg/mL without the application. The system enabled a pulsatile "on-off" release profile, improving drug localization in the brain while minimizing systemic exposure. The applied ES and MF conditions (5V and 0.4 Tesla) were found to be safe and well-tolerated, indicating the potential of this dual-stimuli-responsive platform for effective, non-invasive, and controlled nose-to-brain drug delivery.
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Akilo et al. (2025) studied this question.
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