Chitosan Coated Liposomes for Non-Invasive Brain Delivery in Zebra Finch: Formulation Optimization and Evidence of Blood Brain Barrier Traversal

dc.contributor.advisorDaou, Arij
dc.contributor.advisorEL-Sabban, Marwan
dc.contributor.authorFawaz, Mohamad
dc.contributor.commembersDarwiche, Nadine
dc.contributor.commembersMhanna, Rami
dc.contributor.degreeMSBE
dc.contributor.departmentBiomedical Engineering Program
dc.contributor.facultyFaculty of Medicine
dc.contributor.facultyMaroun Semaan Faculty of Engineering and Architecture
dc.contributor.institutionAmerican University of Beirut
dc.date2026
dc.date.accessioned2026-02-05T13:02:50Z
dc.date.submitted2026-01-03T22:00:00Z
dc.description.abstractZebra finches are a well-established neuroscience model for studying learning and vocalization, yet minimally invasive strategies for delivering pharmacological agents to their brain remain limited. Nanoparticle-based drug delivery systems, particularly liposomes, offer a biocompatible and membrane-mimetic platform that has demonstrated blood–brain barrier (BBB) penetration in mammalian models; however, their ability to access brain tissue in zebra finches has not been previously established. In this study, fluorescently labelled liposomes were formulated using ethanol injection and characterized for size, stability, and morphology using dynamic light scattering, zeta potential measurements, and scanning electron microscopy to confirm the formation of stable vesicular structures. Optimization of the formulation reduced liposome diameter to 67 nm ± 1.53 SEM, significantly smaller than earlier preparations with a size of 85 nm ± 3.76 SEM (p < 0.01), with no significant size increase observed over 30 days, demonstrating stability. Following intravenous administration, brain tissues were analyzed by confocal fluorescence microscopy with z-stack reconstruction to localize liposome-derived lipid signals relative to blood vessels and parenchyma. Injected birds exhibited significantly higher fluorescence intensity in both brain vasculature and parenchyma compared with controls, and threedimensional reconstructions revealed dye colocalization outside blood vessels, indicating extravasation and BBB crossing. Moreover, the visualization of intact vesicular structures using scanning electron microscope further supported the claim that the colocalized entities are in fact liposomes. These findings show that systemically administered liposomes can successfully cross the zebra finch BBB and reach brain tissue while maintaining structural integrity. This delivery approach provides a reliable and minimally invasive platform for future pharmacological and neurobiological interventions in this model.
dc.identifier.urihttps://hdl.handle.net/10938/35167
dc.language.isoen
dc.subject.lcshDrug delivery systems
dc.subject.lcshDrug targeting
dc.subject.lcshBlood-brain barrier
dc.subject.lcshLiposomes
dc.subject.lcshZebra finch
dc.titleChitosan Coated Liposomes for Non-Invasive Brain Delivery in Zebra Finch: Formulation Optimization and Evidence of Blood Brain Barrier Traversal
dc.typeThesis
local.AUBID202471479

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