Overcoming the Blood-Brain Barrier: Advanced Strategies in Targeted Drug Delivery for Neurodegenerative Diseases.
Authors: Yang HM
The increasing global health crisis of neurodegenerative diseases such as Alzheimer's, Parkinson's, amyotrophic lateral sclerosis, and Huntington's disease is worsening because of a rapidly increasing aging population. Disease-modifying therapies continue to face development challenges due to the blood-brain barrier (BBB), which prevents more than 98% of small molecules and all biologics from entering the central nervous system. The therapeutic landscape for neurodegenerative diseases has recently undergone transformation through advances in targeted drug delivery that include ligand-decorated nanoparticles, bispecific antibody shuttles, focused ultrasound-mediated BBB modulation, intranasal exosomes, and mRNA lipid nanoparticles. This review provides an analysis of the molecular pathways that cause major neurodegenerative diseases, discusses the physiological and physicochemical barriers to drug delivery to the brain, and reviews the most recent drug targeting strategies including receptor-mediated transcytosis, cell-based "Trojan horse" approaches, gene-editing vectors, and spatiotemporally controlled physical methods. The review also critically evaluates the limitations such as immunogenicity, scalability, and clinical translation challenges, proposing potential solutions to enhance therapeutic efficacy. The recent clinical trials are assessed in detail, and current and future trends are discussed, including artificial intelligence (AI)-based carrier engineering, combination therapy, and precision neuro-nanomedicine. The successful translation of these innovations into effective treatments for patients with neurodegenerative diseases will require essential interdisciplinary collaboration between neuroscientists, pharmaceutics experts, clinicians, and regulators.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To review and critically evaluate current drug delivery strategies that overcome the blood–brain barrier for treating neurodegenerative diseases, including their mechanisms, limitations, and future translational prospects.
Disease model
Neurodegenerative diseases (Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, Huntington's disease)
Cargo name and characteristics
Ligand-decorated nanoparticles (targeted nanoparticles/nanocarriers), bispecific antibody shuttles (protein biologics/antibodies), intranasal exosomes (extracellular vesicle-based carriers), mRNA lipid nanoparticles (LNPs carrying mRNA), gene‑editing vectors (viral vectors e.g., AAV), cell-based 'Trojan horse' carriers (cellular carriers for therapeutic payloads), and conventional small molecules and biologics delivered via receptor-mediated transcytosis.
Route of administration
intranasal
Outcomes and Safety
Summary of Outcomes
The review concludes that several targeted delivery strategies—ligand-decorated nanoparticles, bispecific antibody shuttles, focused ultrasound-mediated BBB modulation, intranasal exosomes, and mRNA lipid nanoparticles—substantially improve CNS drug access and thus hold promise to enable disease-modifying therapies for neurodegenerative diseases, though immunogenicity, scalability, and clinical translation challenges remain.
Safety-related matter
The review identifies immunogenicity as a safety-related limitation of drug delivery approaches and notes clinical translation challenges; it does not describe specific adverse events or detailed safety data.
Brain Region
Ultrasound Parameters
Focal Characteristics
Focal depth: None, Focal length: None, Aperture size: None
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