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Updated: Jul 29, 2025

Intranasal Administration of CNS Therapeutics to Awake Mice
Published on: April 8, 2013
Intranasal Drug Administration in Alzheimer-Type Dementia: Towards Clinical Applications
Raquel Taléns-Visconti1, Jesus Vicente de Julián-Ortiz2, Ofelia Vila-Busó3
1Department of Pharmacy and Pharmaceutical Technology and Parasitology, Faculty of Pharmacy, University of Valencia, Av. Vicent Andrés Estellés s/n, 46100 Valencia, Spain.
Nanostructured lipid carriers show promise for intranasal Alzheimer-type dementia (ATD) treatment, overcoming blood-brain barrier challenges. Further research is needed to confirm the potential of this direct brain delivery route.
Area of Science:
- Neuroscience
- Pharmacology
- Biotechnology
Background:
- Alzheimer-type dementia (ATD) treatments struggle with blood-brain barrier penetration and systemic side effects.
- The intranasal route offers direct brain access via olfactory and trigeminal pathways, but faces challenges in drug absorption and bioavailability.
- Technological strategies are essential to optimize formulation physicochemical characteristics for effective intranasal drug delivery.
Purpose of the Study:
- To review nanostructured lipid carriers (NLCs) for intranasal administration in Alzheimer-type dementia (ATD) treatment.
- To evaluate the potential of NLCs in overcoming intranasal delivery challenges for ATD therapeutics.
- To summarize current preclinical and clinical investigations of intranasal ATD treatments.
Main Methods:
- Literature review of studies investigating NLCs for intranasal administration in ATD.
- Analysis of preclinical data on NLCs' toxicity and therapeutic efficacy.
- Examination of current clinical trial status for intranasal ATD drug candidates.
Main Results:
- Lipid-based nanosystems, particularly NLCs, demonstrate promise in preclinical ATD research with low toxicity and good efficacy.
- NLCs show potential in overcoming challenges associated with intranasal drug absorption and bioavailability.
- Currently, no intranasal ATD drugs are approved, with only insulin, rivastigmine, and APH-1105 in clinical investigation.
Conclusions:
- Nanostructured lipid carriers are a promising strategy for intranasal delivery of ATD treatments.
- The intranasal route, enhanced by NLCs, has significant potential for future ATD therapy.
- Continued research and clinical trials are necessary to validate the efficacy of intranasal administration for ATD.
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