Answers are grounded in this paper and cite their sources.
Evaluates intranasal delivery of nanoparticle carriers for schizophrenia, suggesting improved outcomes.
INTRODUCTION: Schizophrenia management using conventional oral antipsychotic formulations is constrained by poor bioavailability, extensive first-pass metabolism, and dose-related systemic adverse effects. Intranasal drug delivery using nanocarrier systems has emerged as a promising strategy for direct brain targeting by bypassing the blood-brain barrier (BBB) via olfactory and trigeminal pathways, thereby enhancing therapeutic efficacy while minimizing peripheral exposure. AREAS COVERED: permeation, and stability studies. The optimized NLCs exhibited a particle size of 213.40 ± 46.53 nm, zeta potential of -32.7 mV, and entrapment efficiency of approximately 72%. EXPERT OPINION: This approach has strong potential for enhancing therapeutic outcomes in schizophrenia.
No takes yet. Share an insight, caveat, or question.
Maniar et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: