Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration
<b>Background/Objectives:</b> The intranasal (IN) route of administration is a promising non-invasive approach for brain targeting, bypassing the blood-brain barrier and enhancing bioavailability. Citalopram hydrobromide (CT), a widely prescribed sparingly water-soluble selective serotonin reuptake inhibitor (SSRI), faces challenges with oral and intravenous administration, including delayed onset, adverse effects, and patient compliance issues. <b>Methods:</b> This study aimed to develop a novel thermoresponsive polymeric micelle (PM) system based on Pluronic<sup>®</sup> copolymers (Pluronic F127 and Poloxamer 188) improving CT's solubility, stability, and nasal permeability for enhanced antidepressant efficacy. A preliminary study was conducted to select the optimized formulation. The preparation process involved using the thin-film hydration method, followed by freeze-drying. Comprehensive evaluations of optimized formulation characteristics included Z-average, polydispersity index (PdI), thermal behavior (lower critical solution temperature, LCST), encapsulation efficiency, X-ray powder diffraction (XRPD), thermodynamic solubility, and biological stability. Additionally, in vitro CT release and CT permeability in nasal conditions were studied. Stability under storage was also evaluated. <b>Results:</b> The optimized CT-PM formulation showed nanoscale micelle size (Z-average of 31.41 ± 0.99 nm), narrow size distribution (polydispersity index = 0.241), and a suitable thermal behavior for intranasal delivery (lower critical solution temperature (LCST) ~31 °C). Encapsulation efficiency reached approximately 90%, with an amorphous structure confirmed via XRPD, leading to a 95-fold increase in CT solubility. The formulation demonstrated appropriate biological and physical stability. In vitro studies showed a 25-fold faster CT release from optimized formulation compared to the initial CT, while CT-PM permeability in nasal conditions increased four-fold. <b>Conclusions:</b> This novel nanoscale thermosensitive formulation is a value-added strategy for nasal drug delivery systems, offering enhanced drug solubility, rapid drug release, stability, and improved permeability. This smart nanosystem represents a promising platform to overcome the limitations of conventional CT administration, improving therapeutic outcomes and patient compliance in depression management.
Authors
- Bence Sipos (ORCID: https://orcid.org/0000-0002-0131-4728)
- Ildikó Csóka (ORCID: https://orcid.org/0000-0003-0807-2781)
- Gábor Katona (ORCID: https://orcid.org/0000-0003-1564-4813)
- Fatima Rajab
Institutions
- University of Szeged (HU)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2025-09-01
- DOI
- https://doi.org/10.3390/pharmaceutics17091147
- Citations
- 1
- Primary Topic
- Advanced Drug Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.79
Funders
- Szegedi Tudományegyetem