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Article

Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration

Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös Street 6, H-6720 Szeged, Hungary
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Author to whom correspondence should be addressed.
Pharmaceutics 2025, 17(9), 1147; https://doi.org/10.3390/pharmaceutics17091147
Submission received: 18 July 2025 / Revised: 25 August 2025 / Accepted: 31 August 2025 / Published: 1 September 2025
(This article belongs to the Section Nanomedicine and Nanotechnology)

Abstract

Background/Objectives: 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. Methods: This study aimed to develop a novel thermoresponsive polymeric micelle (PM) system based on Pluronic® 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. Results: 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. Conclusions: 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.
Keywords: intranasal; polymeric micelle; Pluronic F127; Poloxamer 188; thermosensitive; citalopram; nanocarriers intranasal; polymeric micelle; Pluronic F127; Poloxamer 188; thermosensitive; citalopram; nanocarriers

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MDPI and ACS Style

Rajab, F.; Sipos, B.; Katona, G.; Csóka, I. Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration. Pharmaceutics 2025, 17, 1147. https://doi.org/10.3390/pharmaceutics17091147

AMA Style

Rajab F, Sipos B, Katona G, Csóka I. Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration. Pharmaceutics. 2025; 17(9):1147. https://doi.org/10.3390/pharmaceutics17091147

Chicago/Turabian Style

Rajab, Fatima, Bence Sipos, Gábor Katona, and Ildikó Csóka. 2025. "Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration" Pharmaceutics 17, no. 9: 1147. https://doi.org/10.3390/pharmaceutics17091147

APA Style

Rajab, F., Sipos, B., Katona, G., & Csóka, I. (2025). Development and Characterization of Citalopram-Loaded Thermosensitive Polymeric Micelles for Nasal Administration. Pharmaceutics, 17(9), 1147. https://doi.org/10.3390/pharmaceutics17091147

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