EventsThe 1st International Electronic Conference on Medicinal Chemistry and Pharmaceutics
Published
This submission belongs to the session S11. Formulation, Drug Delivery and Controlled Release of the event The 1st International Electronic Conference on Medicinal Chemistry and Pharmaceutics
Published date
29 Oct, 2025
Academic Editor
author-avatarFrancisco Otero-Espinar
Citation
Elena Giuliano, Angela Costagliola di Polidoro, Agnese Gagliardi, Domenico Sorrentino, Emanuela Longo, Sandra Albanese, Francesco Napolitano, Valeria Gaetano, Antonella Zannetti, Donato Cosco, Smart P407-based Thermogels Containing 5-ASA as Next Generation Rectal Formulations for the treatment of Inflammatory Bowel Diseases, in Proceedings of The 1st International Electronic Conference on Medicinal Chemistry and Pharmaceutics, 1 November–30 November 2025, MDPI: Basel, Switzerland
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Smart P407-based Thermogels Containing 5-ASA as Next Generation Rectal Formulations for the treatment of Inflammatory Bowel Diseases

Angela Costagliola di Polidoro 2
Domenico Sorrentino 3
Sandra Albanese 2
Francesco Napolitano 4
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1. Department of Health Sciences, University of Catanzaro “Magna Græcia”, Campus Universitario “S. Venuta”, I-88100 Catanzaro, Italy, Italy
2. Institute of Biostructures and Bioimaging, National Research Council (IBB-CNR), 80145 Napoli, Italy., Italy
3. CEINGE-Biotecnologie Avanzate Franco Salvatore, 80145 Napoli, Italy, Italy
4. Department of Veterinary Medicine and Animal Production, University of Naples Federico II, 81037 Napoli, Italy, Italy
Abstract

Introduction: Inflammatory bowel disease (IBD) is a chronic inflammatory disorder of the gastrointestinal tract that severely compromises quality of life. First-line therapy with 5-aminosalicylic acid (5-ASA) is limited by poor solubility, rapid absorption in the upper gut, and insufficient colonic delivery. Rectal formulations may overcome these issues, but conventional suppositories and enemas often reduce patient compliance.

Methods: Poloxamer 407 (P407)-based thermosensitive hydrogels were prepared using the cold method by dissolving the copolymer (20% w/w) in cold water and incorporating 5-ASA (0.1-0.5% w/w). The systems were characterized by rheological behavior, gelation temperature, mucoadhesive strength, injectability and spreadability. Drug release was evaluated at pH 5.0 and 7.4 by dialysis and membrane-less methods. Anti-inflammatory effects were tested in lipopolysaccharide -activated RAW264.7/Caco-2 co-cultures and in dextran sodium sulfate (DSS)-induced murine colitis model.

Results: The optimized P407-5-ASA hydrogel showed rapid gelation at physiological temperature, mucoadhesion, shear-thinning flow and easy syringeability, ensuring patient-friendly administration. 5-ASA showed prolonged release profiles even under acidic conditions. In vitro tests demonstrated that the formulation decreased both the macrophage infiltration and TNF-α secretion compared to free drug. Rhodamine-labelled gels demonstrated prolonged colon retention and P407-5-ASA markedly improved the therapeutic outcomes in DSS-treated mice with respect to commercial 5-ASA.

Conclusions: P407-based in situ hydrogels provide a high-performance, patient-acceptable platform for localized IBD therapy. They enhance 5-ASA efficacy and retention combining thermo-responsive gelation, mucoadhesion and sustained release while minimizing systemic exposure.

The obtained results support their potential as next-generation rectal formulations to improve the therapeutic outcomes and adherence in IBD patients.

Keywords
5-ASA
IBD
poloxamer 407
thermo-sensitive hydrogels
rectal formulations
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