Engineering PVA-Based Nanofibrous Mats Containing Pramipexole with Anti-Parkinsonian Effects: Fabrication, Characterization, and Pharmacological Study
- Pharmaceutical Sciences Research Center, TeMS.C., Islamic Azad University, Tehran, Iran
- Research School of Chemistry & Applied Biomedical Sciences, Tomsk Polytechnic University, Lenin Avenue 43, 63400, Tomsk, Russian Federation
- Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
- Department of Organic Chemistry, TeMS.C., Islamic Azad University, Tehran, Iran
Received: 2025-09-18
Revised: 2026-03-14
Accepted: 2026-04-29
Published in Issue 2026-07-10
Published Online: 2026-06-09
Copyright (c) 2025 Maryam Ghaffarimoghadam, Mitra Baghali, Majid Motaghinejad, Hakimeh Ziyadi, Danial Sadri (Author)

This work is licensed under a Creative Commons Attribution 4.0 International License.
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Abstract
Parkinson’s disease is a progressive neurodegenerative disorder that requires long-term pharmacotherapy; however, conventional oral administration of pramipexole is associated with fluctuating plasma levels and systemic side effects. In this study, a novel electrospun PVA-based nanofibrous transdermal patch containing pramipexole was developed to enable controlled drug delivery and improved therapeutic efficacy. Pramipexole-loaded PVA and PVA/PVP nanofibers were fabricated via electrospinning and subsequently cross-linked using glutaraldehyde vapor. The nanofibrous mats were characterized in terms of morphology, wettability, rheological behavior, drug release kinetics, and in vivo neuroprotective performance. Smooth and bead-free nanofibers were obtained, confirming suitable solution viscosity and electrospinnability. Water contact angle measurements demonstrated hydrophilic behavior, with contact angles of 33° for PVA, 71° for PVA/PVP, and 43° for cross-linked PVA/PVP/pramipexole nanofibers, indicating tunable surface wettability. In vitro release studies revealed an initial burst release of approximately 43% and 32% of pramipexole within 30 min for PVA and PVA/PVP nanofibers, respectively, followed by sustained release reaching ~52% and ~49% after 24 h. In contrast, cross-linked nanofibers exhibited significantly slower and more controlled drug release due to reduced polymer network permeability. Histopathological analysis of the substantia nigra region in a paraquat-induced Parkinson’s disease model demonstrated a marked reduction in neuronal degeneration in both systemic and transdermal pramipexole-treated groups compared to untreated animals.
Keywords
- Behavioral assessments,
- Nanofiber; Parkinson,
- Poly Vinyl Alcohol (PVA),
- Polyvinylpyrrolidone (PVP),
- Pramipexole,
- Transdermal mat
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