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Stream/Area:
-
Subject:
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Paper ID:
IJSREM65071
Volume:
10 |
6 |
Jun 2026
Pages:
1-4
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
Dept. of Pharmaceutics
Rajesh Bhaiyya Tope College of Pharmacy, Chh.Sambhajinagar.
Dept. of Pharmaceutics
Rajesh Bhaiyya Tope College of Pharmacy, Chh.Sambhajinagar.
Dept. of Pharmaceutics
Rajesh Bhaiyya Tope College of Pharmacy, Chh.Sambhajinagar.
Suzetrigine is a novel, selective sodium channel (Naᵥ1.8) inhibitor developed for the management of moderate to severe pain, offering an effective non-opioid alternative for analgesia. Despite its promising pharmacological profile, conventional delivery of Suzetrigine may face challenges such as variable bioavailability, frequent dosing, and potential systemic side effects. To overcome these limitations, the present work focuses on the development of a novel drug delivery system (NDDS) for Suzetrigine aimed at enhancing therapeutic efficacy and patient compliance. The novel delivery approach is designed to provide controlled and targeted drug release, thereby maintaining optimal plasma drug concentrations over an extended period
KEYWORDS
The present thesis organized a suzetrigine nanoparticle-based gel project into full academic format while preserving the uploaded Result and Discussion section as the core experimental chapter. The combined evidence shows that suzetrigine could be assessed analytically at 250 nm that the drug remained compatible with the main polymeric system on FTIR and DSC interpretation, and that physically acceptable gels with nanosized characteristics could be prepared. A second consideration is the relationship between material selection and patient-facing performance. A semisolid system can appear simple, but its final behavior depends on dispersion quality, polymer hydration, pH control, viscosity, release rate, and storage stability. When these factors are considered together, the dosage form becomes a structured platform for controlled delivery rather than a simple mixture of drug and excipients. The updated thesis presents a coherent project that begins with a current pain-management problem and ends with practical formulation recommendations.
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Publication Date
6/16/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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The authors declare no conflict of interest related to this research work.
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