Abstract
Purpose
The purpose of this research was to employ maltodextrin as a stabilizer to stabilize the zein nanocomplex of paliperidone palmitate.
Method
A zein-maltodextrin nanocomplex was synthesized using an anti-solvent precipitation technique. Box–Behnken Design was utilized for the optimization of drug-loaded zein-maltodextrin nanocomplex. Physiochemical characterization (DSC, XRD, NMR, and FT-IR), surface morphology, and release behavior were carried out.
Results
The inclusion of polysaccharides resulted in spherical stable optimized nanocomplexes with a small particle size (184.30 ± 0.067 nm) and an acceptable zeta potential (23.00 ± 0.124 mV) and improved encapsulation. The solid-state characterization and zeta potential demonstrated that electrostatic interaction was the predominant driving force, with hydrogen bonding and hydrophobic interaction serving as additional driving forces. The release profile of drug-loaded zein-maltodextrin nanocomplex indicated sustained release in vitro. In long-term storage (25 ± 2 °C/60 ± 5% RH and 4 ± 2 °C), the drug-loaded zein-maltodextrin nanocomplex remained stable.
Conclusion
Thus, the protein-polysaccharide nanocomplex can be used to deliver antipsychotic drugs.
Graphical Abstract
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Data Availability
All data generated or analysed during this study are included in this published article.
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Acknowledgements
This work was supported by the Science and Engineering Research Board, File Number: CRG/2018/003176.
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Bhadale, R.S., Londhe, V.Y. Paliperidone Palmitate-Loaded Zein-Maltodextrin Nanocomplex: Fabrication, Characterization, and In Vitro Release. J Pharm Innov 18, 1253–1263 (2023). https://doi.org/10.1007/s12247-023-09717-6
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DOI: https://doi.org/10.1007/s12247-023-09717-6