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Proteins and peptide drugs are easily degraded in the gastrointestinal tract when administered orally, decreasing their bioavailability, and hence are administered intravenously or subcutaneously, creating a demand for how to administer them orally efficiently. The present research aims to develop protein-loaded nanoparticles by the coacervation method using biodegradable polymers and study their different characteristics.
The nanoparticles are prepared using low molecular-weight Chitosan and sodium alginate and characterized using instruments like Zetasizer, Fourier Transform Infrared spectroscopy (FTIR), & UV Spectrophotometer, etc. The nanoparticles are further loaded with egg albumin to study protein loading and release characteristics.
The empty nanoparticles have a size range of 226-589 nm and a Polydispersity Index (PDI) of 0.398-0.298. The minimum size of loaded nanoparticles was 180.2±7.82 nm, with a PDI value of 0.314±0.02. The maximum protein entrapment efficiency and loading percentage were 76.12% and 29.78%, respectively. The maximum in vitro protein release from 29.78% loaded nanoparticles was 42.30% and 12.80% in phosphate buffer solution (PBS) and water as the test medium, respectively.
The particle size, PDI, entrapment statistics, and prolonged protein release profile, etc, show the possibility of the nanoparticulate system to be used as a suitable vehicle for oral delivery of proteins and peptide drugs.
The optimised standard protein-loaded nanoparticles have all the characteristics making them suitable vehicles for administering proteins and peptide drugs orally. The current Nanoparticulate development system offers a promising solution for the effective oral delivery of protein or peptides.
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