Journal
JOURNAL OF NANOPARTICLE RESEARCH
Volume 25, Issue 2, Pages -Publisher
SPRINGER
DOI: 10.1007/s11051-023-05672-y
Keywords
Chitosan; Sodium tripolyphosphate; Nanoparticles; Peptide; Release profile; Targeted drugs; Nanomedicine
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This study aimed to prepare and evaluate walnut meal-derived elastase inhibitory peptide loaded in chitosan-tripolyphosphate (CS-TPP) nanoparticles (NPs). The results showed that the encapsulation efficiency of FFVPF could reach up to 94.58 +/- 0.23%. The CS-TPP FFVPF NPs demonstrated nanometric size, spherical shape, and uniformity, with good stability under various conditions. The in vitro release profile of the peptides indicated explosive initial release followed by gradual slowing down. These findings suggest the potential of CS-TPP NPs as an oral delivery system and the use of peptides in food and pharmaceutical products.
This study is aimed at the preparation and evaluation of walnut meal-derived elastase inhibitory peptide loaded in chitosan-tripolyphosphate (CS-TPP) nanoparticles (NPs). It was shown that the maximum encapsulation efficiency of FFVPF could reach 94.58 +/- 0.23%. TEM microphotographs, polydispersity index, and zeta-sizer reports indicated that FFVPF-loaded CS-TPP NPs were in nanometric range and were spherical, discrete, and uniform in size with PDI less than 0.3. FTIR analysis indicated that the peptides interacted with CS-TPP NPs through strong hydrogen bonds and electrostatic interactions. The CS-TPP FFVPF NPs showed better stability with heating treatment, pH treatment, or photochemical treatment. Moreover, the in vitro release profile of peptides was identified. The release rate of encapsulated FFVPF was released explosively to 77.22 +/- 2.21% and gradually slowed down. These findings highlighted the prospect of CS-TPP NPs as an oral delivery system, and the application of peptides within food and pharmaceutical products.
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