Abstract The purpose of this study was to design and characterize Bovine Serum Albumin (BSA)-loaded chitosan (CHT)-based nanoparticles for the potential delivery of therapeutic proteins. Tripolyphosphate (TPP) was used as… Click to show full abstract
Abstract The purpose of this study was to design and characterize Bovine Serum Albumin (BSA)-loaded chitosan (CHT)-based nanoparticles for the potential delivery of therapeutic proteins. Tripolyphosphate (TPP) was used as a polyanionic agent to synthesize the nanosystem that was characterized for its structural integrity, functional modification, particle size, morphology, zeta potential, thermal stability, protein-loading efficiency and protein release kinetics. H 1 NMR and FT-IR confirmed grafting of co-polymers to the CHT moiety. The average size and morphology of the BSA-loaded nanoparticles - confirmed by TEM, DLS and SEM-showed that the nanoparticles were spherically shape with a narrow particle size distribution (polydispersity index (PDI) = 0.232) and a size of 63.14 ± 31.31 nm. Both TGA and DSC results confirmed the thermal stability of the BSA-loaded nanoparticles compared with native polymers. Protein loading efficiency was 77.2% with an initial burst release due to surface protein desorption and subsequent prolong release through diffusion from sublayers after 2 h up to 30 h at varying pH conditions. The release kinetics at pH 6.8 was higher than at pH 7.4. Conclusively, this nanosystem may be explored as a vehicle for pH-responsive targeting of therapeutic proteins in cancer nanomedicine where tumors are known to have varying pH micro-environments.
               
Click one of the above tabs to view related content.