Design of chitosan-based nanoparticles functionalized with gallic acid

• DOI: 10.1016/j.msec.2016.05.072
• Publication Date: 2016-05-18T18:21:23Z
• Authors: J. Lamarra; S. Rivero; A. Pinotti
• Keywords: QUICKSCAN; Chitosan; RSM; 02 engineering and technology; Drug Delivery Systems; https://purl.org/becyt/ford/2.5; Gallic Acid; CENTRAL COMPOSITE DESIGN; IONOTROPIC GELATION; PERCENTAGE ENCAPSULATION EFFICIENCY; Nanoparticles; https://purl.org/becyt/ford/2; 0210 nano-technology; ZETA POTENTIAL

Active nanoparticles based on chitosan could be applied as a support for the modulation of gallic acid delivery. In this sense, these nanostructures could be employed in different fields such as food, packaging, and pharmaceutical areas. The design parameters of chitosan-based nanoparticles functionalized with gallic acid (GA) were optimized through RSM by means of the analysis of zeta potential (ZP) and percentage encapsulation efficiency (PEE). The nanoparticles were prepared by ionotropic gelation using tripolyphosphate (TPP), at different combinations of chitosan (CH) concentration, CH:TPP ratio and GA. Global desirability methodology allowed finding the optimum formulation that included CH 0.76% (w/w), CH:TPP ratio of 5 and 37mgGA/gCH leading to ZP of +50mV and 82% of PEE. Analysis through QuickScan and turbidity demonstrated that the most stable nanoparticle suspensions were achieved combining concentrations of chitosan ranging between 0.5 and 0.75% with CH:TPP ratios higher than 3. These suspensions had high stability confirmed by means ZP and transmittance values which were higher than +25mV and 0.21 on average, respectively, as well as nanoparticle diameters of about 140nm. FTIR revealed the occurrence of both hydrogen bond and ionic interactions of CH-TPP which allowed the encapsulation and the improvement of the stability of the active agent.