Optimization and characterization of levamisole-loaded chitosan nanoparticles by ionic gelation method using 23factorial design by Minitab®15

2011 ◽  
Vol 2 (2) ◽  
pp. 171-179 ◽  
Author(s):  
Divyen Shah ◽  
Vaishali Londhe
Author(s):  
Sri Atun ◽  
Retno Arianingrum ◽  
Stela Dimitrova

The main objectives of this research are to synthesize chitosan nanoparticles of chloroform fraction of K. rotunda, to characterize the products, and to conduct a biological test on these products as an antioxidant. Chloroform fraction of K. rotunda was loaded on chitosan nanoparticles and then was prepared by ionic gelation of chitosan with sodium tripolyphosphat (Na-TPP) in various compositions. Characterization of the products were investigated for particle size, zeta potential, and morphology by Scanning Electron Microscophy (SEM). The biological activity of the products as an antioxidant was tested by the DPPH method. Results of this study showed that the nanoparticle can be synthesized at the concentration ratio of 10: 1 for chitosan/Na-TPP. The size were in the range of 172 to 877 nm, with a zeta potential of + 28.06 to + 38.03 mV. The nanoparticle was cylinders in shape and smooth in surfaces. The antioxidant activity of chitosan nanoparticles of chloroform fraction of K. rotunda showed less activity compared with the previous fraction.


2019 ◽  
Vol 38 (2) ◽  
pp. 385 ◽  
Author(s):  
Marwa M. El-Naggar ◽  
Wael S. I. Abou-Elmagd ◽  
Ashraf Suloma ◽  
Hamza A. El-Shabaka ◽  
Magdy T. Khalil ◽  
...  

Author(s):  
Fatmanur Tuğcu-Demiröz ◽  
Sinem Saar ◽  
Adnan Altuğ Kara ◽  
Ayşegül Yıldız ◽  
Emre Tunçel ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1375
Author(s):  
María J. Moreno-Vásquez ◽  
Maribel Plascencia-Jatomea ◽  
Saúl Sánchez-Valdes ◽  
Judith C. Tanori-Córdova ◽  
Francisco J. Castillo-Yañez ◽  
...  

Nanoparticles based on chitosan modified with epigallocatechin gallate (EGCG) were synthetized by nanoprecipitation (EGCG-g-chitosan-P). Chitosan was modified by free-radical-induced grafting, which was verified by Fourier transform infrared (FTIR). Furthermore, the morphology, particle size, polydispersity index, and zeta potential of the nanoparticles were investigated. The grafting degree of EGCG, reactive oxygen species (ROS) production, antibacterial and antioxidant activities of EGCG-g-chitosan-P were evaluated and compared with those of pure EGCG and chitosan nanoparticles (Chitosan-P). FTIR results confirmed the modification of the chitosan with EGCG. The EGCG-g-chitosan-P showed spherical shapes and smoother surfaces than those of Chitosan-P. EGCG content of the grafted chitosan nanoparticles was 330 μg/g. Minimal inhibitory concentration (MIC) of EGCG-g-chitosan-P (15.6 μg/mL) was lower than Chitosan-P (31.2 μg/mL) and EGCG (500 μg/mL) against Pseudomonas fluorescens (p < 0.05). Additionally, EGCG-g-chitosan-P and Chitosan-P presented higher Staphylococcus aureus growth inhibition (100%) than EGCG at the lowest concentration tested. The nanoparticles produced an increase of ROS (p < 0.05) in both bacterial species assayed. Furthermore, EGCG-g-chitosan-P exhibited higher antioxidant activity than that of Chitosan-P (p < 0.05) in 2,2′-azino-bis (3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS), 2,2-diphenyl-1-picrylhydrazyl radical (DPPH) and ferric-reducing antioxidant power assays. Based on the above results, EGCG-g-chitosan-P shows the potential for food packaging and biomedical applications.


Sign in / Sign up

Export Citation Format

Share Document