Published: CABEQ 29 (3) (2015) 429-435
Paper type: Original Scientific Paper
T. . Nguyen, T. Hong-Ngan Tran, C. Nguyen, C. Im and C. Dang
Abstract
The aim of this work was to study a novel nanoparticle system formed from alginate
and β-cyclodextrin by ionotropic gelation method and to evaluate their potential for the
association and delivery of drugs. The nanoparticles were prepared by electrostatic interactions
between Ca2+/alginate gel and β-cyclodextrin. Morphology and structure characterization
of nanoparticles was investigated by scanning electron micrographs (SEM),
transmission electron microscope (TEM), Fourier transform infrared spectra (FTIR). The
nanoparticle size was about 50 – 80 nm and their structure quite regular and consistent.
Ketoprofen, chosen as a model drug, was incorporated into the nanocarriers with association efficiency of 50.7 % and loading efficiency of 5.7 %. Ketoprofen released from the nanoparticles was 57 % at pH 7.4 and 69 % at pH 5.0 for 4 h.
This work is licensed under a Creative Commons Attribution 4.0 International License
Keywords
nanoparticle, nanocarrier, drug delivery, β-cyclodextrin, alginate, ketoprofen, drug release