Characterization of N-trimethyl chitosan/alginate complexes and curcumin release

被引:112
|
作者
Martins, Alessandro F. [1 ]
Bueno, Pedro V. A. [1 ]
Almeida, Elizangela A. M. S. [1 ]
Rodrigues, Francisco H. A. [1 ]
Rubira, Adley F. [1 ]
Muniz, Edvani C. [1 ]
机构
[1] Univ Estadual Maringa, Dept Quim, GMPC, Grp Mat Polimer & Compositos, BR-87020900 Maringa, Parana, Brazil
关键词
N-trimethyl chitosan; Sodium alginate; Polyelectrolyte complex; Curcumin; Controlled release; Beads; DRUG ABSORPTION ENHANCEMENT; IN-VITRO EVALUATION; CHITOSAN CHLORIDE; MOLECULAR-WEIGHT; PERORAL DELIVERY; SOLUTE RELEASE; ORAL DELIVERY; QUATERNIZATION; ANTIBACTERIAL; NANOCOMPLEXES;
D O I
10.1016/j.ijbiomac.2013.03.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N-trimethyl chitosan of two quaternization degrees, DQ = 20 and 80 mol% and labeled as TMC20 and TMC80, were synthesized and characterized by H-1 NMR. Polyelectrolyte complexes (PECs) of TMC/alginate (TMC/ALG) were prepared at pHs 2, 7 and 10 by mixing the aqueous solutions of unlike polymers. The PECs were characterized through infrared spectroscopy (FTIR), thermogravimetric analysis (TGA/DTG) and wide-angle X-ray scattering (WAXS). Using the TMC of DQ = 20 mol% and following the same methodology for preparing the PECs, beads of TMC20/ALG were obtained at pH 2 and loaded with curcumin (CUR) at pH 6.0-6.5. The morphology of the beads was evaluated by scanning electron microscopy (SEM). Studies in vitro of the controlled release of CUR from beads were investigated in simulated intestinal fluid (SIF) and simulated gastric fluid (SGF) and treated using conventional and partition-diffusion models. Results indicated that the beads based on TMC20 and ALG presented potential as drug-carrier to improve the solubility and biological activity of CUR at pH close to physiological one. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 184
页数:11
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