A study on sustained release formulations for oral delivery of 5-fluorouracil based on alginate-chitosan/montmorillonite nanocomposite systems

被引:93
作者
Azhar, Fahimeh Farshi [1 ]
Olad, Ali [2 ]
机构
[1] Azarbijan Shahid Madani Univ, Fac Sci, Dept Chem, Tabriz, Iran
[2] Univ Tabriz, Fac Chem, Dept Appl Chem, Polymer Composite Res Lab, Tabriz, Iran
关键词
5-Fluorouracil; Montmorillonite; Sustained release; Oral drug delivery; IN-VITRO EVALUATION; DRUG-RELEASE; CHITOSAN NANOPARTICLES; CALCIUM ALGINATE; MONTMORILLONITE; INTERCALATION; OPTIMIZATION; COMPOSITES; MECHANISMS; THERAPY;
D O I
10.1016/j.clay.2014.09.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The objective of this study was to develop a sustained drug release system for 5-fluorouracil (5-FU), an anticancer drug, to improve its half-life. 5-Fluorouracil was loaded on montmorillonite (Mt) layers through the preparation of 5-FU/Mt nanocomposite by an intercalation method. In order to retard the drug release in the gastric environment, the prepared 5-FU/Mt nanocomposite was compounded with alginate (Alg), and further coated with chitosan (CS). This novel drug delivery system was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) analyses. By in vitro experiments the effects of Mt contents and pH of the release media on the release rate of the drug were investigated. According to the results, the Alg-CS/5-FU/Mt nanocomposite system containing 30 wt.% Mt in the release media with the pH of 7.4 effectively sustained the drug release and the time for 50% release, T-50%, is about 8 h. The release profile of 5-FU from the Alg-CS/5-FU/Mt nanocomposite system was best fitted by the Korsmeyer-Peppas kinetic model suggesting the diffusion controlled release mechanism. The prepared Alg-CS/5-FU/Mt nanocomposite system is suitable for the delivery of 5-FU in the small intestine with a controlled manner. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:288 / 296
页数:9
相关论文
共 50 条
[1]  
[Anonymous], 1963, J PHARM SCI
[2]   Poly(ethylene glycol) layered silicate nanocomposites for retarded drug release prepared by hot-melt extrusion [J].
Campbell, Kayleen ;
Craig, Duncan Q. M. ;
McNally, Tony .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 363 (1-2) :126-131
[3]   Organosilicate-polymer drug delivery systems: controlled release and enhanced mechanical properties [J].
Cypes, SH ;
Saltzman, WM ;
Giannelis, EP .
JOURNAL OF CONTROLLED RELEASE, 2003, 90 (02) :163-169
[4]   Novel microbially triggered colon specific delivery system of 5-Fluorouracil: Statistical optimization, in vitro, in vivo, cytotoxic and stability assessment [J].
Dev, Rakesh Kumar ;
Bali, Vikas ;
Pathak, Kamla .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 411 (1-2) :142-151
[5]   CLINICAL-PHARMACOLOGY OF 5-FLUOROURACIL [J].
DIASIO, RB ;
HARRIS, BE .
CLINICAL PHARMACOKINETICS, 1989, 16 (04) :215-237
[6]   Systemic treatment of gastric cancer [J].
Dickson, JLB ;
Cunningham, D .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2004, 16 (03) :255-263
[7]   Wheat germ agglutinin-conjugated chitosan-Ca-alginate microparticles for local colon delivery of 5-FU: Development and in vitro characterization [J].
Dodov, M. Glavas ;
Calis, S. ;
Crcarevska, M. S. ;
Geskovski, N. ;
Petrovska, V. ;
Goracinova, K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 381 (02) :166-175
[8]   Poly(D,L-lactide-co-glycolide)/montmorillonite nanoparticles for oral delivery of anticancer drugs [J].
Dong, YC ;
Feng, SS .
BIOMATERIALS, 2005, 26 (30) :6068-6076
[9]   Poly(ethylene glycol)-carboxymethyl chitosan-based pH-responsive hydrogels: photo-induced synthesis, characterization, swelling, and in vitro evaluation as potential drug carriers [J].
El-Sherbiny, Ibrahim M. ;
Smyth, Hugh D. C. .
CARBOHYDRATE RESEARCH, 2010, 345 (14) :2004-2012
[10]   Regional chemotherapeutic techniques for liver tumors: current knowledge and future directions [J].
Elias, D ;
de Baere, T ;
Sideris, L ;
Ducreux, M .
SURGICAL CLINICS OF NORTH AMERICA, 2004, 84 (02) :607-+