Gold nanoparticles enhance 5-fluorouracil anticancer efficacy against colorectal cancer cells

被引:82
作者
Safwat, Mohamed A. [1 ,2 ]
Soliman, Ghareb M. [1 ]
Sayed, Douaa [3 ]
Attia, Mohamed A. [1 ]
机构
[1] Assiut Univ, Dept Pharmaceut, Fac Pharm, Assiut 71526, Egypt
[2] Deraya Univ, Dept Pharmaceut & Ind Pharm, El Minia, Egypt
[3] Assiut Univ, South Egypt Canc Inst, Dept Clin Pathol, Assiut, Egypt
关键词
Gold nanoparticles; Colorectal cancer; 5-Fluorouracil; Thioglycolic acid; Glutathione; DRUG-DELIVERY; POLYMERIC NANOPARTICLES; COLLOIDAL STABILITY; AMINO-ACIDS; RELEASE; SIZE; MECHANISMS; SYSTEMS; NANOTECHNOLOGY; GLUTATHIONE;
D O I
10.1016/j.ijpharm.2016.09.076
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5-Fluorouracil (5-FU), an antimetabolite drug, is extensively used in the treatment solid tumors. However, its severe side effects limit its clinical benefits. To enhance 5-FU anticancer efficacy and reduce its side effects it was loaded onto gold nanoparticles (GNPs) using two thiol containing ligands, thioglycolic acid (TGA) and glutathione (GSH). The GNPs were prepared at different 5-FU/ligand molar ratios and evaluated using different techniques. Anticancer efficacy of 5-FU/GSH-GNPs was studied using flow cytometry in cancerous tissue obtained from patients having colorectal cancer. The GNPs were spherical in shape and had a size of similar to 9-17 nm. Stability of the GNPs and drug release were studied as a function of salt concentration and solution pH. Maximum 5-FU loading was achieved at 5-FU/ligand molar ratio of 1:1 and 2:1 for TGA-GNPs and GSH-GNPs, respectively. GNPs coating with pluronic F127 improved their stability against salinity. 5-FU release from GNPs was slow and pH-dependent. 5-FU/GSHGNPs induced apoptosis and stopped the cell cycle progression in colorectal cancer cells. They also had a 2-fold higher anticancer effect compared with free 5-FU. These results confirm the potential of GNPs to enhance 5-FU anticancer efficacy. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:648 / 658
页数:11
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