Investigation of pantoprazole loading and release from a magnetic-coated chitosan-modified zirconium-based metal-organic framework (MOF) as a nanocarrier in targeted drug delivery systems

被引:8
作者
Yaghoubian, Ali [1 ]
Setoodehkhah, Moslem [1 ]
Parsa, Fatemeh [1 ]
机构
[1] Univ Kashan, Fac Chem, Dept Inorgan Chem, Kashan, Iran
关键词
IN-VITRO EVALUATION; ADSORPTION; REMOVAL; NANOCOMPOSITE; NANOPARTICLES; UIO-66; FORMULATION; OMEPRAZOLE; INHIBITOR; PARTICLES;
D O I
10.1039/d4ra04365k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study reports a novel magnetic and porous nanocomposite, Fe3O4@CS@UIO-66-NH2(Zr), developed by growing a zirconium-based metal-organic framework on magnetite-chitosan. It is designed for targeted and delayed pantoprazole delivery, the nanocomposite exhibits pH-sensitive behavior and functions as an efficient nanocarrier. The synthesis process involved coating magnetite nanoparticles with chitosan, followed by the growth of UIO-66-NH2(Zr) on the coated nanoparticles. The nanocomposite demonstrated high drug loading efficiency (DLE) in acetate buffer (pH 5.0) and deionized water, with loading percentages of 79% and 75%, respectively, within 48 hours. The corresponding drug loading content (DLC) was approximately 14% and 10%. The Freundlich and Langmuir models accurately described the multilayer adsorption behavior of pantoprazole on the nanocomposite's active sites. BET and EDX-map analyses confirmed that the drug was loaded into the nanocomposite's pores and uniformly adsorbed on its surface. The drug release kinetics were best described by the pseudo-second-order model. Due to its porosity, magnetic properties, and favorable drug loading characteristics, the Fe3O4@CS@UIO-66-NH2(Zr) nanocomposite shows potential as an efficient targeted drug delivery system for in vivo applications. This study reports a novel magnetic and porous nanocomposite, Fe3O4@CS@UIO-66-NH2(Zr), developed by growing a zirconium-based metal-organic framework on magnetite-chitosan.
引用
收藏
页码:26091 / 26102
页数:12
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