Aspartic-acid-loaded starch-functionalized Mn-Fe-Ca ferrite magnetic nanoparticles as novel green heterogeneous nanomagnetic catalyst for solvent-free synthesis of dihydropyrimidine derivatives as potent antibacterial agents

被引:20
作者
Afradi, Nahid [1 ]
Foroughifar, Naser [2 ]
Pasdar, Hoda [2 ]
Qomi, Mahnaz [3 ]
机构
[1] Islamic Azad Univ, Fac Pharmaceut Chem, Dept Organ Chem, Tehran Med Sci, Tehran, Iran
[2] Islamic Azad Univ, Dept Chem, Tehran North Branch, Tehran, Iran
[3] Islamic Azad Univ, Pharmaceut Sci Branch, APIRC, Tehran, Iran
关键词
Ferrite nanoparticles; Modified amino acid; Multicomponent reaction; Biological activity; Reusable nanocatalyst; CALCIUM-CHANNEL BLOCKERS; ECO-FRIENDLY SYNTHESIS; HIGHLY EFFICIENT; BIOLOGICAL EVALUATION; FE3O4; NANOPARTICLES; REUSABLE CATALYST; FACILE SYNTHESIS; IONIC LIQUIDS; AMINO-ACIDS; DESIGN;
D O I
10.1007/s11164-019-03791-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mn0.5Fe0.25Ca0.25Fe2O4@starch@aspartic acid magnetic nanoparticles (MNPs) as a new green nanocatalyst were designed and synthesized by a coprecipitation procedure. The structure of the aspartic-acid-loaded starch-functionalized Mn0.5Fe0.25Ca0.25Fe2O4 nanoparticles was evaluated by powder X-ray diffraction analysis, Fourier-transform infrared spectroscopy, vibrating-sample magnetometry, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and thermogravimetric analysis. The ferrite magnetic nanoparticles exhibited superparamagnetic nature with saturation magnetization of 35 emu/g. The impact of the MnFeCaFe2O4@starch@aspartic acid MNPs was investigated in synthesis of 3,4-dihydropyrimidine derivatives by multicomponent reaction between thiourea/urea, acetylacetone, and various aryl aldehydes under solvent-free conditions. Facile workup, short reaction time, superb yield, and use of a reusable catalyst are the advantages of this method. The magnetic nanocatalyst was easily recovered and reused six times without considerable reduction in its catalytic activity. The invitro antibacterial activity of all synthesized pyrimidine derivatives was studied by agar well diffusion assay technique against four pathogenic bacterial strains, namely Staphylococcus aureus (ATCC no. 6538) and Staphylococcus epidermidis (ATCC no. 12228) as Gram-positive bacteria and Pseudomonas aeruginosa (ATCC no. 9027) and Escherichia coli (ATCC no. 8739) as Gram-negative bacteria. All compounds exhibited greater antibacterial activity compared with the reference drug ciprofloxacin.
引用
收藏
页码:3251 / 3271
页数:21
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