Synthesis, Characterization, and Biological Evaluation of Chromium(III) Complexes of Alanine and Valine

Shuaibu Musa, S. Idris, David A. Onu, A. Suleiman
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Abstract

Two metal-amino acid complexes, Cr(III)-alanine and Cr(III)-valine, were synthesized and characterized by IR spectroscopy, powder X-ray diffraction (XRD) analysis, magnetic susceptibility, and molar conductivity measurements. Molar conductivity measurements indicated that the composition of the metal complexes corresponds to a metal-amino acid ligand ratio of 1:3. The IR spectra indicated that the amino acids act as bidentate ligands with coordination involving the carboxyl oxygen and the nitrogen of the amino group. Magnetic susceptibility measurements revealed a six-coordinate local symmetry around the Cr(III) ions which depicted that the complexes were paramagnetic with magnetic moment values ranging from 5.10 to 6.00 BM. Powder XRD studies confirmed that the amino acid complexes were crystalline with monoclinic crystal structure. The in vitro biological activity of the investigated chromium(III) complexes with alanine and valine was tested against Bacillus subtilis, Staphylococcus aureus, Salmonella typhi, Pseudomonas aeruginosa, and Escherichia coli. All the microorganisms were standardized using 0.5 McFarland standard. The antimicrobial studies showed that the ligands were biologically active with an inhibition zone range of 10-17 mm and their metal complexes showed significantly enhanced antimicrobial sensitivity with an inhibition zone range of 12-21 mm. The standard drug showed slightly better activity with an inhibition zone range of 24-38 mm.
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丙氨酸和缬氨酸铬(III)配合物的合成、表征及生物学评价
合成了两种金属氨基酸配合物,Cr(III)-丙氨酸和Cr(Ⅲ)-缬氨酸,并通过红外光谱、粉末X射线衍射(XRD)分析、磁化率和摩尔电导率测量对其进行了表征。摩尔电导率测量表明,金属配合物的组成对应于1:3的金属-氨基酸配体比例。红外光谱表明,氨基酸作为双齿配体,与氨基的羧基氧和氮配位。磁化率测量揭示了Cr(III)离子周围的六坐标局部对称性,这表明该配合物是顺磁性的,磁矩值在5.10至6.00BM之间。粉末XRD研究证实,氨基酸配合物是具有单斜晶体结构的晶体。研究了所研究的丙氨酸和缬氨酸铬(III)配合物对枯草芽孢杆菌、金黄色葡萄球菌、伤寒沙门氏菌、铜绿假单胞菌和大肠杆菌的体外生物活性。使用0.5McFarland标准对所有微生物进行标准化。抗菌研究表明,配体具有生物活性,抑制区范围为10-17mm,其金属配合物显示出显著增强的抗菌敏感性,抑制区为12-21mm。标准药物显示出略好的活性,抑制范围为24-38mm。
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来源期刊
Avicenna Journal of Environmental Health Engineering
Avicenna Journal of Environmental Health Engineering Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
1.00
自引率
0.00%
发文量
8
审稿时长
8 weeks
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