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二氨基丙酸三碘化氢配位化合物的合成、理化性质及抗菌活性

Synthesis, physicochemical properties and antimicrobial activity of a di-aminopropionic acid hydrogen tri-iodide coordination compound.

作者信息

Turganbay Seitzhan, Kenesheva Sabina, Jumagaziyeva Аrdak, Ilin Alexandr, Askarova Dana, Azembayev Amir, Kurmanaliyeva Assel

机构信息

Laboratory of New Substances and Materials, JSC Scientific Center for Anti-Infectious Drugs, Almaty, 050060, Kazakhstan.

"One Belt One Road" Petroleum Engineering Institute, Kazakh-British Technical University, Almaty, 050000, Kazakhstan.

出版信息

BMC Res Notes. 2024 Dec 25;17(1):384. doi: 10.1186/s13104-024-07052-8.

Abstract

OBJECTIVE

The objective of this study is to synthesize and comprehensively characterize a novel iodine-containing coordination compound, di-aminopropionic acid hydrogen tri-iodide. This involves determining its structural, physicochemical, and thermal properties, as well as evaluating its antimicrobial activity against a range of bacterial strains, including multidrug-resistant pathogens. The aim is to explore the potential of this compound as a candidate for developing new antibacterial agents to address the challenge of antibiotic resistance.

RESULTS

An original iodine-containing semiorganic coordination compound was synthesized and characterized. The physicochemical properties were studied via diffraction, FTIR spectroscopy and thermogravimetric/differential scanning calorimetry (TG/DSC). In vitro antimicrobial activity evaluation was performed using two-fold serial dilution method. The obtained results demonstrated efficiency against both gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii) bacteria including MDR strains that cause infectious disease. The results of the antibacterial evaluation revealed that the new iodine coordination compound - di-aminopropionic acid hydrogen tri-iodide possesses high bactericidal properties and exhibits better antimicrobial activity against both susceptible and multidrug-resistant strains than does Lugol solution and ampicillin sodium, which are used as reference drugs.

摘要

目的

本研究的目的是合成并全面表征一种新型含碘配位化合物——二氨基丙酸三碘化氢。这包括确定其结构、物理化学和热性质,以及评估其对一系列细菌菌株(包括多重耐药病原体)的抗菌活性。目的是探索该化合物作为开发新型抗菌剂候选物的潜力,以应对抗生素耐药性的挑战。

结果

合成并表征了一种新型含碘半有机配位化合物。通过衍射、傅里叶变换红外光谱和热重/差示扫描量热法(TG/DSC)研究了其物理化学性质。使用两倍系列稀释法进行体外抗菌活性评估。所得结果表明,该化合物对革兰氏阳性菌(金黄色葡萄球菌)和革兰氏阴性菌(大肠杆菌、铜绿假单胞菌、鲍曼不动杆菌)均有效,包括引起传染病的多重耐药菌株。抗菌评估结果显示,新型碘配位化合物——二氨基丙酸三碘化氢具有高杀菌性能,并且与用作参考药物的卢戈氏溶液和氨苄西林钠相比,对敏感菌株和多重耐药菌株均表现出更好的抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ec8/11670392/3d33fca916a1/13104_2024_7052_Fig1_HTML.jpg

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