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银(I)双(菲咯啉-恶嗪)配合物的合成、表征及溶液行为研究及其对致病性酵母白色念珠菌的生物活性评价。

Synthesis, characterisation, and solution behaviour of Ag(I) bis(phenanthroline-oxazine) complexes and the evaluation of their biological activity against the pathogenic yeast Candida albicans.

机构信息

Department of Chemistry, Maynooth University, Co. Kildare, Maynooth, Ireland.

Kathleen Lonsdale Institute for Human Health Research, Maynooth University, Co. Kildare, Maynooth, Ireland.

出版信息

Biometals. 2023 Dec;36(6):1241-1256. doi: 10.1007/s10534-023-00513-w. Epub 2023 Jun 28.

Abstract

Three Ag(I) bis(phenanthroline-oxazine) complexes with varying lipophilicity were synthesised and characterised. The solution stoichiometry of 1:2 Ag(I):ligand was determined for each complex by the continuous variation Job's plot method using NMR spectroscopy. NMR studies were also carried out to investigate the fluxional behaviour of the Ag(I) complexes in solution. The biological activity of the silver(I) complexes and the corresponding ligands towards a clinical strain of Candida albicans MEN was studied using broth microdilution assays. Testing showed the choice of media and the duration of incubation were key determinants of the inhibitory behaviour towards Candida albicans, however, the difference between freshly prepared and pre-prepared solutions was insignificant in minimal media. The activity of the metal-free ligands correlated with the length of the alkyl chain. In minimal media, the methyl ester phenanthroline-oxazine ligand was effective only at 60 μM, limiting growth to 67% of the control, while a 60 μM dose of the propyl ester analogue limited fungal growth at < 20% of the control. MIC and MIC values for the propyl and hexyl ester analogues were calculated to be 45 and 59 µM (propyl), and 18 and 45 µM (hexyl). Moreover, in a study of activity as a function of time it was observed that the hexyl ester ligand maintained its activity for longer than the methyl and propyl analogues; after 48 h a 60 μM dose held fungal growth at 24% of that of the control. Complexation to Ag(I) was much more effective in enhancing biological activity of the ligands than was increasing the ester chain length. Significantly no difference in activity between the three silver(I) complexes was observed under the experimental conditions. All three complexes were substantially more active than their parent ligands against Candida albicans and AgClO and the three silver(I) bis(phen-oxazine) complexes have MIC values of < 15 μM. The ability of the silver(I) complexes to hold fungal growth at about 20% of the control even after 48 h incubation at low dosages (15 μM) showcases their superiority over the simple silver(I) perchlorate salt, which ceased to be effective at dosages below 60 μM at the extended time point.

摘要

三种具有不同亲脂性的 Ag(I) 双(菲咯啉-恶嗪)配合物被合成并进行了表征。通过 NMR 光谱的连续变化 Job 作图法确定了每个配合物的溶液化学计量比为 1:2 Ag(I):配体。NMR 研究还用于研究 Ag(I)配合物在溶液中的动态行为。使用肉汤微量稀释法测定了银(I)配合物及其相应配体对临床白色念珠菌 MEN 的生物活性。测试表明,选择培养基和孵育时间是抑制白色念珠菌的关键决定因素,然而,在最小培养基中,新鲜制备和预制备溶液之间的差异并不显著。金属游离配体的活性与烷基链的长度相关。在最小培养基中,甲基酯菲咯啉-恶嗪配体仅在 60μM 时有效,将生长限制在对照的 67%,而丙基酯类似物的 60μM 剂量将真菌生长限制在对照的<20%。计算出丙基和己基酯类似物的 MIC 和 MIC 值分别为 45 和 59μM(丙基)和 18 和 45μM(己基)。此外,在研究活性随时间的变化时,观察到己基酯配体的活性保持时间长于甲基和丙基类似物;48 小时后,60μM 剂量使真菌生长保持在对照的 24%。与 Ag(I) 配位比增加酯链长度更能有效地增强配体的生物活性。在实验条件下,观察到三种银(I)配合物之间的活性没有显著差异。所有三种配合物对白色念珠菌和 AgClO 的活性都明显高于其母体配体,三种银(I)双(菲咯啉-恶嗪)配合物的 MIC 值均<15μM。即使在低剂量(15μM)孵育 48 小时后,银(I)配合物仍能将真菌生长保持在对照的约 20%,这展示了它们优于简单的银(I)高氯酸盐盐的优势,后者在延长时间点的低剂量(60μM)下不再有效。

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