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聚咔唑-氧化铜(PCz-CuO)纳米复合材料的合成与表征:探究卓越的抗菌性能及FabI/FabH对接相互作用

synthesis and characterization of polycarbazole-copper oxide (PCz-CuO) nanocomposite: investigating superior antibacterial performance and FabI/FabH docking interactions.

作者信息

War Jahangir Ahmad, Ul AIn Qurat, Zargar Mohammed Iqbal, Chisti Hamida-Tun-Nisa

机构信息

Department of Chemistry, National Institute of Technology Srinagar 190006 Jammu & Kashmir India

Department of Pharmaceutical Sciences, University of Kashmir Srinagar 190006 Jammu & Kashmir India.

出版信息

RSC Adv. 2025 Aug 13;15(35):28754-28769. doi: 10.1039/d5ra02065d. eCollection 2025 Aug 11.

Abstract

This research investigated the synthesis of a polycarbazole-copper oxide nanocomposite oxidative polymerization. Various techniques were employed to characterize the structural and morphological properties of both PCz and PCz-CuO. The study evaluated the bactericidal potential of PCz and PCz-CuO against two common pathogens, () and (). Additionally, computational modeling (molecular docking) was performed to understand how these materials might interact with and enzymes, which are crucial for bacterial fatty acid synthesis in both and . The results showed that PCz-CuO was more effective at killing both bacterial strains compared to pure PCz. The inhibition zones observed in the agar well diffusion method were larger for PCz-CuO (4.2-16.2 mm and 4.5-17.1 mm for and , respectively) compared to PCz (3.4-14.5 mm and 3.5-15.2 mm). Docking simulations provided insights into possible binding interactions between the synthesized materials and the target enzymes. The results are consistent with a potential for inhibitory activity, which may help explain the observed differences in antibacterial behavior. Overall, this study demonstrates the potential of PCz-CuO as an antibacterial agent and highlights the complementary role of molecular docking in guiding further mechanistic studies.

摘要

本研究通过氧化聚合反应研究了聚咔唑-氧化铜纳米复合材料的合成。采用了各种技术来表征聚咔唑(PCz)和聚咔唑-氧化铜(PCz-CuO)的结构和形态特性。该研究评估了PCz和PCz-CuO对两种常见病原体(此处括号内容缺失)的杀菌潜力。此外,还进行了计算建模(分子对接),以了解这些材料如何与两种细菌脂肪酸合成中至关重要的(此处酶名称缺失)酶相互作用。结果表明,与纯PCz相比,PCz-CuO对两种细菌菌株的杀灭效果更有效。在琼脂孔扩散法中观察到的PCz-CuO的抑菌圈(分别为(此处细菌名称缺失)的4.2 - 16.2毫米和4.5 - 17.1毫米)比PCz(3.4 - 14.5毫米和3.5 - 15.2毫米)更大。对接模拟提供了关于合成材料与目标酶之间可能的结合相互作用的见解。结果与潜在的抑制活性一致,这可能有助于解释观察到的抗菌行为差异。总体而言,本研究证明了PCz-CuO作为抗菌剂的潜力,并突出了分子对接在指导进一步机理研究中的补充作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7d2/12376980/8a191d9d5e3d/d5ra02065d-s1.jpg

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