Department of Biotechnology, Faculty of Science, Taif University, P.O. Box 888, Taif, 21974, Saudi Arabia.
Department of Botany and Microbiology, Faculty of Science, Assiut University, 71516 Assiut, Egypt.
J Microbiol Biotechnol. 2018 Sep 28;28(9):1563-1572. doi: 10.4014/jmb.1711.11037.
Gold nanoparticles (AuNP) and their conjugates have been gaining a great deal of recognition in the medical field. Meanwhile, extended-spectrum β-lactamases (ESBL)-producing bacteria are also demonstrating a challenging problem for health care. The aim of this study was the biosynthesis of AuNP using petal extract and conjugation of ceftriaxone antibiotic (Cef-AuNP) in inhibiting ESBL-producing bacteria and study of in vitro anticancer activity. Characterization of the synthesized AuNP and Cef-AuNP was studied. ESB-Lproducing strains, ACI1 and PSE4 were used for testing the efficacy of Cef-AuNP. The cells of MCF-7 breast cancer were treated with previous AuNP and Cef-AuNP at different time intervals. Cytotoxicity effects of apoptosis and its molecular mechanism were evaluated. Ultraviolet-visible spectroscopy and Fourier transform infrared spectroscopy established the formation of AuNP and Cef-AuNP. Transmission electron microscope demonstrated that the formed nanoparticles were of different shapes with sizes of 15~35 nm and conjugation was established by a slight increase in size. Minimum inhibitory concentration (MIC) values of Cef-AuNP against tested strains were obtained as 3.6 and 4 μg/ml, respectively. Cef-AuNP demonstrated a decrease in the MIC of ceftriaxone down to more than 27 folds on the studied strains. The biosynthesized AuNP displayed apoptotic and time-dependent cytotoxic effects in the cells of MCF-7 at a concentration of 0.1 μg/ml medium. The Cef-AuNP have low significant effects on MCF-7 cells. These results enhance the conjugating utility in old unresponsive ceftriaxone with AuNP to restore its efficiency against otherwise resistant bacterial pathogens. Additionally, AuNP may be used as an alternative chemotherapeutic treatment of MCF-7 cancer cells.
金纳米粒子(AuNP)及其缀合物在医学领域得到了广泛的认可。与此同时,产生超广谱β-内酰胺酶(ESBL)的细菌也对医疗保健提出了挑战。本研究旨在利用花瓣提取物合成 AuNP,并将头孢曲松抗生素(Cef-AuNP)缀合,以抑制产生 ESBL 的细菌,并研究体外抗癌活性。研究了合成的 AuNP 和 Cef-AuNP 的特性。使用 ACI1 和 PSE4 两种产 ESBL 菌株来测试 Cef-AuNP 的功效。用不同时间间隔的先前的 AuNP 和 Cef-AuNP 处理 MCF-7 乳腺癌细胞。评估了细胞凋亡的细胞毒性作用及其分子机制。紫外-可见光谱和傅里叶变换红外光谱确立了 AuNP 和 Cef-AuNP 的形成。透射电子显微镜证明形成的纳米颗粒具有不同的形状,尺寸为 15~35nm,并且通过尺寸的轻微增加建立了缀合。Cef-AuNP 对测试菌株的最小抑菌浓度(MIC)值分别为 3.6 和 4μg/ml。Cef-AuNP 使头孢曲松的 MIC 对研究菌株降低了 27 倍以上。在 0.1μg/ml 培养基浓度下,生物合成的 AuNP 在 MCF-7 细胞中表现出凋亡和时间依赖性的细胞毒性作用。Cef-AuNP 对 MCF-7 细胞的影响较小。这些结果增强了将旧的无反应性头孢曲松与 AuNP 缀合以恢复其对其他耐药细菌病原体的功效的共轭用途。此外,AuNP 可作为 MCF-7 癌细胞的替代化学治疗方法。