Alshatwi Ali A, Athinarayanan Jegan, Periasamy Vaiyapuri Subbarayan
Nanobiotechnology and Molecular Biology Research Lab, Department of Food Science and Nutrition, College of Food Science and Agriculture, King Saud University, P.O. Box 2460, Riyadh, 11451, Kingdom of Saudi Arabia,
J Mater Sci Mater Med. 2015 Mar;26(3):148. doi: 10.1007/s10856-015-5468-5. Epub 2015 Mar 13.
Bimetallic Au@Pt nanostructures (Au@Pts) are potential candidates for optical, electrical, catalytic and biological applications. However, methods for the fabrication of Au@Pts using total tea polyphenols (TPPs), studies of the mechanism of action of Au@Pts on biological systems and studies on the application of Au@Pts in cancer diagnosis and therapy are sparse. In this study, we developed a simple, eco-friendly and low-cost method for the synthesis of Au@Pts to examine the cytotoxic effect of these Au@Pts on human cervical cancers in vitro. The gold and platinum ions were successfully reduced simultaneously using TPPs at room temperature. The prepared Au@Pts were characterized using UV-Vis spectrophotometery, X-ray diffractometery (XRD), energy-dispersive X-ray spectroscopy (EDS), and transmission electron microscopy (TEM). EDS and XRD confirmed the formation of the Au@Pt. Formation of Au@Pts with a size of 5-20 nm was confirmed using TEM. The cytotoxic properties of the Au@Pts were evaluated in human cervical cancer cells (SiHa). The cell viability results revealed that Au@Pts induce cell death in a dose- and time-dependent manner. The morphological features of the Au@Pt-exposed SiHa cells were observed and indicated cell death via cell shrinkage, intranucleosomal DNA fragmentation and chromatin condensation. During progression of the different phases of the cell cycle, the proportion of cells in the G2/M phase of the treated SiHa cells was significantly increased, which strongly confirmed that the Au@Pts induced apoptosis through the G2/M phase check points. Our findings demonstrate the activity of Au@Pts against cervical cancer cells and reveal strategies for the development of highly active bimetallic nanostructures for cancer therapeutics.
双金属金@铂纳米结构(Au@Pts)是光学、电学、催化和生物应用的潜在候选材料。然而,利用总茶多酚(TPPs)制备Au@Pts的方法、Au@Pts对生物系统的作用机制研究以及Au@Pts在癌症诊断和治疗中的应用研究都很少。在本研究中,我们开发了一种简单、环保且低成本的方法来合成Au@Pts,以检测这些Au@Pts对人宫颈癌的体外细胞毒性作用。在室温下,使用TPPs成功地同时还原了金离子和铂离子。使用紫外-可见分光光度法、X射线衍射仪(XRD)、能量色散X射线光谱仪(EDS)和透射电子显微镜(TEM)对制备的Au@Pts进行了表征。EDS和XRD证实了Au@Pt的形成。使用TEM确认形成了尺寸为5-20 nm的Au@Pts。在人宫颈癌细胞(SiHa)中评估了Au@Pts的细胞毒性特性。细胞活力结果表明,Au@Pts以剂量和时间依赖性方式诱导细胞死亡。观察了暴露于Au@Pt的SiHa细胞的形态特征,表明细胞通过细胞收缩、核小体间DNA片段化和染色质凝聚而死亡。在细胞周期不同阶段的进程中,处理后的SiHa细胞在G2/M期的细胞比例显著增加,这有力地证实了Au@Pts通过G2/M期检查点诱导细胞凋亡。我们的研究结果证明了Au@Pts对宫颈癌细胞的活性,并揭示了开发用于癌症治疗的高活性双金属纳米结构的策略。