Hamida Reham Samir, AlMotwaa Sahar M, Al-Otaibi Waad A, Alqhtani Haifa A, Ali Mohamed Abdelaal, Bin-Meferij Mashael Mohammed
Institute for Protein Research, Osaka University, Osaka 565-0871, Japan.
Department of Chemistry, College of Science and Humanities, Shaqra University, Shaqra 11961, Saudi Arabia.
Biomedicines. 2024 Jul 15;12(7):1570. doi: 10.3390/biomedicines12071570.
strain AB_11_10 was isolated and identified using microscopy and 16s rRNA sequencing, and its phytochemical constituents were determined using liquid chromatography-quadrupole time-of-flight mass spectrometry. The isolate had a segmented filamentous shape with a blue-green color. Many biomolecules, including organic compounds, amino acids, and fatty acids, were detected. strain AB_11_10 was used to synthesize gold nanoparticles (Ph-AuNPs) by adjusting the optimum reaction conditions. The concentration, algal/precursor ratio, temperature, reaction time, and pH significantly influenced the synthesis of the Ph-AuNPs. Mixing 1 mL of 0.5 mM of HAuCl with 1 mL of algal extract and exposing the mixture to 100 °C for 30 min at pH 5.6 were the optimum conditions for the biosynthesis of Ph-AuNPs at a wavelength of 524.5 nm. The Ph-AuNPs were characterized using TEM, SEM, EDX, and mapping Zeta sizer and FTIR. The Ph-AuNPs had quasi-spherical to triangular shapes with an average diameter of 9.6 ± 4.3 nm. Ph-AuNPs composed of 76.10 ± 3.14% of Au and trace amounts of carbon and oxygen were detected, indicating that the strain AB_11_10 successfully synthesized Ph-AuNPs. The hydrodynamic diameter of the Ph-AuNPs was 28.5 nm, and their potential charge was -17.7 mV. O-H, N-H, C=C, N-O, C-H, and C-O were coated onto the surfaces of the Ph-AuNPs. These groups correspond to algal phytochemicals, which may have been the main reducing and stabilizing substances during the Ph-AuNP synthesis. The therapeutic activity of the Ph-AuNPs against osteosarcoma cancers was examined in MG-63 and SAOS-2 cell lines, while their biocompatibility was tested against Vero cell lines using a sulforhodamine B assay. The Ph-AuNPs had potent antitumor activity against the MG-63 and SAOS-2 cells, with a low toxicity toward Vero cells. Flow cytometry and cell cycle arrest analyses revealed that the Ph-AuNPs enhanced the apoptotic pathway and arrested the cell cycle in the MG-63 and SAOS-2 cells. strain AB_11_10 provides a new source to synthesize small, stable, and biocompatible AuNPs that act as apoptotic enhancers in osteosarcoma.
菌株AB_11_10通过显微镜检查和16s rRNA测序进行分离和鉴定,其植物化学成分通过液相色谱-四极杆飞行时间质谱法测定。该分离物呈分段丝状,颜色为蓝绿色。检测到许多生物分子,包括有机化合物、氨基酸和脂肪酸。通过调整最佳反应条件,菌株AB_11_10被用于合成金纳米颗粒(Ph-AuNPs)。浓度、藻类/前驱体比例、温度、反应时间和pH值对Ph-AuNPs的合成有显著影响。将1 mL 0.5 mM的HAuCl与1 mL藻类提取物混合,并在pH 5.6下于100°C暴露30分钟,是在524.5 nm波长下生物合成Ph-AuNPs的最佳条件。使用透射电子显微镜(TEM)、扫描电子显微镜(SEM)、能量色散X射线光谱(EDX)以及Zeta电位分析仪和傅里叶变换红外光谱(FTIR)对Ph-AuNPs进行表征。Ph-AuNPs具有准球形到三角形的形状,平均直径为9.6±4.3 nm。检测到由76.10±3.14%的金以及痕量的碳和氧组成的Ph-AuNPs,表明菌株AB_11_10成功合成了Ph-AuNPs。Ph-AuNPs的流体动力学直径为28.5 nm,其电位电荷为-17.7 mV。O-H、N-H、C=C、N-O、C-H和C-O被包覆在Ph-AuNPs的表面。这些基团对应于藻类植物化学成分,它们可能是Ph-AuNP合成过程中的主要还原和稳定物质。在MG-63和SAOS-2细胞系中检测了Ph-AuNPs对骨肉瘤癌症的治疗活性,同时使用磺基罗丹明B测定法在Vero细胞系中测试了它们的生物相容性。Ph-AuNPs对MG-63和SAOS-2细胞具有强大的抗肿瘤活性,对Vero细胞毒性较低。流式细胞术和细胞周期阻滞分析表明,Ph-AuNPs增强了MG-63和SAOS-2细胞中的凋亡途径并使细胞周期停滞。菌株AB_11_10为合成小尺寸、稳定且生物相容的金纳米颗粒提供了新的来源,这些金纳米颗粒在骨肉瘤中作为凋亡增强剂发挥作用。