Ullah Zakir, Iqbal Javed, Abbasi Banzeer Ahsan, Gul Farhat, Ali Sarfaraz, Kanwal Sobia, Aljowaie Reem M, Murtaza Ghulam, Iqbal Rashid, Mahmood Tariq
Department of Plant Sciences, Faculty of Biological Sciences, Quaid-I-Azam University Islamabad, Islamabad, 45320, Pakistan.
Department of Botany, Bacha Khan University, Charsadda, 24420, Khyber Pakhtunkhwa, Pakistan.
Appl Biochem Biotechnol. 2025 Apr;197(4):2328-2355. doi: 10.1007/s12010-024-05151-7. Epub 2025 Jan 3.
The current research was conducted to synthesize Parietaria alsinifolia-mediated iron oxide nanoparticles (P.A@FeONPs) using the green and eco-friendly protocol. The biosynthesized P.A@FeONPs were characterized using various approaches like UVs, FTIR, SEM, EDX, and DLS. The mean crystallite size was calculated to be ~ 21.48 nm using the Debye-Scherrer equation. Further, various in vitro biological assays were performed to analyze the therapeutic potentials of FeONPs. 2,2-Diphenyl-1-picrylhydrazy (DPPH) antioxidant activity was performed to reveal the DPPH radical scavenging potential of P.A@FeONPs and was calculated as 72%. Similarly, the total reducing power was determined as 65.45 ± 1.77%. In addition, P.A@FeONPs exhibited a significant total antioxidant capacity of 87 ± 4.8%. Antibacterial and antifungal assays were performed using the disc diffusion method. Among the different bacterial strains accession (EFB-10-2023 M.B), Rhodococcus jostii has shown the highest zone of inhibition (23.9 mm at 1000 μg/mL), while Escherichia coli displayed a 22.65 mm zone of inhibition at (1000 μg/mL). Similarly, Aspergillus niger exhibited a substantial zone of inhibition (28.75 mm). A brine shrimp cytotoxicity assay revealed the cytotoxicity potential (LC 244.92 μg/mL). P.A@FeONPs were also tested against red blood cells, HEK-293, and VERO cell lines (< 200 μg/mL) to validate their biocompatibility. An alpha-amylase inhibition assay demonstrated 68.66% inhibition and substantial cytotoxicity against Hep-2 liver cancer cells (IC 100 μg/mL). In conclusion, P.A@FeONPs have shown significant bioactivities. In the future, we recommend other biological and catalytic activities using different animal models to explore its potential further.
本研究采用绿色环保方案合成了墙草介导的氧化铁纳米颗粒(P.A@FeONPs)。通过紫外可见光谱(UVs)、傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、能谱分析(EDX)和动态光散射(DLS)等多种方法对生物合成的P.A@FeONPs进行了表征。使用德拜-谢乐方程计算出平均微晶尺寸约为21.48纳米。此外,还进行了各种体外生物学试验,以分析FeONPs的治疗潜力。进行了2,2-二苯基-1-苦基肼(DPPH)抗氧化活性试验,以揭示P.A@FeONPs清除DPPH自由基的潜力,计算得出为72%。同样,总还原能力测定为65.45±1.77%。此外,P.A@FeONPs表现出显著的总抗氧化能力,为87±4.8%。采用纸片扩散法进行了抗菌和抗真菌试验。在不同的细菌菌株保藏物(EFB-10-2023 M.B)中,约氏红球菌显示出最高的抑菌圈(1000μg/mL时为23.9毫米),而大肠杆菌在1000μg/mL时显示出22.65毫米的抑菌圈。同样,黑曲霉表现出较大的抑菌圈(28.75毫米)。卤虫细胞毒性试验揭示了其细胞毒性潜力(LC 244.92μg/mL)。还针对红细胞、HEK-293和VERO细胞系(<200μg/mL)对P.A@FeONPs进行了测试,以验证其生物相容性。α-淀粉酶抑制试验显示抑制率为68.66%,对Hep-2肝癌细胞具有显著的细胞毒性(IC 100μg/mL)。总之,P.A@FeONPs已显示出显著的生物活性。未来,我们建议使用不同的动物模型进行其他生物学和催化活性研究,以进一步探索其潜力。