Plant used | Metal precursor | Morphology | Cell line | Techniques used | IC50 value | Impact | References |
---|---|---|---|---|---|---|---|
Silver | |||||||
Allium cepa L (A. cepa) extract | Silver nitrate | Cubic shapes 150–250 nm | HT-29 and 0SW620 cells | DPPH scavenging, activity, TAA, FRAP, MTT assay, RT-PCR, Flow cytometry | A. cepa TAA: 55.49 ± 0.91 DPPH-SA: 2.23 ± 0.36 FRAP:14.78 ± 0:20 Ag NPs-CEPA TAA: 58.85 ± 4.39 DPPH-SA: 1.91 ± 0.20 FRAP: 13.37 ± 0.17 | The synthesized NPs inhibited cell proliferation and induced apoptosis by inhibiting Bcl2 family gene expression hence act as a promising anticancer agent for treating colorectal cancer | [267] |
Anthemis atropatana aerial parts | Silver nitrate | Spherical 38.89 nm | HT29 cancer cell | MTT assay, RT-PCR, Flow cytometry, DNA fragmentation assay | 100 µg/mL | Caused the cell to undergo early and delayed apoptosis by 15.64 and 21.32%, respectively | [273] |
Vitex negundo L. leaves extract | Silver nitrate | Spherical 5–47 nm | HCT15 | MTT assay, Propidium iodide staining, Flow cytometry, Comet assay | 20 µg/mL | Ag NPs exerted antiproliferative effects on colon cancer cell line by suppressing its growth, arresting G0/G1-phase, inhibited DNA synthesis and induced apoptosis | [274] |
Gold | |||||||
Albizia lebbeck leaf extract | HAuCl3 | Spherical 20 and 30 nm | HCT-116 colon cancer cell lines | MTT assay, AO/EtBr staining, DCFH-DA staining, Rhodamine 123, Caspases activity assay, Western blotting | 48 µg/mL | HCT-116 cells improved the activity of caspase-9 and caspase-3 in a dose-dependent manner | [268] |