Plant used | Metal precursor | Morphology | Cell line | Techniques used | IC50 value | Impact | References |
---|---|---|---|---|---|---|---|
Silver | |||||||
Citrus sinensis leaf aqueous extract | Silver nitrate | Spherical 78.12 nm | NCI-H661, HLC-1, NCI-H1563, LC-2/ad, NCI-H1299, PC-14, HUVEC | DPPH assay, MTT assay | NCI-H661: 82 µg/mL HLC-1: 139 µg/mL NCI-H1563:170 µg/mL LC-2/ad: 66 µg/mL NCI-H1299: 62 µg/mL PC-14: 50 µg/mL | Dose-dependent decrease in human lung cancer cell viability reported | [238] |
Leucus aspera leaf extract | Silver nitrate | Spherical 40.67–8.17 nm | A549 HUVEC | DPPH assay, MTT assay | 328 µg/mL | No cytotoxicity on the normal cell line (HUVEC) and very low cell viability against the A549 cell line | [239] |
Avicennia marina leaf extract | Silver nitrate | Spherical 10–100 nm | A549 | MTT assay, DCFH-DA assay, Rhodamine 123 | 50 µg/mL | High damages in mitochondrial membrane | [240] |
Cleome viscosa L fruit extract | Silver nitrate | Spherical 20–50 nm | A549 | MTT assay | 28 µg/mL | The ability of green-synthesized silver nanoparticles to inhibit cancer cells growth in vitro could be taken as an indicator of potential anticancer effect | [241] |
Lonicera japonica leaves extract | Silver nitrate | Spherical | A549 | MTT assay | 75 µg/mL | At very low concentrationsAg NPs altered the shape of A549 human lung cancer cells | [235] |
Gold | |||||||
Rabdosia rubescens | Gold (III) chloride trihydrate | Spherical 130 nm | A549 | MTT assay, DAPI staining, TUNEL assay, Western blotting analysis | 50 µg/mL | Caspase levels were found to be 1.5 times higher in the cells treated with 25 µg/mL of RR-AuNP | [242] |
Musa paradisiaca peel extract against | Chloroauric acid | Spherical to triangular 50 nm | A549 | MTT assay | 58 μg/mL | Nuclear morphological changes, such as cell clumping and a lack of membrane stability, after 24 h at 100 μg/mL | [243] |
Marsdenia tenacissima plant extracts | Chloroauric acid | Spherical 40–50 nm | A549 | MTT assay, AO/EtBr staining, Western blotting | 15 µg/mL | Modulates the levels of the proteins Bax and Bcl-2 to cause apoptosis in the lung cancer cell line A549 | [244] |
Magnolia officinalis extract | – | Oval, spherical, hexagonal, and triangular 70–10 nm | A549 | MTT assay, DCFH-DA, TUNEL assay, Western blotting | 50 µg/mL | In A549 cells, Au NPs made from Magnolia officinalis increased the expression of Bax, Beclin-1, and caspase-3 while decreasing the expression of Bcl-2 and Bid | [231] |
Zinc oxide | |||||||
Azadirachta indica leaf extract | Zinc sulfate heptahydrate | Ribbon/strip shaped | A549 | MTT assay, Crystal violet assay, AO/PI staining, Flow cytometry | 138.50 µg/mL | Apoptosis was observed in cells treated with IC50 dose G1 phase accounted for 76.9% cells get arrested in A549 cells after treatment | [245] |
Euphorbia fischeriana root extract | Zinc acetate dehydrate | Spherical 30 nm | A549 | MTT assay, AO/EtBr fluorescence staining, DCFH-DA assay, Rhodamine 123, Cell migration assay, Western blotting analysis | 14.5 µg/mL | EF-ZnO NPs induced cytotoxicity also activated apoptosis during increased ROS formation, decreased MMP, inhibited cell migration, altered AO/EtBr staining and induced pro-apoptotic and inhibited anti-apoptotic protein were observed | [246] |
Mangifera indica leaf extract | Zinc nitrate | Spherical/hexagonal quartzite 45–60 nm | A549 | MTT assay | 25 µg/mL | Anticancer activity of ZnO NPs increased with the increasing concentration of NPs and is comparable to the cytotoxic effects of cyclophosphamide in low doses | [247] |
Copper oxide | |||||||
Calendula officinalis aqueous leaf extract | Copper (II) Nitrate Trihydrate | Spherical 19.64–39.15 nm | LC-2/ad PC-14 HLC-1 | DPPH assay, MTT assay | PC-14: 297 µg/mL LC-2/ad:328 µg/mL HLC-1:514 µg/mL | The viability of malignant lung cell line reduced dose-dependently | [248] |
Ficus religiosa leaf extract | Cupric sulfate | Spherical | A549 | MTT assay, AO/EtBr fluorescence staining, DCFH-DA assay, Rhodamine 123 | 200 μg/mL | When compared to control, A549 cells treated with copper oxide nanoparticles showed loss of membrane integrity, apoptosis induction, and orange fragmented nuclei, all of which were consistent with low cell viability | [249] |
Ilex paraguariensis | Copper(I) sulfate | Spherical 26–40 nm | A549 | MTT assay | 100 μg/mL | In lung cancer A549 cells, Cu NPs with a size of less than 20 nm caused cytotoxicity | [250] |
Beta vulgaris extract | Cupric sulfate | Spherical 33.47 nm | A549 | MTT assay, FACS analysis | 25 μg/mL | In comparison to control, A549 cells decreased at the G0/G1 phase from 52.8 to 20.6%, increased at the S phase from 38.43 to 30.41%, and considerably increased at the G2/M phase from 14.56 to 52.46% | [251] |
Foeniculum vulgare leaves extract | Copper (II) nitrate trihydrate | Spherical 33.62–74.81 nm | NCI-H2126, NCI-H1299, NCIH1437 Normal cell line: HUVEC | MTT assay DPPH assay | Fv-Cu NPs NCI-H2126: 122 µg/mL NCI-H1299: 168 µg/mL NCI-H1437: 108 µg/mL F. vulgare extract NCI-H2126: 594 µg/mL NCI-H1299: 781 µg/mL NCI-H1437: 610 µg/mL | The viability of malignant lung cell lines reduced dose-dependently in the presence of NPs. The IC50 of Cu NPs and BHT against DPPH free radicals were 42 and 26 µg/mL, respectively | [252] |
Titanium oxide | |||||||
Ledebouria revoluta bulb extract | Titanium dioxide | Spherical 47.6 nm | A549 | MTT assay | 53.65 µg/mL | Highly reactive hydroxyl act as a powerful oxidant resulting in oxidative DNA-damage both single and double standard DNA | [232] |