journal article·2026-01-23Open access

Eco-friendly synthesis of silver nanoparticles mediated Crataegus azarolus fruits: biomedical applications and molecular docking insights

Alaa R. Hameed, Butheina A. Hasoon, Ghassan M Sulaiman, Salim Albukhaty, Majid S. Jabir, Hamdoon A. Mohammed, Ines Guidara, Ameni Ben Ammar, Shaymaa Al-Majmaie, Mohamed Trigui, Faizah A. AlMalki, Mariam Siala

Nanotechnology Reviews· Volume 15· Issue 1

Abstract

Abstract Green nanotechnology offers promising opportunities for the development of multifunctional therapeutic agents derived from plant bioresources. In this study, silver nanoparticles (AgNPs) were biosynthesized using Crataegus azarolus fruit extract ( Ca FrE) and characterized by UV–Vis spectroscopy, XRD, FTIR, TEM, zeta potential, and DLS analyses. Biological evaluation revealed that Ca FrE-AgNPs had a greater antioxidant capacity than the plant extract, with DPPH IC 50 values of 47.75 μg/mL, ABTS IC 50 values of 67.4 μg/mL, and FRAP EC 0 . 5 values of 156.25 μg/mL. These values represent an improvement on those of Ca FrE alone. Antimicrobial assays revealed potent bactericidal activity, with minimum inhibitory concentration (MIC) values ranging from 1.95 to 15.62 μg/mL and minimum bactericidal concentration (MBC) values from 3.90 to 31.24 μg/mL, as well as notable antibiofilm efficacy. Additionally, Ca FrE-AgNPs were found to induce cytotoxic effects in A549 lung cancer cells via Annexin V-FITC/PI analysis. This test revealed a substantial increase in early apoptotic cells (38 %) following treatment, confirming apoptosis as the predominant mechanism of cell death. To explore the potential molecular mechanisms, molecular docking was performed using the major phytochemicals identified in C. azarolus . Flavonoids, such as quercetin, exhibited strong binding affinities toward proteins associated with the regulation of oxidative stress, bacterial virulence, and apoptosis pathways. This supports their potential contribution to the biological activity of the nanoparticles. Overall, these results suggest that Ca FrE-AgNPs are a multifunctional, phytochemical-capped nanoplatform that combines antioxidant, antibacterial, and apoptosis-inducing properties. This highlights the potential of plant-mediated nanomaterials in developing sustainable strategies against diseases related to oxidative stress, antimicrobial resistance, and cancer.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Botanical Studies and Applications · Phytochemicals and Antioxidant Activities · Phytochemical and Pharmacological Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Medical Laboratory Techniques , School of Life Sciences, Dijlah University , Baghdad , Iraq

Research Laboratory of Environmental Sciences and Sustainable Development LASED LR18ES32, Sfax Preparatory Institute for Engineering Studies, University of Sfax , Sfax , Tunisia

Department of Biotechnology , College of Applied Sciences, University of Technology , Baghdad , Iraq

Department of Pharmaceutical Sciences , College of Pharmacy, University of Manara , Maysan , Iraq

Department of Pharmaceutical Chemistry and Pharmacognosy , College of Pharmacy, Qassim University , Qassim , 51452 , Saudi Arabia

Department of Biotechnology , College of Science, University of Diyala , Baghdad , Iraq

Department of Biology , College of Science, Taif University , P.O. Box 11099 , Taif , 21944 , Saudi Arabia

References (78)

Show source-provided references
1. Jangid, H, Singh, S, Kashyap, P, Singh, A, Kumar, G. Advancing biomedical applications: an in-depth analysis of silver nanoparticles in antimicrobial, anticancer, and wound healing roles. Front Pharmacol 2024;15:1438227. https://doi.org/10.3389/fphar.2024.1438227.10.3389/fphar.2024.1438227 ↗
2. Mohammed, HA, Amin, MA, Zayed, G, Hassan, Y, El-Mokhtar, M, Saddik, MS. In vitro and in vivo synergistic wound healing and anti-methicillin-resistant Staphylococcus aureus (MRSA) evaluation of liquorice-decorated silver nanoparticles. J Antibiot (Tokyo) 2023;76:1–10. https://doi.org/10.1038/s41429-023-00603-4.10.1038/s41429-023-00603-4 ↗
3. Kirubakaran, D, Wahid, JBA, Karmegam, N, Jeevika, R, Sellapillai, L, Rajkumar, M, et al.. A comprehensive review on the green synthesis of nanoparticles: advancements in biomedical and environmental applications. Biomed Mater Devices [Internet] 2026;4:388–413. https://doi.org/10.1007/s44174-025-00295-4.10.1007/s44174-025-00295-4 ↗
4. Adeyemi, JO, Oriola, AO, Onwudiwe, DC, Oyedeji, AO. Plant extracts mediated metal-based nanoparticles: synthesis and biological applications. Biomolecules 2022;12:627. https://doi.org/10.3390/biom12050627.10.3390/biom12050627 ↗
5. Abu-Hussien, SH, Khan, MA, AL-Farga, A, Soliman, AG, El-Sayed, SM, Adly, E. Biogenic silver nanoparticles synthesized from Pseudomonas fluorescens-mediated olive cake waste: antimicrobial, larvicidal activity against Culex pipiens and cytotoxicity assessment. BMC Biotechnol [Internet] 2025;25:75. https://doi.org/10.1186/s12896-025-01011-2.10.1186/s12896-025-01011-2 ↗
6. Farouk, SM, Abu-Hussien, SH, Abd-Elhalim, BT, Mohamed, RM, Arabe, NM, Hussain, AAT, et al.. Biosynthesis and characterization of silver nanoparticles from Punica granatum (pomegranate) peel waste and its application to inhibit foodborne pathogens. Sci Rep 2023;13:19469. https://doi.org/10.1038/s41598-023-46355-x.10.1038/s41598-023-46355-x ↗
7. Mohamed, EA, Hasoon, BAH, Abdulwahhab, NI, Sulaiman, GM, Jawad, KH, Aljaafari, HAS, et al.. Green synthesis of parsley-derived silver nanoparticles and their enhanced antimicrobial and antioxidant effects against foodborne resistant bacteria. Green Process Synth 2025;14:20250094. https://doi.org/10.1515/gps-2025-0094.10.1515/gps-2025-0094 ↗
8. Ali, E, Abu-Hussien, SH, Hesham, E, Ahmed, S, Mostafa, H, Gamal, A, et al.. Compatibility and antimicrobial activity of silver nanoparticles synthesized using Lycopersicon esculentum peels. AMB Express 2024;14:120. https://doi.org/10.1186/s13568-024-01774-5.10.1186/s13568-024-01774-5 ↗
9. Shafie, NA, David, SR, Mumin, NH, Lim, YC, Chellian, J, Rajabalaya, R. Green synthesis of silver nanoparticles using plant extracts: recent advances in mechanisms, parameters, and characterization methods. Curr Drug Ther 2025. https://doi.org/10.2174/0115748855414247251012171623.10.2174/0115748855414247251012171623 ↗
10. Sammari, H, Jedidi, S, Selmi, H, Jridi, M, Ayari, A, Sebai, H. Phytochemical properties of Crataegus azarolus berries decoction extract and evaluation of its protective activity against acetic acid-induced ulcerative colitis in rats. Dose Res 2024;22:15593258241226890. https://doi.org/10.1177/15593258241226890.10.1177/15593258241226890 ↗
11. Lewis, JM, Janda, KE, Kotter, DB, Grose, JH, McCleary, WR. Characterization of the attachment of three new coliphages onto the Ferrichrome transporter FhuA. J Virol 2023;97:e0066723. https://doi.org/10.1128/jvi.00667-23.10.1128/jvi.00667-23 ↗
12. Li, G-W, Rong, Q-Y, Zhang, W, Rao, G-W, Zheng, Q. FabH (β-Ketoacyl-ACP synthase III)--promising novel antibacterial target and its inhibitors. Med Chem Res 2026;35:1–34. https://doi.org/10.1007/s00044-025-03522-1.10.1007/s00044-025-03522-1 ↗
13. Wu, T, Xia, T, Cao, F, Liu, B, Li, F. Inhibitory effect of hyperin on Staphylococcus aureus pathogenicity though interactions with sortase A and sortase B. Sci Rep 2025;15:39190. https://doi.org/10.1038/s41598-025-23458-1.10.1038/s41598-025-23458-1 ↗
14. Park, SH, Park, C, Chun, H-S, Lee, D-G. Identification of a novel ltaS mutation in daptomycin heteroresistant community-acquired methicillin-resistant Staphylococcus aureus ST72 strains in South Korea. Int J Infect Dis IJID Off Publ Int Soc Infect Dis. 2025;159:108013. https://doi.org/10.1016/j.ijid.2025.108013.10.1016/j.ijid.2025.108013 ↗
15. Pei, J, Pan, X, Wei, G, Hua, Y. Research progress of glutathione peroxidase family (GPX) in redoxidation. Front Pharmacol 2023;14:1147414. https://doi.org/10.3389/fphar.2023.1147414.10.3389/fphar.2023.1147414 ↗
16. El-Saghier, AM, El-Naggar, M, Hussein, AHM, El-Adasy, A-BA, Olish, M, Abdelmonsef, AH. Eco-Friendly synthesis, biological evaluation, and in Silico molecular docking approach of some new quinoline derivatives as potential antioxidant and antibacterial agents. Front Chem 2021;9:679967. https://doi.org/10.3389/fchem.2021.679967.10.3389/fchem.2021.679967 ↗
17. Fadhil, OK, Hassan, FA. Role of LDH, 17-ß-hydroxysteroid dehydrogenase and myloperoxidase enzymes in early diagnosis for lung cancer patients. Int J Pharmacol Res 2020. https://doi.org/10.31838/ijpr/2020.SP1.272.10.31838/ijpr/2020.SP1.272 ↗
18. Palabiyik, AA. The role of Bcl-2 in controlling the transition between autophagy and apoptosis (review). Mol Med Rep 2025;32:1–9. https://doi.org/10.3892/mmr.2025.13537.10.3892/mmr.2025.13537 ↗
19. Shankar, SS, Rai, A, Ahmad, A, Sastry, M. Rapid synthesis of Au, Ag, and bimetallic Au core-Ag shell nanoparticles using Neem (Azadirachta indica) leaf broth. J Colloid Interface Sci 2004;275:496–502. https://doi.org/10.1016/j.jcis.2004.03.003.10.1016/j.jcis.2004.03.003 ↗
20. Trigui, M, Hsouna, AB, Tounsi, S, Jaoua, S. Chemical composition and evaluation of antioxidant and antimicrobial activities of Tunisian Thymelaea hirsuta with special reference to its mode of action. Ind Crops Prod [Internet] 2013;41:150–7. https://doi.org/10.1016/j.indcrop.2012.04.011.10.1016/j.indcrop.2012.04.011 ↗
21. Eloff, JN. A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta Med 1998;64:711–3. https://doi.org/10.1055/s-2006-957563.10.1055/s-2006-957563 ↗
22. Eucast. Routine and extended internal quality control for MIC determination and disk diffusion as recommended by EUCAST. Version. 2021;12.
23. Basumatari, M, Devi, RR, Gupta, MK, Gupta, SK, Raul, PK, Chatterjee, S, et al.. Musa balbisiana Colla pseudostem biowaste mediated zinc oxide nanoparticles: their antibiofilm and antibacterial potentiality. Curr Res Green Sustain Chem 2021;4:100048. https://doi.org/10.1016/j.crgsc.2020.100048.10.1016/j.crgsc.2020.100048 ↗
24. Al-Attar, HM, Mohammad, MH, Majeed, AM, Hussein, HT, Ahmed, AA. Investigating the anticancer activity of cerium nanoparticle decorated on GO produced by green methods against cancerous cell lines. Asian Pac J Cancer Prev 2025;26:541–9. https://doi.org/10.31557/apjcp.2025.26.2.541.10.31557/APJCP.2025.26.2.541 ↗
25. Jasim, AJ, Sulaiman, GM, Ay, H, Mohammed, SAA, Mohammed, HA, Jabir, MS, et al.. Preliminary trials of the gold nanoparticles conjugated chrysin: an assessment of anti-oxidant, anti-microbial, and in vitro cytotoxic activities of a nanoformulated flavonoid. Nanotechnol Rev 2022;11:2726–41. https://doi.org/10.1515/ntrev-2022-0153.10.1515/ntrev-2022-0153 ↗
26. Khorrami, S, Zarrabi, A, Khaleghi, M, Danaei, M, Mozafari, MR. Selective cytotoxicity of green synthesized silver nanoparticles against the MCF-7 tumor cell line and their enhanced antioxidant and antimicrobial properties. Int J Nanomed 2018;13:8013–24. https://doi.org/10.2147/ijn.s189295.10.2147/IJN.S189295 ↗
27. Rakowski, M, Porębski, S, Grzelak, A. Silver nanoparticles modulate the epithelial-to-mesenchymal transition in estrogen-dependent breast cancer cells in vitro. Int J Mol Sci 2021;22:9203. https://doi.org/10.3390/ijms22179203.10.3390/ijms22179203 ↗
28. Singh, M, Prasad, DN, Agnihotri, S. Synthesis, characterization and biological evaluation of novel triazolyl-acridine derivatives as cytotoxic agents. Res J Pharm Technol 2021;14:5101–7. https://doi.org/10.52711/0974-360x.2021.00889.10.52711/0974-360X.2021.00889 ↗
29. Kumar, R, Saneja, A, Panda, AK. An annexin V-FITC-Propidium iodide-based method for detecting apoptosis in a non-small cell lung cancer cell line. Methods Mol Biol 2021;2279:213–23.10.1007/978-1-0716-1278-1_17 ↗
30. Majewska, E, Drużyńska, B. Validation of microplate methods for total phenolic content and antioxidant activity on honeys, and comparison with conventional spectrophotometric methods. Appl Sci 2025;15:11234. https://doi.org/10.3390/app152011234.10.3390/app152011234 ↗
31. Ozgen, M, Reese, RN, Tulio, AZ, Scheerens, JC, Miller, AR. Modified 2, 2-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) method to measure antioxidant capacity of selected small fruits and comparison to ferric reducing antioxidant power (FRAP) and 2, 2′ -diphenyl-1-picrylhydrazyl (DPPH) methods. J Agric Food Chem 2006;54:1151–7. https://doi.org/10.1021/jf051960d.10.1021/jf051960d ↗
32. Affes, S, Ben Younes, A, Frikha, D, Allouche, N, Treilhou, M, Tene, N, et al.. ESI-MS/MS analysis of phenolic compounds from Aeonium arboreum leaf extracts and evaluation of their antioxidant and antimicrobial activities. Molecules 2021;26:4338. https://doi.org/10.3390/molecules26144338.10.3390/molecules26144338 ↗
33. Hanwell, MD, Curtis, DE, Lonie, DC, Vandermeersch, T, Zurek, E, Hutchison, GR. Avogadro: an advanced semantic chemical editor, visualization, and analysis platform. J Cheminf 2012;4:17. https://doi.org/10.1186/1758-2946-4-17.10.1186/1758-2946-4-17 ↗
34. Eberhardt, J, Santos-Martins, D, Tillack, AF, Forli, S. AutoDock Vina 1.2.0: new docking methods, expanded force field, and python bindings. J Chem Inf Model 2021;61:3891–8. https://doi.org/10.1021/acs.jcim.1c00203.10.1021/acs.jcim.1c00203 ↗
35. Trott, O, Olson, AJ. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J Comput Chem 2010;31:455–61. https://doi.org/10.1002/jcc.21334.10.1002/jcc.21334 ↗
36. Morris, GM, Huey, R, Lindstrom, W, Sanner, MF, Belew, RK, Goodsell, DS, et al.. AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility. J Comput Chem 2009;30:2785–91. https://doi.org/10.1002/jcc.21256.10.1002/jcc.21256 ↗
37. Systèmes, D. Biovia discovery studio visualizer. Dassault Systèmes San Diego. 2020.
38. Elshibani, FA, Farouk, A, Naili, EE, Mahmoud, E, Othman, A, Mohammed, HA, et al.. GC-MS and HPLC chemical profile, antioxidant, anti-acetylcholinesterase, and anti-diabetic activities of Libyan Salvia lanigera herb extract and essential oil. Sci Rep 2025;15:31853. https://doi.org/10.1038/s41598-025-12233-x.10.1038/s41598-025-12233-x ↗
39. Mansour, T, Radwan, WH, Mansour, M, Gomaa, M, Farouk, F, Shepl, M, et al.. Larvicidal potential, toxicological assessment, and molecular docking studies of four Egyptian bacterial strains against Culex pipiens L.(Diptera: culicidae). Sci Rep 2023;13:17230. https://doi.org/10.1038/s41598-023-44279-0.10.1038/s41598-023-44279-0 ↗
40. Lasmi, F, Hamitouche, H, Laribi-Habchi, H, Benguerba, Y, Chafai, N. Silver nanoparticles (AgNPs), methods of synthesis, characterization, and their application: a review. Plasmonics 2025;20:9455–88. https://doi.org/10.1007/s11468-025-02894-9.10.1007/s11468-025-02894-9 ↗
41. Naik, LS, Ramana Devi, CV. Phyto-fabricated silver nanoparticles inducing microbial cell death via reactive oxygen species-mediated membrane damage. IET Nanobiotechnol 2021;15:492–504. https://doi.org/10.1049/nbt2.12036.10.1049/nbt2.12036 ↗
42. Pasieczna-Patkowska, S, Cichy, M, Flieger, J. Application of fourier transform infrared (FTIR) spectroscopy in characterization of green synthesized nanoparticles. Molecules 2025;30:684. https://doi.org/10.3390/molecules30030684.10.3390/molecules30030684 ↗
43. Ls, AD, Krishnan, M. Electro-spun nano fiber of carboxymethyl cellulose–curcumin and its applications. World J Curr Med Pharm Res 2021:94–100. https://doi.org/10.37022/wjcmpr.v3i4.184.10.37022/wjcmpr.v3i4.184 ↗
44. Vijeata, A, Chaudhary, GR, Umar, A, Chaudhary, S. Distinctive solvatochromic response of fluorescent carbon dots derived from different components of Aegle Marmelos plant. Eng Sci 2021;15:197–209. https://doi.org/10.30919/es8e512.10.30919/es8e512 ↗
45. Yadav, P, Bharti, N, Kansotiya, AK, Mali, PC. Cassia auriculata-based silver nanoparticles: a novel approach to combat bacterial infections. SSR Inst J Life Sci 2024;10:6360–70. https://doi.org/10.21276/ssr-iijls.2024.10.6.2.10.21276/SSR-IIJLS.2024.10.6.2 ↗
46. Park, K-B, Kim, J-S, Pahlavan, F, Fini, EH. Biomass waste to produce phenolic compounds as antiaging additives for asphalt. ACS Sustain Chem Eng 2022;10:3892–908. https://doi.org/10.1021/acssuschemeng.1c07870.10.1021/acssuschemeng.1c07870 ↗
47. Liu, J, Zhang, Q, Ma, F, Zhang, S, Zhou, Q, Huang, A. Three-step identification of infrared spectra of similar tree species to Pterocarpus santalinus covered with beeswax. J Mol Struct [Internet] 2020;1218:128484. https://doi.org/10.1016/j.molstruc.2020.128484. Available from: https://www.sciencedirect.com/science/article/pii/S0022286020308097.10.1016/j.molstruc.2020.128484 ↗
48. Nallusamy, N, Mohd Kamal Rufadzil, NA, Bala, MJ, Liam, JZ, Wan, FWND, Mohd Jefri, HD, et al.. Green synthesis and characterization of silver nanoparticles using rice (Oryza sativa) and spent coffee (Coffea robusta) grounds from agricultural waste(§). Food Technol Biotechnol 2025;63:159–67. https://doi.org/10.17113/ftb.63.02.25.8925.10.17113/ftb.63.02.25.8925 ↗
49. Sytu, MRC, Camacho, DH. Green synthesis of silver nanoparticles (AgNPs) from Lenzites betulina and the potential synergistic effect of AgNP and capping biomolecules in enhancing antioxidant activity. Bionanoscience [Internet] 2018;8:835–44. https://doi.org/10.1007/s12668-018-0548-x.10.1007/s12668-018-0548-x ↗
50. Ghaffari-Moghaddam, M, Hadi-Dabanlou, R. Plant mediated green synthesis and antibacterial activity of silver nanoparticles using Crataegus douglasii fruit extract. J Ind Eng Chem [Internet] 2014;20:739–44. https://doi.org/10.1016/j.jiec.2013.09.005.10.1016/j.jiec.2013.09.005 ↗
51. Karataş, H, Eker, F, Akdaşçi, E, Bechelany, M, Karav, S. Silver nanoparticles in antibacterial research: mechanisms, applications, and emerging perspectives. Int J Mol Sci 2026;27:927. https://doi.org/10.3390/ijms27020927.10.3390/ijms27020927 ↗
52. Ebrahimzadeh, MA, Naghizadeh, A, Amiri, O, Shirzadi-Ahodashti, M, Mortazavi-Derazkola, S. Green and facile synthesis of Ag nanoparticles using Crataegus pentagyna fruit extract (CP-AgNPs) for organic pollution dyes degradation and antibacterial application. Bioorg Chem 2020;94:103425. https://doi.org/10.1016/j.bioorg.2019.103425.10.1016/j.bioorg.2019.103425 ↗
53. Mehmood, A, Zahir, S, Rauf Khan, MA, Ahmad, KS, Abasi, F, Raffi, M, et al.. Optimization and bio-fabrication of phyto-mediated silver nanoparticles (Ag-NPs) for antibacterial potential. J Biomol Struct Dyn 2024;42:8063–72. https://doi.org/10.1080/07391102.2023.2242960.10.1080/07391102.2023.2242960 ↗
54. Altammar, KA. A review on nanoparticles: characteristics, synthesis, applications, and challenges. Front Microbiol 2023;14:1155622. https://doi.org/10.3389/fmicb.2023.1155622.10.3389/fmicb.2023.1155622 ↗
55. Khalid, HF, Tehseen, B, Sarwar, Y, Hussain, SZ, Khan, WS, Raza, ZA, et al.. Biosurfactant coated silver and iron oxide nanoparticles with enhanced anti-biofilm and anti-adhesive properties. J Hazard Mater 2019;364:441–8. https://doi.org/10.1016/j.jhazmat.2018.10.049.10.1016/j.jhazmat.2018.10.049 ↗
56. Siddique, MH, Aslam, B, Imran, M, Ashraf, A, Nadeem, H, Hayat, S, et al.. Effect of silver nanoparticles on biofilm formation and EPS production of multidrug-resistant Klebsiella pneumoniae. Biomed Res Int 2020;2020:6398165. https://doi.org/10.1155/2020/6398165.10.1155/2020/6398165 ↗
57. Shariati, A, Noei, M, Askarinia, M, Khoshbayan, A, Farahani, A, Chegini, Z. Inhibitory effect of natural compounds on quorum sensing system in Pseudomonas aeruginosa: a helpful promise for managing biofilm community. Front Pharmacol 2024;15:1350391. https://doi.org/10.3389/fphar.2024.1350391.10.3389/fphar.2024.1350391 ↗
58. Philip, N, Bandara, HMHN, Leishman, SJ, Walsh, LJ. Inhibitory effects of fruit berry extracts on Streptococcus mutans biofilms. Eur J Oral Sci 2019;127:122–9. https://doi.org/10.1111/eos.12602.10.1111/eos.12602 ↗
59. Lalsangpuii, F, Rokhum, SL, Nghakliana, F, V, L, Ruatpuia, J, Tochhawng, L, et al.. Mikania micrantha silver nanoparticles exhibit anticancer activities against human lung adenocarcinoma via caspase-mediated apoptotic cell death. Artif cells, nanomedicine. Biotechnol 2024;52:186–200. https://doi.org/10.1080/21691401.2024.2325942.10.1080/21691401.2024.2325942 ↗
60. Mickky, B, Elsaka, H, Abbas, M, Gebreil, A, Shams Eldeen, R. Orange peel-mediated synthesis of silver nanoparticles with antioxidant and antitumor activities. BMC Biotechnol 2024;24:66. https://doi.org/10.1186/s12896-024-00892-z.10.1186/s12896-024-00892-z ↗
61. Xiong, H, Nie, X, Cao, W, Zhu, J, Chen, J, Liu, R, et al.. Investigation of mitochondria-dependent apoptosis pathway and lipid peroxidation level induced by biosynthesized silver nanoparticles: Caspase-3 activation, BAK1/BCLx regulation and malondialdehyde production. Cancer Nanotechnol 2024;15:13. https://doi.org/10.1186/s12645-024-00248-4.10.1186/s12645-024-00248-4 ↗
62. Al-Asiri, WY, Al-Sheddi, ES, Farshori, NN, Al-Oqail, MM, Al-Massarani, SM, Malik, T, et al.. Cytotoxic and apoptotic effects of green synthesized silver nanoparticles via reactive oxygen species–mediated mitochondrial pathway in human breast cancer cells. Cell Biochem Funct 2024;42:e4113. https://doi.org/10.1002/cbf.4113.10.1002/cbf.4113 ↗
63. Thakkar, AB, Subramanian, RB, Thakkar, VR, Bhatt, SV, Chaki, S, Vaidya, YH, et al.. Apoptosis induction capability of silver nanoparticles capped with Acorus calamus L. and Dalbergia sissoo Roxb. Ex DC. Against lung carcinoma cells. Heliyon 2024;10:e24400. https://doi.org/10.1016/j.heliyon.2024.e24400.10.1016/j.heliyon.2024.e24400 ↗
64. Báez, DF, Gallardo-Toledo, E, Oyarzún, MP, Araya, E, Kogan, MJ. The influence of size and chemical composition of silver and gold nanoparticles on in vivo toxicity with potential applications to central nervous system diseases. Int J Nanomed 2021;16:2187–201. https://doi.org/10.2147/ijn.s260375.10.2147/IJN.S260375 ↗
65. Bahri-Sahloul, R, Ben Fredj, R, Boughalleb, N, Shriaa, J, Saguem, S, Hilbert, J-L, et al.. Phenolic composition and antioxidant and antimicrobial activities of extracts obtained from Crataegus azarolus L. var. aronia (Willd.) Batt. ovaries calli. J Bot, Le 2014;2014:623651–11. https://doi.org/10.1155/2014/623651.10.1155/2014/623651 ↗
66. Ganeshpurkar, A, Saluja, AK. The pharmacological potential of rutin. Saudi Pharm J SPJ Off Publ Saudi Pharm Soc 2017;25:149–64. https://doi.org/10.1016/j.jsps.2016.04.025.10.1016/j.jsps.2016.04.025 ↗
67. Zhang, W, Wang, R, Guo, R, Yi, Z, Wang, Y, Wang, H, et al.. The multiple biological activities of hyperoside: from molecular mechanisms to therapeutic perspectives in neoplastic and non-neoplastic diseases. Front Pharmacol 2025;16:1538601. https://doi.org/10.3389/fphar.2025.1538601.10.3389/fphar.2025.1538601 ↗
68. Ademiluyi, AO, Oyeniran, OH, Del Prado-Audelo, ML, Romero-Montero, A, Leyva-Gómez, G, Dini, I, et al.. Procyanidins as potential anticancer agents: mechanisms of action, bioavailability challenges and therapeutic opportunities. Med Oncol 2025;42:251. https://doi.org/10.1007/s12032-025-02814-1.10.1007/s12032-025-02814-1 ↗
69. Mohammed, HA, Khan, RA. Anthocyanins: traditional uses, structural and functional variations, approaches to increase yields and products’ quality, hepatoprotection, liver longevity, and commercial products. Int J Mol Sci 2022;23:2149. https://doi.org/10.3390/ijms23042149.10.3390/ijms23042149 ↗
70. Qubtia, M, Ghumman, SA, Noreen, S, Hameed, H, Noureen, S, Kausar, R, et al.. Evaluation of plant-based silver nanoparticles for antioxidant activity and promising wound-healing applications. ACS Omega 2024;9:12146–57. https://doi.org/10.1021/acsomega.3c10489.10.1021/acsomega.3c10489 ↗
71. Bedlovičová, Z, Strapáč, I, Baláž, M, Salayová, A. A brief overview on antioxidant activity determination of silver nanoparticles. Molecules 2020;25:3191. https://doi.org/10.3390/molecules25143191.10.3390/molecules25143191 ↗
72. Ojemaye, MO, Okoh, SO, Okoh, AI. Silver nanoparticles (AgNPs) facilitated by plant parts of Crataegus ambigua Becker AK extracts and their antibacterial, antioxidant and antimalarial activities. Green Chem Lett Rev 2021;14:51–61. https://doi.org/10.1080/17518253.2020.1861344.10.1080/17518253.2020.1861344 ↗
73. Flieger, J, Franus, W, Panek, R, Szymańska-Chargot, M, Flieger, W, Flieger, M, et al.. Green synthesis of silver nanoparticles using natural extracts with proven antioxidant activity. Molecules 2021;26:4986. https://doi.org/10.3390/molecules26164986.10.3390/molecules26164986 ↗
74. Kim, S, Choi, JE, Choi, J, Chung, K-H, Park, K, Yi, J, et al.. Oxidative stress-dependent toxicity of silver nanoparticles in human hepatoma cells. Toxicol Vitr Int J Publ Assoc BIBRA 2009;23:1076–84. https://doi.org/10.1016/j.tiv.2009.06.001.10.1016/j.tiv.2009.06.001 ↗
75. Foldbjerg, R, Olesen, P, Hougaard, M, Dang, DA, Hoffmann, HJ, Autrup, H. PVP-coated silver nanoparticles and silver ions induce reactive oxygen species, apoptosis and necrosis in THP-1 monocytes. Toxicol Lett 2009;190:156–62. https://doi.org/10.1016/j.toxlet.2009.07.009.10.1016/j.toxlet.2009.07.009 ↗
76. Sarkar, C, Chaudhary, P, Jamaddar, S, Janmeda, P, Mondal, M, Mubarak, MS, et al.. Redox activity of flavonoids: impact on human health, therapeutics, and chemical safety. Chem Res Toxicol 2022;35:140–62. https://doi.org/10.1021/acs.chemrestox.1c00348.10.1021/acs.chemrestox.1c00348 ↗
77. Wypij, M, Jędrzejewski, T, Trzcińska-Wencel, J, Ostrowski, M, Rai, M, Golińska, P. Green synthesized silver nanoparticles: antibacterial and anticancer activities, biocompatibility, and analyses of surface-attached proteins. Front Microbiol 2021;12:632505. https://doi.org/10.3389/fmicb.2021.632505.10.3389/fmicb.2021.632505 ↗
78. Tang, S-M, Deng, X-T, Zhou, J, Li, Q-P, Ge, X-X, Miao, L. Pharmacological basis and new insights of quercetin action in respect to its anti-cancer effects. Biomed Pharmacother 2020;121:109604. https://doi.org/10.1016/j.biopha.2019.109604.10.1016/j.biopha.2019.109604 ↗