Determination of the Cytotoxicity and Antibiofilm Potential Effect of Equisetum arvense Silver Nanoparticles
Özet
This study aimed to synthesize and characterize silver nanoparticles (AgNPs) by green synthesis from Equisetum arvense (Ea) extracts and to investigate their cytotoxicity, antibiofilm activity, and α-glucosidase enzyme inhibition. Diverse characterization techniques were applied to verify the production of nanoparticles. SEM examination confirmed that the size of nanoparticles is in the range of 40–60 nm. Also, interactions between silver and natural compounds of plant extract were confirmed through FT-IR and EDX analyses. It was determined that Equisetum arvense silver nanoparticles had antibiofilm activity against three different clinical strains with high biofilm-forming ability. AgNPs reduced the biofilm-forming capacity of clinical A. baumannii isolate with strong biofilm-forming capacity by approximately twofold, while the capacity of clinical K.pneumonaie and E.coli isolates decreased by 1.5 and 1.2 fold, respectively. The α-glucosidase enzyme inhibition potential of the AgNPs, which is determined as 93.50%, was higher than the plant extract with, and the α- 30.37%. MTT was performed to assess whether incubation of nanoparticles with A549 and ARPE-19 cell lines affected their viability, and a dramatic reduction in cell growth inhibition of both A549 and ARPE-19 cells was observed. It has been shown that A549 cells treated with 200 and 150 µg/mL nanoparticles had less cell proliferation compared to control cells at 24-h and 48-h incubation time. According to these results, Ea-derived AgNPs appear to have potential anticancer activity against A549 cancer cells. Investigating the effects of green synthesis nanoparticles on microbial biofilm and various tumors may be important for developing new therapies. The outcomes of this study have showed that Ea-AgNPsmay have a high potential both in the treatment of pathogenic strains that form biofilms, as well as in anticancer therapy use.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Akar, Zeynep | |
| dc.contributor.author | Akay, Seref | |
| dc.contributor.author | Ejder, Nebahat | |
| dc.contributor.author | Özad Düzgün, Azer | |
| dc.date.accessioned | 2026-10-22T10:20:17.569659581Z | |
| dc.date.available | 2026-10-22T10:20:17.569659581Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | This study aimed to synthesize and characterize silver nanoparticles (AgNPs) by green synthesis from Equisetum arvense (Ea) extracts and to investigate their cytotoxicity, antibiofilm activity, and α-glucosidase enzyme inhibition. Diverse characterization techniques were applied to verify the production of nanoparticles. SEM examination confirmed that the size of nanoparticles is in the range of 40–60 nm. Also, interactions between silver and natural compounds of plant extract were confirmed through FT-IR and EDX analyses. It was determined that Equisetum arvense silver nanoparticles had antibiofilm activity against three different clinical strains with high biofilm-forming ability. AgNPs reduced the biofilm-forming capacity of clinical A. baumannii isolate with strong biofilm-forming capacity by approximately twofold, while the capacity of clinical K.pneumonaie and E.coli isolates decreased by 1.5 and 1.2 fold, respectively. The α-glucosidase enzyme inhibition potential of the AgNPs, which is determined as 93.50%, was higher than the plant extract with, and the α- 30.37%. MTT was performed to assess whether incubation of nanoparticles with A549 and ARPE-19 cell lines affected their viability, and a dramatic reduction in cell growth inhibition of both A549 and ARPE-19 cells was observed. It has been shown that A549 cells treated with 200 and 150 µg/mL nanoparticles had less cell proliferation compared to control cells at 24-h and 48-h incubation time. According to these results, Ea-derived AgNPs appear to have potential anticancer activity against A549 cancer cells. Investigating the effects of green synthesis nanoparticles on microbial biofilm and various tumors may be important for developing new therapies. The outcomes of this study have showed that Ea-AgNPsmay have a high potential both in the treatment of pathogenic strains that form biofilms, as well as in anticancer therapy use. | |
| dc.identifier.doi | 10.1007/s12010-023-04587-7 | |
| dc.identifier.eissn | 1559-0291 | |
| dc.identifier.endpage | 922 | |
| dc.identifier.issn | 0273-2289 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 37273097 | |
| dc.identifier.scopus | 2-s2.0-85160960970 | |
| dc.identifier.startpage | 909 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/gumushane/12580 | |
| dc.identifier.volume | 196 | |
| dc.identifier.wos | WOS:001000891200001 | |
| dc.language.iso | en | |
| dc.publisher | Springer | |
| dc.relation.ispartof | Applied Biochemistry and Biotechnology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Antibiofilm | |
| dc.subject | Anticancer | |
| dc.subject | Green synthesis | |
| dc.subject | Nanotechnology | |
| dc.subject | Silver nanoparticle | |
| dc.subject.classification | Biochemistry & Molecular Biology | |
| dc.subject.classification | Biotechnology & Applied Microbiology | |
| dc.subject.other | alpha-Glucosidases | |
| dc.subject.other | Anti-Bacterial Agents | |
| dc.subject.other | Biofilms | |
| dc.subject.other | Equisetum | |
| dc.subject.other | Escherichia coli | |
| dc.subject.other | Metal Nanoparticles | |
| dc.subject.other | Microbial Sensitivity Tests | |
| dc.subject.other | Plant Extracts | |
| dc.subject.other | Silver | |
| dc.subject.other | Spectroscopy, Fourier Transform Infrared | |
| dc.subject.other | Cancer cells | |
| dc.subject.other | Cell culture | |
| dc.subject.other | Cell proliferation | |
| dc.subject.other | Enzyme inhibition | |
| dc.subject.other | Silver compounds | |
| dc.subject.other | Synthesis (chemical) | |
| dc.subject.other | Equisetum arvense extract | |
| dc.subject.other | glucosidase | |
| dc.subject.other | silver nanoparticle | |
| dc.subject.other | alpha glucosidase | |
| dc.subject.other | antiinfective agent | |
| dc.subject.other | metal nanoparticle | |
| dc.subject.other | plant extract | |
| dc.subject.other | Antibiofilms | |
| dc.subject.other | Anticancer | |
| dc.subject.other | Characterization techniques | |
| dc.subject.other | Clinical strains | |
| dc.subject.other | Equisetum arvense | |
| dc.subject.other | Forming ability | |
| dc.subject.other | Green synthesis | |
| dc.subject.other | Natural compounds | |
| dc.subject.other | Potential effects | |
| dc.subject.other | A-549 cell line | |
| dc.subject.other | Acinetobacter baumannii | |
| dc.subject.other | antibiofilm activity | |
| dc.subject.other | antineoplastic activity | |
| dc.subject.other | ARPE-19 cell line | |
| dc.subject.other | Article | |
| dc.subject.other | bacterial strain | |
| dc.subject.other | bacterium isolate | |
| dc.subject.other | cancer cell | |
| dc.subject.other | cancer inhibition | |
| dc.subject.other | cancer therapy | |
| dc.subject.other | cell growth | |
| dc.subject.other | cell viability | |
| dc.subject.other | controlled study | |
| dc.subject.other | cytotoxicity | |
| dc.subject.other | enzyme activity | |
| dc.subject.other | human | |
| dc.subject.other | human cell | |
| dc.subject.other | incubation time | |
| dc.subject.other | major clinical study | |
| dc.subject.other | nonhuman | |
| dc.subject.other | scanning electron microscopy | |
| dc.subject.other | biofilm | |
| dc.subject.other | Fourier transform infrared spectroscopy | |
| dc.subject.other | microbial sensitivity test | |
| dc.subject.other | Silver nanoparticles | |
| dc.title | Determination of the Cytotoxicity and Antibiofilm Potential Effect of Equisetum arvense Silver Nanoparticles | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.openalex | 7 | |
| rdl.citation.scopus | 10 | |
| rdl.citation.wos | 9 | |
| rdl.department | Department of Genetics and Bioengineering, Faculty of Engineering and Natural Sciences, Gumushane University, 29100, Gümüşhane, Turkey | |
| rdl.oa.status | green | |
| rdl.oa.status | preprint | |
| rdl.oa.url | https://hdl.handle.net/20.500.12868/5571 | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |

