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December 9, 2025BMC Plant Biology10 citationsOpen Access

Green-synthesized silver nanoparticles from Camellia sinensis: mechanistic insights into phenolic-mediated multifunctional biological activities

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ADAdem Demi̇r

Key Points

  • This research aims to explore the biological activities and mechanisms of silver nanoparticles synthesized from Camellia sinensis using green chemistry.
  • Characterization of phenolic compounds in Camellia sinensis using HPLC-DAD.
  • Synthesis of silver nanoparticles using C. sinensis extracts.
  • Characterization of nanoparticles by UV-Vis, FTIR, XRD, SEM, EDX, and DLS.
  • Assessment of biological activities through antioxidant, antibacterial, anti-inflammatory, and enzyme inhibitory assays.
  • Molecular docking analysis to evaluate binding affinity of phenolic compounds with target enzymes.
  • EGCG was identified as the primary phenolic compound, measured at 54.8 ± 2.8 mg/g.
  • CS-AgNPs showed strong antioxidant activity with an IC50 of 28.78 µg/mL for DPPH.
  • Anti-inflammatory activity of CS-AgNPs demonstrated an IC50 of 66.78 µg/mL.
  • CS-AgNPs displayed significant antibacterial effects with inhibition zones of 16.78–25.31 mm.
  • Molecular docking revealed strong binding affinities of EGCG with enzymes at −12.386 and −10.129 kcal/mol.

Abstract

Abstract Background Green synthesis of silver nanoparticles (AgNPs) using plant extracts provides an eco-friendly route that bridges phytochemistry with nanobiotechnology. Camellia sinensis , rich in polyphenols, serves as an effective reducing and stabilizing agent in this process.Ethanolic extracts of C. sinensis leaves were characterized for phenolic composition by HPLC-DAD and utilized for AgNP synthesis (CS-AgNPs). The nanoparticles were characterized by UV-Vis, FTIR, XRD, SEM, EDX, and DLS. Biological properties were assessed through antioxidant (DPPH, ABTS), antibacterial (Gram-positive and Gram-negative strains), anti-inflammatory (BSA denaturation), and enzyme inhibitory (urease, α-glucosidase) assays, supported by molecular docking. Results EGCG was the dominant phenolic compound (54.8 ± 2.8 mg/g). CS-AgNPs displayed strong antioxidant (IC 50 : 28.78 µg/mL for DPPH), anti-inflammatory (IC 50 : 66.78 µg/mL), antibacterial (16.78–25.31 mm inhibition zones), and enzyme inhibitory activities (urease IC 50 : 20.6 µg/mL; α-glucosidase IC 50 : 140.9 µg/mL). Docking analysis confirmed the strong binding affinity of EGCG with target enzymes (−12.386 and −10.129 kcal/mol). Conclusions This study highlights the dual role of C. sinensis phenolics in nanoparticle formation and bioactivity modulation, offering mechanistic insight into phenolic–metal interactions. Future work will focus on cytotoxicity and in vivo evaluations to validate the biomedical potential of CS-AgNPs.

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Adem Demi̇r (2025) studied this question.

synapsesocial.com/papers/69401efa2d562116f28f9931https://doi.org/10.1186/s12870-025-07881-0
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