TY - JOUR
T1 - Chitosan-coated silver nanoparticles synthesized using Moringa oleifera flower extract
T2 - A potential therapeutic approach against triple-negative breast cancer
AU - Anitha, Jaganathan
AU - Muthusankar, Aathi
AU - Sangeetha, Meenakshisundram
AU - Kishore, V. Lokesh
AU - Sherin, Pulikottil Joy
AU - Selvakumar, Rajendran
AU - Chandraprakash, Kumarasamy
AU - Premkumar, Thathan
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/8
Y1 - 2025/8
N2 - Optimizing nanoparticle (NP) synthesis from biological sources for effective anticancer activity remains a challenge in treating triple-negative breast cancer (TNBC) because of the lack of receptors. This study investigates the use of Moringa oleifera (M. oleifera) flower extract to synthesize chitosan (Ch)-coated silver (Ag) nanoparticles (F-Ch-AgNPs) and assesses their efficacy against TNBC cells (MDA-MB-231) in vitro. Gas chromatography–mass spectrometry revealed 31 key components in the extract. Biophysical analysis confirmed the optical properties, with UV–visible spectroscopy showing absorption peaks at 420 nm (F-AgNPs) and 298 nm (F-Ch-AgNPs), respectively. X-ray diffraction confirmed a face-centered cubic (fcc) structure while transmission electron microscopy (TEM) revealed spherical NPs (12–14 nm) with low polydispersity. The F-Ch-AgNPs had a half-maximal inhibitory concentration (IC50) of 27 ± 0.5 μg/mL in a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, causing TNBC cell damage, including shrinkage and rupture, as observed under bright-field microscopy. Fluorescent staining revealed apoptosis with chromatin condensation and nuclear fragmentation. Molecular docking revealed 2,4-pentadienoic acid and 1-cyclopenten-3-on-1-yl ester as potential mammalian target of rapamycin (mTOR) inhibitors. This study highlights the potential of M. oleifera flower extract in nanometal synthesis, as well as the therapeutic relevance of F-Ch-AgNPs in breast cancer research.
AB - Optimizing nanoparticle (NP) synthesis from biological sources for effective anticancer activity remains a challenge in treating triple-negative breast cancer (TNBC) because of the lack of receptors. This study investigates the use of Moringa oleifera (M. oleifera) flower extract to synthesize chitosan (Ch)-coated silver (Ag) nanoparticles (F-Ch-AgNPs) and assesses their efficacy against TNBC cells (MDA-MB-231) in vitro. Gas chromatography–mass spectrometry revealed 31 key components in the extract. Biophysical analysis confirmed the optical properties, with UV–visible spectroscopy showing absorption peaks at 420 nm (F-AgNPs) and 298 nm (F-Ch-AgNPs), respectively. X-ray diffraction confirmed a face-centered cubic (fcc) structure while transmission electron microscopy (TEM) revealed spherical NPs (12–14 nm) with low polydispersity. The F-Ch-AgNPs had a half-maximal inhibitory concentration (IC50) of 27 ± 0.5 μg/mL in a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, causing TNBC cell damage, including shrinkage and rupture, as observed under bright-field microscopy. Fluorescent staining revealed apoptosis with chromatin condensation and nuclear fragmentation. Molecular docking revealed 2,4-pentadienoic acid and 1-cyclopenten-3-on-1-yl ester as potential mammalian target of rapamycin (mTOR) inhibitors. This study highlights the potential of M. oleifera flower extract in nanometal synthesis, as well as the therapeutic relevance of F-Ch-AgNPs in breast cancer research.
KW - Anticancer activity
KW - Chitosan
KW - Molecular docking
KW - Moringa oleifera
KW - Silver nanoparticles
KW - Triple-negative breast cancer
UR - https://www.scopus.com/pages/publications/105010943991
U2 - 10.1016/j.ijbiomac.2025.145995
DO - 10.1016/j.ijbiomac.2025.145995
M3 - Article
C2 - 40669649
AN - SCOPUS:105010943991
SN - 0141-8130
VL - 320
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 145995
ER -