Emerging Antineoplastic Plant-Based Gold Nanoparticle Synthesis: A Mechanistic Exploration of their Anticancer Activity Toward Cervical Cancer Cells

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TitreEmerging Antineoplastic Plant-Based Gold Nanoparticle Synthesis: A Mechanistic Exploration of their Anticancer Activity Toward Cervical Cancer Cells
Type de publicationJournal Article
Year of Publication2020
AuteursKhatua A, Prasad A, Priyadarshini E, Patel AKumar, Naik A, Saravanan M, Barabadi H, Ghosh L, Paul B, Paulraj R, Meena R
JournalJOURNAL OF CLUSTER SCIENCE
Volume31
Pagination1329-1340
Date PublishedNOV
Type of ArticleArticle
ISSN1040-7278
Mots-clésAnticancer activity, Cell cycle analysis, gold nanoparticles, Green synthesis, Mitochondrial membrane potential, Reactive oxygen species
Résumé

In this work, gold nanoparticles (AuNPs) were synthesised using the fresh leaves extract ofPongamia pinnata(PLE) and characterized using various analytical techniques such as UV-visible spectroscopy, TEM, SEM, EDX, and XRD. UV-Visible spectra showed surface plasmon resonance (SPR) peaks in the range of 520-540 nm signifying the synthesis of colloidal AuNPs stabilised by PLE. Further, we investigated the cytotoxic effects of AuNPs against human cervical cancer cell line (HeLa). MTT assay screened IC(50)value of 200 mu g/mL at 24 h for AuNPs formed at varying HAuCl(4)concentration. Flow cytometry measurements using H(2)DCFDA showed that the toxicity of AuNPs was attributed to the generation of reactive oxygen species (ROS). Besides, the in vitro anticancer activities of AuNPs were studied in HeLa cells by several assays which resulted in altered cell morphology, reduced potential of wound healing, inactive mitochondria due to loss of mitochondrial membrane potential (MMP) and cell cycle arrest. AuNPs showed dose-dependent selective toxicity towards HeLa cells and were non-toxic against human embryonic kidney cell line (HEK293). The study revealed an efficient, ecofriendly and simple method for synthesis of multifunctional AuNPs using green synthetic approach with high anticancer potential for cervical cancer cell line.

DOI10.1007/s10876-019-01742-1, Early Access Date = {DEC 2019