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author Vijayakumar, Sekar
González-Sánchez, Zaira I
Amanullah, Mohammed
Sonamuthu, Jegatheeswaran
Rajkumar, Mangaiyarkarasi
Divya, Mani
Durán-Lara, Esteban F
Li, Mingchun
author_facet Vijayakumar, Sekar
González-Sánchez, Zaira I
Amanullah, Mohammed
Sonamuthu, Jegatheeswaran
Rajkumar, Mangaiyarkarasi
Divya, Mani
Durán-Lara, Esteban F
Li, Mingchun
Vijayakumar, Sekar
González-Sánchez, Zaira I
Amanullah, Mohammed
Sonamuthu, Jegatheeswaran
Rajkumar, Mangaiyarkarasi
Divya, Mani
Durán-Lara, Esteban F
Li, Mingchun
collection PubMed - marine biology
contents Shark chondroitin sulfate gold nanoparticles: A biocompatible apoptotic agent for osteosarcoma. Vijayakumar, Sekar González-Sánchez, Zaira I Amanullah, Mohammed Sonamuthu, Jegatheeswaran Rajkumar, Mangaiyarkarasi Divya, Mani Durán-Lara, Esteban F Li, Mingchun Chondroitin Sulfates Gold Animals Osteosarcoma Apoptosis Humans Sharks Metal Nanoparticles Mice Cell Line, Tumor Biocompatible Materials Reactive Oxygen Species Membrane Potential, Mitochondrial NIH 3T3 Cells Antineoplastic Agents Cell Survival Mitochondria Bone Neoplasms Osteosarcoma is a highly aggressive tumor that originates in the bone and often infiltrates nearby bone cells. It is the most prevalent type of primary bone cancer among the various bone malignancies. Traditional cancer treatment methods such as surgery, chemotherapy, immunotherapy, and radiotherapy have had restricted success. However, the integration of nanotechnology into cancer research has led to notable progress. One promising area is the use of marine-derived polysaccharide-based nano formulations for treating various human diseases, including cancer. This study presents a straightforward method for synthesizing biocompatible gold nanoparticles (AuNPs), utilizing sodium borohydride as a reducing agent and a cost-effective, water-soluble chondroitin sulfate (CS) derived from shark cartilage as a stabilizing agent. The synthesized CS-Au NPs appeared purple and were mainly spherical, with 40.768 nm of average size. Cytotoxicity assays (MTT) indicated that CS-Au NPs significantly reduced the viability of human osteosarcoma cells (MG63) at 100 μg/mL, while it showed no cytotoxic effects on mouse embryonic fibroblast cells (NIH3T3) at the same concentration. The observed toxicity of the CS-Au NPs was linked to a rise in the production of reactive oxygen species (ROS) within damaged mitochondria. ROS generation and changes in mitochondrial membrane potential were detected in MG63 cells treated with CS-Au NPs. Furthermore, apoptotic analysis through ethidium bromide dual staining and flow cytometry demonstrated that CS-Au NPs at higher concentrations significantly increased the amount of apoptotic cells, as demonstrated by acridine orange/ethidium bromide staining. Flow cytometry also confirmed that CS-Au NPs activated the apoptotic pathway in MG63 cells.
format Artículo científico
id pubmed_39689798
institution PubMed
language en
publishDate 2025
publisher International journal of biological macromolecules
record_format pubmed
spellingShingle Shark chondroitin sulfate gold nanoparticles: A biocompatible apoptotic agent for osteosarcoma.
Vijayakumar, Sekar
González-Sánchez, Zaira I
Amanullah, Mohammed
Sonamuthu, Jegatheeswaran
Rajkumar, Mangaiyarkarasi
Divya, Mani
Durán-Lara, Esteban F
Li, Mingchun
Chondroitin Sulfates
Gold
Animals
Osteosarcoma
Apoptosis
Humans
Sharks
Metal Nanoparticles
Mice
Cell Line, Tumor
Biocompatible Materials
Reactive Oxygen Species
Membrane Potential, Mitochondrial
NIH 3T3 Cells
Antineoplastic Agents
Cell Survival
Mitochondria
Bone Neoplasms
Shark chondroitin sulfate gold nanoparticles: A biocompatible apoptotic agent for osteosarcoma. Vijayakumar, Sekar González-Sánchez, Zaira I Amanullah, Mohammed Sonamuthu, Jegatheeswaran Rajkumar, Mangaiyarkarasi Divya, Mani Durán-Lara, Esteban F Li, Mingchun Chondroitin Sulfates Gold Animals Osteosarcoma Apoptosis Humans Sharks Metal Nanoparticles Mice Cell Line, Tumor Biocompatible Materials Reactive Oxygen Species Membrane Potential, Mitochondrial NIH 3T3 Cells Antineoplastic Agents Cell Survival Mitochondria Bone Neoplasms Osteosarcoma is a highly aggressive tumor that originates in the bone and often infiltrates nearby bone cells. It is the most prevalent type of primary bone cancer among the various bone malignancies. Traditional cancer treatment methods such as surgery, chemotherapy, immunotherapy, and radiotherapy have had restricted success. However, the integration of nanotechnology into cancer research has led to notable progress. One promising area is the use of marine-derived polysaccharide-based nano formulations for treating various human diseases, including cancer. This study presents a straightforward method for synthesizing biocompatible gold nanoparticles (AuNPs), utilizing sodium borohydride as a reducing agent and a cost-effective, water-soluble chondroitin sulfate (CS) derived from shark cartilage as a stabilizing agent. The synthesized CS-Au NPs appeared purple and were mainly spherical, with 40.768 nm of average size. Cytotoxicity assays (MTT) indicated that CS-Au NPs significantly reduced the viability of human osteosarcoma cells (MG63) at 100 μg/mL, while it showed no cytotoxic effects on mouse embryonic fibroblast cells (NIH3T3) at the same concentration. The observed toxicity of the CS-Au NPs was linked to a rise in the production of reactive oxygen species (ROS) within damaged mitochondria. ROS generation and changes in mitochondrial membrane potential were detected in MG63 cells treated with CS-Au NPs. Furthermore, apoptotic analysis through ethidium bromide dual staining and flow cytometry demonstrated that CS-Au NPs at higher concentrations significantly increased the amount of apoptotic cells, as demonstrated by acridine orange/ethidium bromide staining. Flow cytometry also confirmed that CS-Au NPs activated the apoptotic pathway in MG63 cells.
title Shark chondroitin sulfate gold nanoparticles: A biocompatible apoptotic agent for osteosarcoma.
topic Chondroitin Sulfates
Gold
Animals
Osteosarcoma
Apoptosis
Humans
Sharks
Metal Nanoparticles
Mice
Cell Line, Tumor
Biocompatible Materials
Reactive Oxygen Species
Membrane Potential, Mitochondrial
NIH 3T3 Cells
Antineoplastic Agents
Cell Survival
Mitochondria
Bone Neoplasms
url https://pubmed.ncbi.nlm.nih.gov/39689798/