Biosynthesis of β-D-glucan‑gold nanoparticles, cytotoxicity and oxidative stress in mouse splenocytes
Article
-
- Overview
-
- Research
-
- Identity
-
- Additional Document Info
-
- View All
-
Overview
abstract
-
This study reports biosynthesis of gold-nanoparticles (AuNPs) by using β-D-glucans isolated from the yeast Yarrowia lypolitica D1. β-D-glucans serve as reducing and stabilizing mediators that induce the formation of AuNPs on the outer surface of the own β-D-glucan. The systems were physicochemically characterized by ultraviolet visible (UV–Vis) spectroscopy, high-resolution transmission electron microscopy (HR-TEM), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), and dynamic light scattering (DLS) analyses. The results revealed the generation of AuNPs with quasi-spherical shape or large one dimension (1D) gold-nanostructures (AuNSs) depending on the HAuCl4 concentration. A cytotoxic study was assessed in mouse splenocytes. Contrary to that expected, important cytotoxicity was found in all β-D-gluc AuNPs systems by an oxidative stress increase. This study discusses the cytotoxic mechanism, suggesting that the resulting β-D-gluc AuNPs systems may not be candidates for the formulation of immunostimulants or nanocarriers for biomedical applications. © 2019 Elsevier B.V.
-
This study reports biosynthesis of gold-nanoparticles (AuNPs) by using β-D-glucans isolated from the yeast Yarrowia lypolitica D1. β-D-glucans serve as reducing and stabilizing mediators that induce the formation of AuNPs on the outer surface of the own β-D-glucan. The systems were physicochemically characterized by ultraviolet visible (UV–Vis) spectroscopy, high-resolution transmission electron microscopy (HR-TEM), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), and dynamic light scattering (DLS) analyses. The results revealed the generation of AuNPs with quasi-spherical shape or large one dimension (1D) gold-nanostructures (AuNSs) depending on the HAuCl4 concentration. A cytotoxic study was assessed in mouse splenocytes. Contrary to that expected, important cytotoxicity was found in all β-D-gluc%2bAuNPs systems by an oxidative stress increase. This study discusses the cytotoxic mechanism, suggesting that the resulting β-D-gluc%2bAuNPs systems may not be candidates for the formulation of immunostimulants or nanocarriers for biomedical applications. © 2019 Elsevier B.V.
publication date
funding provided via
published in
Research
keywords
-
Delivery vehicles; Green biosynthesis; Immune system; Mouse splenocytes; Toxicity beta 1,3 glucan; catalase; chemical compound; chloroauric acid; dectin 1; gold nanoparticle; immunoglobulin enhancer binding protein; interleukin 1beta; nitric oxide; peroxidase; superoxide dismutase; tumor necrosis factor; unclassified drug; antioxidant; biological marker; catalase; cytokine; glucan; gold; metal nanoparticle; nitric oxide; adult; animal cell; Article; biosynthesis; concentration (parameter); controlled study; cytotoxicity; green biosynthesis; green chemistry; infant; male; mouse; nanotoxicology; nonhuman; oxidative stress; physical chemistry; spleen cell; surface property; Yarrowia lipolytica; animal; cell survival; chemistry; cytology; gene expression; genetics; green chemistry; immunology; leukocyte; metabolism; phagocytosis; physiology; respiratory burst; spleen; ultrastructure; Animals; Antioxidants; Biomarkers; Catalase; Cell Survival; Cytokines; Cytotoxicity, Immunologic; Gene Expression; Glucans; Gold; Green Chemistry Technology; Leukocytes; Male; Metal Nanoparticles; Mice; Nitric Oxide; Oxidative Stress; Phagocytosis; Respiratory Burst; Spleen
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume