We studied the size dependent toxicity of TiO₂ nanoparticles (TiO₂ NPs; 5-50 nm) of the anatase and rutile crystalline phases (including the mixture of anatase and rutile) against the model organism . All the TiO₂ NPs were characterized and their photocatalytic inactivation of was studied under the solar simulated light irradiation and dark conditions. In addition, the mechanism of toxicity was studied by measurement of reactive oxygen species (ROS), an indicator of oxidative stress. Rutile TiO₂ NPs (TiO₂-R-30 nm) of 30 nm showed the highest photocatalytic activity against (LC of 14.11 mg/L), followed by rutile TiO₂ NPs (TiO₂-R-50 nm) (LC of 35.96 mg/L). The anatase and rutile mixture of 20 nm size produced LC of 17.12 and 27.26 mg/L for A80%-R20% and A20%-R80% respectively, whereas none of the anatase TiO₂ NPs with various sizes (5 nm, 15 nm and 30 nm) showed any toxicity against . The results indicate that the rutile had higher photocatalytic activity than anatase and the toxicity is size dependent, while the mixture of anatase and rutile had the median toxicity. Hydroxyl radical formation is the major ROS causing oxidative stress in , the primary mechanism of toxicity.

Download full-text PDF

Source
http://dx.doi.org/10.1166/jnn.2019.16757DOI Listing

Publication Analysis

Top Keywords

tio₂ nps
20
anatase rutile
16
tio₂ nanoparticles
8
photocatalytic inactivation
8
inactivation studied
8
size dependent
8
mixture anatase
8
mechanism toxicity
8
oxidative stress
8
rutile tio₂
8

Similar Publications

Biomedical Application Prospects of Gadolinium Oxide Nanoparticles for Regenerative Medicine.

Pharmaceutics

December 2024

Department of Hospital Surgery, Department of Plastic and Reconstructive Surgery, Cosmetology and Cell Technology, Pirogov Russian National Research Medical University (RNRMU), 117997 Moscow, Russia.

Background/objectives: The aim was to study the possibilities of biomedical application of gadolinium oxide nanoparticles (GdO NPs) synthesized under industrial conditions, and evaluate their physicochemical properties, redox activity, biological activity, and safety using different human cell lines.

Methods: The powder of GdO NPs was obtained by a process of thermal decomposition of gadolinium carbonate precipitated from nitrate solution, and was studied using transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, mass spectrometry, and scanning electron microscopy (SEM) with energy dispersive X-ray analyzer (EDX). The redox activity of different concentrations of GdO NPs was studied by the optical spectroscopy (OS) method in the photochemical degradation process of methylene blue dye upon irradiation with an optical source.

View Article and Find Full Text PDF

To design a multifunctional nanozyme hydrogel with antibacterial, photo-responsive nitric oxide-releasing, and antioxidative properties for promoting the healing of infected wounds. We first developed ultra-small silver nanoparticles (NPs)-decorated sodium nitroprusside-doped Prussian blue (SNPB) NPs, referred to as SNPB@Ag NPs, which served as a multifunctional nanozyme. Subsequently, this nanozyme, together with geniposide (GE), was incorporated into a thermo-sensitive hydrogel, formulated from Poloxamer 407 and carboxymethyl chitosan, creating a novel antibacterial wound dressing designated as GE/SNPB@Ag hydrogel.

View Article and Find Full Text PDF

Prussian blue nanoparticles (PBNPs) have gained significant attraction in the field of nanomedicine due to their excellent biocompatibility, potential for nanoscale production, exceptional photothermal conversion ability, and multi-enzyme mimicking capabilities. PBNPs have made considerable advancements in their application to biomedical fields. This review embarks with a comprehensive understanding of the physicochemical properties and chemical profiling of PB-based nanoparticles, discussing systematic approaches to tune their dimensions, shapes, and sizes, as well as their biomedical properties.

View Article and Find Full Text PDF

Building of CuO@Cu-TA@DSF/DHA Nanoparticle Targets MAPK Pathway to Achieve Synergetic Chemotherapy and Chemodynamic for Pancreatic Cancer Cells.

Pharmaceutics

December 2024

Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, College of Pharmacy, Shihezi University, Shihezi 832003, China.

With the increase of reactive oxygen species (ROS) production, cancer cells can avoid cell death and damage by up-regulating antioxidant programs. Therefore, it will be more effective to induce cell death by using targeted strategies to further improve ROS levels and drugs that inhibit antioxidant programs. Considering that dihydroartemisinin (DHA) can cause oxidative damage to protein, DNA, or lipids by producing excessive ROS, while, disulfiram (DSF) can inhibit glutathione (GSH) levels and achieve the therapeutic effect by inhibiting antioxidant system and amplifying oxidative stress, they were co-loaded onto the copper peroxide nanoparticles (CuO) coated with copper tannic acid (Cu-TA), to build a drug delivery system of CuO@Cu-TA@DSF/DHA nanoparticles (CCTDD NPs).

View Article and Find Full Text PDF

Glucagon-like peptide-1 (GLP-1) receptor is currently one of the most explored targets exploited for the management of diabetes and obesity, with many aspects of its mechanisms behind cardiovascular protection yet to be fully elucidated. Research dedicated towards the development of oral GLP-1 therapy and non-peptide ligands with broader clinical applications is crucial towards unveiling the full therapeutic capacity of this potent class of medicines. This study describes the virtual screening of a natural product database consisting of 695,133 compounds for positive GLP-1 allosteric modulation.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!