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.2019.16757 | DOI Listing |
Int J Nanomedicine
December 2024
State Key Laboratory of Ophthalmology, Optometry and Visual Science, National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, People's Republic of China.
Background: Developing carrier-free nanomedicines via self-assembly of two antitumor drug molecules is a potential strategy for enhancing the combination treatment of tumors. Similarly, conventional chemotherapy combined with photodynamic therapy may synergistically improve the antitumor effect while minimizing the adverse reactions associated with antitumor treatment. Hyaluronic acid (HA) can bind to overexpressed HA receptors on the tumor cell surface, increasing cell internalization and resulting in good tumor-targeting properties.
View Article and Find Full Text PDFBeilstein J Nanotechnol
December 2024
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Science, Lavrent'ev av., 8, Novosibirsk, 630090, Russian Federation.
A protein corona is present on any nanoparticle (NP) entering biological fluids; however, the existence of a natural protein corona on natural NPs has not been experimentally confirmed. We used our previously developed photomodification method to fix the natural corona on "biological nanoparticles" (bio-NPs) in fetal bovine serum and newborn bovine serum; native sera served as a control. To isolate photomodified bio-NPs, we used ultracentrifugation (UC), sucrose gradient (12%, 30%, and 50%), and sucrose cushion (30%) methods.
View Article and Find Full Text PDFFront Immunol
December 2024
State Key Laboratory for Animal Disease Control and Prevention & Lanzhou Center for Tuberculosis Research, Institute of Pathogen Biology, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China.
Introduction: Vaccines against intracellular pathogens like require the induction of effective cell-mediated immunity. Adjuvants primarily enhance antigen-induced adaptive immunity by promoting the activation of antigen-presenting cells (APCs).This study is to develop an adjuvant targeted to dendritic cells (DCs), one of the main APCs, so as to assist in inducing a long-term cellular immune response to protein antigens.
View Article and Find Full Text PDFACS Appl Bio Mater
January 2025
Institute of Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario M5S 3E2, Canada.
Contemporary therapies following heart failure center on regenerative approaches to account for the loss of cardiomyocytes and limited regenerative capacity of the adult heart. While the delivery of cardiac progenitor cells has been shown to improve cardiac function and repair following injury, recent evidence has suggested that their paracrine effects (or secretome) provides a significant contribution towards modulating regeneration, rather than the progenitor cells intrinsically. The direct delivery of secretory biomolecules, however, remains a challenge due to their lack of stability and tissue retention, limiting their prolonged therapeutic efficacy.
View Article and Find Full Text PDFBMC Biotechnol
January 2025
Department of Microbiology and Immunology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, 62511, Egypt.
Background: Successful treatment of pathogenic bacteria like Enterobacter Cloacae with bacteriophage (phage) counteract some hindrance such as phage stability and immunological clearance. Our research is focused on the encapsulation of phage HK6 within chitosan nanoparticles.
Result: Encapsulation significantly improves stability, efficacy, and delivery of phages.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!