Isidro D Obregon, Brandi S Betts-Obregon, Brian Yust, Francisco Pedraza, Alexandra Ortiz, Dhiraj Sardar, Andrew T Tsin
{"title":"Effect of Silver Coating on Barium Titanium Oxide Nanoparticle Toxicity.","authors":"Isidro D Obregon, Brandi S Betts-Obregon, Brian Yust, Francisco Pedraza, Alexandra Ortiz, Dhiraj Sardar, Andrew T Tsin","doi":"10.4028/www.scientific.net/AMR.787.404","DOIUrl":null,"url":null,"abstract":"<p><p>Nanoparticles are presently being studied for optical and biomedical applications such as medical imaging and drug delivery. Nanoparticles impact the cellular environment due to many variables such as size, shape, and composition. How these factors affect cell viability is not fully understood. The purpose of this study is to test the toxicity effects of silver coating (Ag@) Barium Titanium Oxide (BaTiO<sub>3</sub>) nanoparticles on Rhesus Monkey Retinal Endothelial cells (RhREC's) in culture. The addition of silver to the nanoparticles increases their nonlinear optical properties significantly, making the Ag@BaTiO<sub>3</sub> nanoparticles good candidates for nonlinear microscopy contrast agents. We hypothesize that by silver coating nanoparticles, there will be an increase in cell viability at higher concentrations when compared to non-silver coated nanoparticles. RhREC's were treated with BaTiO<sub>3</sub> and Ag@BaTiO<sub>3</sub> at concentrations of 0, 1.0, 10.0, and 100µg/ml for 24 hours at 37°C + 5%CO<sub>2</sub>. After 24 hour incubation with respective nanoparticles, cell viability was determined using the trypan blue dye-exclusion method. Treatment with 0, 1.0 and 10.0µg/ml of Ag@BaTiO<sub>3</sub> had minimal effect on cell viability, with 90% viable cells remaining at the end of the 24 hours treatment period. However, cells treated with 100µg/ml of Ag@BaTiO<sub>3</sub> resulted in a decrease to 51% viable cells. Comparatively, cells treated with 0, 1.0 and 10µg/ml of BaTiO<sub>3</sub> had no significant effect on cell viability (90% viable cells after treatment) while the 100µg/ml treatment resulted in a decrease to 29% viable cells. These results show that silver coating of BaTiO<sub>3</sub> nanoparticles has a protective effect on cellular toxicity at high concentrations.</p>","PeriodicalId":7271,"journal":{"name":"Advanced Materials Research","volume":"787 ","pages":"404-407"},"PeriodicalIF":0.0000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4028/www.scientific.net/AMR.787.404","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4028/www.scientific.net/AMR.787.404","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Nanoparticles are presently being studied for optical and biomedical applications such as medical imaging and drug delivery. Nanoparticles impact the cellular environment due to many variables such as size, shape, and composition. How these factors affect cell viability is not fully understood. The purpose of this study is to test the toxicity effects of silver coating (Ag@) Barium Titanium Oxide (BaTiO3) nanoparticles on Rhesus Monkey Retinal Endothelial cells (RhREC's) in culture. The addition of silver to the nanoparticles increases their nonlinear optical properties significantly, making the Ag@BaTiO3 nanoparticles good candidates for nonlinear microscopy contrast agents. We hypothesize that by silver coating nanoparticles, there will be an increase in cell viability at higher concentrations when compared to non-silver coated nanoparticles. RhREC's were treated with BaTiO3 and Ag@BaTiO3 at concentrations of 0, 1.0, 10.0, and 100µg/ml for 24 hours at 37°C + 5%CO2. After 24 hour incubation with respective nanoparticles, cell viability was determined using the trypan blue dye-exclusion method. Treatment with 0, 1.0 and 10.0µg/ml of Ag@BaTiO3 had minimal effect on cell viability, with 90% viable cells remaining at the end of the 24 hours treatment period. However, cells treated with 100µg/ml of Ag@BaTiO3 resulted in a decrease to 51% viable cells. Comparatively, cells treated with 0, 1.0 and 10µg/ml of BaTiO3 had no significant effect on cell viability (90% viable cells after treatment) while the 100µg/ml treatment resulted in a decrease to 29% viable cells. These results show that silver coating of BaTiO3 nanoparticles has a protective effect on cellular toxicity at high concentrations.