scholarly journals A Method to Assess the Relevance of Nanomaterial Dissolution during Reactivity Testing

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2235 ◽  
Author(s):  
Willie J. G. M. Peijnenburg ◽  
Emmanuel Ruggiero ◽  
Matthew Boyles ◽  
Fiona Murphy ◽  
Vicki Stone ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Incubation Time ◽  
Epr Spectroscopy ◽  
Particle Concentration ◽  
Dose Range ◽  
Potential Hazard ◽  
Paramagnetic Resonance ◽  
Particle Ratios ◽  
Concentration Of Ions ◽  
Electron Paramagnetic

The reactivity of particle surfaces can be used as a criterion to group nanoforms (NFs) based on similar potential hazard. Since NFs may partially or completely dissolve over the duration of the assays, with the ions themselves inducing a response, reactivity assays commonly measure the additive reactivity of the particles and ions combined. Here, we determine the concentration of ions released over the course of particle testing, and determine the relative contributions of the released ions to the total reactivity measured. We differentiate three classes of reactivity, defined as being (A) dominated by particles, (B) additive of particles and ions, or (C) dominated by ions. We provide examples for each class by analyzing the NF reactivity of Fe2O3, ZnO, CuO, Ag using the ferric reduction ability of serum (FRAS) assay. Furthermore, another two reactivity tests were performed: Dichlorodihydrofluorescin diacetate (DCFH2-DA) assay and electron paramagnetic resonance (EPR) spectroscopy. We compare assays and demonstrate that the dose-response may be almost entirely assigned to ions in one assay (CuO in DCFH2-DA), but to particles in others (CuO in EPR and FRAS). When considering this data, we conclude that one cannot specify the contribution of ions to NF toxicity for a certain NF, but only for a certain NF in a specific assay, medium and dose. The extent of dissolution depends on the buffer used, particle concentration applied, and duration of exposure. This culminates in the DCFH2-DA, EPR, FRAS assays being performed under different ion-to-particle ratios, and differing in their sensitivity towards reactions induced by either ions or particles. If applied for grouping, read-across, or other concepts based on the similarity of partially soluble NFs, results on reactivity should only be compared if measured by the same assay, incubation time, and dose range.

Investigation of Antioxidant Activity of Pomegranate Juices by Means of Electron Paramagnetic Resonance and UV-Vis Spectroscopy

2015 ◽  
Vol 98 (4) ◽  
pp. 866-870 ◽  
Author(s):  
Violetta Kozik ◽  
Krystyna Jarzembek ◽  
Agnieszka Jędrzejowska ◽  
Andrzej Bąk ◽  
Justyna Polak ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Free Radical ◽  
Epr Spectroscopy ◽  
Antioxidant Properties ◽  
Free Radical Scavenger ◽  
Pomegranate Juice ◽  
Radical Scavenger ◽  
Paramagnetic Resonance ◽  
Vis Spectroscopy ◽  
Electron Paramagnetic

Abstract Pomegranate fruit (Punica granatum L.) is a source of numerous phenolic compounds, and it contains flavonoids such as anthocyanins, anthocyanidins, cyanidins, catechins and other complexes of flavonoids, ellagitannins, and hydrolyzed tannins. Pomegranate juice shows antioxidant, antiproliferative, and anti-atherosclerotic properties. The antioxidant capacity (TEAC) of the pomegranate juices was measured using electron paramagnetic resonance (EPR) spectroscopy and 1,1-diphenyl-2-picrylhydrazyl (DPPH•) as a source of free radicals, and the total phenolic (TP) content was measured using UV-Vis spectroscopy. All the examined pomegranate juices exhibited relatively high antioxidant properties. The TEAC values determined by means of EPR spectroscopy using Trolox (TE) as a free radical scavenger were in the range of 463.12 to 1911.91 μmol TE/100 mL juice. The TP content measured by the Folin-Ciocalteu method, using gallic acid (GA) as a free radical scavenger, widely varied in the investigated pomegranate juice samples and ranged from 1673.62 to 5263.87 mg GA/1 L juice. The strongest antioxidant properties were observed with the fresh pomegranate juices obtained from the fruits originating from Israel, Lebanon, and Azerbaijan. Correlation analysis of numerical data obtained by means of EPR spectroscopy (TEAC) and UV-Vis spectroscopy (TP) gave correlation coefficient (r) = 0.90 and determination coefficient (r2) = 0.81 (P <0.05).

scholarly journals Chain initiation

2019 ◽  
Vol 89 (2) ◽  
pp. 179-186
Author(s):  
V. V. Ptushenko
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Epr Spectroscopy ◽  
Paramagnetic Resonance ◽  
Chain Initiation ◽  
Radio Spectroscopy ◽  
Scientific Instrumentation ◽  
History Of ◽  
Scientists And Engineers ◽  
Electron Paramagnetic

This article describes the formation of the chemical electron paramagnetic resonance (EPR) spectroscopy institute established by Academician Vladislav V. Voevodsky (1917–1967) along with the history of the development of the instrumentation basis for this field of science in the Union of Soviet Socialist Republics (USSR). The design of the first EPR spectrometers for the chemical radio spectroscopy initiated the emergence of a new scientific instrumentation field in this country. Based on recollections shared by scientists and engineers and an examination of archive materials, the author reconstructs relevant events and identifies major participants in this process.

A Study of V3+/4+ Levels in Semi-insulating 6H-SiC using Optical Admittance and Electron Paramagnetic Resonance Spectroscopies

2006 ◽  
Vol 911 ◽  
Author(s):  
Wonwoo Lee ◽  
Mary E Zvanut
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Charge State ◽  
Conduction Band ◽  
Epr Spectroscopy ◽  
Admittance Spectroscopy ◽  
Paramagnetic Resonance ◽  
Characteristic Spectrum ◽  
Epr Measurements ◽  
The Individual ◽  
Electron Paramagnetic

AbstractThe purpose of this study is to identify the vanadium acceptor levels in semi-insulating (SI) 6H-SiC using optical admittance spectroscopy (OAS) and electron paramagnetic resonance (EPR) spectroscopy. OAS conductance peaks near at 0.67 ± 0.02 eV and 0.70 ± 0.02 eV are identified as V3+/4+ levels at the quasi-cubic sites. An OAS peak at 0.87 eV is assigned to the same transition at the hexagonal site. EPR measurements before illumination revealed the characteristic spectrum of V3+. The presence of the V3+ signal supports the identification of the OAS peaks as transitions from the V3+/4+ level to the conduction band. Photo-induced EPR measurements reveal a change in the intensity of V3+ and V4+ at 0.8 ± 0.1 eV, where the amplitude of the V3+ charge state decreases and that of V4+ increases by approximately equal amounts. Although the individual sites are not resolved in the photo-induced EPR data, the 0.8 eV feature strongly supports the assignment of the three OAS peaks as acceptor levels.

Ultra-broadband EPR spectroscopy in field and frequency domains

2018 ◽  
Vol 20 (22) ◽  
pp. 15528-15534 ◽  
Author(s):  
P. Neugebauer ◽  
D. Bloos ◽  
R. Marx ◽  
P. Lutz ◽  
M. Kern ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Magnetic Properties ◽  
Epr Spectroscopy ◽  
Paramagnetic Resonance ◽  
Powerful Technique ◽  
Electronic And Magnetic Properties ◽  
Wide Range ◽  
Frequency Domains ◽  
Electron Paramagnetic

Electron paramagnetic resonance (EPR) is a powerful technique to investigate the electronic and magnetic properties of a wide range of materials.

scholarly journals Posttranscriptional site-directed spin labeling of large RNAs with an unnatural base pair system under non-denaturing conditions

2020 ◽  
Vol 11 (35) ◽  
pp. 9655-9664
Author(s):  
Yan Wang ◽  
Venkatesan Kathiresan ◽  
Yaoyi Chen ◽  
Yanping Hu ◽  
Wei Jiang ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Epr Spectroscopy ◽  
Base Pair ◽  
Spin Labeling ◽  
Paramagnetic Resonance ◽  
Site Directed Spin Labeling ◽  
Electron Paramagnetic

Site-directed spin labeling (SDSL) of large RNAs for electron paramagnetic resonance (EPR) spectroscopy has remained challenging to date.

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