Search

Reactive oxygen species comprise oxygen-based free radicals and non-radical species such as peroxynitrite and electronically excited (singlet) oxygen. These reactive species often have short lifetimes, and much of our understanding of their formation and reactivity in biological and especially medical environments has come from complimentary fast reaction methods involving pulsed lasers and high-energy radiation techniques. These and related methods, such as EPR, are discussed with particular reference to singlet oxygen, hydroxy radicals, the superoxide radical anion, and their roles in medical aspects, such as cancer, vision and skin disorders, and especially pro- and anti-oxidative processes.

The interactions of dietary carotenoids, and particularly the xanthophylls in the macula, with singlet oxygen and three different oxy-radicals, (hydroxyl radical, nitrogen dioxide and the superoxide radical anion) are compared using pulsed laser and γ-techniques. The results give possible molecular mechanisms for the switch from anti-oxidant (protection) by carotenoids to pro-oxidant (damage) by carotenoids. The participation of oxygen in radical mechanisms in the presence of different carotenoids is compared for the different radicals. It is shown that the mechanistic role of oxygen differs very significantly for anti-/pro-oxidation by hydroxyl radicals when compared to nitrogen dioxide. Lutein was found to be an extremely good cell protector against hydroxyl radicals at all oxygen concentrations, including under physiological conditions.

Managing certain by-products of the nuclear fuel cycle, such as the radioactive isotopes of caesium: 134Cs, 135Cs and 137Cs is challenging due to their environmental mobility and radioactivity. While a great many materials can isolate Cs+ ions from neutral or basic aqueous solutions via ion exchange, few of these, with the exception of ammonium phosphomolybdate (AMP), function effectively in acidic media. The use of AMP, and its porous composite in polyacrylonitrile (PAN) for management of Cs radioisotopes in various nuclear wastes have been known for decades and are well studied, yet the effects of radiation on the physiochemical properties of such composites have only received limited attention to date. In a previous publication, we demonstrated that a 100 kGy gamma irradiation dose has negligible effect on the ion exchange performance of AMP and AMP&ndash, PAN with respect to capacity or kinetics under the Cs+ concentrations and acidity found in spent nuclear fuel (SNF) recycling. As a continuation of this prior study, in this publication we explore the effects of gamma irradiation on the physiochemical properties of AMP and AMP&ndash, PAN using a range of characterisation methods. The effects of the same gamma dose on the oxidation state of Mo in AMP and AMP&ndash, PAN, the thermal degradation of both AMP and AMP&ndash, PAN, combined with a first study into the high-temperature degradation AMP, are reported. The implications of irradiation, its possible mechanism, the conditions present in SNF recycling, and for the end-of-life disposal or recycling of these materials are also discussed.

Pathogenic bacteria found in low levels in natural water systems can present a hazard to human health, such as through contraction of Legionnaires disease, if conditions are favourable for growth and there is potential to create an aerosol. In this study, gamma radiation using a60Co source was applied to Legionella pneumophila and Pseudomonas aeruginosa bacteria for 60 min at varying dose rates. All L. pneumophila bacteria were eliminated by irradiation at a dose of 1.86 kGy, and all P. aeruginosa at a dose of 0.70 kGy. Approximate D10 values for L. pneumophila and P. aeruginosa bacteria were 166.3 Gy and 70.9 Gy respectively.

Gamma irradiation-induced defects at doses of 0.5 and 5 MGy were studied in lithium sodium-borosilicate (LiNaBSi) and sodium barium-borosilicate (NaBaBSi) glasses, used for high-level radioactive waste immobilisation in the UK and India, respectively. X-band electron paramagnetic resonance (EPR), Raman and UV-Vis-nIR spectroscopies were used to characterise the glasses before and after irradiation. EPR and UV-Vis-nIR absorption spectroscopies revealed the formation of boron-oxygen hole centres (BOHC), electrons trapped at alkali cations or ET centres and peroxy-radicals (PORs) as defects common to both glasses. In addition, E− or polaron centres were observed in NaBaBSi glasses, possibly related to formation of elemental sodium colloids. Time-dependent thermal annealing at a range of temperatures, including those relevant to canister centreline cooling (CCC), which may be of relevance to geological disposal in future technical assessments, was carried out to study thermal stability of these radiation-induced defects. It was observed that PORs are the most thermally-stable defects in both glasses. The influence of glass composition on the segregation of sodium and the possible formation of metal colloids upon irradiation have been discussed.

The interactions of dietary carotenoids, and particularly the xanthophylls in the macula, with singlet oxygen and three different oxy-radicals, (hydroxyl radical, nitrogen dioxide and the superoxide radical anion) are compared using pulsed laser and γ-techniques. The results give possible molecular mechanisms for the switch from anti-oxidant (protection) by carotenoids to pro-oxidant (damage) by carotenoids. The participation of oxygen in radical mechanisms in the presence of different carotenoids is compared for the different radicals. It is shown that the mechanistic role of oxygen differs very significantly for anti-/pro-oxidation by hydroxyl radicals when compared to nitrogen dioxide. Lutein was found to be an extremely good cell protector against hydroxyl radicals at all oxygen concentrations, including under physiological conditions.

Redox active metalloenzymes catalyse a range of biochemical processes essential for life. However, due to their complex reaction mechanisms, and often, their poor optical signals, detailed mechanistic understandings of them are limited. Here, we develop a cryoreduction approach coupled to electron paramagnetic resonance measurements to study electron transfer between the copper centers in the copper nitrite reductase (CuNiR) family of enzymes. Unlike alternative methods used to study electron transfer reactions, the cryoreduction approach presented here allows observation of the redox state of both metal centers, a direct read‐out of electron transfer, determines the presence of the substrate/product in the active site and shows the importance of protein motion in inter‐copper electron transfer catalyzed by CuNiRs. Cryoreduction‐EPR is broadly applicable for the study of electron transfer in other redox enzymes and paves the way to explore transient states in multiple redox‐center containing proteins (homo and hetero metal ions)., Metalloenzyme catalysis: Through the use of cryoreduction and annealing, a method of studying electron transfer in redox active metalloenzymes is developed. Combined with electron paramagnetic resonance spectroscopy, active states in the catalytic cycle of the copper containing nitrite reductases are probed.

The effects of γ-radiation sterilization on the parenteral excipient L-histidine were analysed by means of EPR spectroscopy. The irradiation process was found to induce the formation of a deamination radical which was persistent in the solid state. The nature and reactivity of the radicals following dissolution in water was evaluated using spin-trapping EPR experiments. The deamination radical was found to regenerate in solution in the presence of trace metals, potentially leading to radical induced degradation reactions occurring up to an hour after the dissolution process. Understanding this process is significant for the improved design of parental pharmaceutical formulations in which unwanted radical reactions after γ‐radiation sterilization could lead to degradation of active ingredients.

This work investigates the evolution of the tensile and structural properties of fused filament fabrication (FFF), formed polymers under gamma irradiation. Commercial off-the-shelf print filaments of Poly(lactic acid) (PLA), Thermoplastic polyurethane (TPU), Chlorinated polyethylene elastomer (CPE), Nylon, Acrylonitrile butadiene styrene (ABS) and Polycarbonate (PC) were exposed to gamma-ray doses of up to 5.3 MGy. The suitability of FFF-formed components made from these materials for use in radiation environments is evaluated by considering their structural properties. We identify clear trends in the structural properties of all the materials tested and correlate them with changes in the chemical structure. We find that Nylon shows the best performance under these conditions, with no change in ultimate tensile strength and an increase in stiffness. However, some of our findings suggest that the effect of additives to this type of filament may result in potentially undesirable adhesive properties. The organic polymer PLA was notably more radiation-sensitive than the other materials tested, showing 50% decrease in Young’s Modulus and ultimate tensile strength at order of magnitude lower radiation dose. A mechanism is proposed whereby FFF-processed components would have substantially different radiation tolerances than bulk material.

Reducing radiation damage is important and dietary antioxidants that can protect cells from such damage are of value. Dietary lycopene, a carotenoid found in tomatoes, protects human lymphoid cell membranes from damage by γ-radiation. We report that such protective effects are remarkably reduced as the oxygen concentration increases - near zero at 100% oxygen from fivefold protection at 20% oxygen and, dramatically, from 50-fold protection at 0% oxygen. Such huge differences imply that under higher oxygen concentrations lycopene could lead to improved cancer therapy using γ-radiation. The cells are not efficiently protected from the superoxide radical by lycopene. Noncellular studies suggest molecular mechanisms for the oxygen effect.

Anthraquinones have been the subject of numerous photochemical studies and their photopolymerization activities have been examined under various conditions to improve more efficient photochemical systems. This article involves further detailed investigations into the photophysical, photochemistry and photopolymerisation properties of 4 commercial derivatives of 2-substituted anthraquinone, namely, 2-Bromomethylanthraquinone (2BA), 2 Chloromethylanthraquinone (2CA), 2 Ethylanthraquinone (2EA), 2 Hydroxymethylanthraquinone (2HA) and one novel synthesized anthraquinone, 2 Acryloxymethylanthraquinone (2AA). 2AA is synthesized from 2HA. The results from both spectroscopic and analysis studies proved the 2AA to having the ester link. Absorption spectroscopy and solvent shift data are used to characterise their spectral activity. Luminescence studies involving fluorescence and phosphorescence analysis indicates efficient intersystem crossing to triplet state and n-π* nature of the lowest excited triplet state. The polymerisation activity was studied using methyl methacrylate (MMA) and analysis of the cure rate was measured using the gravimetric method. All the compounds are shown to be highly dependent on the structure. However, the rate of polymerisation (Rp) was reduced in the presence of amine. This is consistent with other results, proving the behaviour of derivatives with n-π* configuration. Hardness tests for all compounds took place using a different formula of acrylated resin/monomer systems. The excited state characteristics of the methyl derivatives have also been examined using micro and nanosecond flash photolysis. Triplet absorption spectra of all the anthraquinone derivatives show a significant red shift in the region of 340–370 nm with increasing solvent polarity due to stabilisation of the lowest triplet state by solvent reorganization. Hydrogen atom abstraction takes place in 2 propanol, forming a semiquinone radical. In the presence of the tertiary amine, triethylamine, all anthraquinone derivatives show the formation of intermediary species related to either the exciplex or the radical ion pair. Under aerobic conditions, the first decay rate for all anthraquinone derivatives increases and showed oxygen to be a good quencher with a bimolecular rate constant of around 2 × 10 mol. dm s. Relative to benzophenone, the molar absorption coefficient, ε, and quantum yield of intersystem crossing, Φisc were calculated, and it is summarised that the value for Φisc for all compound is less than 1.00 and controls to a major extent their photochemical activities., The authors thank the University of Sains Malaysia for funding Hazira Mazah.

We report on studies of reactions of singlet oxygen with carotenoids and retinoids and a range of free radical studies on carotenoids and retinoids with emphasis on recent work, dietary carotenoids and the role of oxygen in biological processes. Many previous reviews are cited and updated together with new data not previously reviewed. The review does not deal with computational studies but the emphasis is on laboratory-based results. We contrast the ease of study of both singlet oxygen and polyene radical cations compared to neutral radicals. Of particular interest is the switch from anti- to pro-oxidant behavior of a carotenoid with change of oxygen concentration: results for lycopene in a cellular model system show total protection of the human cells studied at zero oxygen concentration, but zero protection at 100% oxygen concentration.

An effort has been made to bridge the gap between academic knowledge of polymeric seal degradation and industrial practices. A series of physical and mechanical properties that can be related to the sealing behavior of three commercial samples of nitrile rubber have been studied for their degradation when exposed to gamma radiation. For all samples the glass transition temperature (Tg) and retention factor (RF) were found to increase with total dose whilst percentage change in mass (ΔM%) was found to decrease. The ultimate uptake of carbon dioxide (CO2) did not appear to change with radiation dose but the kinetics of the absorption process were found to decrease, suggesting the formation of crosslinks. The crosslinks formed appear to be dependent on the original material composition and comparison against degradation of material properties supports the theory behind butadiene, BDN, content being linked to a propensity for crosslink clustering. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44618.

The yield of singlet oxygen sensitized by chemically modified, carotenoidless bacterial photosynthetic reaction centres and the ensuing oxidative damage are both shown to be magnetic field-dependent.

The synthesis of metal(II) complexes of a bis(thiosemicarbazonato) ligand derived from 1,2-cyclohexanedione are reported. The compounds have been characterised by a range of techniques including reverse-phase HPLC, cyclic voltammetry, NMR, UV/Vis, IR, Raman and EPR spectroscopy. Xray crystal structures of the proligand and two copper(II) complexes have been obtained, and the electronic structures have been analysed by using DFT calculations. DFT calculations have also been used to map the potential energy surface of a related bis(thiosemicarbdzone) proligand and predict solution-phase one-electron reduction potentials of the copper(H) complex by using three polarisable continuum Solvation models. Electrochemistry experiments show that the copper(II) complex undergoes quasi-reversible one-electron reduction at biologically accessible potentials and is within the range proposed for the complex to be hypoxia-selective. In addition, UV/Vis spectroelectrochemistry experiments have been used to characterise the reduced copper(l) anion, and the reaction between the anion and dioxygen has been characterised by experiments and theory, Observation of this oxidation reaction has important implications for the proposed mechanisms of hypoxia selectivity of bis(thiosemicarbazonato)copper(H) complexes, The copper-64 radiolabelled complex has been prepared in aqueous solution which demonstrates the potential of rise of these complexes as medical imaging agents. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

Raman spectroscopy and microscopy, along with all vibrational spectroscopic techniques, has proven itself to be a valuable analytical technique to quantitatively and qualitatively determine the molecular composition, properties of all kind of material systems. It has been successfully utilized in various fields of science, primarily due to the extraordinary versatility of sampling methods. The technique requires minimal sample preparation and can analyze samples of one monolayer thickness or of low sample concentration. Excellent spectral and spatial resolution and detailed fingerprinting can be derived from Raman spectra. Many technical issues such as fluorescence, poor sensitivity, or reproducibility have been overcome with the advances in instrumentation. Thus, its versatility of applications, rapidness of collection and easy analysis have made Raman spectroscopy an attractive analytical tool.

Carotenoids are known to act as dietary antioxidants and so are of wide interest for their health benefits. Dietary lycopene, the carotenoid pigment in tomatoes, has been shown to protect against human lymphoid cell membrane damage from free radicals produced by gamma radiation and also by the nitrogen dioxide radical, generated photolytically. This protective effect is dramatically reduced as the oxygen concentration increases, particularly for damage due to gamma radiolysis – becoming near zero at 100% oxygen from 5-fold protection at 20% oxygen and 50-fold protection at zero per-cent oxygen. The effect is less pronounced for nitrogen dioxide-induced cell killing falling from 17-fold protection in the absence of oxygen to 9-fold at 100% oxygen. Non-cellular gamma radiation and laser studies were also carried out to support the molecular mechanisms suggested for the effect of oxygen. The remarkable reduction in protection by lycopene against gamma radiation at high oxygen concentrations could be exploited to enhance radiation procedures for therapy and preliminary studies have also been undertaken for irradiations with high energy protons.