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71.
PurposeTo analyse the correlations between the eye lens dose estimates performed with dosimeters placed next to the eyes of paediatric interventional cardiologists working with a biplane system, the personal dose equivalent measured on the thorax and the patient dose.MethodsThe eye lens dose was estimated in terms of Hp(0.07) on a monthly basis, placing optically stimulated luminescence dosimeters (OSLDs) on goggles. The Hp(0.07) personal dose equivalent was measured over aprons with whole-body OSLDs. Data on patient dose as recorded by the kerma-area product (PKA) were collected using an automatic dose management system. The 2 paediatric cardiologists working in the facility were involved in the study, and 222 interventions in a 1-year period were evaluated. The ceiling-suspended screen was often disregarded during interventions.ResultsThe annual eye lens doses estimated on goggles were 4.13 ± 0.93 and 4.98 ± 1.28 mSv. Over the aprons, the doses obtained were 10.83 ± 0.99 and 11.97 ± 1.44 mSv. The correlation between the goggles and the apron dose was R2 = 0.89, with a ratio of 0.38. The correlation with the patient dose was R2 = 0.40, with a ratio of 1.79 μSv Gy−1 cm−2. The dose per procedure obtained over the aprons was 102 ± 16 μSv, and on goggles 40 ± 9 μSv. The eye lens dose normalized to PKA was 2.21 ± 0.58 μSv Gy−1 cm−2.ConclusionsMeasurements of personal dose equivalent over the paediatric cardiologist’s apron are useful to estimate eye lens dose levels if no radiation protection devices are typically used. 相似文献
72.
Rudenko NV Sinegina LL Arzhanov MA Ksenzenko VN Ivashina TV Morenkov OS Shaloiko LA Vinokurov LM 《Journal of biochemical and biophysical methods》2007,70(4):605-611
The effective new variant of "sandwich" bioluminescent enzyme immunoassay (BEIA) for the sensitive detection of glycoprotein B (gB) of pseudorabies virus (PrV) was presently developed. The high affinity interaction of barnase-barstar protein pair and photoprotein obelin as bioluminescent marker were for the first time successfully applied to BEIA development. Preliminary the two monoclonal antibodies, 11/5 and 34/2, were raised against gB for ELISA PrV detection. Presently we used the same immuno-"sandwich" principle for BEIA. To do this the two different bioconjugates were elaborated. Recombinant barnase was chemically conjugated with monoclonal anti-PrV's gB IgG, and also barstar was fused in frame to obelin. The characteristics of BEIA method have been compared to ELISA PrV detection. We have shown the proposed here gB-BEIA was 40-fold more sensitive as opposed to gB-ELISA test. The construction might have a broad promise in multiple potential immunological applications. 相似文献
73.
74.
Nishita Dua Monika Punia Pooja Chhillar Manisha Bedi Satyender Pal Khatkar Vinod Bala Taxak Priti Boora Doon 《Luminescence》2023,38(6):783-795
The present research work entails the synthesis of one binary and four ternary red light−emitting Eu (III)-based complexes with 3-benzylidene-2,4-pentanedione as the main ligand and 1,10-phenanthroline, bathophenanthroline, neocuproine, and 4,4′-′dimethyl-2,2′-′bipyridyl as auxiliary ligands. The metal–organic framework of the series was elucidated using energy dispersive X-ray analysis, elemental analysis, Fourier transform infrared spectroscopy, and proton nuclear magnetic resonance. This Eu (III) series exhibits optimum thermal stability, making them a promising candidate for organic light-emitting diodes. On the basis of emission spectra, their optical parameters such as nonradiative and radiative decay rates, luminescence decay time, intrinsic quantum efficiency, and Judd–Ofelt intensity parameter were determined. The monocentric luminescence and Judd–Ofelt parameters reveal the absence of symmetry around the europium center. CIE chromaticity coordinates, correlated color temperature values, color purity, and asymmetric ratios authenticate the color coordinates of the complexes in red region. Optical band gap values lie within the range of wide band gap semiconductors, indicating their utilization in military radars and biological labeling. 相似文献
75.
The perturbation of the racemic equilibrium of luminescent D3 terbium(III) complexes with chelidamic acid (CDA), a hydroxylated derivative of 2,6-pyridine-dicarboxylic acid (DPA), by added chiral biomolecules such as L-amino acids has been studied using circularly polarized luminescence and 13C NMR spectroscopy. It is shown in this work that the chiral-induced equilibrium shift of [Tb(CDA)3](6-) by L-amino acids (i.e. L-proline or L-arginine) was largely influenced by the hydrogen-bonding networks formed between the ligand interface of racemic [Tb(CDA)3](6-) and these added chiral agents. The capping of potential hydrogen-bonding sites by acetylation in L-proline led to a approximately 100-fold drop in the induced optical activity of the [Tb(CDA)3](6-):N-acetyl-L-proline system. This result suggested that the hydrogen-bonding networks serve as the basis for further noncovalent discriminatory interactions between racemic [Tb(CDA)3](6-) and added L-amino acids. 相似文献
76.
Shiro Yamashoji 《Analytical biochemistry》2009,385(1):115-119
In this study, ethanol inhibited the growth and glucose-induced proton release of yeast cells in a dose-dependent manner. On the other hand, ethanol tolerance of menadione-catalyzed luminol luminescence by yeast cells increased with increasing ethanol concentrations in the growth medium. The intracellular reduced-form nicotinamide adenine dinucleotide (NADH) concentration also increased with increasing ethanol concentrations in the medium and was enough to maintain constant menadione-catalyzed luminol luminescence. These facts suggest that the menadione-catalyzed luminol luminescent assay depending on a NADH:quinone reductase and NADH generation system is useful as a new evaluation assay for assessing the vitality of ethanol-stressed yeast cells, whereas the glucose-induced proton release assay is expected to be useful for the evaluation of cell growth under ethanol stress. 相似文献
77.
Synthesis and luminescence properties of brick‐shaped lanthanum–organic frameworks with mesoporous and macroporous architectures 下载免费PDF全文
Generally, metal–organic frameworks (MOFs) are made up from kinds of repeating microporous structure. Here, a series of Eu3+ ions activated terephthalate‐based lanthanum–organic frameworks (La–MOFs) was synthesized by a hydrothermal reaction. By controlling the reaction time, we obtained some unique brick‐shaped La–MOFs in a micron scale size range, and these La–MOFs showed tunable mesoporous and macroporous architectures. It is speculated that the change in the composition and structure of building units results in the formation of this mesoporous and macroporous heterogeneous architectures. Powder X‐ray diffraction patterns and Eu3+ luminescence behavior support the speculation. 相似文献
78.
Synthesis and photoluminescence properties of red emitting phosphor La2–xEuxLi0.5Al0.5O4 [x = 0.2–2] with K2NiF4 structure 下载免费PDF全文
Europium (Eu)3+‐substituted La2Li0.5Al0.5O4 red emitting phosphors were prepared by a conventional high‐temperature solid‐state reaction method. Powder X‐ray diffraction, diffuse reflectance spectra and spectrofluorometry were used as vital characterizing tools for the phosphors. The Eu concentration dependence luminescence properties and Judd–Ofelt intensity parameters were investigated and calculated, respectively. All compositions showed an orange red emission (due to the magnetic and electric dipole transitions of the Eu3+ ion) with the appropriate Commission Internationale de l'Eclairage (CIE) colour gamut under near ultraviolet or blue ray light excitation. The calculated critical distance showed that the energy transfer occured between Eu to Eu via an exchange mechanism. The Eu1.4La0.6Li0.5Al0.5O4 composition showed the highest red emission intensity with CIE colour saturation compared with that of the commercial Eu‐activated yttrium oxysulfide red phosphor. 相似文献
79.
Photoluminescence properties of Ca2Al2O5:RE3+ (RE = Eu,Dy and Tb) phosphors for solid state lighting 下载免费PDF全文
Atul N. Yerpude Vishal R. Panse Sanjay J. Dhoble Namdeo S. Kokode Mudavath Srinivas 《Luminescence》2017,32(7):1361-1364
Ca2Al2O5:Eu3+, Ca2Al2O5:Dy3+ and Ca2Al2O5:Tb3+ phosphors were synthesized using a combustion synthesis method. The prepared phosphors were characterized by X‐ray powder diffraction for phase purity, by scanning electron microscopy for morphology, and by photoluminescence for emission and excitation measurements. The Ca2Al2O5:Eu3+ phosphors could be efficiently excited at 396 nm and showed red emission at 594 nm and 616 nm due to 5D0 → 7F1 and 5D0 → 7F2 transitions. Dy3+‐doped phosphors showed blue emission at 482 nm and yellow emission at 573 nm. Ca2Al2O5:Tb3+ phosphors showed emission at 545 nm when excited at 352 nm. Concentration quenching occurred in both Eu3+ and Dy3+phosphors at 0.5 mol%. Photoluminescence results suggested that the aluminate‐based phosphor could be a potential candidate for application in environmentally friendly based lighting technologies. 相似文献
80.
Synthesis and luminescence characterization of Y2BaZnO5:RE (RE = Eu3+, Tb3+, Pr3+ and Sm3+) phosphors 下载免费PDF全文
Modified synthesis and luminescence of Y2BaZnO5 phosphors activated with the rare earths (RE) Eu3+, Tb3+, Pr3+ and Sm3+ are reported. RE2BaZnO5 phosphors have attracted attention because of their interesting magnetic and optical properties; and are usually prepared using a two‐step solid‐state reaction. In the first step, carbonates or similar precursors are thoroughly mixed and heated at 900°C to decompose them to oxides. To eliminate the unwanted phases like BaRE2O4, the resulting powders are reheated at 1100°C for a long time. We prepared Y2BaZnO5 phosphors activated with various activators by replacing the first step with combustion synthesis. The photoluminescence results are presented. The photoluminescence results for Eu3+, Tb3+ and Pr3+ are in good agreement with the literature. However, photoluminescence emission from Sm3+ has not been documented previously. The excitation spectrum of Eu3+ is dominated by a charge transfer band around 261 nm, and an additional band around 238 nm is always present, irrespective of the type of activator. The presence of this band for all these different types of activators was interpreted as host absorption. 相似文献