The N=2 Super Yang-Mills Low-Energy Effective Action at Two Loops

We have carried out a two loop computation of the low-energy effective action for the four-dimensional N=2 supersymmetric Yang-Mills system coupled to hypermultiplets, with the chiral superfields of the vector multiplet lying in an abelian subalgebra. We have found a complete cancellation at the level of the integrands of Feynman amplitudes, and therefore the two loop contribution to the action, effective or Wilson, is identically zero.Comment: 8 pages, Latex, 2 .eps figure

Nonholomorphic Corrections to the One-Loop N=2 Super Yang-Mills Action

In addition to the familiar contribution from a holomorphic function \FF, the K\"ahler potential of the scalars in the nonabelian $N=2$ vector multiplet receives contributions from a real function \HH. We determine the latter at the one-loop level, taking into account both supersymmetric matter and gauge loops. The function \HH characterizes the four-point coupling of the $N=2$ vector-multiplet vectors for constant values of their scalar superpartners. We discuss the consequences of our results.Comment: 11 pages, Latex, one Postscript figure. Corrections to equation (24): 1 missing term added and one pair of indices interchange

Reacciones fotoquímicas en Química Analítica. Determinación de peroxodisulfatos

A new method for the determination of peroxidisulphate based on the precipitation of S04Ba from homogenous solutions is presented. The reduction of SzOs^ to SO/" is produced by the action of anión iodide generated «in situ» by the photochemical reaction between EDTA and iodine.The main experimental variables such as pH, ilumination, temperature and concentrations of reagents for the gravimetric determination. The results are accurate enough from 94,93 to 189,9 mg of SjOs^'.Se presenta un nuevo método de determinación de peroxidisulfatos basado en su precipitación homogénea bajo la forma de SOéBa. El paso de S208^ a S04^ es producido por la acción reductora del anión ioduro engendrado «in situ» en la reacción fotoquímica entre el ácido etilenodiaminotetracético y el iodo. Se han estudiado las variables que afectan al proceso analítico pH, temperatura, iluminación, concentración de reactivos y presencia de iones extraños, para establecer las condiciones más favorables para la determinación gravimétrica. Los resultados obtenidos son suficientemente exactos en un rango de 94,93 a 189,9 mg de SíOe'"

Estudios sobre la oxidación de AEDT-Co(ll) con el anión [Fe(CN)6]3-: I. Determinación espectrofotométrica de cobalto como AEDT-Co(lll)

Reaction of cobalt (II) ethylenediaminetetraacetate with hexacyanoferrate (III) ion and the study of the intermediates formed giving Co(EDTA)- and Fe(CN)64- as final producís is described and revised. The redox process were carried out directly at pH 5, and also at pH 3,5 in the presence of AEDT-Zn(II) and zinc (II) ions in excess. In both cases, the spectral characteristics study of reactants supply methods for the spectrophotometric determination of cobalt (II) and Beer's law is obeyed in the range 12 to 120 ppm at 536 nm. Determination of cobalt (II) in the presence of manganese (II) is also possible. Discussion in order to explain the results obtained is reported

A rabbit model of Acanthamoeba keratitis: Use of infected soft contact lenses after corneal epithelium debridement with a diamond burr

PURPOSE. To develop a rabbit model of Acanthamoeba keratitis (AK) as the best method to reproduce the natural course of this disease. METHODS. To induce AK, infected contact lenses (1000 amoebae/mm2, 90% trophozoites) were placed over the previously debrided corneal surface, in combination with a temporary tarsorrhaphy. Environmental and clinical strains of Acanthamoeba spp. (genotype T4) were used. Three groups (1L, n = 32; 2L–21d, n = 5; 2L–3d, n = 23) were established according to the number of contact lenses used (1L, 1 lens; 2L–21d and 2L–3d, 2 lenses) and the placement day of these (1L, day 1; 2L–21d, days 1 and 21; 2L–3d, days 1 and 3). The infection was quantified by a clinical score system and confirmed using corneal cytology and culture, polymerase chain reaction and histopathologic analysis. RESULTS. The infection rate obtained was high (1L, 87.5%; 2L–21d, 100%; 2L–3d, 82.6%), although no clinical signs were observed in the 50% of the infected animals in group 1L. Among groups, group 2L–3d showed more cases of moderate and severe infection. Among strains, no statistically significant differences were found in the infection rate. In the control eyes, cross infection was confirmed when a sterile contact lens was placed in the previously debrided corneas but not if the eye remained intact. CONCLUSIONS. The combination of two infected contact lenses after corneal debridement seems to be an alternative model, clinically and histopathologically similar to its human counterpart, to induce the different AK stages and reproduce the course of the disease in rabbits

Seguridad de la sedación profunda con propofol controlada por el endoscopista en la colangiopancreatografía retrógrada endoscópica (CPRE). Estudio prospectivo en un hospital terciario

Introducción: el propofol, administrado por el endoscopista con una enfermera entrenada, ha evolucionado como alternativa a la monitorización anestésica y es cada vez más frecuente en la práctica clínica habitual, incluso en endoscopia avanzada. Objetivo: evaluar la seguridad de la sedación profunda con propofol controlada por el endoscopista en pacientes sometidos a colangiopancreatografía retrógrada endoscópica (CPRE). Material y métodos: estudio prospectivo en los pacientes a los que se les realizó CPRE bajo sedación profunda con propofol. Se incluyeron diferentes variables relacionadas con el paciente y se registraron los datos iniciales y finales de la saturación de oxígeno (SatO2), la tensión arterial (TA), y la frecuencia cardiaca (FC) para determinar la presencia de eventos adversos a la sedación (hipoxemia, hipotensión o bradicardia). Resultados: un total de 661 pacientes fueron sometidos a CPRE bajo sedación con propofol durante un periodo de 24 meses. La tasa de eventos adversos registrada fue del 9, 7%. La más frecuente fue la hipoxemia (5, 7%), seguida de la bradicardia (2, 4%) y de la hipotensión (1, 6%). En el análisis univariante, la aparición de eventos adversos a la sedación (EAS) se asoció a una clasificación de ASA = III (p = 0, 026), a pacientes de edad más avanzada (p = 0, 009), mayor IMC (p = 0, 002) y a un tiempo de exploración más prolongado (p = 0, 034). La dosis de inducción de propofol también se relacionó con mayor probabilidad de eventos adversos (p = 0, 045), pero no la dosis total de propofol administrado (p = 0, 153). En el análisis de regresión logística multivariante, la edad, el índice de masa corporal (IMC) y la duración de la exploración se registran como predictores independientes de EAS (p < 0, 05). Conclusión: la sedación profunda con propofol controlada por personal de endoscopia entrenado es un método seguro en procedimientos endoscópicos complejos como la CPRE. Introduction: propofol administered by an endoscopist with a trained nurse has evolved as an alternative to anesthesia monitoring and is increasingly common in the routine clinical practice, even in advanced endoscopy. Objective: to evaluate the safety of deep sedation with endoscopist-controlled propofol in patients undergoing endoscopic retrograde cholangiopancreatography (ERCP). Material and methods: this was a prospective study in patients undergoing ERCP under deep sedation with propofol. Different patient-related variables were included and the initial and final data on oxygen saturation (SatO(2)) blood pressure (BP) and heart rate (HR) were recorded in order to determine the presence of adverse events due to sedation (hypoxemia, hypotension, or bradycardia). Results: a total of 661 patients underwent ERCP under sedation with propofol over a 24-month period. The rate of recorded adverse events was 9.7%. The most frequent adverse event was hypoxemia (5.7%), followed by bradycardia (2.4%) and hypotension (1.6%). According to the univariate analysis, the occurrence of adverse events due to sedation (AES) was associated with an ASA score >= III (p = 0.026), older patients (p = 0.009), higher body mass index (BMI) (p = 0.002) and a longer exploration time (p = 0.034). The induction dose of propofol was also associated with a greater likelihood of adverse events (p = 0.045) but not the total dose of propofol administered (p = 0.153). According to the multivariate logistic regression analysis, age, body mass index (BMI) and the duration of the exploration were independent predictors of SAE (p < 0.05). Conclusion: deep sedation with propofol controlled by trained endoscopy staff is a safe method in complex endoscopic procedures such as ERCP

Ruxolitinib in refractory acute and chronic graft-versus-host disease : a multicenter survey study

Graft-versus-host disease is the main cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation. First-line treatment is based on the use of high doses of corticosteroids. Unfortunately, second-line treatment for both acute and chronic graft-versus-host disease, remains a challenge. Ruxolitinib has been shown as an effective and safe treatment option for these patients. Seventy-nine patients received ruxolitinib and were evaluated in this retrospective and multicenter study. Twenty-three patients received ruxolitinib for refractory acute graft-versus-host disease after a median of 3 (range 1-5) previous lines of therapy. Overall response rate was 69.5% (16/23) which was obtained after a median of 2 weeks of treatment, and 21.7% (5/23) reached complete remission. Fifty-six patients were evaluated for refractory chronic graft-versus-host disease. The median number of previous lines of therapy was 3 (range 1-10). Overall response rate was 57.1% (32/56) with 3.5% (2/56) obtaining complete remission after a median of 4 weeks. Tapering of corticosteroids was possible in both acute (17/23, 73%) and chronic graft-versus-host disease (32/56, 57.1%) groups. Overall survival was 47% (CI: 23-67%) at 6 months for patients with aGVHD (62 vs 28% in responders vs non-responders) and 81% (CI: 63-89%) at 1 year for patients with cGVHD (83 vs 76% in responders vs non-responders). Ruxolitinib in the real life setting is an effective and safe treatment option for GVHD, with an ORR of 69.5% and 57.1% for refractory acute and chronic graft-versus-host disease, respectively, in heavily pretreated patients

Analysis of norfloxacin ecotoxicity and the relation with its degradation by means of electrochemical oxidation using different anodes

[EN] In this work, ecotoxicological bioassays based on Lactuca sativa seeds and bioluminescent bacterium (Vibrio fischeri) have been carried out in order to quantify the toxicity of Norfloxacin (NOR) and sodium sulfate solutions, before and after treating them using electrochemical advanced oxidation. The effect of some process variables (anode material, reactor configuration and applied current) on the toxicity evolution of the treated solution has been studied. A NOR solution shows an EC50 (5 days) of 336 mg L-1 towards Lactuca sativa. This threshold NOR concentration decreases with sodium sulfate concentration, in solutions that contain simultaneously Norfloxacin and sodium sulfate. In every case considered in this work, the electrochemical advanced oxidation process increased the toxicity (towards both Lactuca sativa and Vibrio fischeri) of the solution. This toxicity increase is mainly due to the persulfate formation during the electrochemical treatment. From a final solution toxicity point of view, the best results were obtained using a BDD anode in a divided reactor applying the lowest current intensity.The authors are very grateful to the Ministerio de Economia y Competitividad (Projects CTQ2015-65202-C2-1-R and RTI2018-101341-B-C21) for their economic support.Montañés, M.; García Gabaldón, M.; Roca-Pérez, L.; Giner-Sanz, JJ.; Mora-Gómez, J.; Pérez-Herranz, V. (2020). Analysis of norfloxacin ecotoxicity and the relation with its degradation by means of electrochemical oxidation using different anodes. Ecotoxicology and Environmental Safety. 188:1-10. https://doi.org/10.1016/j.ecoenv.2019.109923S110188Banks, M. K., & Schultz, K. E. (2005). Comparison of Plants for Germination Toxicity Tests in Petroleum-Contaminated Soils. Water, Air, and Soil Pollution, 167(1-4), 211-219. doi:10.1007/s11270-005-8553-4Barreto, J. P. d. P., Araujo, K. C. d. F., de Araujo, D. M., & Martinez-Huitle, C. A. (2015). 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Model-independent search for CP violation in D0→K−K+π−π+ and D0→π−π+π+π− decays

A search for CP violation in the phase-space structures of D0 and View the MathML source decays to the final states K−K+π−π+ and π−π+π+π− is presented. The search is carried out with a data set corresponding to an integrated luminosity of 1.0 fb−1 collected in 2011 by the LHCb experiment in pp collisions at a centre-of-mass energy of 7 TeV. For the K−K+π−π+ final state, the four-body phase space is divided into 32 bins, each bin with approximately 1800 decays. The p-value under the hypothesis of no CP violation is 9.1%, and in no bin is a CP asymmetry greater than 6.5% observed. The phase space of the π−π+π+π− final state is partitioned into 128 bins, each bin with approximately 2500 decays. The p-value under the hypothesis of no CP violation is 41%, and in no bin is a CP asymmetry greater than 5.5% observed. All results are consistent with the hypothesis of no CP violation at the current sensitivity

Search for the lepton-flavor-violating decays Bs0→e±μ∓ and B0→e±μ∓

A search for the lepton-flavor-violating decays Bs0→e±μ∓ and B0→e±μ∓ is performed with a data sample, corresponding to an integrated luminosity of 1.0  fb-1 of pp collisions at √s=7  TeV, collected by the LHCb experiment. The observed number of Bs0→e±μ∓ and B0→e±μ∓ candidates is consistent with background expectations. Upper limits on the branching fractions of both decays are determined to be B(Bs0→e±μ∓)101  TeV/c2 and MLQ(B0→e±μ∓)>126  TeV/c2 at 95% C.L., and are a factor of 2 higher than the previous bounds