Eduardo J. Fernández
University of La Rioja
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Featured researches published by Eduardo J. Fernández.
IEEE Transactions on Biomedical Engineering | 2004
Almut Branner; Richard B. Stein; Eduardo J. Fernández; Yoichiro Aoyagi; Richard A. Normann
We studied the consequences of long-term implantation of a penetrating microelectrode array in peripheral nerve over the time course of 4-6 mo. Electrode arrays without lead wires were implanted to test the ability of different containment systems to protect the array and nerve during contractions of surrounding muscles. Treadmill walking was monitored and the animals showed no functional deficits as a result of implantation. In a different set of experiments, electrodes with lead wires were implanted for up to 7 mo and the animals were tested at 2-4 week intervals at which time stimulation thresholds and recorded sensory activity were monitored for every electrode. It was shown that surgical technique highly affected the long-term stimulation results. Results between measurement sessions were compared, and in the best case, the stimulation properties stabilized in 80% of the electrodes over the course of the experiment (162 days). The recorded sensory signals, however, were not stable over time. A histological analysis performed on all implanted tissues indicated that the morphology and fiber density of the nerve around the electrodes were normal.
Journal of Neuroscience Methods | 1995
F. Caserta; William D. Eldred; Eduardo J. Fernández; Robert E. Hausman; L.R. Stanford; S.V. Bulderev; S. Schwarzer; H.E. Stanley
Although there is a growing interest in the application of fractal analysis in neurobiology, questions about the methodology have restricted its wider application. In this report we discuss some of the underlying principles for fractal analysis, we propose the cumulative-mass method as a standard method and we extend the applicability of fractal analysis to both 2 and 3 dimensions. We have examined the relationship between the method of log-log Sholl analysis and fractal analysis and have found that they correlate well. Measurements of physiologically characterized retinal ganglion cells indicate that different cell types can have significantly different fractal dimensions. Such differences may allow the correlation of the physiological type of a neuron with its morphological fractal dimension.
Journal of Neuroscience Methods | 1998
Herbert F. Jelinek; Eduardo J. Fernández
In the past 15 years it has become possible to determine the fractal dimension (Df) of complex objects, including neurons, by automated image analysis methods. However, there are many unresolved issues that need to be addressed. In this paper we discuss how the Df calculated by different methods may vary and how fractal analysis may be of use for retinal ganglion cell characterization. The goal of this work was to acknowledge inherent sources of variation during measurement and evaluate current fractal analysis methods for describing structure. Our results show that different algorithms and even the same algorithm performed by different computer programs and/or experimenters may give different but consistent numerical values. All described methods demonstrated their suitability for classifying cat retinal ganglion cells into distinct groups. Our results reinforce the idea that comparison of measurements of different profiles using the same measurement method may be useful and valid even if an exact numeric value of the dimension is not realised in practice.
Journal of Neuroscience Methods | 2000
Edwin M. Maynard; Eduardo J. Fernández; Richard A. Normann
Minimizing relative movements between neural tissues and arrays of microelectrodes chronically implanted into them is expected to greatly enhance the capacity of the microelectrodes to record from single cortical neurons on a long-term basis. We describe a new surgical technique to minimize the formation of adhesions between the dura and an implanted electrode array using a 12 microm (0.5 mil) thick sheet of Teflon film positioned between the array and the dura. A total of 15 cats were implanted using this technique. Gross examination of 12 implant sites at the time of sacrifice failed to find evidence of adhesions between the arrays and the dura when the Teflon(R) film remained in its initial position. In six implants from which recordings were made, an average of nine of the 11 (81%) connected electrodes in each array recorded evoked neural activity after 180 days post implantation. Further, on average, two separable units were identified on each of the implanted electrodes in these arrays. No significant change was found in the density of cell bodies around implanted electrodes of four of the implanted electrode arrays. However, histological evaluation of the implant sites revealed evidence of meningeal proliferation beneath the arrays. The technique described is shown to be effective at preventing adhesions between implanted electrode arrays and improve the characteristics of chronic recordings obtained with these structures.
Inorganic Chemistry | 2008
Eduardo J. Fernández; José M. López-de-Luzuriaga; Miguel Monge; M. Elena Olmos; Raquel C. Puelles; Antonio Laguna; Ahmed A. Mohamed; John P. Fackler
The vapochromic behaviors of {Ag2L2[Au(C6F5)2]2}n (L = Et2O (1), Me2CO (2), THF (3), CH3CN (4)) were studied. {Ag2L2[Au(C6F5)2]2}n (L = Et2O (1)) was synthesized by the reaction of [Bu4N][Au(C6F5)2] with AgOClO3 in 1:1 molar ratio in CH2Cl2/Et2O (1:2). 1 was used as starting material with THF to form {Ag2L2[Au(C6F5)2]2}n (L = THF (3)). 3 crystallizes in the monoclinic space group C2/c and consists of tetranuclear units linked together via aurophilic contacts resulting in the formation of a 1D polymer that runs parallel to the crystallographic z axis. The gold(I) atoms are linearly coordinated to two pentafluorophenyl groups and display additional Au...Ag close contacts within the tetranuclear units with distances of 2.7582(3) and 2.7709(3) A. Each silver(I) center is bonded to the two oxygen atoms of the THF molecules with a Ag-O bond distance of 2.307(3) A. TGA analysis showed that 1 loses two molecules of the coordinated solvent per molecular unit (1st one: 75-100 degrees, second one: 150-175 degrees C), whereas 2, 3, and 4 lose both volatile organic compounds (VOCs) and fluorinated ligands in a less well defined manner. Each complex loses both the fluorinated ligands and the VOCs by a temperature of about 325 degrees C to give a 1:1 gold/silver product. X-ray powder diffraction studies confirm that the reaction of vapors of VOCs with 1 in the solid state produce complete substitution of the ether molecules by the new VOC. The VOCs are replaced in the order CH3CN > Me2CO > THF > Et2O, with the ether being the easiest to replace. {Ag2(Et2O)2[Au(C6F5)2]2}n and {Ag2(THF)2[Au(C6F5)2]2} n both luminesce at room temperature and at 77 K in the solid state. Emission maxima are independent of the excitation wavelength used below about 500 nm. Emission maxima are obtained at 585 nm (ether) and 544 nm (THF) at room temperature and at 605 nm (ether) and 567 nm (THF) at 77 K.
Brain Research | 2000
Eduardo J. Fernández; José Manuel Ferrández; Josef Ammermüller; Richard A. Normann
To achieve a better understanding of the parallel information processing that takes place in the nervous system, many researchers have recently begun to use multielectrode techniques to obtain high spatial- and temporal-resolution recordings of the firing patterns of neural ensembles. Apart from the complexities of acquiring and storing single unit responses from large numbers of neurons, the multielectrode technique has provided new challenges in the analysis of the responses from many simultaneously recorded neurons. This paper provides insights into the problem of coding/decoding of retinal images by ensembles of retinal ganglion cells. We have simultaneously recorded the responses of 15 ganglion cells to visual stimuli of various intensities and wavelengths and analyzed the data using discriminant analysis. Models of stimulus encoding were generated and discriminant analysis used to estimate the wavelength and intensity of the stimuli. We find that the ganglion cells we have recorded from are non-redundant encoders of these stimulus features. While single ganglion cells are poor classifiers of the stimulus parameters, examination of the responses of only a few ganglion cells greatly enhances our ability to specify the stimulus wavelength and intensity. Of the parameters studied, we find that the rate of firing of the ganglion cells provides the most information about these stimulus parameters, while the timing of the first action potential provides almost as much information. While we are not suggesting that the brain is using these variables, our results show how a population of sensory neurons can encode stimulus features and suggest that the brain could potentially deduce reliable information about stimulus features from response patterns of retinal ganglion cell populations.
Chemical Communications | 2007
Eduardo J. Fernández; Antonio Laguna; José M. López-de-Luzuriaga; Miguel Monge; Mihai G. Nema; M. Elena Olmos; Javier Pérez; Cristian Silvestru
Complex [Au(C6F5)2][Bi(C6H4CH2NMe(2)-2)2] displays the first example of an interaction between Au(I) and Bi(III), the nature of which is shown to be consistent with the presence of a high ionic contribution (79%) and a dispersion type (van der Waals) interaction (21%).
Journal of Organometallic Chemistry | 1988
Rafael Usón; Antonio Laguna; Eduardo J. Fernández; Aránzazu Mendía; Peter G. Jones
Abstract The arylsilver derivatives AgR (R = C6F5, 2,4,6-C6F3H2 or C6Cl5) react with chlorogold(I) precursors [AuCl(tht), AuCl(PPh3), ClAu(dppm)AuCl (tht = tetrahydrothiophene, dppm = bis(diphenylphosphino)methane], to give the corresponding arylgold complexes in good yield. With gold precursors in higher oxidation state, AgC6Cl5 either causes reduction to gold(I) or gives no reaction, whereas AgC6F5 and AgC6F3H2 lead to gold(II) complexes (R2Au(dppm)AuR2) or gold (III) complexes [Au(C6F3H2)(C6F5)2(PPh3); Au(C6F3H2)2(C6F5)(tht); Au(C6F5)3(tht); Au(C6F3H2)3(tht)].
Dalton Transactions | 2009
Eduardo J. Fernández; Antonio Laguna; José M. López-de-Luzuriaga; Miguel Monge; Manuel Montiel; M. Elena Olmos; María Rodríguez-Castillo
The synthesis, structural characterization and the study of the photophysical properties of complexes [AuCu(C6F5)2(N[triple bond]C-CH3)2] 1, [AuCu(C6F5)2(N[triple bond]C-Ph)2]2 2, and [AuCu(C6F5)2(N[triple bond]C-CH=CH-Ph)2] 3 have been carried out. The crystal structures of complexes 1-3 consist of dinuclear Au-Cu units built from mediated metallophilic Au(I)...Cu(I) interactions. In the case of complex 2 two dinuclear units interact via an aurophilic interaction leading to a tetranuclear Cu-Au-Au-Cu arrangement. Complex 2 is brightly luminescent in solid state at room temperature and at 77 K with a lifetime in the nanoseconds range, while complexes 1 and 3 do not display luminescence under the same conditions. The presence of the aurophilic interaction in complex 2 seems to be responsible for the blue luminescence observed. DFT and time-dependent DFT calculations agree with the experimental results and support the idea that the origin of the luminescence of these complexes arise from orbitals located in the interacting metals.
Journal of Organometallic Chemistry | 1995
Elena Cerrada; Eduardo J. Fernández; M. Concepción Gimeno; Antonio Laguna; Mariano Laguna; Raquel Terroba; M. Dolores Villacampa
Abstract The reaction of ethanolic solutions of Na 2 (SS) {SS &.dbnd; 1,2-S 2 C 6 H 4 or 3,4-S 2 C 6 H 3 (CH 3 )} with [Sn(CH 3 ) 2 Cl 2 ] or (PPN) 2 [ZnCl 4 ] gives [Sn(CH 3 ) 2 (SS)] and (PPN) 2 [Zn(SS) 2 ], respectively. The tin derivative with 1,3-dithiol-2-thione-4,5-dithiolate (dmit), [Sn(CH 3 ) 2 (dmit)], is obtained by reaction of [Sn(CH 3 ) 2 Cl 2 ] with (NEt 4 ) 2 [Zn(dmit) 2 ]. The tin and zinc complexes further react with the gold(III) derivatives cis -[Au(C 6 F 5 )Cl 2 L] giving rise to dithiolate gold(III) complexes [Au(C 6 F 5 )(SS)L]. The structure of [Au(C 6 F 5 )(S 2 C 6 H 4 )(PPh 3 )] has been established by an X-ray diffraction study, and shows a square-planar coordination of the gold with the dithiolate chelating.