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1.
J Neural Eng ; 12(1): 016014, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25588201

ABSTRACT

OBJECTIVE: The aim of this study was to compare two different microelectrode materials--the conductive polymer composite poly-3,4-ethylenedioxythiophene (PEDOT)-carbon nanotube(CNT) and titanium nitride (TiN)--at activating spikes in retinal ganglion cells in whole mount rat retina through stimulation of the local retinal network. Stimulation efficacy of the microelectrodes was analyzed by comparing voltage, current and transferred charge at stimulation threshold. APPROACH: Retinal ganglion cell spikes were recorded by a central electrode (30 µm diameter) in the planar grid of an electrode array. Extracellular stimulation (monophasic, cathodic, 0.1-1.0 ms) of the retinal network was performed using constant voltage pulses applied to the eight surrounding electrodes. The stimulation electrodes were equally spaced on the four sides of a square (400 × 400 µm). Threshold voltage was determined as the pulse amplitude required to evoke network-mediated ganglion cell spiking in a defined post stimulus time window in 50% of identical stimulus repetitions. For the two electrode materials threshold voltage, transferred charge at threshold, maximum current and the residual current at the end of the pulse were compared. MAIN RESULTS: Stimulation of retinal interneurons using PEDOT-CNT electrodes is achieved with lower stimulation voltage and requires lower charge transfer as compared to TiN. The key parameter for effective stimulation is a constant current over at least 0.5 ms, which is obtained by PEDOT-CNT electrodes at lower stimulation voltage due to its faradaic charge transfer mechanism. SIGNIFICANCE: In neuroprosthetic implants, PEDOT-CNT may allow for smaller electrodes, effective stimulation in a safe voltage regime and lower energy-consumption. Our study also indicates, that the charge transferred at threshold or the charge injection capacity per se does not determine stimulation efficacy.


Subject(s)
Action Potentials/physiology , Bridged Bicyclo Compounds, Heterocyclic/chemistry , Electric Stimulation Therapy/instrumentation , Microelectrodes , Nanotubes, Carbon/chemistry , Polymers/chemistry , Retinal Ganglion Cells/physiology , Animals , Coated Materials, Biocompatible/chemical synthesis , Electric Impedance , Electrodes, Implanted , Equipment Failure Analysis , Female , Materials Testing , Prosthesis Design , Rats , Rats, Sprague-Dawley , Reproducibility of Results , Sensitivity and Specificity , Static Electricity , Titanium/chemistry , Visual Prosthesis
2.
Can J Microbiol ; 47(6): 503-8, 2001 Jun.
Article in French | MEDLINE | ID: mdl-11469252

ABSTRACT

We studied a collection of 126 rhizobial isolates from eight species of Crotalaria (C. comosa, C. glaucoides, C. goreensis, C. hyssopifolia, C. lathyroides, C. perrottetii, C. podocarpa, and C. retusa) growing in Senegal. Nodulation and nitrogen-fixation tests on nine Crotalaria species revealed two specificity groups within the genus Crotalaria. Group I consists of plants solely nodulated by very specific fast-growing strains. Group II plants are nodulated by slow-growing strains similar to promiscuous Bradyrhizobium spp. strains already reported to nodulate many tropical legumes. SDS-PAGE studies showed that slow-growing strains grouped with Bradyrhizobium while fast-growing strains constituted a homogeneous group distinct from all known rhizobia. Amplified ribosomal DNA restriction analysis (ARDRA) of 10 representative strains of this group using four restriction enzymes showed a single pattern for each enzyme confirming the high homogeneity of group I. The 16S rDNA sequence analysis revealed that this specific group belonged to the genus Methylobacterium, thus constituting a new branch of nodulating bacteria.


Subject(s)
Crotalaria/microbiology , Methylobacterium/classification , Methylobacterium/genetics , Symbiosis , Bradyrhizobium/classification , Bradyrhizobium/genetics , Crotalaria/classification , DNA, Ribosomal/analysis , Electrophoresis, Polyacrylamide Gel , Phylogeny , RNA, Ribosomal, 16S/genetics , Restriction Mapping
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