Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:Q86TM3 (cage)
 29,987 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

To assess abrasive wear of mechanical valve prostheses containing pyrolytic carbon components, we recovered at necropsy or surgery and analyzed by scanning electron microscopy and surface profilometry eight prostheses. Seven were implanted for 30-85 (mean 50 months. Valves included DeBakey aortic (2), DeBakey mitral (1), Beall mitral (2), Bjork-Shiley aortic (1), Cooley-Cutter mitral (1), and Lillehei-Kaster (L-K) tricuspid (1). All carbon occluders had undetectable wear. Carbon cage struts had a superficial burnish. Metallic struts had insignificant wear marks. In contrast, a Teflon Beall Model 104 valve implanted for 34 days and similarly analyzed had considerable material loss from the cage struts. This study suggests that clinically important abrasive wear will not be a late complication of cardiac valve replacement with pyrolytic carbon prostheses.
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PMID:Durability of pyrolytic carbon-containing heart valve prostheses. 713 Feb 12

Carbon fiber and titanium cage implantation for anterior column support during spinal fusions is an alternative to the use of more traditional structural allografts and autografts. The authors report instrumentation and cage failure for patients who underwent spinal fusion with structural titanium mesh cages implanted into the anterior column a minimum of 2 years after surgery. They wanted to determine whether plain radiographic techniques can be used to critically assess disk space and corpectomy fusions after implantation of these radioopaque cages. Fifty patients having undergone spinal fusions using structural titanium mesh cages in the anterior column had 99 anterior levels fused with at least 1 (maximum of 2) titanium mesh cage, resulting in a total of 131 cages used. The cages were examined for evidence of settling, migration, or failure. The anterior and posterior instrumentation was assessed for evidence of failure, and the spine was examined for evidence of successful fusion. Radiographic cage settling (>2 mm) into the vertebral body end plates was observed, but cage migration or failure were not. An average lordotic correction of 10 degrees was observed, with loss of correction into kyphosis from immediately after operation to final follow-up averaging 2 degrees. As an average of all reviewers, using a strict radiographic fusion assessment, definite or probable anterior fusion was graded at 81% of the levels, probably not or no at 5% of the levels, and could not be assessed at 14% of the levels. Definite or probable posterior fusion as an average of all reviewers was graded at 44% of the posterior fusion levels, questionable at 4%, no at 5%, and could not be assessed at 47%. The use of anterior-only, posterior-only, or anterior and posterior instrumentation with structural titanium mesh cages in the anterior spine along with proper autogenous bone grafting techniques provided anterior column support with a low rate of radiographic complications. Acceptable anterior spinal fusion rates, as assessed by a consensus agreement of reviewers, were observed primarily by evaluation of the fusion mass around the cages (extracage fusion), because intracage fusion was difficult to assess.
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PMID:Radiographic assessment of anterior titanium mesh cages. 1113 81

Three different surgical methods were used to treat single-segment degenerative cervical spine disease, and the radiological and clinical outcomes were compared. The three groups compared were: 21 cases of anterior interbody fusion with iliac autograft (group A); 20 cases of anterior plate fixation with iliac autograft (group B); and 19 cases of carbon cage fusion and anterior plate fixation (group C). Bone union and changes in Cobb's angle and interbody space were evaluated using radiographs and clinical results by the method of Odom et al. Cobb's angle increased in group C, which was significantly better than the decrease in groups A and B. The interbody space decreased in group C, but was significantly less than the decrease in groups A and B. Carbon cage and anterior plate fixation can be used as an alternative surgical treatment modality for single-segment degenerative cervical spine and can provide early stability, maintain the interbody space and cervical lordosis, reduce operation time and minimize complications at the bone graft donor site.
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PMID:A preliminary study of the use of cage and plating for single-segment fusion in degenerative cervical spine disease. 1645 86

Carbon-cluster anions, CN-, are very reactive toward SO2 (sticking probability of 0.012 +/- 0.005 for C27- at 25 degrees C), in contrast to their inertness toward other common atmospheric gases and pollutants. In flow reactor experiments at ambient temperature and near atmospheric pressure, primary adsorption of SO2 by the carbon cluster anions, N = 4-60, yields CNSO2- or CN-1S-. The inferred elimination of neutral CO2 is also detected as meta-stable decay in collision-induced dissociation. At higher temperatures, the reaction of SO2 with nascent carbon clusters yields CN-1SO- as well as undetected CO. The size-dependent initial reactivity reflects the previously established structural transitions (i.e., from chain to cyclic to cage structures). Such carbon clusters are formed in sooting flames and may act as nuclei for the formation of primary soot particles and serve as models for the local structural features of active soot particle sites for black-carbon soot. The facile generation of reactive carbon-sulfide and -sulfinate units may therefore have implications for understanding the health and environmental effects attributed to the coincidence of soot and SO2.
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PMID:Efficient low-temperature oxidation of carbon-cluster anions by SO2. 1683 61

Carbon nanocage, a three dimensional cage type mesoporous carbon with very high surface area and pore volume, has been functionalized with carboxyl groups for the first time via a simple oxidation using ammonium persulfate solution (APS). The carboxyl groups functionalized carbon nanocage materials have been unambiguously characterized by various sophisticated instruments such as FT-IR, HRSEM-EDX, XRD, nitrogen adsorption, and HRTEM. The degree of carboxyl group functionalization has been controlled by the simple adjustment of the oxidation parameters such as oxidation time, APS concentration and oxidation temperature. FT-IR spectroscopy combined with the HRSEM-EDX has been used to provide a quantitative analysis of the carboxyl groups on the surface of the carbon nanocage materials before and after the APS treatment. In addition, the effect of the oxidation parameters on the structural order and the textural parameters of the carbon nanocage materials has been studied. It has been found that the role of oxidation parameters is highly critical to obtain carbon nanocage materials with a high density of carboxyl groups without affecting the structural order and the pore parameters. Thus, the reaction parameters have been carefully optimized and the best condition for the preparation of carboxyl group functionalized carbon nanocage with well-ordered structure has been proposed.
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PMID:Carboxyl group functionalization of mesoporous carbon nanocage through reaction with ammonium persulfate. 1801 58

Reduction of 1,12-closo-C2B10H12 followed by reaction with the appropriate metal halide and metathesis with either [K(18-crown-6)]Br or [BTMA]Cl ([BTMA] = [C6H5CH2N(CH3)3]+) affords isolable salts of the supraicosahedral metallacarborane sandwich anions [4,4-M-(1,10-closo-C2B10H12)2]n- in moderate to good yield. Compounds prepared are [BTMA][4,4-Co-(1,10-closo-C2B10H12)2] ( 1), [K(18-crown-6)][4,4-Co-(1,10-closo-C2B10H12)2] ( 2), [K(18-crown-6)]2[4,4-Ni-(1,10-closo-C2B10H12)2] ( 3), [K(18-crown-6)]2[4,4-Fe-(1,10-closo-C2B10H12)2] ( 4), [BTMA]2[4,4-Fe-(1,10-closo-C2B10H12)2] ( 5) and [K(18-crown-6)]2[4,4-Ti-(1,10-closo-C2B10H12)2] ( 6). Oxidation of the iron(II) species 4 and 5 with FeCl3 in THF generates the iron(III) analogues [K(18-crown-6)][4,4-Fe-(1,10-closo-C2B10H12)2] ( 7) and [BTMA][4,4-Fe-(1,10-closo-C2B10H12)2] ( 8), respectively. All diamagnetic compounds were characterised spectroscopically and the structures of 1, 3, 4, 6, 7 and 8 were established by single crystal X-ray diffraction. All anions have the anticipated cluster structures with two docosahedral 13-vertex cages joined at the central metal atom (the common degree-six vertex 4). Carbon atoms occupy the degree-four vertex 1 and the degree-five vertex 10. 11B NMR spectroscopy suggests the anions have, on the NMR timescale, C2h symmetry in solution at room temperature, consistent with free rotation, or at least substantial libration, of cage units about the long molecular axis. In the solid state the relative conformations of the two cages may be rationalised by simple bonding arguments, the single exception being the conformation of 4, in which both cages are subject to directional B-H...K+ interactions to the [K(18-crown-6)]+ counterion. The salts 3, 6 and 7 also show B-H...K+ interactions but involving one cage only.
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PMID:New 13-vertex metallacarborane sandwich compounds; synthetic and structural studies. 1827 81

Carbon 1s shake-up spectra of fullerenes C(60), C(70), and C(82) and single-walled carbon nanotubes (SWCNTs) of (5,5), (6,5), and (7,6) have been investigated by using equivalent core hole Kohn-Sham density functional theory approach, in which only one-electron transition between molecular orbitals within core-hole potential is considered. The calculated spectra are generally in good agreement with results of equivalent core-hole time-dependent density functional theory calculations and available experiments, and reliable assignments for the complicated shake-up spectra of such large systems are provided. Calculations have also been performed for endohedral metallofullerene Gd@C(82) to demonstrate the possible use of shake-up processes to identify the charge transfer between the metal ion and the carbon cage. It is found that the exciton binding energy of all systems under investigation is around 0.5 eV.
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PMID:A density functional theory study of shake-up satellites in photoemission of carbon fullerenes and nanotubes. 1857 May 16

Carbon atoms self-assemble into the famous soccer-ball shaped Buckminsterfullerene (C(60)), the smallest fullerene cage that obeys the isolated-pentagon rule (IPR). Carbon atoms self-assemble into larger (n > 60 vertices) empty cages as well-but only the few that obey the IPR-and at least 1 small fullerene (n <or= 60) with adjacent pentagons. Clathrin protein also self-assembles into small fullerene cages with adjacent pentagons, but just a few of those. We asked why carbon atoms and clathrin proteins self-assembled into just those IPR and small cage isomers. In answer, we described a geometric constraint-the head-to-tail exclusion rule-that permits self-assembly of just the following fullerene cages: among the 5,769 possible small cages (n <or= 60 vertices) with adjacent pentagons, only 15; the soccer ball (n = 60); and among the 216,739 large cages with 60 < n <or= 84 vertices, only the 50 IPR ones. The last finding was a complete surprise. Here, by showing that the largest permitted fullerene with adjacent pentagons is one with 60 vertices and a ring of interleaved hexagons and pentagon pairs, we prove that for all n > 60, the head-to-tail exclusion rule permits only (and all) fullerene cages and nanotubes that obey the IPR. We therefore suggest that self-assembly that obeys the IPR may be explained by the head-to-tail exclusion rule, a geometric constraint.
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PMID:A geometric constraint, the head-to-tail exclusion rule, may be the basis for the isolated-pentagon rule in fullerenes with more than 60 vertices. 1905 75

Structures and relative stabilities of carbon clusters belonging to different families have been investigated for diameters d < or = 5 nm based on an efficient semiempirical molecular dynamics (MD) scheme as well as a density functional theory based simulation. Carbon clusters studied include fullerenes and fullerene-derived structures (e.g., cages and onions), icosahedral structures, bucky-diamond structures, and clusters cut from the bulk diamond with spherical and facetted truncations. The reason for using a semiempirical MD is partly due to the large number of different cases (or carbon allotropes) investigated and partly due to the size of the clusters investigated in this work. The particular flavor of the semiempirical MD scheme is based on a self-consistent and environment-dependent Hamiltonian developed in the framework of linear combination of atomic orbitals. We find that (i) among the families of carbon clusters investigated, fullerene structures have the lowest energy with the relative energy ordering being E(fullerene) < E(onion) < E(icosahedral) < E(bucky-diamond) < E(bulk-truncated), (ii) a crossover between bucky-diamond and icosahedral structures is likely at d approximately 8 nm, (iii) the highest occupied molecular orbital-lowest unoccupied molecular orbital gap as a function of the diameter for the case of fullerenes shows an oscillatory behavior with the gap ranging from 2 eV to 6 meV, and the gap approaching that of gapless graphite for d > 3.5 nm, and (iv) there can be three types of phase transformations depending on the manner of heating and cooling in our simulated annealing studies: (a) a bucky-diamond structure --> an onionlike structure, (b) an onionlike --> a cage structure, and (c) a bucky-diamond --> a cage structure.
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PMID:Energetics, relative stabilities, and size-dependent properties of nanosized carbon clusters of different families: fullerenes, bucky-diamond, icosahedral, and bulk-truncated structures. 1944 44

Carbon nitride materials have extraordinary potential in various applications, including catalysts, filled-particles, and superhard materials. Carbon nitride nanoclusters have been prepared under mild solvothermal conditions by a reaction between 1,3,5-trichlotriazine and sodium azide in toluene. The bulk material formed has a C(3)N(4) composition and consists of spheres with diameters ranging from approximately 1 nm to 4 mum. Nanometer-sized clusters of C(3)N(4) stoichiometry have been isolated on surfaces by sublimation or simple physicochemical methods. The clusters have then been characterized by atomic force microscopy and X-ray photoelectron spectroscopy. The laser desorption ionization mass spectra show peaks assignable to the C(12)N(16), C(21)N(28), and C(33)N(44) molecules which could correspond to cage structures with 4, 7, and 11 units of the C(3)N(4) subunit, respectively. The structure and stability of these new nitrogen-rich carbon nitride nanocages has been investigated using density functional theory calculations.
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PMID:Azafullerene-like nanosized clusters. 1986 Mar 86


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