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Biomedical subjects

Karsten Meyer

Publications and source records attributed to Karsten Meyer.

At least 19 recordsLinked to original sources
PubMed2006

Small molecule activation at uranium coordination complexes: control of reactivity via molecular architecture.

Electron-rich uranium coordination complexes display a pronounced reactivity toward small molecules. In this Feature article, the exciting chemistry of trivalent uranium ions coordinated to classic Werner-type ligand environments is reviewed. Three fundamentally important reactions of the [(((R)ArO)3tacn)U]-system are presented that result in alkane coordination, CO/CO2 activation, and nitrogen atom-transfer chemistry.

Alkanes↗
PubMed2005

Carbon dioxide reduction and carbon monoxide activation employing a reactive uranium(III) complex.

The highly reactive, six-coordinate tris-aryloxide U(III) species, [((t-BuArO)3tacn)U] (1) reacts with CO2 in a 2e- reduction to produce CO and a dinuclear U(IV/IV) mu-oxygen bridged complex [{((t-BuArO)3tacn)U}2(mu-O)] (2). This reaction proceeds via a dinuclear CO2-bridged intermediate 3. Also, mononuclear 1 was treated with 1 atm of CO to yield dinuclear [{((t-BuArO)3tacn)U}2(mu-CO)] (4) with a CO ligand bridging two uranium ions in an unprecedented mu:eta1,eta1 fashion. The mixed-valent azido-bridged U(III/IV) complex 5 was synthesized from trivalent 1 and tetravalent [((t-BuArO)3tacn)U(N3)] and serves as an isostructural analogue of triatomic-bridged intermediate 3 as well as an electronic model for mixed-valent 4.

Journal Article↗
PubMed2005

Influence of organically or conventionally produced wheat on health, performance and mycotoxin residues in tissues and bile of growing pigs.

From 1999-2001 three different varieties of wheat [Contur (susceptible to Fusarium), Batis and Petrus (less susceptible to Fusarium)] were cultivated under organic and conventional conditions in order to determine mycotoxin burden. Soil quality, preceding crop and weather conditions were comparable in the different production systems. The wheat batches were analysed for moulds, and the contents of zearalenone (ZEN) and deoxynivalenol (DON). Feeding trials were carried out with growing pigs (n = 96; average initial live weight 22.2 +/- 1.5 kg [mean +/- SD]) to examine a possible influence on the animal performance and on mycotoxin residues. The data recorded were clinical conditions, performance, biochemical and hematological data. Residues of ZEN, alpha- and beta-zearalenol (ZEL) and of DON were determined in bile, liver and muscle after slaughtering. Conventionally cultivated wheat was more frequently contaminated with Fusarium and contained more frequently ZEN and DON in higher concentrations than the organically produced wheat. Hematological and biochemical parameters of pigs fed with organically cultivated diets were not different from those of conventionally fed pigs. Pigs fed with organically produced wheat showed a slightly higher daily weight gain, but a lower carcass yield than the conventionally fed animals. The highest residues of DON and total-ZEN (ZEN + alpha-ZEL + beta-ZEL) were found in bile. Bile samples of organically fed pigs contained lower concentrations of total-ZEN than those of conventionally fed pigs. Altogether, these data suggest that wheat from an organic farming does not have higher mycotoxin-contamination than wheat from the conventional farming system.

Agriculture↗
PubMed2004

Terminal cobalt(III) imido complexes supported by tris(carbene) ligands: imido insertion into the cobalt-carbene bond.

Highly reactive tris-carbene Co(I) complexes [(TIMENaryl)Co]Cl react with organic azides to yield monomeric Co(III) imido complexes [(TIMENaryl)Co(NAr')](BPh4) (aryl = mes, xyl; Ar = -C6H4-CH3, -C6H4-OCH3). The cobalt-imido fragment in these complexes is electrophilic and, as a result, the imido group readily inserts into the cobalt-carbene bond, yielding bis-carbene imine cobalt complexes.

Journal Article↗
PubMed2004

Dioxygen activation by a low-valent cobalt complex employing a flexible tripodal N-heterocyclic carbene ligand.

The novel versatile cobalt(I) tris-carbene complex [(TIMEN(xyl))Co]Cl (1) (where TIMEN = (tris[2-(3-arylimidazol-2-ylidene)ethyl]amine) reacts with CO, one-electron oxidizers such as CH(2)Cl(2), and O(2) to yield the cobalt complexes [(TIMEN(xyl))Co(CO)]Cl (2), [(TIMEN(xyl))Co(Cl)]Cl (3), and peroxo species [(TIMEN(xyl))Co(O(2))](BPh(4)) (5). All new complexes were fully characterized by (1)H NMR, UV/vis, and IR spectroscopy as well as superconducting quantum interference device (SQUID) magnetization measurements and single-crystal X-ray crystallography. The nucleophilic character of the eta(2)-bound dioxygen ligand in 5 was confirmed by density functional theory (DFT) studies and allows for oxygen-transfer reactions with electron-deficient organic substrates, such as benzoyl chloride.

Cobalt↗
PubMed2004

A linear, O-coordinated eta1-CO2 bound to uranium.

The electron-rich, six-coordinate tris-aryloxide uranium(III) complex [((AdArO)3tacn)U(III)] [where (AdArOH)3tacn = 1,4,7-tris(3-adamantyl-5-tert-butyl-2-hydroxybenzyl)1,4,7-triazacyclononane] reacts rapidly with CO2 to yield [((AdArO)3tacn)U(IV)(CO2)], a complex in which the CO(2) ligand is linearly coordinated to the metal through its oxygen atom (eta1-OCO). The latter complex has been crystallographically and spectroscopically characterized. The inequivalent O-C-O bond lengths [1.122 angstroms (A) for the O-C bond adjacent to uranium and 1.277 A for the other], considered together with magnetization data and electronic and vibrational spectra, support the following bonding model: U(IV)=O=C*-O- <--> U(IV)-OC-O-. In these charge-separated resonance structures, the uranium center is oxidized to uranium(IV) and the CO2 ligand reduced by one electron.

Carbon Dioxide↗
PubMed2004

Mobility of the growth promoters trenbolone and melengestrol acetate in agricultural soil: column studies.

There is growing concern about environmentally released man-made chemicals suspected to be responsible for a number of adverse effects on endocrine function in wildlife species and possibly also in humans. Sex hormones are of particular interest due to their regulatory role in developmental processes such as sexual differentiation. Endogenous hormones of human or animal origin as well as exogenous sex steroids used for contraception or as anabolics for farm animals are excreted and reach the environment. We investigated the transport of the synthetic growth promoters trenbolone (TbOH) and melengestrol acetate (MGA) in agricultural soil by means of column experiments with aggregated soil materials (Ap and Bt horizons of a Luvisol). Column effluent concentrations and depth profiles of TbOH and MGA were determined with sensitive enzyme immunoassay systems and HPLC (RP-18), respectively. All procedures were confirmed by liquid chromatography-mass spectrometry. Small amounts of TbOH and MGA passed the columns very quickly. However, both hormones exhibited a high affinity to the organic matter of both horizons leading to a high retardation within the upper layers of the soil columns. Although we cannot deduce whether hormones of animal origin reach the ground water under field conditions, our model experiments show that their transition can be presumed.

Adsorption↗
PubMed2004

Synthesis and characterization of N-heterocyclic carbene complexes of uranium(III).

Reaction of [(((Ad)ArO)(3)tacn)U(III)] (1) or [((Me(3)Si)(2)N)(3)U(III)] (3) with tetramethylimidazol-2-ylidene (Me(4)IMC:) yields novel N-heterocyclic carbene complexes [(((Ad)ArO)(3)tacn)U(III)(Me(4)IMC:)] (2) and [((Me(3)Si)(2)N)(3)U(III)(Me(4)IMC:)] (4). Uranium complexes 2 and 4 represent the first examples of compounds with an N-heterocyclic carbene ligand coordinated to a low-valent uranium center. The paramagnetic complexes 1, 2, and 4 were characterized by (1)H NMR, UV-vis-NIR, and EPR spectroscopy as well as SQUID magnetization measurements and X-ray diffraction analyses. DFT studies indicate a significant degree of pi-bonding in the U(III)-carbene entity.

Journal Article↗
PubMed2004

Parametric perfusion imaging with contrast-enhanced ultrasound in acute ischemic stroke.

BACKGROUND AND PURPOSE: Color-coded perfusion maps can be calculated from ultrasound harmonic gray-scale imaging data after ultrasound contrast agent bolus injection to analyze brain tissue perfusion. First reports indicate that this method can display cerebral perfusion deficits in acute ischemic stroke. We performed a prospective patient study to evaluate this approach. METHODS: Thirty consecutive patients suffering from acute middle cerebral artery infarction who presented to our department within 12 hours after symptom onset were investigated with ultrasound perfusion harmonic imaging (PHI) after Levovist bolus injection. Color-coded perfusion maps were calculated from the ultrasound data. In addition, the original gray-scale images were analyzed in cine mode. Findings were compared with those of cranial CT. RESULTS: All 30 patients suffered from acute ischemic stroke of the middle cerebral artery territory (median National Institutes of Health Stroke Scale score, 16 points). Twenty-three of the 30 patients (76.7%) had sufficient PHI insonation conditions. In 19 of these 23 patients (82.6%), a marked deficit in contrast enhancement could be visualized by initial PHI with the color-coded parameter images and cine-mode images. In 17 of the 23 (73.9%), the perfusion deficit was found on the parameter images. The area of hypoperfusion in the initial PHI investigation corresponded to the definite area of infarction in follow-up cranial CT. In 3 of 23 patients (13.0%), a perfusion deficit could be demonstrated in PHI, although the supplying artery was found patent by transcranial color-coded duplex sonography. CONCLUSIONS: With PHI, it is possible to display cerebral perfusion deficits in acute ischemic stroke. PHI yields additional information on the perfusion state of the human brain compared with extracranial and transcranial color-coded duplex sonography.

Acute Disease↗
PubMed2004

Effects of mycophenolic acid (MPA) treatment on expression of Fc receptor (FcRn) and polymeric immunoglobulin receptor (pIgR) mRNA in adult sheep tissues.

AIM: To quantify the expression of Fc receptor (FcRn) and polymeric immunoglobulin receptor (pIgR) mRNA under a long-term influence of mycotoxin mycophenolic acid (MPA), which is used in human transplantation medicine due to its immunosuppressive properties and is a common contaminant in silage. METHOD: We applied 300 mg MPA/day in nine sheep for nine weeks and compared them with untreated animals (n=9). The expression level of Ig receptor mRNA was determined in eight different adult ovine tissues (liver, kidney, jejunum, ileum, spleen, thymus, mesenteric and pharyngeal lymph nodes). For a reliable and sensitive mRNA quantification of Ig receptor subtypes, a real-time reverse transcriptase-polymerase chain reaction (RT-PCR) was used with a relative- and tissue-specific efficiency corrected quantification model (REST). RESULTS: Each tissue exhibited an individual expression pattern of FcRn and pIgR mRNA. Both types of Ig receptors were highly expressed in the liver, kidney, and gastrointestinal tract. Medium-to-low expressions were found in the spleen, thymus, mesenteric and pharyngeal lymph nodes. FcRn mRNA was significantly down-regulated by MPA in the liver (p=0.02). After MPA treatment, a significant up-regulation of pIgR mRNA expression was observed in the ileum and liver (p=0.04 for both). Expression level of FcRn mRNA in the tissues in decreasing order was as follows: liver > kidney > jejunum > ileum > spleen > thymus > mesenterial lymph node > pharyngeal lymph node; whereas expression level for pIgR mRNA was the following: liver > kidney > jejunum > ileum > pharyngeal lymph node > spleen > thymus > mesenterial lymph node. CONCLUSION: The MPA exhibited immunomodulatory effects in the liver and ileum of treated sheep. Its possible immunosuppressive effects may be explained by lowering the level of FcRn expression in the liver, which resulted in a lower IgG serum-to-bile transport. However, MPA showed stimulatory effects on pIgR expression in the liver and ileum, suggesting good IgA and IgM transport in these tissues.

Animals↗
PubMed2003

Evidence for alkane coordination to an electron-rich uranium center.

A series of five uranium-alkane complexes of the general formula [(ArO)3tacn)U(alkane)].(cy-alkane) has been synthesized and crystallographically characterized. In all cases, X-ray diffraction studies revealed a pseudo-six-coordinate trivalent uranium core structure, [(ArO)3tacn)U], with a coordinated alkane ligand at the axial position. The average U-C bond distance to the bound alkane was determined to be 3.798 A, which is considerably shorter than the sum of the van der Waals radii of the U atom and a CH2 or CH3 unit (3.9 A). In all complexes, the alkane is coordinated in an eta2-H,C fashion.

Journal Article↗
PubMed2003

Copper complexes of nitrogen-anchored tripodal N-heterocyclic carbene ligands.

Incorporation of a nitrogen functionality into a tripodal N-heterocyclic carbene ligand system affords the first N-anchored tetradentate tris-carbene ligands TIMEN(R) (R = Me (5a), t-Bu (5b), Bz (5c)). Treatment of the methyl derivatized [H(3)TIMEN(Me)](PF(6))(3) imidazolium salt (H(3)5a) with silver oxide yields the silver complex [(TIMEN(Me))(2)Ag(3)](PF(6))(3) (9), which, in a ligand transfer reaction, reacts with copper(I) bromide to give the trinuclear copper(I) complex [(TIMEN(Me))(2)Cu(3)](PF(6))(3) (10). Deprotonation of the tert-butyl and benzyl derivatives [H(3)TIMEN(t-Bu)](PF(6))(3) and [H(3)TIMEN(Bz)](PF(6))(3) yields the free tris-carbenes TIMEN(t-Bu) (5b) and TIMEN(Bz) (5c), which react readily with copper(I) salts to give mononuclear complexes [(TIMEN(t-Bu))Cu](PF(6)) (11b) and [(TIMEN(Bz))Cu]Br (11c). The solid-state structures of 10, 11b, and 11c were determined by single-crystal X-ray diffraction. While the TIMEN(Me) ligand yields trinuclear complex 10, with both T-shaped three-coordinate and linear two-coordinate copper(I) centers, the TIMEN(t-Bu) and TIMEN(Bz) ligands induce mononuclear complexes 11b and 11c, rendering the cuprous ion in a trigonal planar ligand environment of three carbenoid carbon centers and an additional, weak axial nitrogen interaction. Complexes 11b and 11c exhibit reversible one-electron redox events at half-wave potentials of 110 and -100 mV vs Fc/Fc(+), respectively, indicating sufficient electronic and structural flexibility of both TIMEN(R) ligands (R = t-Bu, Bz) to stabilize copper(I) and copper(II) oxidation states. Accordingly, a copper(II) NHC complex, [(TIMEN(Bz))Cu](OTf)(2) (12), was synthesized. Paramagnetic complex 12 was characterized by elemental analysis, EPR spectroscopy, and SQUID magnetization measurements.

Journal Article↗
PubMed2003

Uranium tris-aryloxide derivatives supported by triazacyclononane: engendering a reactive uranium(III) center with a single pocket for reactivity.

The synthesis and spectroscopic characterization of the mononuclear uranium complex [((ArO)(3)tacn)U(III)(NCCH(3))] is reported. The uranium(III) complex reacts with organic azides to yield uranium(IV) azido as well as uranium(V) imido complexes, [((ArO)(3)tacn)U(IV)(N(3))] and [((ArO)(3)tacn)U(V)(NSi(CH(3))(3))]. Single-crystal X-ray diffraction, spectroscopic, and computational studies of this analogous series of uranium tris-aryloxide complexes supported by triazacyclononane are described. The hexadentate, tris-anionic ligand coordinates to the large uranium ion in unprecedented fashion, engendering coordinatively unsaturated and highly reactive uranium centers. The macrocyclic triazacyclononane tris-aryloxide derivative occupies six coordination sites, with the three aryloxide pendant arms forming a trigonal plane at the metal center. DFT quantum mechanic methods were applied to rationalize the reactivity and to elucidate the electronic structure of the newly synthesized compounds. It is shown that the deeply colored uranium(III) and uranium(V) species are stabilized via pi-bonding interaction, involving uranium f-orbitals and the axial acetonitrile and imido ligand, respectively. In contrast, the bonding in the colorless uranium(IV) azido complex is purely ionic in nature. The magnetism of the series of complexes with an [N3O3-N(ax)] core structure and oxidation states +III, +IV, and +V is discussed in context of the electronic structures.

Heterocyclic Compounds, Bridged-Ring↗
PubMed2003

Effect of ultrasound on thrombolysis of middle cerebral artery occlusion.

We studied the effect of transcranial 2 MHz Doppler ultrasound (US) on the recanalization and outcome of stroke patients suffering from acute middle cerebral artery occlusion. All patients underwent intravenous recombinant tissue-type plasminogen activator thrombolysis. Eleven patients were randomly selected for continuous US monitoring (C-US) over 1 hour; 14 patients were selected for the control group. The C-US group showed a higher grade of recanalization after 1 hour but also a higher number of intraparenchymal bleedings. Overall, a favorable functional outcome occurred more frequently in the C-US group (Barthel index, p = 0.037) after 3 months.

Brain↗