Search Results - "Theiss, U"

Twenty-four-hour intragastric pH profiles and pharmacokinetics following single and repeated oral administration of the proton pump inhibitor pantoprazole in comparison to omeprazole by Hartmann, M, Theiss, U, Huber, R, Lühmann, R, Bliesath, H, Wurst, W, Lücker, P W

“…Pantoprazole is a proton pump inhibitor characterized by a low potential to interact with the cytochrome P450 enzyme system in man. Its effect on intragastric…”
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PP03.09 SIMULATING THE OXIDATION PROCESS OF FE(II) TO FE(III) DURING WATER RADIOLYSIS WITHIN AN IRRADIATED FRICKE SOLUTION WITH TOPAS-nBIO AND COMPARISON TO EXPERIMENTAL DATA by Breitenbach, C., Weishaar, D., Erdmann, R., Derksen, L., Zink, K., Theiß, U., Adeberg, S., Baumann, K.S.

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PP05.09 DOSE RATE DEPENDENCE OF HYDROGEN PEROXIDE PRODUCTION IN RADIOLYSIS by Weishaar, D., Erdmann, R., Derksen, L., Witt, M., Adeberg, S., Zink, K., Keil, B., Theiß, U., Baumann, K.S.

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Voglibose (AO-128) is an efficient alpha-glucosidase inhibitor and mobilizes the endogenous GLP-1 reserve by Göke, B, Fuder, H, Wieckhorst, G, Theiss, U, Stridde, E, Littke, T, Kleist, P, Arnold, R, Lücker, P W

“…The alpha-glucosidase inhibitor voglibose (AO-128) was designed to prevent rapid postprandial blood glucose rises in non-insulin-dependent diabetics. We…”
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Pharmacological characterization of nicorandil by 86Rb efflux and isometric vasorelaxation studies in vascular smooth muscle by Kreye, V A, Lenz, T, Pfründer, D, Theiss, U

“…Nicorandil and cromakalim were found to stimulate 86Rb efflux (a marker of K+ ions) from resting preparations of rabbit aorta. This action was suppressed by…”
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Iontophoresis--is there a future for clinical application? by Theiss, U, Kuhn, I, Lücker, P W

“…Transdermal application of drugs is a field of great importance in medical therapy. The application is painless and may be controlled at any time…”
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Renal elimination of magnesium as a parameter of bioavailability of oral magnesium therapy by Kuhn, I, Jost, V, Wieckhorst, G, Theiss, U, Lücker, P W

“…Magnesium is an important cation in human physiology, especially in the regulation of membrane proteins, as a cofactor for various enzyme systems and in…”
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Dialysability of dimethindene maleate (Fenistil) from blood after intravenous injection by Kuhn, I, Theiss, U, Rehn, D, Gegenheimer, L, Lücker, P W

“…Dimethindene, an antihistaminic drug, is the treatment of choice in dialysis patients suffering from skin itching. During hemodialysis procedures not only…”
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A17-4 Initiating mechanisms of paroxysmal atrial fibrillation in patients with implantable cardiac defibrillators: First results of the European GEM III at registry by Janko, S., Hahnefeld, A., Mermi, J., Follner, G., Theiss, U., Galler, M., Farges, E., Hoffmann, E.

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Efficacy and tolerability of a “suprabioavailable” formulation of fenofibrate in patients with dyslipidemia: a pooled analysis of two open-label trials by Ramjattan, Brian R., Callaghan, Denis J.G., Theiss, Uwe

“…Background: Newer fibrates such as micronized fenofibrate lower triglyceride (TG) levels, raise high-density lipoprotein cholesterol (HDL-C) levels, and lower…”
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24-Hour Recording of Intragastric pH in Clinical Trials: Preconditions, Methodology, and Standardization Strategies by Timmer, Wolfgang, Wehling, Martin, Theiss, Uwe

“…At present, intragastric pH recording by stomach probe is the standard method for the assessment of the pharmacodynamic effect of newly developed antisecretory…”
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Effects of the K super(+) channel blocker tedisamil on super(86)Rb efflux induced by cromakalim, high potassium and noradrenaline, and on mechanical tension in rabbit isolated vascular smooth muscle by Kreye, VAW, Pfruender, D, Theiss, U

“…Tedisamil, a new bradycardic agent with an inhibitory action on K super(+) channels in cardiac muscle, was found to inhibit in a non-competitive manner the…”
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The dualistic mode of action of the vasodilator drug, nicorandil, differentiated by glibenclamide in 86Rb flux studies in rabbit isolated vascular smooth muscle by KREYE, V. A. W, LENZ, T, THEISS, U

“…(1) In rabbit isolated aorta, the effects of the antianginal drug, nicorandil, of the K+ channel opener, cromakalim, and of the nitrovasodilator, sodium…”
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Effects of the K+ channel blocker tedisamil on 86Rb efflux induced by cromakalim, high potassium and noradrenaline, and on mechanical tension in rabbit isolated vascular smooth muscle by KREYE, V. A. W, PFRÜNDER, D, THEISS, U

“…Tedisamil, a new bradycardic agent with an inhibitory action on K+ channels in cardiac muscle, was found to inhibit in a non-competitive manner the relaxation…”
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The bioequivalence of two different batches of two nifedipine controlled-release preparations with deficient batch conformity in in vitro liberation studies by Theiss, U, Gebhardt, E, Müller, J

“…The pharmacokinetics of two batches of two different nifedipine (CAS 21829-25-4) controlled release formulations (product 1 or 2, respectively) were…”
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Gastric potential difference measurement as a quantification of gastrointestinal tolerability comparing a buffered acetylsalicylic acid formulation versus plain acetylsalicylic acid by Jost, V, Kuhn, I, Rogalla, K, Theiss, U, Lücker, P W

“…Two different acetylsalicylic acid (ASA, CAS 50-78-2) formulations (Aspirin) were compared regarding their gastric mucosal tolerability. After administration…”
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