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of 42
pro vyhledávání: '"H R Ha"'
Autor:
Simon Hebeisen, Stephan Krähenbühl, D Konrad, H R Ha, Katri Maria Waldhauser, Daniel Bur, Karin Brecht
Publikováno v:
British Journal of Pharmacology. 155:585-595
Background and purpose: Amiodarone (2-n-butyl-3-[3,5 diiodo-4-diethylaminoethoxybenzoyl]-benzofuran, B2-O-CH2CH2-N-diethyl) is an effective class III antiarrhythmic drug demonstrating potentially life-threatening organ toxicity. The principal aim of
Publikováno v:
PLoS ONE, Vol 18, Iss 8, p e0290733 (2023)
BackgroundOlder adults frequently attend the Emergency Department (ED) with poorly defined symptoms, often called nonspecific complaints (NSC). NSC such as 'weakness' and 'not feeling well', often lead to an extensive differential diagnosis. Patients
Externí odkaz:
https://doaj.org/article/5b1a59b9f28f4b7ab0909bd9fc7a0d98
Publikováno v:
Xenobiotica. 31:239-248
1. Amiodarone (AMI) is a potent anti-arrhythmic drug and mono-N-desethylamiodarone (MDEA) is its only known metabolite. It was found recently that in rabbit liver microsomes MDEA was biotransformed to n-3-hydroxybutyl-MDEA (3OH-MDEA). 2. In liver mic
Publikováno v:
Journal of Liquid Chromatography. 18:2243-2255
An isocratic, rapid, sensitive and selective reversed phase high-performance liquid chromatographic (HPLC) assay with ultraviolet detection has been used to quantify the in vitro nimodipine metabolism in rat liver microsomes. (±) Nimodipine and its
Akademický článek
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Publikováno v:
British Journal of Clinical Pharmacology. 31:279-286
1. Population pharmacokinetic parameters of quinidine were determined based on 260 serum drug concentration measurements in 60 patients treated for arrhythmias with quinidine sulphate or quinidine bisulphate (Kinidin duriles) orally. 2. Quinidine kin
Publikováno v:
European Journal of Clinical Pharmacology. 38:509-513
The pharmacokinetics of oral and i.v. propafenone and its major metabolites have been investigated in 8 healthy subjects. The total body clearance of propafenone was 963 ml/min, the terminal half-life 198 min and its absolute bioavailability was 15.5
Publikováno v:
Journal of chromatography. B, Biomedical sciences and applications. 757(2)
Amiodarone (AMI) is a potent antiarrhythmic drug. In vivo and in vitro, AMI is biotransformed to mono-N-desethylamiodarone (MDEA). Recently, it was observed that MDEA was further hydroxylated to n-3'-hydroxybutyl-MDEA (3'OH-MDEA). The performance of
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 29(2)
Amiodarone (AMI) is a potent antiarrhythmic drug, but its metabolism has not yet been fully documented. Mono-N-desethylamiodarone (MDEA) is its only known metabolite. Our preliminary investigations using rabbit liver microsomes had shown that in vitr