Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Harold T. Smith"'
Publikováno v:
Bioanalysis. 4:1429-1443
Background: In support of a pilot clinical trial using acetaminophen as the model compound to assess dried blood spot (DBS) sampling as the method for clinical pharmacokinetic sample collection, a novel sensitive LC–MS/MS method was developed and v
Autor:
Rajesh Karan, Karin Meiser, Jingli Duan, Qi Yin, Gangadhar Sunkara, Harold T. Smith, Jin Chen
Publikováno v:
Int. Journal of Clinical Pharmacology and Therapeutics. 50:33-43
Objective The efficacy and safety of valsartan/amlodipine combination have been demonstrated for the treatment of hypertension. In China, where the prevalence of hypertension is increasing the pharmacokinetic study of valsartan, amlodipine assumes si
Publikováno v:
Bioanalysis. 3:967-972
Background: In this case study, urine samples were collected and transferred before the presence of a small degree of nonspecific binding was identified for the analyte of interest in human urine. The approach taken to address the issue was to use st
Publikováno v:
Journal of Chromatography B. 878:583-589
Analyte loss due to non-specific binding, especially container surface adsorption, is not uncommon in the quantitative analysis of urine samples. In developing a sensitive LC-MS/MS method for the determination of a drug candidate, BAF312, in human ur
Publikováno v:
Toxicology. 213:1-12
Transplantation in nonhuman primates, in particular using solid organs from porcine donors, requires an efficacious induction immunosuppression. Besides biologicals, the low molecular weight drugs used include cyclophosphamide (CyP) and methotrexate
Autor:
Harold T. Smith, Henk-Jan Schuurman
Publikováno v:
Xenotransplantation. 12:72-75
Background: In vivo xenotransplantation modeling in large animal species is often performed in nonhuman primates, including baboons. For proper data interpretation, reference values for clinical chemistry and hematology are required. Methods: These v
Autor:
James F. McLeod, Harold T. Smith, Pratapa Prasad, Hilde Bigler, Gangadhar Sunkara, Yibin Wang, Monica Ligueros-Saylan
Publikováno v:
Current Medical Research and Opinion. 20:41-48
The potential for a drug interaction was investigated between nateglinide, an oral antidiabetic agent, and acenocoumarol, an oral anticoagulant, as these drugs are primarily metabolized via CYP2C9.A two-period, randomized, double-blind, two-way cross
Autor:
James F. McLeod, James Lee, Harold T. Smith, Damayanthi Devineni, Pratapa Prasad, Yulia H. Walter
Publikováno v:
The Journal of Clinical Pharmacology. 43:163-170
Treatment of hyperglycemia in patients with diabetes mellitus and renal insufficiency is complicated by altered pharmacokinetics of hypoglycemic agents. This study evaluated the pharmacokinetic profile and safety of nateglinide, an amino acid derivat
Publikováno v:
Journal of Cardiovascular Pharmacology. 37:502-511
Fluvastatin sodium (Lescol, Novartis Pharmaceutical Corp., East Hanover, NJ, U.S.A.), a potent 3-hydroxy-3-methylglutaryl coenzyme A (HMG Co-A) reductase inhibitor that limits cholesterol biosynthesis, is available as a 40-mg immediate-release formul
Autor:
Jordan M. Dunitz, Ramona L. Doyle, David Tudor, James E. Loyd, John M. Kovarik, Marshall I. Hertz, R. Wong, Lin Dou, Silke Appel-Dingemanse, Kimberly A Chappell, Arlene A. Stecenko, Harold T. Smith, Timothy R. Brazelton, Randall E. Morris
Publikováno v:
The Journal of Heart and Lung Transplantation. 20:330-339
Background RAD is a novel macrolide with potent immunosuppressive and antiproliferative activities. This study characterizes the safety, tolerability, and pharmacokinetics of two different single oral doses of RAD in stable lung and heart/lung transp