8 edition of Drug metabolism and transport found in the catalog.
|Statement||edited by Lawrence H. Lash.|
|Series||Methods in pharmacology and toxicology|
|Contributions||Lash, Lawrence H.|
|LC Classifications||RM301.55 .D7625 2005, RM301.55 .D7625 2005|
|The Physical Object|
|Pagination||x, 387 p. :|
|Number of Pages||387|
|ISBN 10||1588293246, 1592598323|
|LC Control Number||2004013419|
The Drug Interaction Database (referred to as DIDB), part of UW Drug Interaction Solutions, is designed to support research and regulatory scientists in their decision-making when evaluating PK-based drug interactions and drug safety. In vitro drug metabolism, drug transport and drug-drug interactions (DDIs) (involving human metabolizing. Silymarin, the extract of milk thistle, and its major active flavonolignan silybin, are common products widely used in the phytotherapy of liver diseases. They also have promising effects in protecting the pancreas, kidney, myocardium, and the central nervous system. However, inconsistent results are noted in the different clinical studies due to the low bioavailability of silymarin. Extensive Cited by: 1.
the need for drug metabolism Many cells in tissues that act as portals for entry of external molecules into the body (eg, pulmonary epithelium, intestinal epithelium) contain transporter molecules (MDR family [P-glycoproteins], MRP family, others) that expel unwanted molecules immediately after absorption. A series of chemical modifications of a drug compound by enzymatic activity that make the substrate (drug) more water soluble to allow its clearance from the body. Drug metabolism occurs in two phases: Phase I (biotransformation) involves oxidation, hydroxylation reduction, and hydrolysis. Phase II (conjugation) involves synthesis and conjugation.
drug metabolism Definition (NCI) A series of chemical modifications of a drug compound by enzymatic activity that make the substrate (drug) more water soluble to allow its clearance from the body. Drug metabolism occurs in two phases: Phase I (biotransformation) involves oxidation, hydroxylation reduction, and . Human Drug Metabolism, An Introduction, Second Edition provides an accessible introduction to the subject and will be particularly invaluable to those who already have some understanding of the life sciences. Completely revised and updated throughout, the new edition focuses only on essential chemical detail and includes patient case histories to illustrate the clinical consequences of changes.
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13 rows Among the key topics covered are: the interplay between drug transport and metabolism in oral bioavailability; the influence of genetic and epigenetic factors on drug metabolism; impact of disease on transport and metabolism; and the use of novel microdosing techniques and novel LC/MS and genomic technologies to predict the metabolic parameters Cited by: 8.
Human Drug Metabolism, An Introduction, Second Edition provides an accessible introduction to the subject and will be particularly invaluable to those who already have some understanding of the life sciences.
Completely revised and updated throughout, the new edition focuses only on essential chemical detail and includes patient case histories to illustrate the clinical.
In Drug Metabolism and Transport: Molecular Methods and Mechanisms, well-established investigators describe their best experimental approaches and strategies for studying the bioactivation, detoxification, tissue distribution, and elimination of xenobiotics in the metabolism and/or Drug metabolism and transport book of various chemicals.
In Drug Metabolism and Transport: Molecular Methods and Mechanisms, well-established investigators describe their best experimental approaches and strategies for studying the bioactivation, detoxification, tissue distribution, and elimination of xenobiotics in the metabolism and/or transport of various chemicals.
The authors address several of Format: Hardcover. This special theme issue of Pharmaceutical Research entitled “Disease, Drug Metabolism and Transporter Interactions” focuses on the molecular impact that specific pathological states have upon the transport and metabolism of drugs in the body, with particular emphasis on disease states that affect the entero-hepatic system.
Experts from Cited by: 5. Human Drug Metabolism, 3rd Edition is an excellent book for advanced undergraduate and graduate students in molecular biology, biochemistry, pharmacology, pharmacy, and toxicology.
It will also appeal to professionals interested in an introduction to this field, or who want to learn more about these bench-to-bedside topics to apply it to their Author: Michael D.
Coleman. Topics on Drug Metabolism. This book presents some in-depth reviews of selected topics in drug metabolism. Topics covered includes: Oral Absorption, Intestinal Metabolism and Human Oral Bioavailability, Pharmacogenetics and Metabolism, Altered Drug Metabolism and Transport in Pathophysiological Conditions, Anticancer Drug Metabolism: Chemotherapy Resistance and New.
Jian-Da Lu, Jun Xue, in Critical Care Nephrology (Third Edition), Metabolism. Drug metabolism is the chemical alteration of a drug by the body. The liver is the principal, but not the sole, site of most drug metabolism in the body.
The cytochrome P enzyme system is particularly important because many different drugs also can induce or inhibit these enzymes, resulting in changing. Recently, interactions involving drug transporters, including P-glycoprotein and the organic anion transporting polypeptide, have also been identified.
Further research is needed to determine the scope, magnitude and clinical importance of Cited by: metabolism necessitate on-going studies of its biotransformation.
In the first chapter, the principles underlying drug absorption, distribution, metabolism and elimination are described, with drug metabolism highlighted within the context of these fundamental processes.
Chapters 2 and 3 deal with the chemistry of drug biotransformation,File Size: 2MB. Drug Metabolism and Pharmacokinetics (DMPK) is an official online journal of the Japanese Society for the Study of Xenobiotics (JSSX), and it replaces the JSSX's former journal, Xenobiotic Metabolism and Disposition.
The journal will accept original submissions in English on the understanding that the work is unpublished and is not being considered for publication elsewhere.
DMD presents important research in pharmacology and toxicology and is a valuable resource in drug design, drug metabolism, drug transport, expression of drug metabolizing enzymes and transporters, and regulation of drug metabolizing enzyme and transporter gene expression.
Drug Metabolism and Disposition. Vol. 48, Issue 3. Table of Contents. Altered drug metabolism and transport in pathophysiological conditions.
Several studies have shown that drug metabolism and transport is disrupted during diseases and altered pathophysiological conditions primarily due to reductions in gene expression of these enzymes and transporters (Aitken et al.,Kato, ).The transcription factors such as nuclear factor-κB (NF Cited by: 2.
Drug Metabolism Handbook is dedicated to helping bench scientists take full advantage of the latest and most advanced tools and techniques in the field of drug metabolism. From creating new molecular entities to drug development to troubleshooting, the book explains the concepts of drug metabolism and guides readers through its applications in Cited by: This new edition overviews drug transporters and presents the principles of drug transport and associated techniques, featuring new chapters on multidrug and toxin extrusion proteins, placental transport, in silico approaches in drug discovery, and regulatory guidance for drug transport studies in drug development.
Pharmaceutics, an international, peer-reviewed Open Access journal. Dear Colleagues, Clinically important phase I and II metabolizing enzymes and transporters from two major superfamilies, ABC (ATP binding cassette) and SLC (Solute carrier) transporters, are designated and the pivotal roles of drug metabolizing enzymes and drug transporters in the pharmacokinetics, pharmacogenomics, and drug.
Most tablets and capsules have a code or number stamped onto them for identification purposes. Most extensive reference book available, with more than listings. Drugs listed by identifiable codes, colors, shapes, and whether the tablet is scored.
Book provides the manufacturer, generic and brand names, strength, and use of the drug. The liver expresses P monooxygenase systems for drug metabolism and detoxification.
Metabolism and detoxification protect liver from injury by drugs and toxic metabolites. Drug Metabolism and Disposition is a peer-reviewed scientific journal covering the fields of pharmacology and was established in and is published monthly by the American Society for Pharmacology and Experimental Therapeutics.
The journal publishes articles on in vitro and in vivo studies of the metabolism, transport, and disposition of drugs and environmental chemicals Discipline: Pharmacology, toxicology. The processes of drug absorption, distribution, metabolism, and elimination include membrane transport steps that traditionally have been thought of as being mediated by passive diffusion.
Research in vitro and in vivo has defined four basic mechanisms of transport across biological membranes: passive diffusion, facilitated diffusion, carrier. Drug Metabolism Letters publishes letters, original research articles, mini-reviews, thematic issues based on mini-reviews and letters, commentaries, technical notes and drug clinical trial studies on major advances in all areas of drug metabolism and disposition.
In vitro systems including CYP; enzyme induction and inhibition; drug-drug interactions and enzyme kinetics; pharmacokinetics.Phenotypic and genotypic characterization of n-acetylation / Craig K.
Svensson and David W. Hein --Methods and approaches to study metabolism and toxicity of acetaminophen / Sam A. Bruschi --Modulation of drug metabolism and antiviral therapies / Bernhard H. Lauterburg --Modulation of thiols and other low-molecular-weight cofactors: effects on.Liver is the primary site where majority of drug metabolism occurs in two phases.
During phase 1, the inactive drug is made active by a set of drug metabolising enzymes. This is done by adding a functional group (OH here) on to the drug compound. In phase 2, the active drug is made inactive and transformed in such a way that it is now suitable.