Farmaceutisk kemi og teknologi

This book, Clinical Biochemistry and Drug Development: From Fundamentals to Output, focuses on clinical biochemistry fundamentals, cell culture techniques, and drug discovery and development concepts. It deals with three different fields of clinical research: cell culture, clinical biochemistry, and drug discovery and development.

This new volume explores biologically active natural products and their use in microbial technologies and as phyto-pharmaceuticals in drug development. It presents detailed scientific principles and recent research on applications of nanotechnology in diagnostics and drug delivery.

This volume on applied pharmaceutical science and microbiology looks at the latest research on the applications of natural products for drug uses. It focuses on understanding how to apply the principles of novel green chemistry methods in the vital area of pharmaceuticals.

This book details the latest research and development in the use of magnetic resonance imaging and spectroscopy as tools to give quantitative insights concerning late stage pharmaceutical formulation, tablet manufacturing and drug dissolution behaviour. The book combines different facets of magnetic resonance and highlights the use of spatial resolution (MRI) and how this adds to the knowledge base to further our understanding of the microscopic physicochemical processes occurring during drug release from solid dosage forms. New topics, that have not been thoroughly reviewed elsewhere, are covered including the applications of solution state magnetic resonance in process scale up, reaction monitoring/understanding and process analytical technologies (PAT); dissolution testing; and counterfeit analysis. Solid state NMR and its role in understanding phase separation in dispersions, polymorphism and crystallography is included and magnetic resonance imaging and its use in assessing tablet dissolution performance, mass transport and mixing in hot melt extrusion (HME) are covered.Focusing on late stage development rather than molecular drug discovery provides a unique approach and the book will appeal to a diversity of disciplines using spectroscopy for study. Aimed at researchers in drug development, manufacture and formulation in both industry (pharmaceutical companies) and academia (pharmacy program), it includes examples, where appropriate, of studies on commercially available pharmaceutical products.

Unverzichtbar im Herstellungs- und Verarbeitungsbetrieb:Fehlerbewertungslisten von PackmittelnDie Packmittel-Fehlerbewertungslisten sind für eine effiziente und strukturierte Durchführung der Qualitätssicherung obligatorisch. Die Fehlerbwertungslisten bieten eine Hilfestellung für den Umgang zwischen Hersteller bzw. Lieferant und Verwender (Kunde). Namhafte Experten aus der Verpackungsprüfung in der Pharmaindustrie haben für die Qualitätssicherung von Packmitteln jeweils umfangreiche und detaillierte Unterlagen erarbeitet. Die Fehlerbewertungslisten orientieren sich an den GMP-Regeln, Arzneibüchern (EP, USP, JP), gesetzlichen Vorgaben und Direktiven sowie technischen Normen EN ISO 2859-1, DIN EN ISO 15378, ANSI Z1.4 (ehemals MILSTD 105). Fehlerklassifizierungen, Stichprobentabellen sowie detaillierte Beschreibungen der Prüfungsmethoden erleichtern die praktische Arbeit. Die vorliegende Neuauflage wurde in Zusammenarbeit mit namhaften Herstellern der Röhrenglas-Industrie sowie mit dem Bundesverband Glasindustrie e.V. gemäß den aktuellen Vorgaben sowie dem heutigen Stand der Technik und des Wissens grundlegend überarbeitet und erweitert um Fehlermerkmale für Spritzen sowie einen bebilderten vierfarbigen Anhang mit Beispielen spezifischer Fehlermerkmale.

Consumer interest in diet and nutritional supplements is increasing dramatically. This book is designed to meet the needs of those professionals who are called upon to advise patients and the general public. It provides a valuable text for those who are researchers or decision-makers in the food and pharmaceutical industries. The text presents a thorough account of this topical subject and enables the reader to appreciate the functions of nutrients in health and common disease states, to understand the current debates over the roles of nutrients and supplements in the diet, and to answer those questions frequently asked by patients and consumers.

Updated and revised, this new edition provides an overview of the design concepts and statistical practices involved in therapeutic drug development. The latest advancements in the realm of drug safety are discussed, and the text includes expanded coverage of clinical trials.