Quantitative Analysis of Drugs in Pharmaceutical Formulations, 3e PDF Download
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Author: P. D. Sethi
Publisher:
ISBN: 9788123905600
Category : Drugs
Languages : en
Pages : 692
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Book Description
Author: P. D. Sethi
Publisher:
ISBN: 9788123905600
Category : Drugs
Languages : en
Pages : 692
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Book Description
Author: Prabhu Dayal Sethi
Publisher:
ISBN: 9788190000505
Category :
Languages : en
Pages : 478
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Book Description
Author: Anette Müllertz
Publisher: Springer
ISBN: 1493940295
Category : Medical
Languages : en
Pages : 829
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Book Description
The aim of this book is to present a range of analytical methods that can be used in formulation design and development and focus on how these systems can be applied to understand formulation components and the dosage form these build. To effectively design and exploit drug delivery systems, the underlying characteristic of a dosage form must be understood--from the characteristics of the individual formulation components, to how they act and interact within the formulation, and finally, to how this formulation responds in different biological environments. To achieve this, there is a wide range of analytical techniques that can be adopted to understand and elucidate the mechanics of drug delivery and drug formulation. Such methods include e.g. spectroscopic analysis, diffractometric analysis, thermal investigations, surface analytical techniques, particle size analysis, rheological techniques, methods to characterize drug stability and release, and biological analysis in appropriate cell and animal models. Whilst each of these methods can encompass a full research area in their own right, formulation scientists must be able to effectively apply these methods to the delivery system they are considering. The information in this book is designed to support researchers in their ability to fully characterize and analyze a range of delivery systems, using an appropriate selection of analytical techniques. Due to its consideration of regulatory approval, this book will also be suitable for industrial researchers both at early stage up to pre-clinical research.
Author: Joachim Ermer
Publisher: John Wiley & Sons
ISBN: 3527604472
Category : Science
Languages : en
Pages : 418
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Book Description
Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness. Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends. With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.
Author: Eustace George Coverley Clarke
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 1258
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Book Description
Provides the means to identify and quantify drugs and other toxic substances in situations of overdose or poisoning and to interpret analytical results. Includes an analysis of toxic metals and pesticides.
Author: Dr. Amit Kumar Verma Ms. Raina Kulshrestha
Publisher: Blue Rose Publishers
ISBN:
Category : Language Arts & Disciplines
Languages : en
Pages : 72
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Book Description
Author: Donald Clarence. Garratt
Publisher: Springer Science & Business Media
ISBN: 1461333806
Category : Science
Languages : en
Pages : 937
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Book Description
General Monographs, Alphabetically Arranged and Consisting of Methods for Quantitative Determination of the Substance, its Salts, and Preparations of Which it is a Principal Con- Stituent.- Synthetic Organic Compounds, Methods for Determination of Substances not Included in the General Monographs.- Essential Oils.- Oils, Fats and Waxes.- Appendices.- I. Determination of Alcohol Content.- II. Complexometric Titrations.- III. Non-aqueous Titrations.- IV. The Oxygen-Flask Combustion Technique.- V. Determination of Water.- VI. Extraneous Matter in Food and Drugs.- VII. Microbiological Assays.- VII.
Author: AK Jaiswal
Publisher: Jaypee Brothers Medical Publishers
ISBN: 939059538X
Category : Medical
Languages : en
Pages : 694
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Book Description
This book is a comprehensive guide to forensic analytical toxicology for trainees in forensic medicine and forensic scientists. The second edition has been fully revised to provide clinicians with the latest developments and research in the field. New chapters covering the latest analytical instruments have been added to this edition. Beginning with guidance on setting up a modern toxicology laboratory, the next sections, with the help of flow charts, explain the procedures for collection, preservation, extraction, and clean up; and screening and colour tests for various poisons. The following chapters describe numerous major and minor analytical instruments and techniques, and their application in forensic toxicology. The text is further enhanced by clinical images, figures and tables. The previous edition (9789351522249) published in 2014.
Author: David G. Watson
Publisher: Elsevier Health Sciences
ISBN: 0702069884
Category : Medical
Languages : en
Pages : 598
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Book Description
Pharmaceutical analysis determines the purity, concentration, active compounds, shelf life, rate of absorption in the body, identity, stability, rate of release etc. of a drug. Testing a pharmaceutical product involves a variety of chemical, physical and microbiological analyses. It is reckoned that over £10 billion is spent annually in the UK alone on pharmaceutical analysis, and the analytical processes described in this book are used in industries as diverse as food, beverages, cosmetics, detergents, metals, paints, water, agrochemicals, biotechnological products and pharmaceuticals. This is the key textbook in pharmaceutical analysis, now revised and updated for its fourth edition. Worked calculation examples Self-assessment Additional problems (self tests) Practical boxes Key points boxes New chapter on electrochemical biosensors. New chapter on the quality control of biotechnologically produced drugs. Extended chapter on molecular emission spectroscopy. Now comes with an e-book on StudentConsult. Self-assessment is interactive in the accompanying online e-book. 65 online animations show concepts such as ionization partitioning of drug molecules etc. ~
Author: Bernd Spangenberg
Publisher: Springer Science & Business Media
ISBN: 364210729X
Category : Science
Languages : en
Pages : 399
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Book Description
Thin-layer chromatography (TLC) is widely used particularly for pharmaceutical and food analysis. While there are a number of books on the qualitative identification of chemical substances by TLC, the unique focus here is on quantitative analysis. The authors describe all steps of the analytical procedure, beginning with the basics and equipment for quantitative TLC followed by sample pretreatment and sample application, development and staining, scanning, and finally statistical and chemometric data evaluation and validation. An important feature is the coverage of effect-directed biological detection methods. Chapters are organized in a modular fashion facilitating the easy location of information about individual procedural steps.
