Pharmaceutical Analysis E Book
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Author | : David G. Watson |
Publisher | : Elsevier Health Sciences |
Total Pages | : 598 |
Release | : 2015-12-24 |
Genre | : Medical |
ISBN | : 0702069884 |
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 | : David G. Watson |
Publisher | : Churchill Livingstone |
Total Pages | : 0 |
Release | : 2017 |
Genre | : Chromatographic analysis |
ISBN | : 9780702069895 |
'Pharmaceutical Analysis' is aimed primarily at pharmacy students and pharmaceutical chemists. It highlights the most important aspects of a wide range of techniques used in the control of the quality of pharmaceuticals.
Author | : David G. Watson |
Publisher | : Elsevier Health Sciences |
Total Pages | : 0 |
Release | : 2017 |
Genre | : Drugs |
ISBN | : 9780702070297 |
'Pharmaceutical Analysis' is aimed primarily at pharmacy students and pharmaceutical chemists. It highlights the most important aspects of a wide range of techniques used in the control of the quality of pharmaceuticals.
Author | : Satinder Ahuja |
Publisher | : Academic Press |
Total Pages | : 604 |
Release | : 2010-11-11 |
Genre | : Medical |
ISBN | : 0123759811 |
Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. - Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it - Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations - Features detailed coverage of QA, ethics, and regulatory guidance (quality by design, good manufacturing practice), as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS
Author | : David C Lee |
Publisher | : John Wiley & Sons |
Total Pages | : 384 |
Release | : 2009-02-12 |
Genre | : Science |
ISBN | : 1405172991 |
The use of analytical sciences in the discovery, development andmanufacture of pharmaceuticals is wide-ranging. From the analysisof minute amounts of complex biological materials to the qualitycontrol of the final dosage form, the use of analytical technologycovers an immense range of techniques and disciplines. This book concentrates on the analytical aspects of drugdevelopment and manufacture, focusing on the analysis of the activeingredient or drug substance. It provides those joining theindustry or other areas of pharmaceutical research with a source ofreference to a broad range of techniques and their applications,allowing them to choose the most appropriate analytical techniquefor a particular purpose. The volume is directed at analytical chemists, industrialpharmacists, organic chemists, pharmaceutical chemists andbiochemists.
Author | : David G. Watson |
Publisher | : Churchill Livingstone |
Total Pages | : 400 |
Release | : 2005 |
Genre | : Medical |
ISBN | : |
This introductory text highlights the most important aspects of a wide range of techniques used in the control of the quality of pharmaceuticals. Written with the needs of the student in mind, this clear, practical guide includes self-testing sections with arithmetical examples and tests to help students brush up on their arithmetical skills in an applied context.
Author | : Joachim Ermer |
Publisher | : John Wiley & Sons |
Total Pages | : 418 |
Release | : 2006-03-06 |
Genre | : Science |
ISBN | : 3527604472 |
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 | : P. D. Chaithanya Sudha |
Publisher | : Pearson Education India |
Total Pages | : 770 |
Release | : 2012 |
Genre | : |
ISBN | : 8131799506 |
Pharmaceutical Analysis is a compulsory subject offered to all the under graduate students of Pharmacy. This book on Pharmaceutical Analysis has been designed considering the syllabi requirements laid down by AICTE and other premier institutes/universities. The book covers both the Titrimetric and Instrumental aspects of Pharmaceutical analysis which is helpful for use in multiple semesters.
Author | : Lena Ohannesian |
Publisher | : CRC Press |
Total Pages | : 605 |
Release | : 2001-11-09 |
Genre | : Medical |
ISBN | : 0824741943 |
Exploring the analysis of pharmaceuticals, including polymorphic forms, this book discusses regulatory requirements in pharmaceutical product development and pharmaceutical testing. It covers methods of drug separation and procedures such as capillary electrophoresis for chromatographic separation of molecules. Additional topics include drug formulation analysis using vibrational and magnetic resonance spectroscopy and identification of drug metabolites and decomposition products using such techniques as mass spectrometry. The book provides more than 300 tables, equations, drawings, and photographs, and convenient, easy-to-use indices, facilitating quick access to each topic.
Author | : Ole Pedersen |
Publisher | : CRC Press |
Total Pages | : 168 |
Release | : 2006-01-13 |
Genre | : Medical |
ISBN | : 0203492269 |
Complete, referenced information in an easy-to-use formatMany of the monographs in the European Pharmacopiea, the industry standard test for certain groups of ingredients and excipients, do not describe the tests in full, but reference general methods based on test-tube chemistry. When a test fails, you need to know what went wrong, how it can be f