Pharmaceutical Analysis A Textbook for Pharmacy Students and Pharmaceutical Chemists 4th Edition by David G Watson – Ebook PDF Instant Download/Delivery: 0702069892, 978-0702069895
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Product details:
ISBN 10: 0702069892
ISBN 13: 978-0702069895
Author: David G Watson
Pharmaceutical analysis forms a core part of any pharmacy programme, as well as being essential for pharmacology and medicinal chemistry courses.
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 analyses, 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.
The mathematics involved is notoriously difficult, but this much-praised textbook, now revised and updated for its fourth edition, guides a student through the complexities with clear writing and the author’s expertise from many years’ teaching pharmacy students. There is continuous learning reinforcement throughout the book by way of worked calculation examples and self-assessment test questions.
Pharmaceutical Analysis A Textbook for Pharmacy Students and Pharmaceutical Chemists 4th Table of contents:
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Introduction to Pharmaceutical Analysis
- The role of pharmaceutical analysis in drug development and manufacturing
- Importance of analytical techniques in ensuring drug quality, safety, and efficacy
- Overview of the regulatory requirements for pharmaceutical analysis
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Fundamentals of Analytical Chemistry
- Basic principles of analytical chemistry: accuracy, precision, sensitivity, and specificity
- Types of analytical techniques: qualitative and quantitative analysis
- Good laboratory practices (GLP) and standard operating procedures (SOPs)
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Pharmaceutical Quality Control
- Principles and practices in quality control (QC) of pharmaceutical products
- The role of quality control in ensuring drug safety and compliance with regulatory standards
- Good manufacturing practices (GMP) and their connection to pharmaceutical analysis
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Instruments and Techniques in Pharmaceutical Analysis
- Overview of instrumental analysis: spectroscopy, chromatography, and mass spectrometry
- Techniques for separation and identification: high-performance liquid chromatography (HPLC), gas chromatography (GC)
- Spectroscopic methods: ultraviolet (UV), infrared (IR), nuclear magnetic resonance (NMR), and atomic absorption spectroscopy (AAS)
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Titrimetric and Gravimetric Methods
- Principles and applications of volumetric (titrimetric) analysis
- Types of titrations: acid-base, redox, complexometric, and precipitation titrations
- Gravimetric analysis: the process of weighing to determine the concentration of a substance
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Chromatographic Techniques
- Fundamentals of chromatography: stationary phase, mobile phase, and separation principles
- Types of chromatography: column chromatography, thin-layer chromatography (TLC), HPLC, and GC
- Applications of chromatography in pharmaceutical analysis and drug quality control
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Spectroscopic Methods in Pharmaceutical Analysis
- UV and visible spectroscopy: principles, applications, and methods of quantitative analysis
- Infrared (IR) spectroscopy: characterizing functional groups and molecular structures
- NMR spectroscopy: its role in determining the structure of pharmaceuticals
- Mass spectrometry: principles and use in molecular identification and quantification
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Microbiological and Biological Testing of Pharmaceuticals
- Microbiological assays for sterility and microbial content in pharmaceutical products
- Biologic testing of drug products, including vaccines and biologics
- Testing for endotoxins and other biological contaminants in pharmaceuticals
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Analysis of Drug Dosage Forms
- Techniques for analyzing solid dosage forms: tablets, capsules, and powders
- Analysis of liquid dosage forms: solutions, suspensions, and emulsions
- Parenteral products: analysis of injectables, ophthalmic solutions, and other sterile preparations
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Stability Testing of Pharmaceuticals
- The importance of stability testing in drug formulation and shelf life
- Factors affecting drug stability: temperature, humidity, light, and packaging
- Methods for conducting stability studies and interpreting stability data
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Pharmacokinetic and Bioanalytical Testing
- Methods for analyzing drug absorption, distribution, metabolism, and excretion (ADME)
- Bioanalytical testing: measuring drug concentrations in biological samples
- Techniques for pharmacokinetic studies: blood plasma analysis, bioavailability testing
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Regulatory and Legal Aspects of Pharmaceutical Analysis
- Overview of regulatory agencies: FDA, EMA, ICH, and their guidelines for pharmaceutical analysis
- International pharmacopoeias and the role they play in pharmaceutical testing
- Legal considerations in pharmaceutical analysis, including compliance with GMP and GLP standards
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Recent Advances in Pharmaceutical Analysis
- Emerging analytical techniques and technologies in pharmaceutical testing
- The role of automation and high-throughput screening in modern pharmaceutical analysis
- Nanotechnology and its impact on pharmaceutical analysis and drug delivery
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Case Studies and Applications
- Practical examples and case studies of pharmaceutical analysis in drug development and quality control
- Analytical challenges in drug formulation and the importance of accurate analysis
- Discussion of real-world applications in pharmaceutical manufacturing and regulation
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Conclusion
- Summary of key principles in pharmaceutical analysis
- Future trends and developments in pharmaceutical analysis and drug testing
- The importance of continued research and innovation in pharmaceutical quality control
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