A Textbook Of Pharmaceutics Technology
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| Author | : Ajay Semalty |
| Publisher | : Pharmamed Press |
| Total Pages | : 364 |
| Release | : 2019-09-03 |
| Genre | : Medical |
| ISBN | : 9789385433177 |
Delivering the active medicament to the body system for a certain therapeutic action is the central idea of Pharmaceutical technology. A Pharmaceutical drug is delivered through various routes of administration with the help of various kinds of dosage forms. Moreover a drug product should be effective, safe and stable. All the aspects of pharmaceutical texts, dealing with drug delivery basically target these three issues The book covers -Basics of dissolution study, bioavailability and stability studies (and ICH guidelines) in detail with recent guidelines -Most common and popular dosage forms viz. tablet, capsule, parenterals, suspension and emulsion have been discussed Other topics discussed include controlled release products, oral protein delivery etc -USPs of the book are easy language, to the point coverage of topics, pictorial/graphical, tabular presentation and a glossary of official definitions of all important key words of Pharmaceutics. We hope that this book shall be very useful to students as well as teachers as ready source of basics of each and every covered topic.
| Author | : Alfred Fahr |
| Publisher | : John Wiley & Sons |
| Total Pages | : 885 |
| Release | : 2018-01-17 |
| Genre | : Medical |
| ISBN | : 1118972430 |
A textbook which is both comprehensive and comprehensible and that offers easy but scientifically sound reading to both students and professionals Now in its 12th edition in its native German, Voigt's Pharmaceutical Technology is an interdisciplinary textbook covering the fundamental principles of pharmaceutical technology. Available for the first time in English, this edition is produced in full colour throughout, with a concise, clear structure developed after consultation with students, instructors and researchers. This book: Features clear chapter layouts and easily digestible content Presents novel trends, devices and processes Discusses classical and modern manufacturing processes Covers all formulation principles including tablets, ointments, capsules, nanosystems and biopharmaceutics Takes account of legal requirements for both qualitative and quantitative composition Addresses quality assurance considerations Uniquely relates contrasting international pharmacopeia from EU, US and Japan to formulation principles Includes examples and text boxes for quicker data assimilation Written for both students studying pharmacy and industry professionals in the field as well as toxicologists, biochemists, medical lab technicians, Voigt’s Pharmaceutical Technology is the essential resource for understanding the various aspects of pharmaceutical technology.
| Author | : Michael E. Aulton |
| Publisher | : Elsevier Health Sciences |
| Total Pages | : 909 |
| Release | : 2013 |
| Genre | : Medical |
| ISBN | : 0702042900 |
"Pharmaceutics is the art of pharmaceutical preparations. It encompasses design of drugs, their manufacture and the elimination of micro-organisms from the products. This book encompasses all of these areas."--Provided by publisher.
| Author | : Walkiria S. Schlindwein |
| Publisher | : John Wiley & Sons |
| Total Pages | : 319 |
| Release | : 2018-01-05 |
| Genre | : Science |
| ISBN | : 1118895215 |
A practical guide to Quality by Design for pharmaceutical product development Pharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative approach is based on the application of product and process understanding underpinned by a systematic methodology which can enable pharmaceutical companies to ensure that quality is built into the product. Familiarity with Quality by Design is essential for scientists working in the pharmaceutical industry. The authors take a practical approach and put the focus on the industrial aspects of the new QbD approach to pharmaceutical product development and manufacturing. The text covers quality risk management tools and analysis, applications of QbD to analytical methods, regulatory aspects, quality systems and knowledge management. In addition, the book explores the development and manufacture of drug substance and product, design of experiments, the role of excipients, multivariate analysis, and include several examples of applications of QbD in actual practice. This important resource: Covers the essential information about Quality by Design (QbD) that is at the heart of modern pharmaceutical development Puts the focus on the industrial aspects of the new QbD approach Includes several illustrative examples of applications of QbD in practice Offers advanced specialist topics that can be systematically applied to industry Pharmaceutical Quality by Design offers a guide to the principles and application of Quality by Design (QbD), the holistic approach to manufacturing that offers a complete understanding of the manufacturing processes involved, in order to yield consistent and high quality products.
| Author | : Geoffrey D Tovey |
| Publisher | : Royal Society of Chemistry |
| Total Pages | : 432 |
| Release | : 2018-06-25 |
| Genre | : Medical |
| ISBN | : 1849739412 |
Formulation is a key step in the drug design process, where the active drug is combined with other substances that maximise the therapeutic potential, safety and stability of the final medicinal product. Modern formulation science deals with biologics as well as small molecules. Regulatory and quality demands, in addition to advances in processing technologies, result in growing challenges as well as possibilities for the field. Pharmaceutical Formulation provides an up to date source of information for all who wish to understand the principles and practice of formulation in the drug industry. The book provides an understanding of the links between formulation theory and the practicalities of processing in a commercial environment, giving researchers the knowledge to produce effective pharmaceutical products that can be approved and manufactured. The first chapters introduce readers to different dosage forms, including oral liquid products, topical products and solid dosage forms such as tablets and capsules. Subsequent chapters cover pharmaceutical coatings, controlled release drug delivery and dosage forms designed specifically for paediatric and geriatric patients. The final chapter provides an introduction to the vital role intellectual property plays in drug development. Covering modern processing methods and recent changes in the regulatory and quality demands of the industry, Pharmaceutical Formulation is an essential, up to date resource for students and researchers working in academia and in the pharmaceutical industry.
| Author | : Jiben Roy |
| Publisher | : Elsevier |
| Total Pages | : 449 |
| Release | : 2011-07-25 |
| Genre | : Medical |
| ISBN | : 1908818042 |
This textbook is written as a unified approach to various topics, ranging from drug discovery to manufacturing, techniques and technology, regulation and marketing. The key theme of the book is pharmaceuticals - what every student of pharmaceutical sciences should know: from the active pharmaceutical ingredients to the preparation of various dosage forms along with the relevant chemistry, this book makes pharmaceuticals relevant to undergraduate students of pharmacy and pharmaceutical sciences.This book explains how a particular drug was discovered and then converted from lab-scale to manufacturing scale, to the market. It explains the motivation for drug discovery, the reaction chemistry involved, experimental difficulties, various dosage forms and the reasoning behind them, mechanism of action, quality assurance and role of regulatory agencies. After having a course based on this book, the student will be able to understand: 1) the career prospects in the pharmaceutical industry, 2) the need for interdisciplinary teamwork in science, 3) the techniques and technology involved in making pharmaceuticals starting from bulk drugs, and 4) different dosage forms and critical factors in the development of pharmaceutical formulations in relation to the principles of chemistry.A few blockbuster drugs including atorvastatin, sildanefil, ranitidine, ciprofloxacin, amoxicillin, and the longest serving drugs such as aspirin and paracetamol are discussed in detail. Finally, the book also covers the important current pharmaceutical issues like quality control, safety, counterfeiting and abuse of drugs, and future prospects for pharmaceutical industry. - Unified approach explaining drug discovery, bulk drug manufacturing, formulation of dosage forms, with pharmacological and therapeutic actions - Manufacturing processes of representative active pharmaceutical ingredients and their chemistry plus formulation of dosage forms presented in this book are based on actual industrial processes - Covers many aspects relevant to students of the pharmaceutical sciences or newly employed pharmaceutical researchers/employees. It contains summary information about regulatory agencies of different countries
| Author | : Defang Ouyang |
| Publisher | : John Wiley & Sons |
| Total Pages | : 350 |
| Release | : 2015-07-20 |
| Genre | : Science |
| ISBN | : 1118573994 |
Molecular modeling techniques have been widely used in drug discovery fields for rational drug design and compound screening. Now these techniques are used to model or mimic the behavior of molecules, and help us study formulation at the molecular level. Computational pharmaceutics enables us to understand the mechanism of drug delivery, and to develop new drug delivery systems. The book discusses the modeling of different drug delivery systems, including cyclodextrins, solid dispersions, polymorphism prediction, dendrimer-based delivery systems, surfactant-based micelle, polymeric drug delivery systems, liposome, protein/peptide formulations, non-viral gene delivery systems, drug-protein binding, silica nanoparticles, carbon nanotube-based drug delivery systems, diamond nanoparticles and layered double hydroxides (LDHs) drug delivery systems. Although there are a number of existing books about rational drug design with molecular modeling techniques, these techniques still look mysterious and daunting for pharmaceutical scientists. This book fills the gap between pharmaceutics and molecular modeling, and presents a systematic and overall introduction to computational pharmaceutics. It covers all introductory, advanced and specialist levels. It provides a totally different perspective to pharmaceutical scientists, and will greatly facilitate the development of pharmaceutics. It also helps computational chemists to look for the important questions in the drug delivery field. This book is included in the Advances in Pharmaceutical Technology book series.
| Author | : Stephen Goundrey-Smith |
| Publisher | : Springer Science & Business Media |
| Total Pages | : 249 |
| Release | : 2012-10-05 |
| Genre | : Medical |
| ISBN | : 1447127803 |
IT in Pharmacy: An Integrated Approach aims to describe and discuss the major areas of pharmacy IT innovation (e-prescribing, drug databases, electronic patient records, clinical decision support, pharmacy management systems, robots and automation etc) from a systems and a professional perspective. It will also consider how the areas of pharmacy IT link together and can be used to enable and develop pharmacy professional practice. The book will examine pharmacy IT from an international perspective, taking into account all parts of the world where IT systems are used in pharmacy practice – namely – North America, the UK, Western Europe and Australia – and will compare pharmacy IT in the different regions. This book is from the author of Principles of Electronic Prescribing (Springer, 2008)
| Author | : Dr. Niranjan Panda |
| Publisher | : Academic Guru Publishing House |
| Total Pages | : 216 |
| Release | : 2023-03-02 |
| Genre | : Study Aids |
| ISBN | : 811915200X |
Graduates in Pharmaceutical Technology are needed worldwide, from the development of medications through their manufacture and packaging. There are excellent employment options in every area of the pharmaceutical industry, both in India and overseas. A "Pharmaceutical Technology" graduate is required at several stages of drug development, including drug research, validation, delivery systems, scaling up manufacturing process, etc. A graduate of the Pharmaceutical technology program has the ability, depending on their level of expertise, to work in the disciplines of chemical engineering, chemistry, bioprocesses engineering, or education in addition to the pharmaceutical industry. The potential in this sector is quite vast since India is one of leading producers of pharmaceuticals. While it is possible to get work in other countries, it is preferable to look for work in India. A "Pharmaceutical Technology Engineer" may readily find work in research and development labs, where their responsibilities include the design of quality pharmaceuticals, as well as the manufacture and inspection of drugs. The scope is quite vast and is expanding on an annual basis. Every industry is evolving more quickly than ever thanks to emerging technology. The pharmaceutical technology industry has also benefited from this, expanding to new heights. These next trends cover a wide range of topics, including artificial intelligence, automation, and more. The trends also indicate that new work possibilities are being created in the industry of the pharmaceutical technology. The technology has offered society several boons while lessening the man’s work.
| Author | : Dilip M. Parikh |
| Publisher | : CRC Press |
| Total Pages | : 905 |
| Release | : 2021-05-11 |
| Genre | : Medical |
| ISBN | : 1000366383 |
Theoretical discussions covering granulation and engineering perspectives. Covers new advances in expert systems, process modelling and bioavailability Chapters on emerging technologies in particle engineering Updated Current research and developments in granulation technologies
