De Gruyter, 2023. — 108 p. This book discusses the effects of prolonged hypoventilation, or a pulmonary condition on hypoxia, and hypercapnia, its effect on the formation of some joint diseases, and the types of natural medicine used in the treatment of each joint disease. You will also find methods used to calculate thermodynamic parameters. You can also learn optimized...
Informa Healthcare USA, Inc., 2008. — 616 p. — (Drugs and the Pharmaceutical Sciences 178) — ISBN: 9780824758097 During the onset of any clinical trial there are many factors and variables to consider. Funding, time restraints, and regulatory agency guidelines are factors that often influence which variables will be studied, leaving other important information out of the study....
CRC Press, Taylor & Francis Group, Informa, 2010. — XI, 481 p. — ISBN13: 978-1-4398-2544-0 (eBook - PDF). The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has witnessed continual improvement over the last half century. New approaches that have transformed classical aseptic production...
Second Edition. — Universities Press (India), 2012. — 835 p. — eISBN 978-81-7371-789-5. The second edition of the textbook Herbal Drug Technology, based on the curriculum of various universities, caters to both bachelor''s and master''s courses in pharmacy and allied sciences. It contains detailed information on Indian systems of medicine, herbal therapeutics, crude drugs and...
Second Edition. — Universities Press (India), 2012. — 835 p. — eISBN 978-81-7371-789-5. The second edition of the textbook Herbal Drug Technology, based on the curriculum of various universities, caters to both bachelor''s and master''s courses in pharmacy and allied sciences. It contains detailed information on Indian systems of medicine, herbal therapeutics, crude drugs and...
Second Edition. — Universities Press (India), 2012. — 835 p. — eISBN 978-81-7371-789-5. The second edition of the textbook Herbal Drug Technology, based on the curriculum of various universities, caters to both bachelor''s and master''s courses in pharmacy and allied sciences. It contains detailed information on Indian systems of medicine, herbal therapeutics, crude drugs and...
2nd Edition. — Academic Press, 2011. — 582 p. — (Separation Science and Technology 10). — ISBN: 978-0-12-045555-3. Handbook 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,...
Academic Press, 2001. — 586 p. — (Separation Science and Technology 3). — ISBN: 978-0-12-045555-3. This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art...
New York – London: Informa Healthcare, 2010. — 505 p. — ISBN13: 9780849339936. Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high quality sterile dosage forms. The author has many years of experience in the development and manufacture of sterile dosage forms including solutions,...
The 10th ed. — Philadelphia-Baltimore-NY: Wolters Kluwer, 2014. — 794 p. The purpose of this text is to introduce pharmacy students to the principles, practices, and technologies applied in the preparation of pharmaceutical dosage forms and drug delivery systems. An integrated presentation is used in this textbook to demonstrate the interrelationships between pharmaceutical and...
Walter de Gruyter, 2023. — 393 p. — ISBN: 978-3-11-079176-1. Benefitting from phytochemicals in medicinal plants has lately gained increasingly more global relevance. The medicinal bioactivity might range from wound healing activity to anti-inflammatory and anti-viral effects. This work describes the challenging scientific process of systematic identification and taxonomy...
CRC Press, 2018. — 436 p. — ISBN: 978-1-84184-976-8. Pharmaceutical Dosage Forms: Capsules covers the development, composition, and manufacture of capsules. Despite the important role that capsules play in drug delivery and product development, few comprehensive texts on the science and technology of capsules have been available for the research and academic environments. This...
3rd edition. — CRC Press, 2008. — 328 p. Preface. Tooling for Pharmaceutical Processing. Tablet Press Instrumentation in the Research and Development Environment. Pharmaceutical Manufacturing: Changes in Paradigms. A Forward-Looking Approach to Process Scale-Up for Solid Dose Manufacturing. Dissolution and Drug Release. Setting Dissolution Specifications. Mechanical Strength of...
3rd edition. — CRC Press, 2008. — 570 p. Preface. Mass Transfer (from solid oral dosage forms). Approaches for Improving Bioavailability of Poorly Soluble Drugs. Experimental Design and Multivariate Optimization Tools in Formulation and Process Development. Knowledge-Based Systems and Other AI Applications for Tableting. Direct Compression and the Role of Filler-Binders....
3rd edition. — CRC Press, 2008. — 570 p. Preface. Mass Transfer (from solid oral dosage forms). Approaches for Improving Bioavailability of Poorly Soluble Drugs. Experimental Design and Multivariate Optimization Tools in Formulation and Process Development. Knowledge-Based Systems and Other AI Applications for Tableting. Direct Compression and the Role of Filler-Binders....
5th edition. — Churchill Livingstone, 2017. — 933 p. For all the pharmacy students out there part of your pharmacy degree will be to study formulation design and pharmaceutics. This is the holy grail of pharmaceutical technology books. The text reads well and introduces difficult concepts in a more easy-to-understand way, it is definitely worth the money to help you get through...
4th edition. — Churchill Livingstone, 2013. — 912 p. Pharmaceutics is one of the most diverse subject areas in all of pharmaceutical science. In brief, it is concerned with the scientific and technological aspects of the design and manufacture of dosage forms or medicines. An understanding of pharmaceutics is therefore vital for all pharmacists and those pharmaceutical...
Wiley, 2014. - 492 p. - Polymers have played a critical role in the rational design and application of drug delivery systems that increase the efficacy and reduce the toxicity of new and conventional therapeutics. Beginning with an introduction to the fundamentals of drug delivery, Engineering Polymer Systems for Improved Drug Delivery explores traditional drug delivery...
CRC Press, 1991. — 442 p. — ISBN: 0824785673. Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Dissolution Testing Devices Automation in Dissolution Testing Factors That Influence Dissolution Testing Interpretation of Dissolution Rate Data and Techniques of In Vivo Dissolution Chetan D. Lathia, and John H. Wood Dissolution of...
4th Edition. — Marcel Dekker, Inc., USA, 2002. — 826 p. — (Drugs and the Pharmaceutical Sciences 121) — ISBN: 0824706749 The fourth edition of Modern Pharmaceutics follows the same format and has the same goals as previous editions. Chapter 1 sets the stage by reviewing the role of drugs and drug products in treating and preventing disease, while also summarizing their primary...
Springer, 2012. — 135 p. MicroRNAs are small, non-coding RNA molecules that interact with target mRNAs to modulate their translation. They are now recognized as widespread and critical regulators of gene expression in the cell. This book is aimed at both industry- and academic-based researchers in the Biopharmaceutical production space who wish to learn more about these...
Wiley, 2022. — 309 p. — (Advances in Pharmaceutical Technology). — ISBN: 9781119678281. In Biopharmaceutics - From Fundamentals to Industrial Practice, distinguished Scientists from the UK's Academy of Pharmaceutical Sciences Biopharmaceutical Focus Group deliver a comprehensive examination of the tools used within the field of biopharmaceutics and their applications to drug...
Institution of Chemical Engineers, 2007. — 450 p. Written by a IChemE Working Party, made up of industrial experts, this guide aims to give a complete overview of pharmaceutical engineering. It provides authoritative guidance for newcomers to the industry, as well as being a comprehensive reference guide for more experienced personnel. Chapters in the book focus on engineering...
Wiley, 2022. — 579 p. — ISBN: 9781119769606. A comprehensive guide to the current research, major challenges, and prospects of controlled drug delivery systems. Controlled drug delivery has the potential to significantly improve therapeutic outcomes, increase clinical benefits, and enhance the safety of drugs in a wide range of diseases and health conditions. Fundamentals of...
Springer, 2016. — 235 p. This book describes 200 bio-polymers, including the most recent and advanced nanotechnology applications. The applications of various bio-medical and other future potential uses are covered and examined in depth. Systematic discussion of current leading natural polymers is also included. - Covers 200 bio-polymers with the most recent and advanced...
CreateSpace Independent Publishing Platform, 2013. — 134 p., ISBN: 1492393495 The United States Pharmacopeia (USP) defines several types of water including: Purified Water, Water for Injection, Sterile Purified Water, Sterile Water for Injection, Sterile Bacteriostatic Water for Injection, Sterile Water for Inhalation, and Sterile Water for Irrigation. Water For Pharmaceutical...
The Royal Society of Chemistry (RSC) Publishing, Cambridge, 2011, 354 p., ISBN: 978-1-84973-146-1 RSC Drug Discovery series Pharmaceutical process research and development is an exacting, multidisciplinary effort but a somewhat neglected discipline in the chemical curriculum. This book presents an overview of the many facets of process development and how recent advances in...
Fine Chemicals, 1998. — 544 p. A selection of about 500 formulations of human and veterinary drugs are presented in this booklet. They have all been developed in the last 20 years in the Applications Laboratories of BASF AG and are in solid, liquid, and semi-solid form. However, emphasis is placed on tablets. Human and veterinary medicines have not been dealt with in separate...
2nd Edition. — CRC Press, 2015. — 180 p. Since the completion of the first edition of this book, major developments have occurred in the pharmaceutical industry that have shaped the field of near-infrared (NIR) spectroscopy. A new initiative from the U.S. Food and Drug Administration (FDA) to modernize regulations of pharmaceutical manufacturing and drug quality has helped...
Marcel Dekker, 2002. — 189 p. — ISBN: 0824794532. This book discusses the theory, instrumentation, validation, and implementation of near-infrared spectroscopy for pharmaceutical and medical applications. It showcases a diverse range of contemporary methods for the production, screening, and analysis of new drug products and pharmaceuticals. Presents current approaches in...
Springer, 2013. - 432 p. - This book is part of a series dedicated to recent advances on preventive, predictive and personalised medicine (PPPM). It focuses on the theme of Drug delivery systems: advanced technologies potentially applicable in personalised treatments. The critical topics involving the development and preparation of effective drug delivery systems, such as:...
Wiley-Interscience, 2008. — 856 p. — ISBN: 978-0-470-25959-7. This Handbook of Manufacturing: Regulations and Quality focuses on all regulatory aspects and requirements that govern how drugs are produced for evaluation (and later, sale to and use in) humans. The coverage ranges from what the issues are at the early stages (when the amounts are small and the materials of limited...
Nova Science Publishers, 2017. — 295 p. — (New Developments in Medical Research) — ISBN: 9781536119770 Phytomedicines have been playing an important role since the beginning of civilization, curing many diseases and alleviating different symptoms for the wellbeing of humans and animals. The millenary history of medicinal plant use and its derivatives give credibility to the...
Springer, 2016. — 224 p. This textbook explains the fundamental aspects of nanotechnology and fills the gap between bio-inspired nanotechnological systems and functionality of living organisms, introducing new insights to their physicochemical, biophysical and thermodynamic behaviour. Addressed to all those involved in recent advances in pharmaceutics, this book is divided in...
Wiley-VCH Verlag & Co., 2012. — 354 p. — ISBN: 3527333959. The chemistry of heterocycles is an important branch of organic chemistry. This is due to the fact that a large number of natural products, e. g. hormones, antibiotics, vitamins, etc. are composed of heterocyclic structures. The Significance of Heterocycles for Pharmaceuticals and Agrochemicals Neurological Disorders...
Published by Woodhead Publishing Limited, 2013. — 299 p. ISBN: 1907568271 Research and development in the pharmaceutical industry is a time-consuming and expensive process, making it difficult for newly developed drugs to be formulated into commercially available products. Both formulation and process development can be optimized by means of statistically organized experiments,...
Hoboken, USA; West Sussex, UK: JohnWiley & Sons Ltd, 2018. — 343 p. — ISBN: 1119305144. . Provides comprehensive coverage of microneedles for delivering and monitoring patient drugs and vaccines. Microneedles are an incredibly active research area and have the potential to revolutionize the way many medicines and vaccines are delivered. This comprehensive research book covers...
CRC Press, 2003. — 246 p. — (Medicinal and Aromatic Plants - Industrial Profiles) — ISBN: 978-0415369541 St. John's wort (Hypericum perforatum) is one of the best-selling herbal medicines in the world. For that reason, research into all aspects of St. John's wort continues to intensify. Hypericum: The Genus Hypericum summarizes the current knowledge on a wide range of issues,...
12th edition. — John Wiley & Sons, 2018. — 888 p. 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...
4th edition. — CRC Press, 2017. — 407 p. Aqueous-based film coating has become routine in the pharmaceutical industry. This process eliminates the use of organic solvents and thus avoids economic, environmental, and toxicological issues related to residual solvents and solvent recovery. Aqueous-based coating, however, is complex and many variables may impact the final product...
Wiley-VCH, 2017. — 293 p. — ISBN: 3527341153 Retaining the successful approach found in the previous volume in this series, the inventors and primary developers of drugs that successfully made it to market tell the story of the drug's discovery and development and relate the often twisted route from the first candidate molecule to the final marketed drug. 11 selected case...
Wiley, 2006. — 610 p. The first authoritative overview of past and current strategies for successful drug development by analog generation, this unique resource spans all important drug classes and all major therapeutic fields, including histamine antagonists, ACE inhibitors, beta blockers, opioids, quinolone antibiotics, steroids and anticancer platinum compounds. Of the 19...
Wiley, 2010. — 551 p. Born out of a project of the IUPAC's committee on Medicinal Chemistry and Drug Development, this reference addresses past and current strategies for successful drug analog development, extending the previously published volume by nine new analog classes and eight case studies. Like its precursor, this volume also contains a general section discussing...
Wiley, 2013. — 390 p. Most drugs are analogue drugs. There are no general rules how a new drug can be discovered, nevertheless, there are some observations which help to find a new drug, and also an individual story of a drug discovery can initiate and help new discoveries. Volume III is a continuation of the successful book series with new examples of established and recently...
CRC Press, 2020. — 211 p. The lyophilization equipment market is forecasted to double its value from $2.7 billion to $4.8 billion in 2020 as a consequence of development in the biopharma industry and the introduction of new drugs. The registration of new products with an expected high return, in particular, can be beneficial for introducing new technologies to production...
Springer, 2015. — 433 p. — (Advances in Delivery Science and Technology) — ISBN: 978-1-4939-1416-6 This comprehensive volume compiles the concepts essential for the understanding of the pharmaceutical science and technology associated with the delivery of subunit vaccines. Twenty-one chapters are divided into four main parts: (I) Background; (2) Delivery Systems for Subunit...
Wiley, 2019. — 299 p. — (Advances in Pharmaceutical Technology) — ISBN: 978-1-118-34147-6 In the last decade, the application of drug release testing has widened to a variety of novel/special dosage forms. In order to predict the in vivo behavior of such dosage forms, the design and development of the in vitro test methods need to take into account various aspects, including...
RSC Publishing, 2007. — 211 p. This book describes the technology of freeze-drying with particular emphasis on the properties of the material to be processed, pre-freezing (formulation) and post-drying (stability and shelf life). It is the first single-author publication, centred mainly on the properties of the materials to be processed, stored and marketed. The book aims to...
Second Edition. — CRC Press, 2018. — 413 p. — (Drugs and the Pharmaceutical Sciences). — ISBN: 9781498704915. Features Reviews how extrusion has become an accepted technology to continuously mix active pharmaceutical ingredients with excipients. Focuses on equipment and process technology. Explains various extrusion system configurations as a manufacturing methodology for a...
Second Edition, Informa Healthcare, 2009. - 560 p. This timely Second Edition reflects the mounting pressure on pharmaceutical companies to accelerate the new drug development and launch process, and the shift from developing small molecules to the growth of biopharmaceuticals. It meets the need for up-to-date and advanced information for drug preformulation and formulation,...
Informa, 2001. - 596 p. Written by a panel of experts, this book covers every stage of drug development, from candidate drug selection to commercial formulation. It provides practical reference and pragmatic guide on what studies need to be undertaken, for what reasons, and at what key stages of the drug development process. Going beyond coverage of preformulation, the book...
De Gruyter, 2021. — 348 p. — ISBN: 978-3-11-061687-3. Biopharmaceuticals, medicines made by or from living organisms (including cells from living organisms), are extremely effective in treating a broad range of diseases. Their importance to human health has grown significantly over the years as more biopharmaceutical products have entered the market, and now the biggest-selling...
Academic Press, 2020. — 288 p. — (Expertise in Pharmaceutical Process Technology). — ISBN: 978-0-12-809412-9. This book covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to...
2nd ed. — Wiley, 2017. — 737 p. — ISBN10: 1119126916. — ISBN13: 978-1119126911. Stay on the cutting edge of antibody purification with the insights of industry experts Biopharmaceutical companies are under extreme pressure to develop robust and economical large-scale processes while consistently meeting regulatory standards for safety and purity. Unfortunately, while upstream...
Elsevier, 2018. — 680 p. — (Pharmaceutical Nanotechnology). — ISBN: 978-0-12-813629-4. This book focuses on the fabrication, optimization, scale-up and biological aspects of pharmaceutical nanotechnology. In particular, the following aspects of nanoparticle preparation methods are discussed: the need for less toxic reagents, simplification of the procedure to allow economic...
William Andrew, 2018. — 614 p. — (Pharmaceutical Nanotechnology). — ISBN: 978-0-12-813665-2. This book showcases recent advances in pharmaceutical nanotechnology, with particular emphasis on tissue engineering, organ and cell applications. The book provides an up-to-date overview of organ targeting and cell targeting using nanotechnology. In addition, tissue engineering...
5th Edition. — Informa Healthcare USA, Inc., New York, USA, 2009. — 550 p. — (Drugs and the Pharmaceutical Sciences 190) — ISBN13: 9781420088496. Global registration of pharmaceutical drug, biologic, and device products is now the way pharmaceutical development and marketing are strategically planned. Since the publication of the fourth edition of New Drug Approval Process,...
CRC Press, 2006. — 429 p. This book was designed and written for validation professionals responsible for writing and maintaining quality management systems for the successful operation of their companies. It provides a set of standard operating procedures (SOPs) that can be used to manage and document critical validation and revalidation tasks in a pharmaceutical manufacturing...
Wiley, 2006. - 371 p. From skilful handling of the wide range of technologies to successful applications in drug discovery — this handbook has all the information professional proteomics users need. Edited by experts working at one of the hot spots in European proteomic research, the numerous contributions by experts from the pharmaceutical industry and public proteomics...
Wiley, 2013. — 236 p. This text is an essential study guide for undergraduates studying microbiology modules on degree courses in pharmacy and the pharmaceutical sciences. Written by two pharmacists each with over 30 years experience of teaching, research and publishing in pharmaceutical microbiology, it distills the subject down into the essential elements that pharmacists and...
John Wiley & Sons, Inc. 2011. — 377 p. ISBN: 978-0-470-57755-4 (cloth) There is a need explain that generic versions of a drug may not be manufactured by the same process as brand-name drugs and that the different processes may have dramatically different environmental impacts. Two global forces are at odds today — the push for "greener" processes and the push for lower drug...
Third, Completely Revised and Enlarged Edition. — Wiley-VCH, 2018. — 431 p. — ISBN: 978-3-527-34306-5. This completely updated and enlarged third edition of the classic text adopts a practical approach to describe the fundamentals of freeze-drying, backed by many explanatory examples. Following an introduction to the fundamentals, the book goes on to discuss process and plant...
2 ed. — CRC Press, 2009. — 236 p. With step-by-step methods of drug production and knowledge of major unit operations and key concepts of pharmaceutical engineering, this guide will help to improve communication among the varied professionals working in the pharmaceutical industry. Key features: Revision of a bestseller - updates include recent advances in the field to keep...
Elsevier, 2018. — 103 p. — (Emerging Issues in Analytical Chemistry). — ISBN: 978-0-12-812209-9. This book describes methods and procedures for consideration when developing inhaled pharmaceuticals, while commenting on product development strategies and their suitability to support regulatory submission. It bridges the gap between the aspirations of scientists invested in new...
CRC Press, 2001. — 286 p. Summarizing fundamental engineering principles and operations critical to converting bulk pharmaceutical products into patient-ready and appropriate drug delivery dosage forms, Pharmaceutical Process Engineering facilitates comprehensive understanding of the practical aspects of drug production in an accessible, step-by-step format. It provides a...
3rd ed. — CRC Press, 2019. — 730 p. — ISBN: 978-1-1380-6307-5. This fully revised and updated third edition of Pharmaceutical Inhalation Aerosol Technology encompasses the scientific and technical foundation for the rationale, design, componentry, assembly and quality performance metrics of therapeutic inhalers in their delivery of pharmaceutical aerosols to treat symptoms or...
CRC Press, 2024. — 255 p. — (Advances in Drying Science and Technology). — ISBN: 978-1-032-21616-4. Drying is a key operation in the processing of many plant-based foods and medicines for preservation and retention of key attributes and active compounds. Therefore, it is essential to select suitable drying techniques to ensure a product is processed under optimal operating...
Academic Press, 2020. — 312 p. — ISBN: 978-0-12-822550-9. Transdermal Drug Delivery: Concepts and Application provides comprehensive background knowledge and documents the most recent advances made in the field of transdermal drug delivery. It provides comprehensive and updated information regarding most technologies and formulation strategies used for transdermal drug...
Elsevier, 2018. — 1310 p. Biopharmaceutical Processing: Development, Design, and Implementation of Manufacturing Processes covers bioprocessing from cell line development to bulk drug substances. The methods and strategies described are essential learning for every scientist, engineer or manager in the biopharmaceutical and vaccines industry. The integrity of the bioprocess...
Elsevier, 2018. — 1310 p. Biopharmaceutical Processing: Development, Design, and Implementation of Manufacturing Processes covers bioprocessing from cell line development to bulk drug substances. The methods and strategies described are essential learning for every scientist, engineer or manager in the biopharmaceutical and vaccines industry. The integrity of the bioprocess...
3rd Edition. — CRC Press, 2019. — 673 p. — (Drugs and the Pharmaceutical Sciences). — ISBN: 9781138056749. Since sterile filtration and purification steps are becoming more prevalent and critical within medicinal drug manufacturing, the third edition of Filtration and Purification in the Biopharmaceutical Industry greatly expands its focus with extensive new material on the...
2nd Edition. – CRC Press — 2007. — 816 c. — (Drugs and the Pharmaceutical Sciences 174) — ISBN: 978-0849379536 Filtration and Purification in the Biopharmaceutical Industry, First Edition greatly expands its focus with extensive new material on the critical role of purification and the significant advances in filtration science and technology. This new edition provides...
Springer-Verlag, Berlin, Heidelberg, 2006. — 210 p. — (Advances in Biochemical Engineering/Biotechnology. Volume 98) — ISBN: 354028625X Filtration,whether pre- or final-, ultra- or diafiltration, is widely used within the biopharmaceutical industry. Especially sterilizing grade filtration, an essential part of aseptic processing, is increasing in importance due to the...
Boca Raton: CRC Press, 2024. — 251 p. 3D Printing, Drug Delivery Systems, and Application Domain Overview. Advancements in Tailoring Medication Using 3D Printing. Innovative and Modified Additive Manufacturing Processes: Extended Applications in the Pharmaceutical Industry. Quality Characteristics’ Challenge in 3D Printing of Pharmaceutical Products. Navigating the Terrain of...
4th edition. — CBS Publishers & Distributors, 2016. — 1856 p. — ISBN13: 9788123922898. The Theory and practice of Industrial Pharmacy Fourth Edition, edited by Roop K. Khar, s. P. Vyas, Farhan j. Ahmad and Gaurav k. Jain, published by CBS publishers and distributors, is a comprehensive book for students of pharmacy and also practitioners. It is thoroughly revised and updated...
Springer, 2019. — 163 p. This monograph covers a novel technology to deliver drugs and cosmetics through the skin in a minimally invasive manner. Microneedles – a bed of miniaturized needles is one of the most studied topics in delivering actives through the skin barrier. This book enables readers to understand the delivery of ingredients through the skin, describes a novel and...
Wiley, 2017. — 348 p. — ISBN10: 111814564X. Considered essential to pharmaceutical drug product development, pharmaceutical excipients are materials, other than the active moiety, intentionally included in a drug product for the purpose of ensuring it is acceptable to regulatory authorities and patients in terms of manufacturability and performance. Pharmaceutical excipients...
William Andrew, 2010. — 313 p. With the improvements in formulation science and certain transdermal delivery technologies, the non-invasive mode of drug delivery is now ready to compete with traditional methods of oral and injectible routes of drug delivery. The Handbook of Non-Invasive Drug Delivery Systems encompasses the broad field of non-invasive drug delivery systems that...
CRC Press, 2017. — 240 p. — ISBN10: 1498758045. The respiratory tract has been used to deliver biologically active chemicals into the human body for centuries. However, the lungs are complex in their anatomy and physiology, which poses challenges to drug delivery. Inhaled formulations are generally more sophisticated than those for oral and parenteral administration. Pulmonary...
Pharmaceutical Press, 2008. — 214 p. This book has been written as a student guide to extemporaneous pharmaceutical compounding and dispensing. It has been designed to assist the student compounder in understanding the key dosage forms encountered within extemporaneous dispensing. Included is a summary of the key principles relating to labelling and packaging, along with a...
Paris: Elsevier Masson SAS, 2009. — 394 p. La pharmacie galénique est la « science et l’art de préparer, conserver et présenter les médicaments ». C’est la définition qu’en donnait mon maître le professeur Maurice-Marie Janot et que j’ai transmis à mes élèves, tout en leur faisant remarquer que si cette discipline reste un art du fait des multiples aspects du médicament, c’est...
Boca Raton: CRC Press. – 2000. – 304 p. This text is based on my experience with validated cleaning applications in pharmaceutical process manufacturing for the past 10 years. This book is designed for those who face the difficult task of designing validatable cleaning processes, and then validating those processes, in pharmaceutical process manufacturing settings. It is...
CRC Press, 2015. — 524 p. A great deal of confusion and uncertainty over genotoxic impurity (GTI) identification, assessment, and control exists in the pharmaceutical industry today. Pharmaceutical Industry Practices on Genotoxic Impurities strives to facilitate scientific and systematic consensus on GTI management by presenting rationales, strategies, methods, interpretations,...
Academic Press, 2015. — 88 p. — ISBN: 9780128035603; ISBN: 9780128035221. How to Scale-Up a Wet Granulation End Point Scientifically provides a single-source devoted to all relevant information on the scale-up of a wet granulation end point. Key Features Thoroughly referenced and based on the latest research and literature of the Expertise in Pharmaceutical Process Technology...
John Wiley & Sons, Inc, 2017. — 704 p. — ISBN: 1118662318. Addressing a significant need by describing the science and process involved to develop biosimilars of monoclonal antibody (mAb) drugs, this book covers all aspects of biosimilar development: preclinical, clinical, regulatory, manufacturing. Guides readers through the complex landscape involved with developing...
Third Edition, Revised and Expanded. — CRC Press, 2018. — 729 p. — ISBN: 978-1-4822-5362-7. Completely revised and updated, this third edition of Pharmaceutical Dosage Forms and Drug Delivery elucidates the basic principles of pharmaceutics, biopharmaceutics, dosage form design, and drug delivery – including emerging new biotechnology-based treatment modalities. The authors...
4th edition. — Boca Raton: CRC Press, 2024. — 567 p. Completely revised and updated, this fourth edition elucidates the principles of pharmaceutics, biopharmaceutics, dosage form design, and drug delivery – including emerging new biotechnology-based treatment modalities. The authors integrate aspects of physical pharmacy, chemistry, biology, and biopharmaceutics into drug...
Woodhead Publishing, 2018. - 694 p. Stimuli Responsive Polymeric Nanocarriers for Drug Delivery Applications, Volume One: Types and Triggers discusses, in detail, the recent trends in designing biodegradable and biocompatible single-responsive polymers and nanoparticles for safe drug delivery. Focusing on the most advanced materials and technologies, evaluation methods, and...
Taylor & Francis, 1996. — XII, 394 p. — ISBN: 0-203-79140-1 (Adobe eReader Format); ISBN: 0-7484-0445-7 (formerly ISBN: 013-290-818-2). A critical review of published papers, this volume presents theoretical and fundamental aspects of FIA-pharmaceutical analyses. Dividing the material into chapters based on measurement technique or type of detector, each chapter provides
NY Springer Science and Business Media, 2015 — 459 p. — ISBN: 978-94-017-9809-9. Medicinal and aromatic plants (MAPs) have accompanied mankind from its very early beginnings. Their utilization has co-evolved with homo sapiens itself bringing about a profound increase in our scientific knowledge of these species enabling them to be used in many facets of our life (e.g....
2nd edition. — CRC Press, 2003. — 847 p. The second edition of this text assembles significant ophthalmic advances and encompasses breakthroughs in gene therapy, ocular microdialysis, vitreous drug disposition modeling, and receptor/transporter targeted drug delivery. A major goal of pharmacotherapeutics is the attainment of an effective drug concentration at the intended site...
Academic Press, 2020. — 257 p. — (Expertise in Pharmaceutical Process Technology). — ISBN: 978-0-12-816813-4. The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor...
Academic Press, 2016. — 190 p. — ISBN: 9780128047323; ISBN: 9780128047316. How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains...
Academic Press, 2019. — 862 p. — ISBN: 978-0-12-810460-6. This Handbook offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide...
CRC Press, 2010. — 629 p. Site-specific drug delivery and targeting is attracting much research interest from both academia and industry, but because of the many challenges faced in the development of these systems, only a handful of targeted therapies have successfully made it into clinical practice. Bringing together leading field experts, Targeted Delivery of Small and...
3rd edition. — Informa Healthcare, 2010. — 312 p. - ISBN13: 9781420086478 This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it is...
Facts on File Incorporated , 2007. - 191 p. ISBN10: 0-8160-5276-X. ISBN13: 978-0-8160-5276-9. The six books in the set — Chemistry of Drugs, Chemistry of New Materials, Forensic Chemistry, Chemistry of the Environment, Food Chemistry, and Chemistry of Space — are designed to provide a broad, general introduction to some fi elds of chemistry that are less commonly mentioned in...
2nd Edition. — CRC Press, Taylor & Francis Group, 2015. — 1009 p. – (Drugs and the Pharmaceutical Sciences 213) — ISBN13: 978-1-4822-2638-6. This second edition of the Handbook of Bioequivalence Testing brings significant and substantial updates to the first edition, which was a great success. Understanding of the scientific principles behind bioequivalence testing has evolved...
2nd ed. — Informa Healthcare USA, Inc., 2009. XXI, 361 p. — ISBN10: 1-4200-8118-7 (Volume 2; Hardcover), ISBN13: 978-1-4200-8118-3 (Volume 2: Hardcover). U.S. FDA Good Manufacturing Practices Good Manufacturing Practices (GMPs) is a universal concept with a dual purpose: to make pharmaceutical products both safe and consistent in their effectiveness. Remarkable changes are...
2nd ed. — Informa Healthcare USA, Inc., 2009. XXI, 345 p. — ISBN10: 1-4200-8126-8 (Volume 4; Hardcover), ISBN13: 978-1-4200-8126-8 (Volume 4: Hardcover). The fourth volume in the series covers the techniques and technologies involved in the preparation of semisolid products such as ointments, creams, gels, suppositories, and special topical dosage forms. Drug manufacturers need...
Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2004. - 395 p. Many modern pharmaceutical and biological products, e.g. blood derivatives, vaccines, cytostatic drugs, antibiotics, bacteria cultures but also consumer goods such as soluble coffe are freeze-dryed to transform perishable substances into a form that can be stored and reconstituted to their almost original state without...
Academic Press, 2016. — 218 p. — ISBN: 9780128096536; ISBN: 9780128041482. How to Validate a Pharmaceutical Process provides a “how to” approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes...
Woodhead Publishing, 2018. - 404 p. Engineering of Biomaterials for Drug Delivery Systems: Beyond Polyethylene Glycol examines the combined issues of PEGylation and viable biomaterials as alternatives. With a strong focus on polymeric biomaterials, the book first reviews the major issues associated with PEGylation and its use in vivo. Chapters then focus on alternative polymer...
Academic Press, 2017. — 210 p. — (Expertise in Pharmaceutical Process Technology). — ISBN: 9780128047279 ; ISBN: 9780128047286. How to Optimize Fluid Bed Processing Technology: Part of the Expertise in Pharmaceutical Process Technology Series addresses the important components of fluid bed granulation, providing answers to problems that commonly arise and using numerous...
Academic Press, 2017. — 465 p. — ISBN: 978-0-12-801814-9 Despite considerable technological advances, the pharmaceutical industry is experiencing a severe innovation deficit, especially in the discovery of new drugs. Innovative Approaches in Drug Discovery: Ethnopharmacology, Systems Biology and Holistic Targeting provides a critical review and analysis of health, disease and...
Cambridge University Press, 2018. — 349 p. — ISBN: 978-1-108-42022-8. This innovative reference provides a coherent and critical view on the potential benefits of a transition from batch to continuous processes in the biopharmaceutical industry, with the main focus on chromatography. It also covers the key topics of protein stability and protein conjugation, addressing the...
9th edition. Cengage Learning; January 1, 2012. — 720 p. ISBN13: 978-1-4390-5847-3 ISBN10: 1-4390-5847-4 Best-selling DOSAGE CALCULATIONS, 9th Edition features the three-step approach to basic and advanced Formula Method calculations that nursing and other health care professionals prefer, along with a reader-friendly writing style and handy "work text" format. In addition to...
CRC Press, 2020. — 241 p. Mathematical and Statistical Skills in the Biopharmaceutical Industry: A Pragmatic Approach describes a philosophy of efficient problem solving showcased using examples pertinent to the biostatistics function in clinical drug development. It was written to share a quintessence of the authors’ experiences acquired during many years of relevant work in...
Chichester: John Wiley & Sons. – 2008. – 301 p. This book contains procedural documents we have developed to describe factors that should be taken into general consideration while setting up cellbased assays, and for the development, optimization and validation of cell assays. A number of actual validations are presented including ELISPOT, flow metric analysis, proliferation...
Academic Press, 2009. — 978 p. This book is intended for pharmaceutical professionals engaged in research and development of oral dosage forms It covers essential principles of physical pharmacy, biopharmaceutics and industrial pharmacy as well as various aspects of state-of-the-art techniques and approaches in pharmaceutical sciences and technologies along with examples and/or...
3rd Ed. — Boca Raton УСА, CRC Press Taylor & Francis Group, 2012. — 531 p. Process Validation in Manufacturing of Biopharmaceuticals, Third Edition delves into the key aspects and current practices of process validation. It includes discussion on the final version of the FDA 2011 Guidance for Industry on Process Validation Principles and Practices, commonly referred to as the...
CRC Press Book, Taylor&Francis Group, 2005. - 578 p. Written by top authorities in process validation, this reference explores current trends in the field and strategies for selecting the most appropriate quality control scheme. It offers practical guidelines, recommendations, and an abundance of case studies that showcase various techniques and approaches in the validation of...
3rd Edition. - Informa Healthcare, 2010. - 580 p. Highlights the application of freeze-drying to pharmaceuticals, illustrating practical and industry-tested methods of preserving and reactivating delicate biologicals and biochemicals. The text discusses the basic principles and engineering aspects of lyophilization, and also the role of bulking agents, cryoprotectants,...
CRC Press, 2017. — 623 p. Integrating the clinical and engineering aspects of drug delivery, this book offers a much needed comprehensive overview and patient-oriented approach for enhanced drug delivery optimization and advancement. Starting with an introduction to the subject and pharmacokinetics, it explores advances for such topics as oral, gastroretentive, intravitreal,...
Monograph, Oxford Cambridge UK, Woodhead Publishing Limited, 2013. - 370 p. Failure to adequately control any microbial challenge associated within process or product by robust sterilisation will result in a contaminated marketed product, with potential harm to the patient. Sterilisation is therefore of great importance to healthcare and the manufacturers of medical devices and...
Wiley, 2013. - 207 p. - Pharmaceutical Emulsions: A Drug Developer's Toolbag covers all the key aspects of pharmaceutical emulsions, starting from the fundamental scientific basics, to the pharmaceutical forms and the chemical tests for its application. The author uses his extensive experience in both industry and academic experience to provide a concise, student friendly guide...
Springer, 2018. — 199 p. — ISBN: 981130288X. Natural Products have always played a pivotal rle as sources for drug lead compounds. This book is aimed at providing inside purview of the scope of natural products (including herbal and marine) in the possible treatment of neurological disorders. The book explains pre-clinical neuropharmacological investigations done on herbs...
Springer, 2018. — 199 p. — ISBN: 981130288X. Natural Products have always played a pivotal rle as sources for drug lead compounds. This book is aimed at providing inside purview of the scope of natural products (including herbal and marine) in the possible treatment of neurological disorders. The book explains pre-clinical neuropharmacological investigations done on herbs...
Springer, 2005. — 436 p. The second edition of this concise hands-on guide to implementing Good Laboratory Practice standards has been fully updated to include the latest changes in the regulatory framework. Particularly the areas of in vitro testing and multi-site studies have undergone considerable developments in recent years. This practice-oriented guide introduces the...
1 edition. — Informa Healthcare, 2004. — 503 p. Introduction: Status and Applicability of US Regulations. EU Guidelines — General Quality Issues. Personnel, Organization, and T raining. Premises/Buildings and Facilities. Contamination and Contamination Control. Equipment. Materials Control. Production and Process Controls. Packaging and Labeling Control. Holding and...
CRC Press, 2007. - 574 p. The biopharmaceutical industry has become an increasingly important player in the global economy, and the success of these products depends on the development and implementation of cost-effective, robust and scaleable production processes. Bioseparations-also called downstream processing- can be a key source of competitive advantageto biopharmaceutical...
Boca Raton: Taylor & Francis Group. - 2005. - 550 p. A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, design, build, validate, and implement pharmaceutical plant and system designs — demonstrating how advances in technology...
Springer International Publishing, Switzerland, 2017. — 308 p. — ISBN: 3319397737. This book provides comprehensive coverage of corneal collagen cross-linking (CXL), a major management modality for keratoconus and ectatic corneal disorders. All aspects are covered, including refractive and non-refractive surgery indications, models of application, safety, efficacy, performance,...
2009 Wiley-VCH Verlag CmbH & Co KGaA, Weinheim, c. 390; ISBN: 978-3-527-3244-6 The present book introduces the basin knowledge of industrial manufacturing of biopharmaceuticals. It is written for those wanting to understand tha landscape, interfaces and interactions between the differend disciplines relevant for production; as such, aspects of technology and analytics,...
3rd edition. — Wiley-VCH, 2022. — 471 p. — ISBN: 978-3-527-34947-0. In the newly revised Third Edition of Manufacturing of Pharmaceutical Proteins: From Technology to Economy, renowned chemical engineer Dr. Stefan Behme delivers a comprehensive text covering all aspects of biopharmaceutical manufacturing, including legal and regulatory considerations, production facility...
Wiley, 2013. — 518 p. The field of solid state characterization is central to the pharmaceutical industry, as drug products are, in an overwhelming number of cases, produced as solid materials. Selection of the optimum solid form is a critical aspect of the development of pharmaceutical compounds, due to their ability to exist in more than one form or crystal structure...
World Scientific Publishing, 2018. — 384 p. — (From Biomaterials Towards Medical Devices: Vol. 1). — ISBN: 978-981-3201-04-0. With the alarming increase in cancer diagnoses and genetic illnesses, traditional drug agents and their delivery media need to be re-evaluated to address a quickly evolving field. With newer smart materials for the controlled release of macromolecules,...
Wiley, 2012. - 886 p. - Cost-effective manufacturing of biopharmaceutical products is rapidly gaining in importance, while healthcare systems across the globe are looking to contain costs and improve efficiency. To adapt to these changes, industries need to review and streamline their manufacturing processes. This two volume handbook systematically addresses the key steps and...
Woodhead Publishing, 2016. - 366 p. Pharmaceutical Drug Delivery Systems and Vehicles focuses on the fundamental principles while touching upon the advances in the pharma field with coverage of the basic concepts, fundamental principles, biomedical rationales, preparative and characterization techniques, and potential applications of pharmaceutical drug delivery systems and...
Warszawa: PZWL, 2017. — 730 s. Każdy lek wprowadzany jest do lecznictwa w określonej postaci farmaceutycznej, którą tworzy się, stosując odpowiednie substancje pomocnicze i technologie. Książka w sposób przystępny wprowadza Czytelnika w tajemnice technologii postaci leku. Dobór właściwej postaci leku to ważny, a czasami podstawowy warunek skutecznej farmakoterapii. Wiedza na...
CRC Press, 2007. — 272 p. This title demonstrates how designed experiments are the most scientific, efficient, and cost effective method of data collection for validation in a laboratory setting. Intended as a learn-by-example guide, Pharmaceutical and Medical Device Validation by Experimental Design demonstrates why designed experiments are the most logical and rational...
The Royal Society of Chemistry, 2018. — 431 p. 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...
Elsevier B.V., 2016. — 831 p. This book represents our effort to give a panoramic view of the most popular medications on the pharmaceutical market, accenting the reader’s attention on the uses of these medications and schemes of synthesis of the best-selling pharmaceutical drugs in 2010s. Although there are numerous books on the medicinal chemistry and drug design, this book...
Tucson:Elsevier, 2006. - 600 p. This book, as is often the case with many others, represents an attempt to express a long overdue need of compiling information which has accumulated over the course of more than 30 years of our work in the area of the synthesis of medical drugs and 7 years of work on the book itself. In our opinion, the result can fill obvious gaps that exist in...
World Scientific Publishing, 2017. — 181 p. – ISBN: 9781786342973. This book is an excursion into the drug development process, from the initial conception in a chemical or molecular biology lab, via tests in isolated cells and animals, to the stage of clinical trials. The human body is a complex ecosystem where little is conclusively known in terms of its response to...
Humana Press, 2019. — 387 p. This detailed volume brings together leading practitioners in the freeze-drying community to address recent progress, not only in new analytical tools and applications of the data derived in cycle design but also in the manufacturing of lyophilized products in the healthcare sector – whether these be therapeutics, vaccines or diagnostic products -...
Woodhead Publishing Limited, 2013. — 360 p. Quality assurance is necessary to maintain quality and services in the pharmaceutical and life science industries. Gordon Welty demonstrates that the logic and practice of problem solving can integrate both program efficacy and regulatory compliance. This book explains how a problem in regulated industry is identified, reviews the...
Wiley, 2015. — 455 p. Vaccine Manufacturing and Production is an invaluable reference on how to produce a vaccine - from beginning to end - addressing all classes of vaccines from a processing, production, and regulatory viewpoint. It will provide comprehensive information on the various fields involved in the production of vaccines, from fermentation, purification,...
New York: Marcel Dekker. – 2004. −. 670 p. (Drugs and the Pharmaceutical Sciences. Volume 140) Parenteral drugs require sterility in every case; there is no gray area in that regard. What, then, is the relevance of contamination control in parenteral manufacturing? Contamination control occurs at a multitude of sites along the series of processes that lead invariably to the...
Academic Press, 2012. — 370 p. — (Methods in Enzymology 502). This volume of Methods in Enzymology looks at Protein Engineering for Therapeutics. The chapters provide an invaluable resource for academics, researchers and students alike. With an international board of authors, this volume is split into sections that cover subjects such as Antibodies, Protein conjugates,...
Academic Press, 2012. — 399 p. — (Methods in Enzymology 502). This volume of Methods in Enzymology looks at Protein Engineering for Therapeutics. The chapters provide an invaluable resource for academics, researchers and students alike. With an international board of authors, this volume is split into sections that cover subjects such as Peptides, and Scaffolds. Key Features -...
Tutorial for laboratory classes for students of speciality “Pharmacy” / Yu. V. Yudina, Yu. V. Shmyrova, S. V. Stepanenko et al. – Kh. : NUPh : Original, 2012. – 254 p. The questions of traditional medicines, industrial manufacture and the new generation of medicinal forms are considered. The information about classification, auxiliary substances, generally accepted...
Comments