Drug Stability for Pharmaceutical Scientists

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Publisher : Academic Press
ISBN 13 : 0124115624
Total Pages : 170 pages
Book Rating : 4.1/5 (241 download)

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Book Synopsis Drug Stability for Pharmaceutical Scientists by : Thorsteinn Loftsson

Download or read book Drug Stability for Pharmaceutical Scientists written by Thorsteinn Loftsson and published by Academic Press. This book was released on 2014-01-25 with total page 170 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug Stability for Pharmaceutical Scientists is a clear and easy-to-follow guide on drug degradation in pharmaceutical formulation. This book features valuable content on both aqueous and solid drug solutions, the stability of proteins and peptides, acid-base catalyzed and solvent catalyzed reactions, how drug formulation can influence drug stability, the influence of external factors on reaction rates and much more. Full of examples of real-life formulation problems and step-by-step calculations, this book is the ideal resource for graduate students, as well as scientists in the pharmaceutical and related industries. Illustrates important theoretical concepts with numerous examples, figures, calculations, learning problems and questions for self-study and retention of material Provides answers and explanations to test your knowledge Enables you to better understand key concepts such as rate and order of reaction, reaction equilibrium, complex reaction mechanisms and more Includes an in-depth discussion of both aqueous and solid drug solutions and contains the latest international regulatory requirements on drug stability

Drug Stability and Chemical Kinetics

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Author :
Publisher : Springer Nature
ISBN 13 : 9811564264
Total Pages : 284 pages
Book Rating : 4.8/5 (115 download)

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Book Synopsis Drug Stability and Chemical Kinetics by : Muhammad Sajid Hamid Akash

Download or read book Drug Stability and Chemical Kinetics written by Muhammad Sajid Hamid Akash and published by Springer Nature. This book was released on 2020-11-01 with total page 284 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book comprehensively reviews drug stability and chemical kinetics: how external factors can influence the stability of drugs, and the reaction rates that trigger these effects. Explaining the important theoretical concepts of drug stability and chemical kinetics, and providing numerous examples in the form of illustrations, tables and calculations, the book helps readers gain a better understanding of the rates of reactions, order of reactions, types of degradation and how to prevent it, as well as types of stability studies. It also offers insights into the importance of the rate at which the drug is degraded and/or decomposed under various external and internal conditions, including temperature, pH, humidity and light. This book is intended for researchers, PhD students and scientists working in the field of pharmacy, pharmacology, pharmaceutical chemistry, medicinal chemistry and biopharmaceutics.

Extended Stability for Parenteral Drugs

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Publisher :
ISBN 13 : 9781585283408
Total Pages : 0 pages
Book Rating : 4.2/5 (834 download)

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Book Synopsis Extended Stability for Parenteral Drugs by : Caryn M. Bing

Download or read book Extended Stability for Parenteral Drugs written by Caryn M. Bing and published by . This book was released on 2013 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: When caring for patients, medication stability should be the least of your worries. Extended Stability for Parenteral Drugs, Fifth Edition, is the indispensable go-to reference for anyone working in alternate site infusion or preparing sterile compounds. This new edition will help you safely extend beyond-use dating of parenteral medications to minimize waste and reduce costs. What''s New in This Edition? � 160 updated monographs, including 10 new to this edition: o Acetaminophen o Ceftaroline fosamil o Coagulation Factor XIII o Doripenem o Ethanol lock o Ibuprofen o Pantoprazole o Telavancin o Toclizumab o Ziconotide acetate � 24 parenteral nutrition monographs include additional considerations for calcium and phosphate solubility. � Monograph updates include revisions to several container types and new information for elastometric infusion device brands. The Applying Stability Data in Patient Care section now includes a nursing perspective, a primer on the types of vascular access devices used in medication administration, and important considerations for pH, osmolality, concentration, and administration devices. With expanded tables and enhanced references, Extended Stability for Parenteral Drugs, Fifth Edition, is the only publication that brings key stability data on the most commonly used IV solutions, medications, and administration devices, together in one convenient, easy-to-use guide.

Stability of Drugs and Dosage Forms

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Author :
Publisher : Springer Science & Business Media
ISBN 13 : 0306468298
Total Pages : 274 pages
Book Rating : 4.3/5 (64 download)

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Book Synopsis Stability of Drugs and Dosage Forms by : Sumie Yoshioka

Download or read book Stability of Drugs and Dosage Forms written by Sumie Yoshioka and published by Springer Science & Business Media. This book was released on 2007-05-08 with total page 274 pages. Available in PDF, EPUB and Kindle. Book excerpt: Drug products are complex mixtures of drugs and excipients and, as such, their chemical and physical stability kinetics are complex. This book discusses the stability of these dosage forms with preformulation studies through to the studies on the final products. The book is intended for graduate students, researchers and professionals in the field of Pharmaceutics and Pharmaceutical Chemistry.

Pharmaceutical Stability Testing to Support Global Markets

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Publisher : Springer Science & Business Media
ISBN 13 : 1441908897
Total Pages : 261 pages
Book Rating : 4.4/5 (419 download)

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Book Synopsis Pharmaceutical Stability Testing to Support Global Markets by : Kim Huynh-Ba

Download or read book Pharmaceutical Stability Testing to Support Global Markets written by Kim Huynh-Ba and published by Springer Science & Business Media. This book was released on 2009-12-04 with total page 261 pages. Available in PDF, EPUB and Kindle. Book excerpt: The International Conference of Harmonization (ICH) has worked on har- nizing the stability regulations in the US, Europe, and Japan since the early 1990s. Even though the Stability Guidelines Q1A (R2) was issued over a decade ago, issues surrounding this arena continue to surface as the principles described in the guideline are applied to different technical concentrations. As a result, the stability community has continued to discuss concerns and find ways of harmonizing regulatory requirements, streamlining practices, improving processes in order to bring safe and effective medical supplies to the patients around the world. In 2007, the American Association of Pharmaceutical Scientists (AAPS) Stability Focus Group organized two workshops – the Stability Workshop and the Degradation Mechanism Workshop. These meetings attracted many industry scientists as well as representatives from several regulatory agencies in the world to discuss important topics related to pharmaceutical stability practices. Recognizing the importance of documenting these discussions and with the permission of AAPS, I have worked with speakers to assemble a collection of 30 articles from presentations given at these two meetings, mainly the Stability Workshop. I trust that this book will be beneficial to all of you in providing guidance and up-to-date information for building quality stability programs. v Freedom of our mind is Mother of all inventions.

Handbook of Stability Testing in Pharmaceutical Development

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Author :
Publisher : Springer Science & Business Media
ISBN 13 : 0387856277
Total Pages : 389 pages
Book Rating : 4.3/5 (878 download)

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Book Synopsis Handbook of Stability Testing in Pharmaceutical Development by : Kim Huynh-Ba

Download or read book Handbook of Stability Testing in Pharmaceutical Development written by Kim Huynh-Ba and published by Springer Science & Business Media. This book was released on 2008-11-16 with total page 389 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook is the first to cover all aspects of stability testing in pharmaceutical development. Written by a group of international experts, the book presents a scientific understanding of regulations and balances methodologies and best practices.

Pharmaceutical Technology--drug Stability

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Publisher :
ISBN 13 :
Total Pages : 178 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Pharmaceutical Technology--drug Stability by : Michael Henry Rubinstein

Download or read book Pharmaceutical Technology--drug Stability written by Michael Henry Rubinstein and published by . This book was released on 1989 with total page 178 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Accelerated Predictive Stability (APS)

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Publisher : Academic Press
ISBN 13 : 0128027851
Total Pages : 512 pages
Book Rating : 4.1/5 (28 download)

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Book Synopsis Accelerated Predictive Stability (APS) by : Fenghe Qiu

Download or read book Accelerated Predictive Stability (APS) written by Fenghe Qiu and published by Academic Press. This book was released on 2018-06-28 with total page 512 pages. Available in PDF, EPUB and Kindle. Book excerpt: Accelerated Predictive Stability (APS): Fundamentals and Pharmaceutical Industry Practices provides coverage of both the fundamental principles and pharmaceutical industry applications of the APS approach. Fundamental chapters explain the scientific basis of the APS approach, while case study chapters from many innovative pharmaceutical companies provide a thorough overview of the current status of APS applications in the pharmaceutical industry. In addition, up-to-date experiences in utilizing APS data for regulatory submissions in many regions and countries highlight the potential of APS in support of registration stability testing for certain regulatory submissions. This book provides high level strategies for the successful implementation of APS in a pharmaceutical company. It offers scientists and regulators a comprehensive resource on how the pharmaceutical industry can enhance their understanding of a product’s stability and predict drug expiry more accurately and quickly. Provides a comprehensive, one-stop-shop resource for accelerated predictive stability (APS) Presents the scientific basis of different APS models Includes the applications and utilities of APS that are demonstrated through numerous case studies Covers up-to-date regulatory experience

Chemical Stability of Pharmaceuticals

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Author :
Publisher : John Wiley & Sons
ISBN 13 : 9780471879558
Total Pages : 884 pages
Book Rating : 4.8/5 (795 download)

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Book Synopsis Chemical Stability of Pharmaceuticals by : Kenneth A. Connors

Download or read book Chemical Stability of Pharmaceuticals written by Kenneth A. Connors and published by John Wiley & Sons. This book was released on 1986-10-13 with total page 884 pages. Available in PDF, EPUB and Kindle. Book excerpt: Provides a sound theoretical basis for understanding chemical kinetics and its uses in studying drug stability. Treats the calculations, approximations, and estimates that are useful to the pharmacist in professional practice, and presents a collection of selected drug-stability data from the pharmaceutical literature. This Handbook makes accessible to the pharmacist much of the information necessary to make pharmaceutical decisions about drug stability. Changes in this edition include thorough revision of the chapter on oxidation, addition of a new chapter on solid-state stability, and a tripling of the number of stability monographs. All monographs figures have been redrawn, most of them from published data, and all sources are cited.

Drug Stability

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Publisher :
ISBN 13 :
Total Pages : 544 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Drug Stability by : Jens Thurø Carstensen

Download or read book Drug Stability written by Jens Thurø Carstensen and published by . This book was released on 1990 with total page 544 pages. Available in PDF, EPUB and Kindle. Book excerpt: Practical advice on the problems of carrying out a testing program, written with the stability scientist in mind. Presents basic theory, industrial practice, and regulatory aspects, taking the reader from stability principles of the drug in dissolved, dispersed, and solid states through data analysis of the packaged drug's stability and experimental methods for achieving stable marketed products. Features computer programs, many diagrams and tables, and some 500 references. Annotation(c) 2003 Book News, Inc., Portland, OR (booknews.com)

Formulation, Characterization, and Stability of Protein Drugs

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Publisher : Springer Science & Business Media
ISBN 13 : 0306474522
Total Pages : 432 pages
Book Rating : 4.3/5 (64 download)

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Book Synopsis Formulation, Characterization, and Stability of Protein Drugs by : Rodney Pearlman

Download or read book Formulation, Characterization, and Stability of Protein Drugs written by Rodney Pearlman and published by Springer Science & Business Media. This book was released on 2006-04-11 with total page 432 pages. Available in PDF, EPUB and Kindle. Book excerpt: Leading scientists offer detailed profiles of ten protein drugs currently in development. The case histories of these important new compounds are described from the perspective of their formulation, characterization, and stability. This ready reference also features recent data and an abundance of previously unpublished information. The in-depth coverage includes a highly useful compendium of degradation sites occurring in over 70 proteins. An invaluable aid in the rapid identification of potential `hot spots' in proteins, this accessible compilation allows for inspection of the protein's primary structure and preparation of a hydroflex plot.

Drug Stability

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Publisher :
ISBN 13 : 9780585393261
Total Pages : 773 pages
Book Rating : 4.3/5 (932 download)

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Book Synopsis Drug Stability by : Christopher T. Rhodes

Download or read book Drug Stability written by Christopher T. Rhodes and published by . This book was released on 2000-01-01 with total page 773 pages. Available in PDF, EPUB and Kindle. Book excerpt: Addressing concerns for patient welfare while protecting producer reputation, and providing a database for formulation of other products, this multiauthored reference blends fundamental theory and practical advice on drug product stability in scientific, technical, and regulatory environments, covering development of indicating assays, computer use, clinical trial materials, strategic planning, and packaging. Describing the documentation required to minimize the changes of regulatory citations, the book lists manufacturers of photostability testing chambers, stability system software, and laboratory information management systems for pharmaceutical applications.

Methods for Stability Testing of Pharmaceuticals

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Author :
Publisher : Humana Press
ISBN 13 : 9781493976850
Total Pages : 358 pages
Book Rating : 4.9/5 (768 download)

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Book Synopsis Methods for Stability Testing of Pharmaceuticals by : Sanjay Bajaj

Download or read book Methods for Stability Testing of Pharmaceuticals written by Sanjay Bajaj and published by Humana Press. This book was released on 2018-05-25 with total page 358 pages. Available in PDF, EPUB and Kindle. Book excerpt: This detailed volume collects numerous methods and protocols related to different aspects of stability programs that are followed in pharmaceutical development laboratories. Implementation of a successful stability program, vital in preventing product failures and recalls, requires critical and logical thinking that goes beyond the regular documented protocols and methods, so the experiences of the book’s internationally-based expert contributors fill the chapters with practical guidance. As a volume in the Methods in Pharmacology and Toxicology series, this book presents the kind of real-world advice that is essential for advancing laboratory research. Authoritative and thorough, Methods for Stability Testing of Pharmaceuticals serves as a valuable addition to the existing armamentarium of resources available to stability testing personnel in research and industry.

Drug Stability, Third Edition, Revised, and Expanded

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Publisher : CRC Press
ISBN 13 : 9780824703769
Total Pages : 792 pages
Book Rating : 4.7/5 (37 download)

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Book Synopsis Drug Stability, Third Edition, Revised, and Expanded by : Jens T. Carstensen

Download or read book Drug Stability, Third Edition, Revised, and Expanded written by Jens T. Carstensen and published by CRC Press. This book was released on 2000-07-28 with total page 792 pages. Available in PDF, EPUB and Kindle. Book excerpt: Addressing concerns for patient welfare while protecting producer reputation, and providing a database for formulation of other products, this multiauthored reference blends fundamental theory and practical advice on drug product stability in scientific, technical, and regulatory environments, covering development of indicating assays, computer use, clinical trial materials, strategic planning, and packaging. Describing the documentation required to minimize the changes of regulatory citations, the book lists manufacturers of photostability testing chambers, stability system software, and laboratory information management systems for pharmaceutical applications.

Trissel's Stability of Compounded Formulations

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Publisher : American Pharmacists Association (APhA)
ISBN 13 :
Total Pages : 456 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Trissel's Stability of Compounded Formulations by : Lawrence A. Trissel

Download or read book Trissel's Stability of Compounded Formulations written by Lawrence A. Trissel and published by American Pharmacists Association (APhA). This book was released on 2000 with total page 456 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Helps readers determine whether formulated compounds will be stable for the anticipated duration of use; properly store and repackage compounded formulations; formulate in accordance with documented standards; and, counsel patients on the use and storate of comounded medications." -- Back cover.

Stability-indicating HPLC Methods for Drug Analysis

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Publisher : American Pharmacists Association (APhA)
ISBN 13 : 9781582121093
Total Pages : 0 pages
Book Rating : 4.1/5 (21 download)

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Book Synopsis Stability-indicating HPLC Methods for Drug Analysis by : Quanyun A. Xu

Download or read book Stability-indicating HPLC Methods for Drug Analysis written by Quanyun A. Xu and published by American Pharmacists Association (APhA). This book was released on 2008 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Monoclonal Antibodies

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Publisher : Woodhead Publishing
ISBN 13 : 0081002971
Total Pages : 224 pages
Book Rating : 4.0/5 (81 download)

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Book Synopsis Monoclonal Antibodies by : Steven Shire

Download or read book Monoclonal Antibodies written by Steven Shire and published by Woodhead Publishing. This book was released on 2015-04-24 with total page 224 pages. Available in PDF, EPUB and Kindle. Book excerpt: Monoclonal antibodies (MAbs) are currently the major class of protein bio therapeutic being developed by biotechnology and pharmaceutical companies. Monoclonal Antibodies discusses the challenges and issues revolving around development of a monoclonal antibody produced by recombinant DNA technology into a therapeutic agent.This book covers downstream processing which includes design of processes to manufacture the formulation, formulation design, fill and finish into closure systems and routes of administration. The characterization of the final drug product is covered where the use of biophysical methods combined with genetic engineering is used to understand the solution properties of the formulation. The latter has become very important since many indications such as arthritis and asthma require the development of formulations for subcutaneous delivery (SC). The development of formulations for IV delivery is also important and comes with a different set of challenges. The challenges and strategies that can overcome these limitations are discussed in this book, starting with an introduction to these issues, followed by chapters detailing strategies to deal with them. Subsequent chapters explore the processing and storage of mAbs, development of delivery device technologies and conclude with a chapter on the future of mAbs in therapeutic remedies. Discusses the challenges to develop MAbs for intravenous (IV) and subcutaneous delivery (SC) Presents strategies to meet the challenges in development of MAbs for SC and IV administration Discusses the use of biophysical analytical tools coupled with MAb engineering to understand what governs MAb properties at high concentration