HPLC Method Development for Pharmaceuticals Book

HPLC Method Development for Pharmaceuticals


  • Author : Satinder Ahuja
  • Publisher : Elsevier
  • Release Date : 2011-09-21
  • Genre: Medical
  • Pages : 532
  • ISBN 10 : 9780080554198

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HPLC Method Development for Pharmaceuticals Excerpt :

High pressure, or high performance, liquid chromatography (HPLC) is the method of choice for checking purity of new drug candidates, monitoring changes during scale up or revision of synthetic procedures, evaluating new formulations, and running control/assurance of the final drug product. HPLC Method Development for Pharmaceuticals provides an extensive overview of modern HPLC method development that addresses these unique concerns. Includes a review and update of the current state of the art and science of HPLC, including theory, modes of HPLC, column chemistry, retention mechanisms, chiral separations, modern instrumentation (including ultrahigh-pressure systems), and sample preparation. Emphasis has been placed on implementation in a pharmaceutical setting and on providing a practical perspective. HPLC Method Development for Pharmaceuticals is intended to be particularly useful for both novice and experienced HPLC method development chemists in the pharmaceutical industry and for managers who are seeking to update their knowledge. Covers the requirements for HPLC in a pharmaceutical setting including strategies for software and hardware validation to allow for use in a regulated laboratory Provides an overview of the pharmaceutical development process (clinical phases, chemical and pharmaceutical development activities) Discusses how HPLC is used in each phase of pharmaceutical development and how methods are developed to support activities in each phase

HPLC Method Development for Pharmaceuticals Book

HPLC Method Development for Pharmaceuticals


  • Author : Satinder Ahuja
  • Publisher : Academic Press
  • Release Date : 2007
  • Genre: Medical
  • Pages : 513
  • ISBN 10 : 0123705401

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HPLC Method Development for Pharmaceuticals Excerpt :

High pressure, or high performance, liquid chromatography (HPLC) is the method of choice for checking purity of new drug candidates, monitoring changes during scale up or revision of synthetic procedures, evaluating new formulations, and running control/assurance of the final drug product. HPLC Method Development for Pharmaceuticals provides an extensive overview of modern HPLC method development that addresses these unique concerns. Includes a review and update of the current state of the art and science of HPLC, including theory, modes of HPLC, column chemistry, retention mechanisms, chiral separations, modern instrumentation (including ultrahigh-pressure systems), and sample preparation. Emphasis has been placed on implementation in a pharmaceutical setting and on providing a practical perspective. HPLC Method Development for Pharmaceuticals is intended to be particularly useful for both novice and experienced HPLC method development chemists in the pharmaceutical industry and for managers who are seeking to update their knowledge. * Covers the requirements for HPLC in a pharmaceutical setting including strategies for software and hardware validation to allow for use in a regulated laboratory * Provides an overview of the pharmaceutical development process (clinical phases, chemical and pharmaceutical development activities) * Discusses how HPLC is used in each phase of pharmaceutical development and how methods are developed to support activities in each phase

Analytical Method Development and Validation Book

Analytical Method Development and Validation


  • Author : Michael E. Swartz
  • Publisher : CRC Press
  • Release Date : 2018-10-03
  • Genre: Science
  • Pages : 96
  • ISBN 10 : 9781482229776

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Analytical Method Development and Validation Excerpt :

Describes analytical methods development, optimization and validation, and provides examples of successful methods development and validation in high-performance liquid chromatography (HPLC) areas. The text presents an overview of Food and Drug Administration (FDA)/International Conference on Harmonization (ICH) regulatory guidelines, compliance with validation requirements for regulatory agencies, and methods validation criteria stipulated by the US Pharmacopia, FDA and ICH.

Handbook of Pharmaceutical Analysis by HPLC Book

Handbook of Pharmaceutical Analysis by HPLC


  • Author : Satinder Ahuja
  • Publisher : Elsevier
  • Release Date : 2005-02-09
  • Genre: Medical
  • Pages : 600
  • ISBN 10 : 0080455182

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Handbook of Pharmaceutical Analysis by HPLC Excerpt :

High pressure liquid chromatography–frequently called high performance liquid chromatography (HPLC or, LC) is the premier analytical technique in pharmaceutical analysis and is predominantly used in the pharmaceutical industry. Written by selected experts in their respective fields, the Handbook of Pharmaceutical Analysis by HPLC Volume 6, provides a complete yet concise reference guide for utilizing the versatility of HPLC in drug development and quality control. Highlighting novel approaches in HPLC and the latest developments in hyphenated techniques, the book captures the essence of major pharmaceutical applications (assays, stability testing, impurity testing, dissolution testing, cleaning validation, high-throughput screening). A complete reference guide to HPLC Describes best practices in HPLC and offers 'tricks of the trade' in HPLC operation and method development Reviews key HPLC pharmaceutical applications and highlights currents trends in HPLC ancillary techniques, sample preparations, and data handling

HPLC for Pharmaceutical Scientists Book
Score: 4
From 4 Ratings

HPLC for Pharmaceutical Scientists


  • Author : Yuri V. Kazakevich
  • Publisher : John Wiley & Sons
  • Release Date : 2007-02-16
  • Genre: Science
  • Pages : 1080
  • ISBN 10 : 9780470087947

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HPLC for Pharmaceutical Scientists Excerpt :

HPLC for Pharmaceutical Scientists is an excellent book for both novice and experienced pharmaceutical chemists who regularly use HPLC as an analytical tool to solve challenging problems in the pharmaceutical industry. It provides a unified approach to HPLC with an equal and balanced treatment of the theory and practice of HPLC in the pharmaceutical industry. In-depth discussion of retention processes, modern HPLC separation theory, properties of stationary phases and columns are well blended with the practical aspects of fast and effective method development and method validation. Practical and pragmatic approaches and actual examples of effective development of selective and rugged HPLC methods from a physico-chemical point of view are provided. This book elucidates the role of HPLC throughout the entire drug development process from drug candidate inception to marketed drug product and gives detailed specifics of HPLC application in each stage of drug development. The latest advancements and trends in hyphenated and specialized HPLC techniques (LC-MS, LC-NMR, Preparative HPLC, High temperature HPLC, high pressure liquid chromatography) are also discussed.

Handbook of Analytical Quality by Design Book

Handbook of Analytical Quality by Design


  • Author : Sarwar Beg
  • Publisher : Academic Press
  • Release Date : 2021-01-09
  • Genre: Business & Economics
  • Pages : 222
  • ISBN 10 : 9780128203330

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Handbook of Analytical Quality by Design Excerpt :

Handbook of Analytical Quality by Design addresses the steps involved in analytical method development and validation in an effort to avoid quality crises in later stages. The AQbD approach significantly enhances method performance and robustness which are crucial during inter-laboratory studies and also affect the analytical lifecycle of the developed method. Sections cover sample preparation problems and the usefulness of the QbD concept involving Quality Risk Management (QRM), Design of Experiments (DoE) and Multivariate (MVT) Statistical Approaches to solve by optimizing the developed method, along with validation for different techniques like HPLC, UPLC, UFLC, LC-MS and electrophoresis. This will be an ideal resource for graduate students and professionals working in the pharmaceutical industry, analytical chemistry, regulatory agencies, and those in related academic fields. Concise language for easy understanding of the novel and holistic concept Covers key aspects of analytical development and validation Provides a robust, flexible, operable range for an analytical method with greater excellence and regulatory compliance

Biochemical Analysis Tools Book

Biochemical Analysis Tools


  • Author : Oana-Maria Boldura
  • Publisher : BoD – Books on Demand
  • Release Date : 2020-06-24
  • Genre: Science
  • Pages : 206
  • ISBN 10 : 9781789848564

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Biochemical Analysis Tools Excerpt :

This book explores the role of nucleic acid analysis and the advances it has led to in the field of life sciences. The first section is a collection of chapters covering experimental methods used in molecular biology, the techniques adjacent to these methods, and the steps of analysis before and after obtaining raw DNA data. The second section deals with the principles of chromatography, method development, sample preparation, and industrial applications.

An Introduction to HPLC for Pharmaceutical Analysis Book

An Introduction to HPLC for Pharmaceutical Analysis


  • Author : Oona McPolin
  • Publisher : Lulu.com
  • Release Date : 2009-03-01
  • Genre: Medical
  • Pages : 150
  • ISBN 10 : 9780956152800

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An Introduction to HPLC for Pharmaceutical Analysis Excerpt :

If you are new to HPLC, this book provides an invaluable guide to how HPLC is actually used when analysing pharmaceuticals. It is full of practical advice on the operation of HPLC systems combined with the necessary theoretical knowledge to ensure understanding of the technique. Key features include: A thorough discussion of the stationary phase enabling the reader to make sense of the many parameters used to describe a HPLC column; Practical advice and helpful hints for the preparation and use of mobile phase; A complete overview of each of the different components which together make up a HPLC system; A description of the contents of a typical HPLC analytical method and how to interpret these; A step-by-step guide on how to follow a method and set up a HPLC analysis; A discussion of system suitability criteria and how to interpret the values obtained during an analysis; Explanation of the common methods of calibration and quantification used for pharmaceutical analysis.

HPLC Methods for Recently Approved Pharmaceuticals Book
Score: 5
From 1 Ratings

HPLC Methods for Recently Approved Pharmaceuticals


  • Author : George Lunn
  • Publisher : John Wiley & Sons
  • Release Date : 2005-05-06
  • Genre: Science
  • Pages : 640
  • ISBN 10 : 9780471711674

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HPLC Methods for Recently Approved Pharmaceuticals Excerpt :

An indispensable resource for busy researchers Your time is valuable-too valuable to spend hunting through thetechnical literature in search of the right HPLC assay techniquesfor your projects. With HPLC Methods for Recently ApprovedPharmaceuticals, you'll quickly identify and replicate the idealprocedures for your project needs, without having to refer tooriginal source publications. More of your time can then be spentin the lab, not the library. Covering the relevant world literature through 2003, this bookpicks up where Dr. Lunn's acclaimed HPLC Methods for PharmaceuticalAnalysis left off. It arms you with established HPLC assaytechniques for hundreds of newly approved drugs, as well as drugsfor which assay methods were only recently developed. Combiningdetailed descriptions of procedures with specially annotatedreferences, this practical handbook gives you: * HPLC methods for 390 commonly prescribed pharmaceuticalcompounds * Various procedures for each drug listed together-making it easyto mix and match for customized approaches * Methods for drugs in biological fluids and for bulk andformulated drugs * Chemical structures, molecular weights and formulas, and CASRegistry Numbers * Cross-references to The Merck Index * Retention times of other drugs that can be assayed using the samemethods

Development And Validation Of Chromatographic Methods For Simultaneous Quantification Of Drugs In Bulk And In Their Formulations  HPLC And HPTLC Techniques Book

Development And Validation Of Chromatographic Methods For Simultaneous Quantification Of Drugs In Bulk And In Their Formulations HPLC And HPTLC Techniques


  • Author : Satish Y. Gabhe
  • Publisher : diplom.de
  • Release Date : 2015-08-01
  • Genre: Science
  • Pages : 108
  • ISBN 10 : 9783954898077

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Development And Validation Of Chromatographic Methods For Simultaneous Quantification Of Drugs In Bulk And In Their Formulations HPLC And HPTLC Techniques Excerpt :

This book details: 1. Development and validation of a HPTLC-densitometric method for concurrent estimation of metformin hydrochloride, pioglitazone hydrochloride and gliclazide in combined dosage form. 2. Development and validation of a HPTLC method for simultaneous estimation of moxifloxacin hydrochloride and dexamethasone sodium phosphate in combined pharmaceutical dosage form. 3. Development and validation of a RP-HPLC method for simultaneous estimation of ciprofloxacin hydrochloride and dexamethasone in combined dosage form, which is a better alternative to existing ones. The developed analytical methods are simple, selective, accurate, robust, and precise with shorter analysis time for the analysis of drug/s in combined pharmaceutical dosage forms. All the developed HPTLC and HPLC methods have been validated as per ICH Q2 (R1) guideline. Developed analytical methods could boost analytical researchers to work more efficiently in the field of analytical method development and validation of Pharmaceutical dosage forms.

Practical HPLC Method Development Book

Practical HPLC Method Development


  • Author : Lloyd R. Snyder
  • Publisher : John Wiley & Sons
  • Release Date : 2012-12-03
  • Genre: Science
  • Pages : 800
  • ISBN 10 : 9781118591512

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Practical HPLC Method Development Excerpt :

This revision brings the reader completely up to date on the evolving methods associated with increasingly more complex sample types analyzed using high-performance liquid chromatography, or HPLC. The book also incorporates updated discussions of many of the fundamental components of HPLC systems and practical issues associated with the use of this analytical method. This edition includes new or expanded treatments of sample preparation, computer assisted method development, as well as biochemical samples, and chiral separations.

HPLC Method Development and Validation in Pharmaceutical Analysis Book

HPLC Method Development and Validation in Pharmaceutical Analysis


  • Author : Ghulam Shabir
  • Publisher : LAP Lambert Academic Publishing
  • Release Date : 2013-01
  • Genre: Uncategoriezed
  • Pages : 492
  • ISBN 10 : 3659321206

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HPLC Method Development and Validation in Pharmaceutical Analysis Excerpt :

This handbook is concerned with new chromatographic method development and validation using novel systematic approaches for pharmaceutical compounds. The first stage of the research was to study how method development and validation are typically carried out at present and to formulate this into a simple step-by-step approach. Such a template and protocol was not only used as the foundation of this research programme but could also serve as a simple systematic guide for other practitioners in the pharmaceutical industry. Furthermore, it was recognised that this protocol should satisfy the requirements of the major regulatory agencies. The second stage of this research involved evaluation and application of the above validation approach to new methods that were developed for a diverse range of analytes using HPLC, LC-MS and GC. In essence, the critical review of the requirements for method validation for various agencies and the subsequent preparation of single guidelines on how to go about method validation have had a significant impact on analytical practitioners worldwide.

HPLC and UHPLC for Practicing Scientists Book

HPLC and UHPLC for Practicing Scientists


  • Author : Michael W. Dong
  • Publisher : John Wiley & Sons
  • Release Date : 2019-07-23
  • Genre: Science
  • Pages : 410
  • ISBN 10 : 9781119313762

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HPLC and UHPLC for Practicing Scientists Excerpt :

A concise yet comprehensive reference guide on HPLC/UHPLC that focuses on its fundamentals, latest developments, and best practices in the pharmaceutical and biotechnology industries Written for practitioners by an expert practitioner, this new edition of HPLC and UHPLC for Practicing Scientists adds numerous updates to its coverage of high-performance liquid chromatography, including comprehensive information on UHPLC (ultra-high-pressure liquid chromatography) and the continuing migration of HPLC to UHPLC, the modern standard platform. In addition to introducing readers to HPLC’s fundamentals, applications, and developments, the book describes basic theory and terminology for the novice, and reviews relevant concepts, best practices, and modern trends for the experienced practitioner. HPLC and UHPLC for Practicing Scientists, Second Edition offers three new chapters. One is a standalone chapter on UHPLC, covering concepts, benefits, practices, and potential issues. Another examines liquid chromatography/mass spectrometry (LC/MS). The third reviews at the analysis of recombinant biologics, particularly monoclonal antibodies (mAbs), used as therapeutics. While all chapters are revised in the new edition, five chapters are essentially rewritten (HPLC columns, instrumentation, pharmaceutical analysis, method development, and regulatory aspects). The book also includes problem and answer sections at the end of each chapter. Overviews fundamentals of HPLC to UHPLC, including theories, columns, and instruments with an abundance of tables, figures, and key references Features brand new chapters on UHPLC, LC/MS, and analysis of recombinant biologics Presents updated information on the best practices in method development, validation, operation, troubleshooting, and maintaining regulatory compliance for both HPLC and UHPLC Contains major revisions to all chapters of the first edition and substantial rewrites of chapters on HPLC columns, instrumentation, pharmaceutical ana

Modern HPLC for Practicing Scientists Book

Modern HPLC for Practicing Scientists


  • Author : Michael W. Dong
  • Publisher : John Wiley & Sons
  • Release Date : 2016-04-06
  • Genre: Science
  • Pages : 304
  • ISBN 10 : 9781119293606

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Modern HPLC for Practicing Scientists Excerpt :

A comprehesive yet concise guide to Modern HPLC Written for practitioners by a practitioner, Modern HPLC for Practicing Scientists is a concise text which presents the most important High-Performance Liquid Chromatography (HPLC) fundamentals, applications, and developments. It describes basic theory and terminology for the novice, and reviews relevant concepts, best practices, and modern trends for the experienced practitioner. Moreover, the book serves well as an updated reference guide for busy laboratory analysts and researchers. Topics covered include: HPLC operation Method development Maintenance and troubleshooting Modern trends in HPLC such as quick-turnaround and "greener" methods Regulatory aspects While broad in scope, this book focuses particularly on reversed-phase HPLC, the most common separation mode, and on applications for the pharmaceutical industry, the largest user segment. Accessible to both novice and intermedate HPLC users, information is delivered in a straightforward manner illustrated with an abundance of diagrams, chromatograms, tables, and case studies, and supported with selected key references and Web resources. With intuitive explanations and clear figures, Modern HPLC for Practicing Scientists is an essential resource for practitioners of all levels who need to understand and utilize this versatile analytical technology.

Method Validation in Pharmaceutical Analysis Book
Score: 5
From 1 Ratings

Method Validation in Pharmaceutical Analysis


  • Author : Joachim Ermer
  • Publisher : John Wiley & Sons
  • Release Date : 2006-03-06
  • Genre: Science
  • Pages : 418
  • ISBN 10 : 9783527604470

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Method Validation in Pharmaceutical Analysis Excerpt :

Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness. Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends. With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.