HPLC Method Development for Pharmaceuticals

Written By Satinder Ahuja
HPLC Method Development for Pharmaceuticals
  • Publsiher : Elsevier
  • Release : 21 September 2011
  • ISBN : 0080554199
  • Pages : 532 pages
  • Rating : /5 from reviews
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Download or read book entitled HPLC Method Development for Pharmaceuticals by author: Satinder Ahuja which was release on 21 September 2011 and published by Elsevier with total page 532 pages . This book available in PDF, EPUB and Kindle Format. 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

HPLC Method Development for Pharmaceuticals
  • Author : Satinder Ahuja,Henrik Rasmussen
  • Publisher : Elsevier
  • Release Date : 2011-09-21
  • Total pages : 532
  • ISBN : 0080554199
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Summary : 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 ...

Analytical Method Development and Validation

Analytical Method Development and Validation
  • Author : Michael E. Swartz,Ira S. Krull
  • Publisher : CRC Press
  • Release Date : 2018-10-03
  • Total pages : 96
  • ISBN : 0080554199
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Summary : 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 ...

Handbook of Pharmaceutical Analysis by HPLC

Handbook of Pharmaceutical Analysis by HPLC
  • Author : Satinder Ahuja,Michael Dong
  • Publisher : Elsevier
  • Release Date : 2005-02-09
  • Total pages : 600
  • ISBN : 0080554199
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Summary : 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 ...

HPLC Method Development and Validation in Pharmaceutical Analysis

HPLC Method Development and Validation in Pharmaceutical Analysis
  • Author : Ghulam Shabir
  • Publisher : LAP Lambert Academic Publishing
  • Release Date : 2013-01
  • Total pages : 492
  • ISBN : 0080554199
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Summary : 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 ...

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

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,Kakasaheb R. Mahadik,Sachin E. Potawale,Anirudh B. Thati
  • Publisher : Anchor Academic Publishing (aap_verlag)
  • Release Date : 2014-08
  • Total pages : 112
  • ISBN : 0080554199
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Summary : 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 ...

HPLC for Pharmaceutical Scientists

HPLC for Pharmaceutical Scientists
  • Author : Yuri V. Kazakevich,Rosario LoBrutto
  • Publisher : John Wiley & Sons
  • Release Date : 2007-02-16
  • Total pages : 1080
  • ISBN : 0080554199
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Summary : 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 ...

An Introduction to HPLC for Pharmaceutical Analysis

An Introduction to HPLC for Pharmaceutical Analysis
  • Author : Oona McPolin
  • Publisher : Lulu.com
  • Release Date : 2009-03-01
  • Total pages : 139
  • ISBN : 0080554199
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Summary : 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 ...

Development of Novel Stability Indicating Methods Using Liquid Chromatography

Development of Novel Stability Indicating Methods Using Liquid Chromatography
  • Author : Mukesh Maithani,Parveen Bansal
  • Publisher : Springer
  • Release Date : 2019-08-07
  • Total pages : 101
  • ISBN : 0080554199
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Summary : Reversed-phase high-performance liquid chromatography (RP-HPLC) has become the most widely used method for pharmaceutical analysis, as it ensures accuracy, specificity and reproducibility for the quantification of drugs, while avoiding interference from any of the excipients that are normally present in pharmaceutical dosage forms. This book presents a simple methodology for ...

HPLC Method for Determination of APIs in pharmaceutical formulation

HPLC Method for Determination of APIs in pharmaceutical formulation
  • Author : Parimal Chatrabhuji,Chintan Pandya,Mukesh Patel
  • Publisher : Lulu.com
  • Release Date : 2021-05-10
  • Total pages : 212
  • ISBN : 0080554199
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Summary : Read online HPLC Method for Determination of APIs in pharmaceutical formulation written by Parimal Chatrabhuji,Chintan Pandya,Mukesh Patel, published by Lulu.com which was released on . Download full HPLC Method for Determination of APIs in pharmaceutical formulation Books now! Available in PDF, ePub and Kindle....

Capillary Electrophoresis Methods for Pharmaceutical Analysis

Capillary Electrophoresis Methods for Pharmaceutical Analysis
  • Author : Satinder Ahuja,Mohamedilias Jimidar
  • Publisher : Elsevier
  • Release Date : 2011-08-09
  • Total pages : 546
  • ISBN : 0080554199
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Summary : Capillary electrophoresis (CE) is a powerful analytical technique that is widely used in research and development and in quality control of pharmaceuticals. Many reports of highly efficient separations and methods have been published over the past 15 years. CE offers several advantages over high-pressure or high-performance liquid chromatography (HPLC). These include ...

Method Validation in Pharmaceutical Analysis

Method Validation in Pharmaceutical Analysis
  • Author : Joachim Ermer,John H. McB. Miller
  • Publisher : John Wiley & Sons
  • Release Date : 2006-03-06
  • Total pages : 418
  • ISBN : 0080554199
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Summary : 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 ...

Handbook of Modern Pharmaceutical Analysis

Handbook of Modern Pharmaceutical Analysis
  • Author : Satinder Ahuja,Stephen Scypinski
  • Publisher : Academic Press
  • Release Date : 2010-11-11
  • Total pages : 598
  • ISBN : 0080554199
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Summary : Handbook of Modern Pharmaceutical Analysis, Second Edition, 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, providing complete coverage of quality assurance from the point of ...

Software assisted Method Development In High Performance Liquid Chromatography

Software assisted Method Development In High Performance Liquid Chromatography
  • Author : Szabolcs Fekete,Imre Molnar
  • Publisher : World Scientific
  • Release Date : 2018-08-01
  • Total pages : 364
  • ISBN : 0080554199
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Summary : 'The book is a useful contribution in the field of HPLC, and may represent a valuable tool for chromatography practitioners in different fields, as well as teachers and instructors. The 12 chapters provide comprehensive insights of current day retention and resolution modelling in HPLC, and its applications for small and large ...

Practical Hplc and Lc Ms Method Development and Validation

Practical Hplc and Lc Ms Method Development and Validation
  • Author : Ghulam A. Shabir
  • Publisher : LAP Lambert Academic Publishing
  • Release Date : 2012-06
  • Total pages : 308
  • ISBN : 0080554199
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Summary : The coherent body of research described in this book is concerned with new HPLC method development and validation using novel systematic approaches for pharmaceutical and diagnostic compounds. The first stage of the research was to study how analytical method development and validation are typically carried out at present and to ...

Validation of Analytical Methods for Pharmaceutical Analysis

Validation of Analytical Methods for Pharmaceutical Analysis
  • Author : Oona McPolin
  • Publisher : Lulu.com
  • Release Date : 2009-05-01
  • Total pages : 152
  • ISBN : 0080554199
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Summary : This book provides a comprehensive guide on validating analytical methods. Key features: Full review of the available regulatory guidelines on validation and in particular, ICH. Sections of the guideline, Q2(R1), have been reproduced in this book with the kind permission of the ICH Secretariat; Thorough discussion of each of ...