Sample Preparation of Pharmaceutical Dosage Forms: Challenges and Strategies for Sample Preparation and Extraction
Editat de Beverly Nickersonen Limba Engleză Paperback – 26 noi 2014
This book is divided into four parts:
• Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.
• Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.
• Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.
• Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.
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Specificații
ISBN-13: 9781489995827
ISBN-10: 148999582X
Pagini: 412
Ilustrații: XIV, 397 p.
Dimensiuni: 155 x 235 x 22 mm
Greutate: 0.58 kg
Ediția:2011
Editura: Springer Us
Colecția Springer
Locul publicării:New York, NY, United States
ISBN-10: 148999582X
Pagini: 412
Ilustrații: XIV, 397 p.
Dimensiuni: 155 x 235 x 22 mm
Greutate: 0.58 kg
Ediția:2011
Editura: Springer Us
Colecția Springer
Locul publicării:New York, NY, United States
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Public țintă
ResearchDescriere
Accurate analytical data is critical in the pharmaceutical industry. During drug development this information is used to evaluate and select formulations for use in toxicology and clinical studies, to assess manufacturing processes and to assess the suitability and stability of clinical supplies. For marketed products, analytical data is used to assess the suitability and stability of the commercial product.
Development and use of robust analytical methods is critical for the ability to generate accurate analytical data. Sample preparation is an integral part of the analytical method. In a survey conducted by LC-GC1, responses indicated that approximately two-thirds of the time spent testing and analyzing samples was spent on the sample preparation portion of the method. In addition, issues related to sample preparation accounted for one-third of the errors generated while performing an analytical method.
A number of challenges exist in the sample preparation/extraction of pharmaceutical dosage forms for potency and purity analysis as well as isolation and identification of impurities and degradants. These challenges increase for complex dosage forms such as some controlled release formulations and other challenging formulations such as suspensions, ointments, transdermal patches, etc. Challenges in developing rapid and rugged sample preparation methods include complete dispersion of the dosage form to facilitate extraction and solubilization of the analytes of interest, dealing with extracted interfering components and addressing drug-excipient interactions. A number of factors must be considered and addressed in each of these areas.
The objective of Sample Preparation of Pharmaceutical Dosage Forms is to provide an overview of the various sample preparation and extraction techniques available for pharmaceutical dosage forms. In addition to the review and discussion of specific techniques, sample preparation method development and trouble shooting strategies are discussed. Multiple examples and case studies are presented to highlight various potential issues and solutions.
Development and use of robust analytical methods is critical for the ability to generate accurate analytical data. Sample preparation is an integral part of the analytical method. In a survey conducted by LC-GC1, responses indicated that approximately two-thirds of the time spent testing and analyzing samples was spent on the sample preparation portion of the method. In addition, issues related to sample preparation accounted for one-third of the errors generated while performing an analytical method.
A number of challenges exist in the sample preparation/extraction of pharmaceutical dosage forms for potency and purity analysis as well as isolation and identification of impurities and degradants. These challenges increase for complex dosage forms such as some controlled release formulations and other challenging formulations such as suspensions, ointments, transdermal patches, etc. Challenges in developing rapid and rugged sample preparation methods include complete dispersion of the dosage form to facilitate extraction and solubilization of the analytes of interest, dealing with extracted interfering components and addressing drug-excipient interactions. A number of factors must be considered and addressed in each of these areas.
The objective of Sample Preparation of Pharmaceutical Dosage Forms is to provide an overview of the various sample preparation and extraction techniques available for pharmaceutical dosage forms. In addition to the review and discussion of specific techniques, sample preparation method development and trouble shooting strategies are discussed. Multiple examples and case studies are presented to highlight various potential issues and solutions.
Cuprins
Properties that Impact Sample Preparation and Extraction of Pharmaceutical Dosage Forms.- Sampling Considerations.- Agitation and Particle Size Reduction Techniques.- Liquid-Liquid and Solid-Phase Extraction Techniques.- Extraction Techniques Leveraging Elevated Temperature and Pressure.- Addressing Drug-Excipient Interactions.- Sample Preparation for Solid Oral Dosage Forms.- Sample Preparation for Select Non Solid Dosage Forms.- Post-Extraction Considerations.- Sample Preparation Method Validation.- Application of Quality by Design (QbD) Principles for Sample Preparation.- Automation and Sample Preparation.- A Systematic Approach for Investigating Aberrant Potency Values.- Green Chemistry Considerations for Sample Preparation.- No Sample Preparation
Notă biografică
Beverly Nickerson, Ph.D., is Associate Research Fellow in Analytical Development in Pfizer Global Research and Development, Pfizer Inc. Dr. Nickerson is well published in peer-reviewed journals, is author of several book chapters and has presented at various scientific meetings. She has extensive experience in early stage and late stage drug development.
Textul de pe ultima copertă
Designed as a resource guide for analytical scientists working in the pharmaceutical industry, this comprehensive guide is focused entirely on sample preparation and extraction of pharmaceutical dosage forms.
This book is divided into four parts:
• Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.
• Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.
• Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.
• Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.
Analytical scientists in the pharmaceutical industry as well as in analytical testing laboratories will find this book a valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug product.
Beverly Nickerson, Ph.D., is Associate Research Fellow in Analytical Development in Pfizer Global Research and Development, Pfizer Inc. Dr. Nickerson is well published in peer-reviewed journals, is author of several book chapters and has presented at various scientific meetings. She has extensive experience in early stage and late stage drug development.
This book is divided into four parts:
• Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.
• Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.
• Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.
• Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.
Analytical scientists in the pharmaceutical industry as well as in analytical testing laboratories will find this book a valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug product.
Beverly Nickerson, Ph.D., is Associate Research Fellow in Analytical Development in Pfizer Global Research and Development, Pfizer Inc. Dr. Nickerson is well published in peer-reviewed journals, is author of several book chapters and has presented at various scientific meetings. She has extensive experience in early stage and late stage drug development.
Caracteristici
Volume focused entirely on sample preparation and extraction of pharmaceutical dosage forms
A valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug product
Presents multiple examples and case studies to highlight various potential issues and solutions
A valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug product
Presents multiple examples and case studies to highlight various potential issues and solutions