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Springer Protocols eBook Series

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  • Metabolic Profiling

    Methods and Protocols

    Edited by Olga Deda, Helen G. Gika, Ian D. Wilson ...
    Series series Springer Protocols
    This second edition volume expands on the previous edition with new chapters and updated discussions on the latest advancements in the development and practice of metabolic phenotyping. The chapters in this book cover topics such as quality control in untargeted metabolic phenotyping; implementation of quality assurances processes; careful bio- and chemoinformatic data analysis; using reversed ... Read more

    PHP10,979.59

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  • Specification of Drug Substances and Products

    Development and Validation of Analytical Methods

    Edited by Thomas W. Rosanske, Christopher M. Riley ...
    Specification of Drug Substances and Products: Development and Validation of Analytical Methods is a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on phase-appropriate development and validation of analytical methods. This book is intended as more than a review of new regional guidelines, existing ... Read more

    PHP6,432.99

  • Handbook of Modern Pharmaceutical Analysis

    Edited by Satinder Ahuja, Stephen Scypinski ...
    Series Book 3 - Separation Science and Technology
    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 topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability ... Read more

    PHP13,675.49

  • Mass Spectrometry for the Clinical Laboratory

    Edited by Hari Nair, William Clarke ...
    Mass Spectrometry for the Clinical Laboratory is an accessible guide to mass spectrometry and the development, validation, and implementation of the most common assays seen in clinical labs. It provides readers with practical examples for assay development, and experimental design for validation to meet CLIA requirements, appropriate interference testing, measuring, validation of ion suppression ... Read more

    PHP5,359.99

  • Peptide Therapeutics

    Strategy and Tactics for Chemistry, Manufacturing, and Controls

    Edited by Ved Srivastava ...
    Series Book 72 - Drug Discovery Series
    Peptide therapy has become a key strategy in innovative drug development, however, one of the potential barriers for the development of novel peptide drugs in the clinic is their deficiencies in clearly defined chemistry, manufacturing and controls (CMC) strategy from clinical development to commercialization. CMC can often become a rate-limiting step due to lack of knowledge and lack of a formal ... Read more

    PHP13,859.69

  • Applied Computer-Aided Drug Design: Models and Methods

    by Igor José dos Santos Nascimento ...
    Designing and developing new drugs is an expensive and time-consuming process, and there is a need to discover new tools or approaches that can optimize this process. Applied Computer-Aided Drug Design: Models and Methods compiles information about the main advances in computational tools for discovering new drugs in a simple and accessible language for academic students to early career ... Read more

    PHP3,060.29

  • Developing Solid Oral Dosage Forms

    Pharmaceutical Theory and Practice

    Edited by Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang, Lawrence Yu, Rao V. Mantri ...
    Developing Solid Oral Dosage Forms: Pharmaceutical Theory and Practice, Second Edition illustrates how to develop high-quality, safe, and effective pharmaceutical products by discussing the latest techniques, tools, and scientific advances in preformulation investigation, formulation, process design, characterization, scale-up, and production operations. This book covers the essential principles ... Read more

    PHP16,089.29

  • Handbook of Modern Pharmaceutical Analysis

    Edited by Satinder Ahuja, Stephen Scypinski ...
    Series Book 10 - Separation Science and Technology
    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 discovery to the ... Read more

    PHP13,139.29

  • Antimicrobial Peptides

    A Roadmap for Accelerating Discovery and Development

    Edited by Gregory R. Wiedman, Luis H. Reyes, Juan C. Cruz ...
    Antimicrobial Peptides: A Roadmap for Accelerating Discovery and Development covers the most important efforts of scientists and engineers worldwide to accelerate the process of discovery, production, and eventual market penetration of more potent antimicrobial peptides. These efforts have been fueled by emerging technologies such as artificial intelligence and data science, molecular and CFD ... Read more

    PHP10,726.19

  • Regulated Bioanalysis: Fundamentals and Practice

    Edited by Mario L. Rocci Jr., Stephen Lowes ...
    Series series Biomedical and Life Sciences (R0)
    The editors have engaged leading scientists in the field to participate in the development of this book, which is envisioned as a “one of a kind” contribution to the field. The book is a comprehensive text that puts fundamental bioanalytical science in context with current practice, its challenges and ongoing developments. It expands on existing texts on the subject by covering regulated ... Read more

    PHP8,395.99

  • Quality by Design for Biopharmaceutical Drug Product Development

    Edited by Mansoor A. Khan, Feroz Jameel, Sheryl Martin-Moe, Susan Hershenson ...
    Series series Biomedical and Life Sciences (R0)
    This volume explores the application of Quality by Design (QbD) to biopharmaceutical drug product development. Twenty-eight comprehensive chapters cover dosage forms, liquid and lyophilized drug products. The introductory chapters of this book define key elements of QbD and examine how these elements are integrated into drug product development. These chapters also discuss lessons learned from the ... Read more

    PHP14,790.99

  • Pharmaceutical Stress Testing

    Predicting Drug Degradation, Second Edition

    Edited by Steven W. Baertschi, Karen M. Alsante, Robert A. Reed ...
    Series series Drugs and the Pharmaceutical Sciences
    The second edition of Pharmaceutical Stress Testing: Predicting Drug Degradation provides a practical and scientific guide to designing, executing and interpreting stress testing studies for drug substance and drug product. This is the only guide available to tackle this subject in-depth. The Second Edition expands coverage from chemical stability ... Read more

    PHP4,249.67