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    1. Naturvetenskap och teknik
    2. Matematik och naturvetenskap
    3. Biologi
    4. Biokemi

    Therapeutic Protein Drug Products

    Practical Approaches to formulation in the Laboratory, Manufacturing, and the Clinic

    AvBrian K Meyer

    Inbunden, Engelska, 2012

    Del i serien Woodhead Publishing Series in Biomedicine

    1 735 kr

    Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

    Beskrivning

    Therapeutic protein drug products provides a comprehensive overview of therapeutic protein drug products, with an emphasis on formulation beginning in the laboratory, followed by manufacturing and administration in the clinic. A list of many commercial therapeutic drug products are described and include the product name, dosages, active concentration, buffer, excipients, Ph, container type and route of administration. The laboratory formulation sections focus on the most common buffers, excipients, and Ph ranges that are commonly tested in addition to systematic approaches. A brief section on biophysical and analytical analysis is also provided. Properties of therapeutic protein formulations are described and include opalescence, phase separation, color, and subvisible particles. An emphasis is placed on material and process testing to ensure success during manufacturing. The drug product manufacturing process, which includes the process of compounding to filling, is also covered. Methods of delivery in the clinic are addressed, as well as delivery strategies. Finally, a perspective on the regulatory requirements for therapeutic protein formulations is discussed.

    • Provides a list and description of commercially available therapeutic drug products and their formulations
    • A comprehensive and practical overview of protein formulation in the laboratory, manufacturing, and the clinic
    • Discusses recent topics including high protein concentration, phase separation, opalescence, and subvisible particles

    Produktinformation

    • Utgivningsdatum:2012-01-02
    • Mått:156 x 234 x undefined mm
    • Vikt:480 g
    • Format:Inbunden
    • Språk:Engelska
    • Serie:Woodhead Publishing Series in Biomedicine
    • Antal sidor:200
    • Förlag:Elsevier Science
    • ISBN:9781907568183

    Utforska kategorier

    • Biokemi inom Naturvetenskap och teknik
    • Farmakologi inom Medicin
    • Tillverkningsteknik inom Naturvetenskap och teknik

    Mer om författaren

    Dr Brian K. Meyer is a Research Fellow in Bioprocess Research and Development, Merck Research Laboratories (MRL). Dr Meyer's current position is leading a group in Vaccine Drug Product Development. Previously, Dr Meyer's team was responsible for formulating therapeutic proteins in pre-clinical development. Prior to joining MRL, Dr Meyer was a Process Scientist in Vaccine Technology and Engineering, Merck Manufacturing Division. He has a Ph.D. in Biochemistry, Microbiology, and Molecular Biology from The Pennsylvania State University and a B.S.E. in Biomedical Engineering from Tulane University.

    Innehållsförteckning

    • List of figures and tablesPrefaceAbout the authorsChapter 1: Commercial therapeutic protein drug productsAbstract1.1 Introduction1.2 Lyophilized formulations1.3 Liquid formulations1.4 Protein formulations for radiologic and diagnostic use1.5 SummaryChapter 2: A formulation method to improve the physical stability of macromolecular-based drug productsAbstract2.1 Introduction2.2 Common techniques used for the construction of EPDs2.3 The peptide drug pramlintide2.4 Monoclonal antibodies at low and high concentration2.5 Static vs. dynamic EPDs: a case study using a humanized immunoglobulin (IgG1)2.6 Conclusion and future studiesChapter 3: Properties of protein formulationsAbstract3.1 Introduction3.2 Opalescence3.3 Phase separation3.4 Color3.5 Subvisible particlesChapter 4: Material and process compatibility testingAbstract4.1 Introduction4.2 Material compatibility4.3 Process compatibility testing4.4 Antimicrobial preservative compatibility testingChapter 5: Compounding and filling: drug substance to drug productAbstract5.1 Introduction5.2 Aseptic processing5.3 Bulk drug substance5.4 Compounding of drug product5.5 Filling the drug productChapter 6: Administration in the clinicAbstract6.1 Introduction and background6.2 Diluents6.3 Components6.4 Construction materials6.5 Clinical dosing strategy: fixed volume versus fixed concentration6.6 Representative admixture concentration levels6.7 Exposure temperature and time6.8 Option of using syringes6.9 Analytical tests and acceptance criteria6.10 Sample preparation considerations6.11 Role of probe studies6.12 Bag overfill volume6.13 Pharmacy instructions6.14 ConclusionsChapter 7: Regulatory guidelines for the development of a biotechnology drug productAbstract7.1 Introduction7.2 ICH overview7.3 Common Technical Document (CTD)7.4 Drug product dossier7.5 Regulatory considerations through the biotechnology product lifecycle7.6 ConclusionsAppendixRecommended readingIndex