Denise Bohrer

Contamination

• Gebundenes Buch

Produktbeschreibung

Contamination in pharmaceutical manufacturing poses significant health risks, yet it is not fully addressed in existing compendia. This book provides for the first time a one-stop reference on the subject. It surveys the sources of contamination, explaining how to identify contaminants and impurities in pharmaceutical products, methods to avoid and remove contaminants, and regulatory guidelines to determine contamination. An absolute must for pharmaceutical and biotechnology researchers working in the area of quality control, as well as quality managers, regulators, chemists, and toxicologists in the field.

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The first one-volume guide to sources of contamination in pharmaceuticals and medical devices

Most books dealing with contaminants in medicinal products often focus on analytical methods for detecting nonspecific impurities. Key to the work of the pharmaceutical chemist, this unique reference helps identify the sources of contamination in medicinal and pharmaceutical products and medical devices. Divided into three parts, Sources of Contamination in Medicinal Products and Medical Devices covers chemical, microbiological, and physical (particulate matter) contamination, including those originating from sterilization procedures.

As compelling as a medical documentary, the book sheds light on how impurities and contaminants can enter the human body transported via a specific product or treatment. Focusing on only those medicinal products and medical devices that may lead to exposure to contaminants harmful to human health, the book offers a comprehensive, systematic look at the entire universe of medical contamination:
Chemical contaminants including residual solvents, catalyst residuals, and genotoxic impurities in active pharmaceutical ingredients (APIs)
Diagnostic imaging agents (i.e., radiopharmaceuticals and contrast agents)
Microbiological and endotoxin contamination involving single and multiple dose products, medical devices, and biofilms
Contamination from sterilization procedures, residuals from radiation sterilization, ionizing radiation on packaging materials and medical devices
Medicinal gases and volatile anesthetics
Biopharmaceuticals including recombinant DNA technology products
Extractables and leachables from containers made of glass, plastics, and metal

Each section of the book contains information on what contaminants could be expected in a particular product, and how they were generated and reached that product. With up-to-date regulatory guidelines for determining contamination, as well as methods for assessing, quantifying, avoiding and removing contaminants, Sources of Contamination in Medicinal Products and Medical Devices is essential to fully understanding the specific threats that undermine the safety of medicines and medical devices.

Produktdetails

• Verlag: Wiley & Sons
• 1. Auflage
• Seitenzahl: 592
• Erscheinungstermin: 19. November 2012
• Englisch
• Abmessung: 240mm x 161mm x 36mm
• Gewicht: 948g
• ISBN-13: 9780470487501
• ISBN-10: 047048750X
• Artikelnr.: 36273790

Autorenporträt

DENISE BOHRER, PhD, is Professor of Analytical Chemistry at the Federal University of Santa Maria, Brazil. Her research has focused on sources of contamination in pharmaceutical products, specifically, infusion solutions for patients with kidney disease and preterm infants. She has published sixty-eight papers and two book chapters on pharmaceutical manufacturing.

Inhaltsangabe

1. Introduction 2. Directives for contamination control PART I: CHEMICAL
CONTAMINATION 3. Raw Materials 3.1 Water 3.2 Inorganic Impurities 3.3
Organic Impurities 3.4 Additives 3.5 Residual solvents Concluding remarks
References 4. Medicinal gases and volatile anesthetics 4.1 Medicinal gases
4.2 Volatile anesthetics Concluding remarks References 1. Introduction 2.
Directives for contamination control PART I: CHEMICAL CONTAMINATION 3. Raw
Materials 3.1 Water 3.2 Inorganic Impurities 3.3 Organic Impurities 3.4
Additives 3.5 Residual solvents Concluding remarks References 4. Medicinal
gases and volatile anesthetics 4.1 Medicinal gases 4.2 Volatile anesthetics
Concluding remarks References 5. Diagnostic imaging agents 5.1
Radiopharmaceuticals 5.2 Contrast agents Concluding remarks References 6.
Containers 6.1 Glass containers 6.2 Plastics containers 6.3 Metal
containers Concluding remarks References 7. Closures Concluding remarks
References 8. Delivery systems and filters 8.1 Delivery systems made of PVC
8.2 Delivery systems made of other plastic materials 8.3 Filters Concluding
remarks References 9. Medical devices 9.1 General use devices 9.1.1 Medical
gloves 9.1.2 Syringes 9.2 Extracorporeal circuits 9.3 Devices for
administration of aerosolized drugs 9.4 Reprocessed medical devices 9.5
Tissue substitutes Concluding remarks References PART II: PHYSICAL
CONTAMINATION 10. Particulate matter Concluding remarks References PART
III: MICROBIOLOGICAL CONTAMINATION 11. Microbiological and endotoxin
contamination 11.1 Water 11.2 Raw materials 11.3 Sterile products 11.4
Medicinal gases 11.5 Medical devices 11.6 Biofilms 11.7 Dialysis circuits
11.8 Nosocomial infections Concluding remarks References PART IV:
MISCELLANEOUS 12. Contamination from sterilization procedures 12.1
Residuals from radiation sterilization 12.2 Heat sterilization 12.3
Residuals from chemical disinfection/sterilization agents Concluding
remarks References 13. Biotechnological products 13.1 DNA and Host cell
proteins residuals 13.2 Viruses and mycoplasma 13.3 Endotoxin 13.4 Protein
degradation 13.5 Protein aggregation Concluding remarks References Appendix