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Sinopsis
The pharmaceutical industry faces significant challenges due to impurities in pharmaceutical substances. These impurities can originate from various sources, including raw materials, manufacturing processes, and storage conditions. Types of impurities include organic, inorganic, and residual solvents, each requiring stringent control to ensure drug safety and efficacy. The historical evolution of Pharmacopoeia has played a crucial role in standardizing drug quality, with significant milestones including the publication of national and international pharmacopoeias that set the standards for drug purity, strength, and consistency. In pharmaceutical analysis, limit tests are vital for detecting impurities such as chloride, sulphate, iron, arsenic, lead, and heavy metals. Each test involves specific principles and methods, like precipitation reactions for chlorides and colorimetric methods for iron. Modified limit tests for chloride and sulphate offer enhanced sensitivity, while specialized tests for heavy metals and lead ensure trace amounts are kept within safe limits.
Acids, bases, and buffers are essential components in pharmaceutical systems, ensuring the stability and efficacy of formulations. Buffer equations and buffer capacity are fundamental concepts, with buffers playing a critical role in maintaining the pH of solutions. The preparation and stability of buffers, as well as their use in creating buffered isotonic solutions, are crucial for pharmaceutical applications.
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- EditorialNotion Press
- Año de publicación2024
- ISBN 13 9798894758497
- EncuadernaciónTapa blanda
- IdiomaInglés
- Número de páginas246
- Contacto del fabricanteno disponible
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Edited Book of Pharmaceutical Inorganic Chemistry
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EDITED BOOK OF PHARMACEUTICAL INORGANIC CHEMISTRY
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Edited Book of Pharmaceutical Inorganic Chemistry
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PAP. Condición: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. Nº de ref. del artículo: L0-9798894758497
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Edited Book of Pharmaceutical Inorganic Chemistry (Paperback)
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Calificación del vendedor: 5 de 5 estrellas
Paperback. Condición: new. Paperback. The pharmaceutical industry faces significant challenges due to impurities in pharmaceutical substances. These impurities can originate from various sources, including raw materials, manufacturing processes, and storage conditions. Types of impurities include organic, inorganic, and residual solvents, each requiring stringent control to ensure drug safety and efficacy. The historical evolution of Pharmacopoeia has played a crucial role in standardizing drug quality, with significant milestones including the publication of national and international pharmacopoeias that set the standards for drug purity, strength, and consistency. In pharmaceutical analysis, limit tests are vital for detecting impurities such as chloride, sulphate, iron, arsenic, lead, and heavy metals. Each test involves specific principles and methods, like precipitation reactions for chlorides and colorimetric methods for iron. Modified limit tests for chloride and sulphate offer enhanced sensitivity, while specialized tests for heavy metals and lead ensure trace amounts are kept within safe limits.Acids, bases, and buffers are essential components in pharmaceutical systems, ensuring the stability and efficacy of formulations. Buffer equations and buffer capacity are fundamental concepts, with buffers playing a critical role in maintaining the pH of solutions. The preparation and stability of buffers, as well as their use in creating buffered isotonic solutions, are crucial for pharmaceutical applications. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Nº de ref. del artículo: 9798894758497
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Edited Book of Pharmaceutical Inorganic Chemistry (Paperback)
Librería: Grand Eagle Retail, Fairfield, OH, Estados Unidos de America
Calificación del vendedor: 5 de 5 estrellas
Paperback. Condición: new. Paperback. The pharmaceutical industry faces significant challenges due to impurities in pharmaceutical substances. These impurities can originate from various sources, including raw materials, manufacturing processes, and storage conditions. Types of impurities include organic, inorganic, and residual solvents, each requiring stringent control to ensure drug safety and efficacy. The historical evolution of Pharmacopoeia has played a crucial role in standardizing drug quality, with significant milestones including the publication of national and international pharmacopoeias that set the standards for drug purity, strength, and consistency. In pharmaceutical analysis, limit tests are vital for detecting impurities such as chloride, sulphate, iron, arsenic, lead, and heavy metals. Each test involves specific principles and methods, like precipitation reactions for chlorides and colorimetric methods for iron. Modified limit tests for chloride and sulphate offer enhanced sensitivity, while specialized tests for heavy metals and lead ensure trace amounts are kept within safe limits.Acids, bases, and buffers are essential components in pharmaceutical systems, ensuring the stability and efficacy of formulations. Buffer equations and buffer capacity are fundamental concepts, with buffers playing a critical role in maintaining the pH of solutions. The preparation and stability of buffers, as well as their use in creating buffered isotonic solutions, are crucial for pharmaceutical applications. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Nº de ref. del artículo: 9798894758497
Cantidad disponible: 1 disponibles