Pharmaceutics: The Science of Dosage Form Design

Pharmaceutics: The Science of Dosage Form Design

Edited by M. E. Aulton

A comprehensive textbook covering the design of dosage forms and all aspects of drug delivery systems. 'Pharmaceutics' in its broadest sense is the 'art of the apothecary' or, in simple terms, pharmaceutical preparations. It remains a diverse subject in the pharmacy curriculum, encompassing design of drugs, their manufacture, and the elimination of micro-organisms from the products. This books encompasses all those areas and pays particular attention to the design of dosage forms and their manufacture

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Excipient Development for Pharmaceutical, Biotechnology and Drug Delivery Systems

Excipient Development for Pharmaceutical, Biotechnology and Drug Delivery Systems

Edited by Ashok Katdare & Mahesh V. Chaubal

To facilitate the development of novel drug delivery systems and biotechnology-oriented drugs, the need for new excipients to be developed and approved continues to increase. Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems serves as a comprehensive source to improve understanding of excipients and forge new avenues for regulatory review and allowance to use. This book presents detailed, up-to-date information on various aspects of excipient development, testing, and technological considerations for their use. It addresses specific details such as historical perspective, preclinical testing, safety, and toxicology evaluation, as well as regulatory, quality, and utility aspects. The text also describes best practices for use of various functional excipients and extensive literature references for all topics

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Pharmaceutical Manufacturing Encyclopedia

Pharmaceutical Manufacturing Encyclopedia

This industry standard encyclopedia on pharmaceutical manufacturing processes has been completely updated to include FDA drugs approved up to the summer of 2004. The encyclopedia gives details for the manufacture of 2226 pharmaceuticals that are being marketed as a trade-named product somewhere in the world. Each entry includes:

ò Therapeutic function
ò Chemical and common name
ò Structural Formula
ò Chemical Abstracts Registry no.
ò Trade name, manufacturer, country, and year introduced
ò Raw Materials
ò Manufacturing Process

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Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems

Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems

Succeed in your course with the most comprehensive source on pharmaceutical dosage forms and drug delivery systems available today. Reflecting the CAPE, APhA, and NAPLEX? competencies, this trusted resource covers physical pharmacy, pharmacy practice, pharmaceutics, compounding, and dosage forms and the clinical application of the various dosing forms in patient care. The 10th edition features a dynamic new full color design, new coverage of prescription flavoring, and additional coverage of expiration dates. ? See pharmaceutical concepts in action through the two case studies (one pharmaceutical and one clinical) in each dosing forms chapter. Practice applying material using the group and individual activities in Applying the Principles and Concepts sections in every chapter. Master important underlying pharmaceutical principles through Physical Pharmacy Capsules . Extend your learning beyond the book with the online glossary and the online quiz bank that features 300 NAPLEX-style questions. Focus on what's important with Chapter Objectives that highlight key material you need to master.

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The Theory and Practice of Industrial Pharmacy

The Theory and Practice of Industrial Pharmacy

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Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial Case Studies

Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial Case Studies

A study of biopharmaceutical process validation. It aims to enable developers and producers to ensure safe products, reduce the risk of adverse reactions in patients, and avoid recalls by outlining sophisticated validation approaches to characterize processes, process intermediates, and final product fully. The text emphasizes cost effectiveness while determining what level of validation is required for different phases of development, license application, and process improvements.


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Analysis of Drug Impurities

Analysis of Drug Impurities

This book is intended for student and practitioners alike and is structured to bring the relevant disciplines together in one reference book.

A key component of the quality of pharmaceutical drugs is the control of impurities. It is important to identify and quantify levels of impurities that may be present to provide safe, effective and well-controlled medicines.

The measurement and identification of impurities to today’s standards presents significant challenges to the analytical chemist. The development of modern quantitative methods is driven by these challenges, and the rapid development
of spectrometers has provided increasing opportunity to identify the structure, and therefore the origin and safety potential, of such impurities. This book provides a source of information for the analytical chemist to understand the challenges and the techniques available to permit accurate identification and quantification of drug impurities.
This is a unique book; the editors are to be conrgatulated on persuading their industrial colleagues to write chapters, providing an industrial focus on analytical issues. This is a useful volume which fills a gap in the literature… I would recommend the book to all process and analytical chemists.

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Aerosols Handbook: Measurement, Dosimetry, and Health Effects

Aerosols Handbook: Measurement, Dosimetry, and Health Effects

As more attention is dedicated to understanding the occupational health risks associated with the industrial manufacture and use of nanotechnology, Aerosols Handbook: Measurement, Dosimetry, and Health Effects is a timely presentation of the latest research in the field of aerosol science. The book covers a multitude of topics on indoor, outdoor, and industrial aerosols, including aerosol measurement, deposition, particle size distribution, and biokinetic processes. Where harmful exposure to ultrafine particles may occur through inhalation, dermal contact, and ingestion, this book discusses how the size, shape, and chemical properties of particles affect aerosol deposition in the lungs, possibly other organs, and the overall toxicity. The book covers all relevant aspects of aerosols, from epidemiology to molecular biology, and emphasizes the importance of accurate aerosol measurement. The authors discuss Chernobyl accident and miners' lungs in detail to illustrate the effects of radioactive aerosols. The final section focuses on the health effects of specific aerosols, such as diesel aerosols and ultrafine particles. By converging research from both radioactive and non-radioactive aerosols, the editors give the book a unique and more complete perspective of how aerosols behave in the lungs. Aerosols Handbook: Measurement, Dosimetry, and Health Effects is an essential resource for those who study exposure, dosages, and toxicity to develop treatments for exposure, reduce air pollution, and establish better safety regulations, particularly in industries using nanotechnologies.


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Dielectric Analysis of Pharmaceutical Systems

Dielectric Analysis of Pharmaceutical Systems

Dielectric analysis is a technique used particularly in quality controlling drug samples. This guide to the dielectric analysis of pharmaceutical systems serves both as an introduction to the technique and as a spring board for further studies of Pharmaceutical Systems.


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Oral Delivery of Macromolecular Drugs: Barriers, Strategies and Future Trends

Oral Delivery of Macromolecular Drugs: Barriers, Strategies and Future Trends

Recent and rapid progress in the field of biotechnology has resulted in an increasing number of novel macromolecular drugs with great promise for further advanced research and clinical application. However, the delivery of these macromolecular drugs by routes other than the parenteral route is difficult. The pipeline of macromolecular drugs derived from biotechnology presents a challenging opportunity to develop practical dosage forms that could be dosed via the oral route. Given this, the successful oral delivery of macromolecular drugs presents an enormous opportunity. Oral Delivery of Macromolecular Drugs will provide an overview of the innovative oral delivery technologies that have demonstrated success in human testing and will go on to cite the challenges, strategies, and future trends that are to be expected.


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HandBook Of Isolation And Characterization Of Impurities In Pharmaceuticals

HandBook Of Isolation And Characterization Of Impurities In Pharmaceuticals


Book Description:

A Volume in the Separation Science and Technology Series. The United States Food and Drug Administration (FDA) and other regulatory bodies around the world require that impurities in drug substance and drug product levels recommended by the International Conference on Harmonisation (ICH) be isolated and characterized.

Identifying process-related impurities and degradation products also helps us to understand the production of impurities and assists in defining degradation mechanisms. When this process is performed at an early stage, there is ample time to address various aspects of drug development to prevent or control the production of impurities and degradation products well before the regulatory filing and thus assure production of a high-quality drug product.

This book, therefore, has been designed to meet the need for a reference text on the complex process of isolation and characterization of process-related (synthesis and formulation) impurities and degradation products to meet critical requlatory requirements.

It's objective is to provide guidance on isolating and characterizing impurities of pharmaceuticals such as drug candidates, drug substances, and drug products. The book outlines impurity identification processes and will be a key resource document for impurity analysis, isolation/synthesis, and characterization.

- Provides valuable information on isolation and characterization of impurities.
- Gives a regulatory perspective on the subject.
- Describes various considerations involved in meeting regulatory requirements.
- Discusses various sources of impurities and degredation products.


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Micro-encapsulation Methods And Industrial Applications

Micro-encapsulation Methods And Industrial Applications

The second edition of Microencapsulation, Methods and Industrial Applications
comprises 11 expanded and revised chapters and 12 new chapters that reflect
the evolution of this discipline in the past decade.The second edition of Microencapsulation, Methods and Industrial Applications
comprises 11 expanded and revised chapters and 12 new chapters that reflect
the evolution of this discipline in the past decade.


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Lubricant Additives: Chemistry and Applications

Lubricant Additives: Chemistry and Applications (Chemical Industries)

CRC | ISBN: 0824708571 | 2003-01-29 | PDF (OCR) | 758 pages | 40.5 Mb

This text details the design of cost-effective, environmentally friendly lubricant additive technologies and components for the automotive, industrial, manufacturing, food, and aerospace industries. It examines the mechanisms, functions, advantages and limitations of lubricant additives such as antioxidants, antiwear agents, detergents and dispersants, friction modifiers and metalworking fluids. It contains a disk displaying Internet resources for the lubricant industry.

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Pharmaceutical Emulsions and Suspensions: Second Edition, Revised and Expanded

Pharmaceutical Emulsions and Suspensions: Second Edition, Revised and Expanded

University Montpellier, France. Covers fundamental and applied knowledge of emulsions and suspensions. Assists those working in all spheres of pharmacy in solving the problems posed by by emulsion and suspension formulations and applications. Diagrams, charts.

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Ophthalmic Drug Delivery Systems, Second Edition

Ophthalmic Drug Delivery Systems, Second Edition

Extensively revised and updated, this second edition compares conventional and innovative drug delivery systems. The book covers significant ophthalmic advances and breakthroughs in gene therapy, ocular microdialysis, vitreous drug disposition modelling, and receptor/transporter targeted drug delivery. It examines procedures in pharmacokinetic/pharmacodynamic modeling for the determination of appropriate dosing regimens, covers new developments in animal modeling, and discusses current regulations governing patenting, commercial product release, and human testing. This in-depth reference lays the groundwork for overcoming constraints on the delivery of ophthalmic drugs.

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Remington: The Science and Practice of Pharmacy

Remington: The Science and Practice of Pharmacy

For over 100 years, Remington has been the definitive textbook and reference on the science and practice of pharmacy. This Twenty-First Edition keeps pace with recent changes in the pharmacy curriculum and professional pharmacy practice. More than 95 new contributors and 5 new section editors provide fresh perspectives on the field. New chapters include pharmacogenomics, application of ethical principles to practice dilemmas, technology and automation, professional communication, medication errors, re-engineering pharmacy practice, management of special risk medicines, specialization in pharmacy practice, disease state management, emergency patient care, and wound care. Purchasers of this textbook are entitled to a new, fully indexed Bonus CD-ROM, affording instant access to the full content of Remington in a convenient and portable format.

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ENCYCLOPEDIA OF PHARMACEUTICAL TECHNOLOGY,THIRD EDITION

ENCYCLOPEDIA OF PHARMACEUTICAL TECHNOLOGY,THIRD EDITION


Presenting official and attractive articles on every aspects of take development, dosage, manufacturing, and regulation, this Third Edition enables the caregiver doc and initiate like to ready abreast of developments in this apace evolving and highly combative field. A secure meaning agency and unceasing consort for eld to come, the Third Edition module substance completely newborn entries that counterbalance grave issues in the earth much as the effect of genomics, biotechnology, and implants on take discovery, targeting, delivery, and formulation. In addition, it module come newborn restrictive issues, much as the changes in business regulations, and aborning bureau procedures.

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