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- Taylor and Francis 2004; US$ 283.00
Newcomers to the field of biopharmaceuticals require an understanding of the basic principles and underlying methodology involved in developing protein- and nucleic acid-based therapies for genetic and acquired diseases. Biomaterials for Delivery and Targeting of Proteins and Nucleic Acids introduces the principles of polymer science and chemistry,... more...
- Wiley 2007; US$ 120.00
This comprehensive resource covers the fundamentals, formulation, and biopharmaceutical issues of lipid-based drug delivery. It presents the principles of lipid absorption and covers formulation issues, such as dissolution testing and stability testing, and physiological and biopharmaceutical issues, including the role of specific enzymes, the evaluation... more...
- McGraw-Hill Education 2005; US$ 135.00
The goal of every drug delivery system is to deliver the precise amount of a drug at a pre-programmed rate to the desired location in order to achieve the drug level necessary for the treatment. An essential guide for biomedical engineers and pharmaceutical designers, this resource combines physicochemical principles with physiological processes to... more...
- Taylor and Francis 2008; US$ 378.00
From a world-class team of experts, "Water-Insoluble Drug Formulation" provides step-by-step guidance and scientific background on drug and water properties, discussing how they contribute to solubilization and dissolution. The second edition features three brand new chapters on regulatory aspects of water-insoluble drugs, water-insoluble... more...
- Pharmaceutical Press 2007; US$ 240.00
A combination of a sound formulation with a proper control of the tabletting or capsule filling process is necessary to produce a satisfactory tablet or capsule. These considerations require accurate measurements. Tablet and Capsule Machine Instrumentation is a practical guide to the techniques and applications of instrumentation used to make these... more...
- Springer 2007; US$ 319.00
Solvent systems are integral to drug development and pharmaceutical technology. This single topic encompasses numerous allied subjects running the gamut from recrystallization solvents to biorelevant media. The goal of this contribution to the AAPS Biotechnology: Pharmaceutical Aspects series is to generate both a practical handbook as well as a reference... more...
- Springer 2008; US$ 199.00
In spite of the potential use of nanomaterials as tissue engineering devices, implants, biosensors, and drug delivery devices, there has yet to be a compilation of the risks associated with the in vivo use of nanomaterials. This book intends to provide detailed views of how cells and tissues in the body deal with nanoparticles. more...
- Taylor and Francis 2009; US$ 294.00
Aqueous solubility is one of the major challenges in the early stages of drug discovery. One of the most common and effective methods for enhancing solubility is the addition of an organic solvent to the aqueous solution. Along with an introduction to cosolvency models, the Handbook of Solubility Data for Pharmaceuticals provides an extensive database... more...
- Wiley 2011; US$ 125.00
This book describes the theories, applications, and challenges for different oral controlled release formulations. This book differs from most in its focus on oral controlled release formulation design and process development. It also covers the related areas like preformulation, biopharmaceutics, in vitro-in vivo correlations (IVIVC), quality by design... more...
- Wiley 2012; US$ 135.00
A practical and science-based approach for addressing toxicological concerns related to leachables and extractables associated with inhalation drug products Packaging and device components of Orally Inhaled and Nasal Drug Products (OINDP)such as metered dose inhalers, dry powder inhalers, and nasal sprayspose potential safety risks from... more...