By Donald L. Wise
He guide of Pharmaceutical managed liberate know-how experiences the layout, fabrication, technique, management, and classifications of assorted drug supply structures, together with matrices, and membrane managed reservoir, bioerodible, and pendant chain structures. comprises state-of-the-art learn at the managed supply of biomolecules! Discussing the benefits and barriers of managed unlock structures, the guide of Pharmaceutical managed liberate expertise· covers oral, transdermal, parenteral, and implantable supply of substances· discusses amendment the way to in achieving wanted unencumber kinetics· highlights constraints of procedure layout for useful scientific software· analyzes diffusion equations and mathematical modeling· considers environmental reputation and tissue compatibility of biopolymeric platforms for biologically energetic brokers· evaluates polymers as drug supply vendors· describes peptide, protein, micro-, and nanoparticulate free up platforms· examines the fee, convenience, ailment regulate, uncomfortable side effects, and sufferer compliance of diverse supply platforms and units· and extra!
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Additional info for Handbook of Pharmaceutical Controlled Release Technology
While research is all about generating new knowledge, development is (mostly) about engineering new products. For example, we might study the physiological mechanisms and molecular pathways of cancer, which will later be used in the development phase as potential drug targets. In a typical approach, when university researchers identify a protein, whose activation is associated with cancer, this knowledge can be licensed out to a pharmaceutical company, which then tests its huge chemical libraries to identify compounds, which inhibit the target molecule (Angell, 2004; LaMattina, 2008).
Chapter | 1 23 that look at the same clearly defined research question. Usually the objective is to critically evaluate all the available evidence that a single treatment works. This is very different from the conventional review format in biology, where the object is to give a review of the results (but usually not the methodology or biases) of recent studies in a wider field of science. Biological reviews usually assume that the individual studies under review are correct, while medical systematic reviews make no such assumption and try to critically compare all relevant independent studies.
China’s R&D spending is growing at the incredible rate of 18% (inflation-adjusted) and in 2011 it constituted 15% of the world’s R&D spending. In 2009 Asia held 34%, the United States 30%, and the EU 22% of the global R&D (National Science Board, 2013). If future manifests itself in the number of first university degrees awarded, then China, which awards 24% of the global total, should celebrate its victory over the EU (17%), and the United States with its 10% share is a spent force. 5% of global R&D, respectively.
Handbook of Pharmaceutical Controlled Release Technology by Donald L. Wise