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dc.contributor.authorEdited by Waterbeemd, Han van de
dc.contributor.authorTesta, Bernard
dc.date.accessioned2019-12-04T06:48:48Z
dc.date.available2019-12-04T06:48:48Z
dc.date.issued2009
dc.identifier.citationEdited by Waterbeemd, Han van de and Testa, Bernard (2009). Drug bioavailability: estimation of solubility, permeability, absorption and bioavailability. Second, completely revised ed. Weinheim : WILEY-VCH Verlag GmbH.en_US
dc.identifier.isbn9783527320516
dc.identifier.urihttp://hdl.handle.net/123456789/1339
dc.description.abstractIn order to reach its intended site of action, the drug molecules in every pill that we swallow must first be absorbed, transported via the bloodstream and evade various mechanisms that eliminate drugs from the body. Those drug properties that determine, for example, its stability in the gut or its ease of uptake into the bloodstream, are therefore of central importance in drug development. In fact, many potentially useful drugs fail because of insufficient availability at the biological target site. This second edition of the gold standard for industrial research is thoroughly revised in line with current trends in the field, with all contributions extensively updated or rewritten. No other publication offers the same level of treatment on this crucial topic.en_US
dc.language.isoenen_US
dc.publisherWILEY-VCH Verlag GmbHen_US
dc.subjectDrug bioavailabilityen_US
dc.titleDrug bioavailability: estimation of solubility, permeability, absorption and bioavailabilityen_US
dc.typeBooken_US


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