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020 _a9783319426099
024 7 _a10.1007/978-3-319-42609-9
_2doi
040 _aES-MaUEC
050 4 _aRM301.25
_bF676 2016 EB
245 1 0 _aFormulating Poorly Water Soluble Drugs
_cedited by Robert O. Williams III, Alan B. Watts, Dave A. Miller.
250 _a2nd ed. 2016.
260 _aCham, Switzerland
_bSpringer
_c2016
300 _a1 recurso en línea (XIV, 779 p.)
_b210 ilustraciones, 84 ilustraciones en color
336 _aTexto (visual)
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 1 _aAAPS Advances in the Pharmaceutical Sciences Series
_x2210-7371
_v22
505 0 _aRoute-Specific Challenges in Delivery of Poorly Water Soluble Drugs -- Optimizing the Formulation of Poorly Water Soluble Drugs -- Solid-State Techniques for Improving Solubility -- Mechanical Particle Size Reduction Techniques -- Solubilized Formulations -- Injectable Formulations of Poorly Water Soluble Drugs -- Design and Development of Self-Emulsifying Lipid Formulations for Improving Oral Bioavailability of Poorly Water-Soluble and Lipophilic Drugs -- Structured Development Approach for Amorphous Systems -- Melt Extrusion -- Spray Drying Technology -- Pharmaceutical Cryogenic Technologies -- Precipitation Technologies for Nanoparticle Production -- Emerging Technologies to Increase the Bioavailability of Poorly Water Soluble Drugs -- Regulatory Considerations for Development and Commercialization of Poorly Water Soluble Drugs.
520 _aThe objective of this volume is to consolidate within a single text the most current knowledge, practical methods, and regulatory considerations pertaining to formulations development with poorly water-soluble molecules. A pharmaceutical scientist�s approach toward solubility enhancement of a poorly water-soluble molecule typically includes detailed characterization of the compound�s physiochemical properties, solid-state modifications, advanced formulation design, non-conventional process technologies, advanced analytical characterization, and specialized product performance analysis techniques. The scientist must also be aware of the unique regulatory considerations pertaining to the non-conventional approaches often utilized for poorly water-soluble drugs. One faced with the challenge of developing a drug product from a poorly soluble compound must possess at minimum a working knowledge of each of the abovementioned facets and detailed knowledge of most. In light of the magnitude of the growing solubility problem to drug development, this is a significant burden especially when considering that knowledge in most of these areas is relatively new and continues to develop.
650 0 7 _aTecnología farmacéutica
_0http://id.loc.gov/authorities/subjects/sh85100590
_0LocalZ
_2embne
_9161127
650 0 7 _aFarmacia
_0LocalZ
_2embne
_9137891
650 7 _aMedicina
_0comprobar BNE19900959047
_2embne
_9405021
650 7 _aTecnología farmacéutica
_0comprobar BNE20030698632
_2embne
_9161127
650 0 7 _aCiencias biomédicas
_0LocalZ
_2embne
_9143729
700 1 _aWilliams III, Robert O.
_eeditor literario
_9101601
_0Local
700 1 _aWatts, Alan B.
_eeditor literario
_9101602
_0Local
700 1 _aMiller, Dave A.
_eeditor literario
_9101603
_0Local
830 0 _aAAPS Advances in the Pharmaceutical Sciences Series
_x2210-7371
_v22
_0http://id.loc.gov/authorities/names/n2011180825
_9133175
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-42609-9zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
901 _ai9783319426099
907 _a.b12981400
_b10-10-17
_c08-03-17
942 _2lcc
_cLE
945 _aRM301.25 F676 2016 EB
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