dc.creatorLima, Ádley A. N.
dc.creatorSobrinho, José L.S.
dc.creatorCorrêa Jr, Roberto A.C.
dc.creatorRolim Neto, Pedró José
dc.date2009-06-16T03:00:00Z
dc.date2008
dc.date.accessioned2017-03-08T20:12:11Z
dc.date.available2017-03-08T20:12:11Z
dc.identifierhttp://hdl.handle.net/10915/7693
dc.identifierhttp://www.latamjpharm.org/trabajos/27/5/LAJOP_27_5_4_2_7QVYB4J43B.pdf
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/7693
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/429760
dc.descriptionThe solubility behaviour of drugs remains one of the most challenging aspects in formulation development. Solid dispersions (SD) and inclusion complexes (IC) are two of the most promising strategies to improve the oral bioavailability of poorly water soluble drugs. By reducing drug particle size to the absolute minimum, and hence improving drug wettability, bioavailability may be significantly improved. The basis for this popularity from a pharmaceutical standpoint, is the ability of these materials to interact with poorly water-soluble drugs and drug candidates resulting in an increase in their apparent water solubility. This review is intended to give a general background to the use of cyclodextrins (CD) and solid dispersions as alternative technologies in the study of drug solubilization.
dc.languageen
dc.relationLatin American Journal of Pharmacy
dc.relationvol. 27, no. 5
dc.subjectcyclodextrins; inclusion complexes; polymers; solid dispersion; solubility
dc.subjectFarmacia
dc.subjectFarmacología
dc.subjectEvaluación de medicamentos
dc.subjectSolubilidad
dc.titleAlternative technologies to improve solubility of poorly water soluble drugs
dc.typeArtículos de revistas
dc.typeRevision


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