000 01418 a2200421 4500
005 20250516005307.0
264 0 _c20110411
008 201104s 0 0 eng d
022 _a1573-9686
024 7 _a10.1007/s10439-010-0169-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGamsiz, Ece Dilber
245 0 0 _aDrug salts and solubilization: modeling the influence of cyclodextrins on oral absorption.
_h[electronic resource]
260 _bAnnals of biomedical engineering
_cJan 2011
300 _a455-68 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAbsorption
650 0 4 _aAdministration, Oral
650 0 4 _aAnimals
650 0 4 _aBiological Availability
650 0 4 _aComputer Simulation
650 0 4 _aCyclodextrins
_xadministration & dosage
650 0 4 _aDiffusion
650 0 4 _aDrug Carriers
_xchemistry
650 0 4 _aDrug Compounding
_xmethods
650 0 4 _aHumans
650 0 4 _aIntestinal Absorption
_xphysiology
650 0 4 _aIntestines
_xchemistry
650 0 4 _aModels, Biological
650 0 4 _aModels, Chemical
650 0 4 _aSalts
_xchemistry
650 0 4 _aSolubility
700 1 _aThombre, Avinash G
700 1 _aAhmed, Imran
700 1 _aCarrier, Rebecca Lyn
773 0 _tAnnals of biomedical engineering
_gvol. 39
_gno. 1
_gp. 455-68
856 4 0 _uhttps://doi.org/10.1007/s10439-010-0169-1
_zAvailable from publisher's website
999 _c20262858
_d20262858