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dc.contributor.author최한곤-
dc.date.accessioned2018-12-17T07:34:48Z-
dc.date.available2018-12-17T07:34:48Z-
dc.date.issued2018-01-
dc.identifier.citationCOLLOIDS AND SURFACES B-BIOINTERFACES, v. 162, Page. 420-426en_US
dc.identifier.issn0927-7765-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0927776517308573-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/80904-
dc.description.abstractThe aim of this research was to compare three strategies for enhancing the solubility of poorly water-soluble revaprazan hydrochloride: solid dispersion, solid SNEDDS and inclusion compound. The influence of polymers, surfactants and oils on the drug solubility was assessed, and via the chosen carriers, the three types of formulations were prepared utilising spray drying technique. Their physicochemical properties, solubility, dissolution and pharmacokinetics in rats were performed compared with revaprazan powder. Among the liquid SNEDDS formulations assessed, the compositions of revaprazan, peceol, Tweed 80 and Labrasol (10:15:55:30, weight ratio) provided the smallest emulsion size. Moreover, this liquid SNEDDS and dextran were suspended/dissolved in distilled water, and spray-dried, producing an optimal revaprazan-loaded solid SNEDDS. The appropriate solid dispersion and inclusion compound were composed of revaprazan, hydroxypropylmethylcellulose and cremophor A25 (5:1.4:5.6) and drug and hydroxyl-beta-cyclodextrin (2.5:8.77), respectively. The crystalline drug was converted to an amorphous state in all formulations. In the solid dispersion, the drug was attached to the hydrophilic carrier. The solid SNEDDS and inclusion compound contained aggregate microspheres and separate microspheres, respectively. All formulations significantly increased the drug solubility, dissolution, plasma concentration and AUC compared with revaprazan powder. These properties were ranked in the order solid dispersion >= solid SNEDDS > inclusion compound. Particularly, the solid dispersion improved about 9500 fold drug solubility and 10-fold oral bioavailability. Thus, the improved properties were considerably dependent upon these techniques, although all of the techniques employed similar mechanisms. Among the strategies checked, the solid dispersion system would be recommended as an oral revaprazan-loaded pharmaceutical product. (C) 2017 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis work was supported by National Research Foundation (NRF) of South Korea, grants funded by the South Korea government (MEST) (No. 2015R1A2A2A05027872), and a grant (16173MFDS542) from the Ministry of Food and Drug Safety in 2016.en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.subjectRevaprazan hydrochlorideen_US
dc.subjectSolid dispersionen_US
dc.subjectSolid SNEDDSen_US
dc.subjectinclusion compounden_US
dc.subjectSolubilityen_US
dc.subjectCrystallinityen_US
dc.subjectBioavailabilityen_US
dc.titleComparison of a revaprazan-loaded solid dispersion, solid SNEDDS and inclusion compound: Physicochemical characterisation and pharmacokineticsen_US
dc.typeArticleen_US
dc.relation.volume162-
dc.identifier.doi10.1016/j.colsurfb.2017.12.017-
dc.relation.page420-426-
dc.relation.journalCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.contributor.googleauthorPark, Jong Hyuck-
dc.contributor.googleauthorPark, Jong Hyuck-
dc.contributor.googleauthorMustapha, Omer-
dc.contributor.googleauthorYousaf, Abid Mehmood-
dc.contributor.googleauthorKim, Jung Suk-
dc.contributor.googleauthorKim, Dong Wuk-
dc.contributor.googleauthorYong, Chul Soon-
dc.contributor.googleauthorYoun, Yu Seok-
dc.contributor.googleauthorOh, Kyung Taek-
dc.contributor.googleauthorChoi, Han-Gon-
dc.contributor.googleauthorLim, Soo-Jeong-
dc.contributor.googleauthorKim, Jong Oh-
dc.relation.code2018001466-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidhangon-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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