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dc.contributor.author최한곤-
dc.date.accessioned2019-05-23T00:31:05Z-
dc.date.available2019-05-23T00:31:05Z-
dc.date.issued2018-09-
dc.identifier.citationPHARMAZIE, v. 73, No. 9, Page. 498-502en_US
dc.identifier.issn0031-7144-
dc.identifier.urihttps://www.ingentaconnect.com/contentone/govi/pharmaz/2018/00000073/00000009/art00003-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/105712-
dc.description.abstractTo develop a novel celecoxib (CXB)-loaded drug delivery system, numerous nanosuspensions were prepared with various polymers and surfactants using a wet media milling process, and their particle sizes were subsequently determined. A 24 full factorial design was used to identify the most appropriate preparation conditions. Pharmacokinetics of the selected nanosuspension were performed in rats and compared with those of a drug powder and a commercial CXB-loaded product. Among the carriers investigated, copovidone and sodium lauryl sulphate gave the smallest particle size of the drug in the nanosuspension. In particular, the nanosuspension prepared with 5% CXB, 4% copovidone, and 0.1% sodium lauryl sulphate, under the appropriate conditions, showed a particle size of approximately 190 nm, which was physically stable for at least 8 weeks. This nano-suspension provided a significantly higher plasma concentration and AUC in rats as compared with the drug powder and the commercial product. Thus, this novel CXB-loaded nanosuspension is a promising candidate with excellent stability and enhanced oral bioavailability. © 2018 Govi-Verlag Pharmazeutischer Verlag GmbH. All rights reserved.en_US
dc.description.sponsorshipAcknowledgements: This work was supported by the National Research Foundation (NRF) of South Korea grants funded by the South Korean government (MEST) (No. 2018R1A2B2004668) and a grant (16173MFDS542) from the Ministry of Food and Drug Safety in 2016.en_US
dc.language.isoen_USen_US
dc.publisherGOVI-VERLAG PHARMAZEUTISCHER VERLAG GMBHen_US
dc.titleDevelopment of a novel celecoxib-loaded nanosuspension using a wet media milling processen_US
dc.typeArticleen_US
dc.relation.volume73-
dc.identifier.doi10.1691/ph.2018.8035-
dc.relation.page498-502-
dc.relation.journalPHARMAZIE-
dc.contributor.googleauthorJeong, Sung Chan-
dc.contributor.googleauthorKim, Dong Shik-
dc.contributor.googleauthorJin, Sung Giu-
dc.contributor.googleauthorYoun, Yu Seok-
dc.contributor.googleauthorOh, Kyung Taek-
dc.contributor.googleauthorLi, Dong Xun-
dc.contributor.googleauthorYong, Chul Soon-
dc.contributor.googleauthorKim, Jong Oh-
dc.contributor.googleauthorKim, Kyeong Soo-
dc.contributor.googleauthorChoi, Han-Gon-
dc.relation.code2018002917-
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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