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dc.contributor.author Hetenyi, G
dc.contributor.author Griesser, J
dc.contributor.author Fontana, S
dc.contributor.author Gutierrez, AM
dc.contributor.author Ellemunter, H
dc.contributor.author Niedermayr, K
dc.contributor.author Szabó, Péter
dc.contributor.author Bernkop-Schnurch, A
dc.date.accessioned 2019-10-02T19:33:25Z
dc.date.available 2019-10-02T19:33:25Z
dc.date.issued 2018
dc.identifier.citation journalVolume=13;journalIssueNumber=7;journalTitle=NANOMEDICINE;pagerange=717-732;journalAbbreviatedTitle=NANOMEDICINE-UK;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/7760
dc.identifier.uri doi:10.2217/nnm-2017-0307
dc.description.abstract AIM: The aim of the study was to develop self-emulsifying delivery systems (SEDDS) exhibiting improved permeation rate for pulmonary delivery of amikacin for treatment of cystic fibrosis (CF) patients. MATERIALS & METHODS: Solubility of amikacin in lipids was improved by hydrophobic ion pairing with sodium myristyl sulfate. The complex was loaded into SEDDS. Drug-release studies were performed and the permeation properties of SEDDS through human CF mucus were examined. RESULTS: A total of 10% complex could be loaded into SEDDS. SEDDS exhibited sustained release. Up to twofold more amounts of amikacin permeated through the CF mucus compared with reference. CONCLUSION: The developed SEDDS with amikacin may be a promising tool for the treatment of certain bacterial infections of CF patients.
dc.format.extent 717-732
dc.title Amikacin containing self-emulsifying delivery systems via pulmonary administration for treatment of bacterial infections of cystic fibrosis patients.
dc.type Journal Article
dc.date.updated 2019-09-15T14:56:01Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 3352190
dc.identifier.wos 000432823900005
dc.identifier.pubmed 29488425
dc.contributor.department SE/GYTK/Egyetemi Gyógyszertár Gyógyszerügyi Szervezési Intézet
dc.contributor.institution Semmelweis Egyetem


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