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29篇 您的检索式:作者名="Reppas C"
    题名 作者 年代 出处 被引量
1Dissolutiontesting as a prognostic tool for oral drug absorption:Immediate release dosage forms显示文摘DRESSMAN J B AMIDON G L REPPAS C 1998Pharm Res1998,15,1:1
2Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms 显示文摘Dressman J B Amidon G L Reppas C 1998Pharm Res1998,15,1:1
3In vitro versus canine data for predicting input profiles of isosorbide-5-mononitrate from oral extended release products on a confidence interval basis显示文摘FOTAKI N SYMILLIDES M REPPAS C 2005Eur J Pharm Sci2005,24,1:1
4Determination of intralumenal individual bile acids by HPLC with charged aerosol detection显示文摘Vertzoni M Archontaki H Reppas C 2008J Lipid Res2008,49,12:1
5Enhancement of cyclosporine A solubility by d-α-tocopheryl-polyethy-lene-glycol- 1000 succinate (TPGS) 显示文摘Ismailos G Reppas C Macheras P 1994Eur J Pharm Sci1994,,1:1
6In vitro-in vivo correlations for lipophilic,poorly water-soluble drugs显示文摘Dressman JB Reppas C 2000Eur J Pharm Sci2000,11,:1
7Unusual solubility behavior of cyclosporin A in aqueous media显示文摘Ismailos G Reppas C Dressman JB 1991J Pharm Pharmacol1991,43,4:1
8Dissolution media simuXafing conditions in the proximal human gastrointesti- nal tract: an update显示文摘JANTRATID E JANSSEN N REPPAS C 2008Pharm Res2008,25,7:1
9Solubilization andquantification of lycopene in aqueous media in the form of cyclodextrinbinary systems显示文摘VERTZONI M KARTEZINI T REPPAS C 2006International Journal of Pharmaceutics2006,309,12:1
10Dissolution testing as a prognostic tool for oral drug absorption:immediaterelease dosage form显示文摘DRESSMAN J B AMIDON G L REPPAS C 1998Pharmaceut Res1998,15,1:1
11New media discriminate dissolution properties of poorly soluble drugs显示文摘Galia E Nieolaides E Reppas C 1996Pharm Res1996,13,:1
12Tuning the average path length of complex networks and its influence to the emergent dynamics of the majority-rule model显示文摘Reppas A I Spiliotis K Siettos C I 2015Mathematics and Com- puters in Simulation2015,109,3:1
13Dissolution testing as a prognostic tool for oral drug absorption:Immediate release dosage forms显示文摘Dressman JB Amidon GL Reppas C 1998Pharm Res1998,15,1:1
14In vitro versus canine data for predicting input profiles of isosorbide- 5-mononitrate from oral extended release products on a confidence interval basis显示文摘Fotaki N Symillides M Reppas C 2005Eur J Pharm Sci2005,24,1:1
15Solubilization and quantification of lycopene in aqueous media in the form of cyclodextrin binary systems显示文摘Vertzoni M Kartezini T Reppas C 2006International Journal of Pharmaeeuties2006,309,1:1
16Paired-Spike interactions And Synaptic Efficacy Of Retinal Inputs To The Thalamus显示文摘 Reppas J B Reid R C 1998Nature1998,395,:1
17Enhancement of cyclosporine A solubility by d-α-tocopheryl-polyethylene-glycol- 1000 succinate(TPGS) 显示文摘ISMAILOS G REPPAS C MACHERAS P 1994Eur J Pharm Scl1994,1,5:1
18Optimized deterruination of lycopene in canine plasma using reversed-phase high-perfor- mance liquid chromatography显示文摘VERTZONI M V REPPAS C ARCHONTAKI H A 2005J Chromatogr B2005,819,1:1
19Dissolution testing as a prognostic tool for oral drug absorption: Immediate release dosage forms显示文摘DRESSMAN J B AMIDON G L REPPAS C 1998Pharm Res1998,15,1:1
20Dissolution testing as a prognostic tool for oral drug absorption:immediate release dosage form 显示文摘DRESSMAN JB AMIDON GL REPPAS C 1998Pharm Res1998,15,1:1
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