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55篇 您的检索式:作者名="DRESSMAN JB"
    题名 作者 年代 出处 被引量
1Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: comparison with commercial preparations 显示文摘Vogt M Kunath K Dressman JB 2008Eur J Pharm Biopharm2008,68,2:1
2New formulation approaches to improve solubility and drug release from fixed dose combinations: case examples pioglitazone/glimepiride and ezetimibe/simvastatin 显示文摘Taupitz T Dressman JB Klein S 2013Eur JPharm Biopharm2013,84,1:1
3Classification of orally ad- ministered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classifica- tion system显示文摘Lindenberg M Kopp S Dressman JB 2004Eur J Pharm Biopharm2004,58,:1
4Gastrointestinal parameters that influence oral medications显示文摘Dressman JB Bass P Ritschel WA 1993J Pharm Sci1993,82,9:1
5Comparison of canine and human gastrointestinal physiology显示文摘Dressman JB 1986Pharm Res1986,3,3:1
6Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations显示文摘Vogtm Kunath K Dressman JB 2008European Journal of Pharmaceutics and Biopharmaeeutics2008,68,2:1
7Comparison of canine and human gastrointestinal physiology显示文摘Dressman JB 1986Pharmacol Res1986,3,:1
8Cytochrome P450-mediated metabolism in the human gut wall 显示文摘Thelen K Dressman JB 2009J Pharm Pharmacol2009,61,5:1
9A comparative analysis of biopharmaceutics classification system and biopharmaceutics drug disposition classification system: A cross- sectional survey with 500 bioequivalence studies 显示文摘CRISTOFOLETTI R CHIANN C DRESSMAN JB 2013J Pharm Sci2013,102,9:1
10In vitro-in vivo correlations for lipophilic,poorly water-soluble drugs显示文摘Dressman JB Reppas C 2000Eur J Pharm Sci2000,11,:1
11Unusual solubility behavior of cyclosporin A in aqueous media显示文摘Ismailos G Reppas C Dressman JB 1991J Pharm Pharmacol1991,43,4:1
12Comparison of canine and human gastrointesti- nal physiology显示文摘DRESSMAN JB 1986Pharm Res1986,3,3:1
13Dissolution improvement of four poorly water soluble drugs by cogrinding with commonly used excipients 显示文摘Vogt M Kunath K Dressman JB 2008Eur J Pharm Biopharm2008,68,2:1
14Development and validation of a physiology-based model for the prediction of oral absorption in monkeys 显示文摘Willmann S Edginton AN Dressman JB 2007Pharm Res2007,24,7:1
15Influence of physicochemical properties on dissolution of drugs in the gastrointesti- nal tract显示文摘Horter D Dressman JB 2001Adv Drug Deliv Rev2001,46,13:1
16Classilication of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics clas- sification system 显示文摘LINDENBERG M KOPP S DRESSMAN JB 2004Eur J Pharm Biopharm2004,58,2:1
17Comparison ofWHO and US FDA biowaiver dissolution test conditions using bio-equivalent doxycycline hyclate drug products 显示文摘STRAUCH S JANTRATID E DRESSMAN JB 2009J Pharm Phar-macol2009,61,3:1
18Dissolution improvement of four poorly water soluble drugs by cogrinding with commonly used excipients 显示文摘Vogt M Kunath K Dressman JB 2008Eur J Pharm Biopharm2008,68,2:1
19Drug release character- istics of different mesalazine products using USP apparatus 3 to simulate passage through the GI tract显示文摘Klein S Rudolph MW Dressman JB 2002Dissolution Technolo- gies2002,9,9:1
20Classification of orally administered drugs on the World Health Organization model llst of essential medicines according to the biopharmaceutics clas- sification system 显示文摘LINDENBERG M KOPP S DRESSMAN JB 2004Eur J Pharm Biopharm2004,58,2:1
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