Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fried Faassen"'
Autor:
Ashley R. Johnson, Jeanine E. Ballard, Andrew Leithead, Corin Miller, Fried Faassen, Xiaowei Zang, Rebecca Nofsinger, Angela M. Wagner
Publikováno v:
Pharmaceutical Research.
Publikováno v:
Journal of pharmaceutical sciences.
Amorphous solid dispersions (ASDs) have been widely utilized to enhance the bioavailability of pharmaceutical drugs with poor aqueous solubility. The role of various excipients on the amorphous drug to crystalline form conversion in ASDs has been wid
Publikováno v:
Part.Part.Syst.Charact., 22(2), 133-140. WILEY-V C H VERLAG GMBH
The particle size distribution of pharmaceutically active materials and other fine chemicals determines the performance of the final product to a large extent. Often milling of these particles is necessary. It is not possible to determine the milling
Publikováno v:
Pharmaceutical Research. 20:177-186
Purpose. The purpose of this work was to study the relevant physicochemical properties for the absorption of steroids. Methods. Various physicochemical properties of steroids were calculated (molecular weight, ClogP, static polar surface area [PSA],
Autor:
Glenn A. Edwards, Christopher J.H. Porter, Karen L. White, W A (Fried) Faassen, William N. Charman, Gary Nguyen
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 331(2)
The contribution of lymphatic transport to the oral bioavailability of methylnortestosterone (M) after oral administration of the lipophilic prodrug methylnortestosterone undecanoate (MU) has been evaluated, and the sensitivity of lymphatic MU transp
Publikováno v:
Current drug delivery. 6(4)
Org 45697 (MW 600.7, clogP 7.92, soybean oil solubility 50 mg/g) and Org 46035 (MW 601.6, clog P 8.46, soybean oil solubility 40 mg/g) are two poorly water soluble (0.1 microg/ml), highly lipophilic drug candidates with immunomodulator activity and h
Publikováno v:
Part.Part.Syst.Charact., 22, 261-267. WILEY-V C H VERLAG GMBH
Particle & Particle Systems Characterization, 22(4), 261-267. WILEY-V C H VERLAG GMBH
Particle & Particle Systems Characterization, 22(4), 261-267. WILEY-V C H VERLAG GMBH
The particle size distribution of fine chemicals in the solid state, like active pharmaceutical ingredients, is often a critical parameter. To achieve the desired particle size distribution, milling of such materials is usually the method of choice.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bdf40fc3c088007967f2be3d0fd74b
https://research.rug.nl/en/publications/36c92696-7162-4cc1-a245-294ad28cd16e
https://research.rug.nl/en/publications/36c92696-7162-4cc1-a245-294ad28cd16e
Autor:
Fried Faassen, Herman Vromans
Publikováno v:
Clinical pharmacokinetics. 43(15)
Bioequivalence of drug formulations plays an important role in drug development. Recently, the Biopharmaceutical Classification System (BCS) has been implemented for the purpose of waiving bioequivalence studies on the basis of the solubility and gas
Publikováno v:
International journal of pharmaceutics. 278(1)
Milling of agglomerates is one of the common unit operations during preparation of oral dosage forms like capsules and tablets. In literature the breakage of granules is mostly determined after single impact at an ideally formed granule or of single
Publikováno v:
International journal of pharmaceutics. 263(1-2)
In this study the gastrointestinal absorption and P-glycoprotein (Pgp) efflux transport of heterocyclic drugs was investigated with the Caco-2 cell model. Based on the calculation of the physico-chemical properties a good oral absorption was predicte