Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation.
about
Relative bioavailability of a new oral form of cyclosporin A in patients with rheumatoid arthritis.Lipid-based formulations for oral administration: opportunities for bioavailability enhancement and lipoprotein targeting of lipophilic drugs.Clinical studies with oral lipid based formulations of poorly soluble compoundsTherapeutic drug monitoring of cyclosporine and area under the curve prediction using a single time point strategy: appraisal using peak concentration data.Generic cyclosporine formulations: more open questions than answers.The use of ciclosporin in psoriasis.Lipids and lipid-based formulations: optimizing the oral delivery of lipophilic drugs.Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption.Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.Self-nano-emulsifying drug delivery systems: an update of the biopharmaceutical aspects.Clinical determinants of calcineurin inhibitor disposition: a mechanistic review.Quantitative Analyses of Hepatic OATP-Mediated Interactions Between Statins and Inhibitors Using PBPK Modeling With a Parameter Optimization Method.A comparative evaluation of mono-, di- and triglyceride of medium chain fatty acids by lipid/surfactant/water phase diagram, solubility determination and dispersion testing for application in pharmaceutical dosage form development.Effect of food on everolimus absorption: quantification in healthy subjects and a confirmatory screening in patients with renal transplants.Supersaturated self-nanoemulsifying drug delivery systems (Super-SNEDDS) enhance the bioavailability of the poorly water-soluble drug simvastatin in dogs.Optimization of self nanoemulsifying drug delivery system for poorly water-soluble drug using response surface methodology.Improved oral bioavailability of BCS class 2 compounds by self nano-emulsifying drug delivery systems (SNEDDS): the underlying mechanisms for amiodarone and talinolol.Nanomemulsion of megestrol acetate for improved oral bioavailability and reduced food effect.Age effect on whole blood cyclosporine concentrations following oral administration in children with nephrotic syndrome.Optimizing the absorption of valspodar, a P-glycoprotein modulator, Part I: Selecting an oral formulation and exploring its clinical pharmacokinetics/dynamics.Comparison of the steady state pharmacokinetics of two formulations of cyclosporin in patients with atopic dermatitis.Development of Self-Emulsifying Drug Delivery Systems (SEDDS) for Oral Bioavailability Enhancement of Poorly Soluble Drugs
P2860
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P2860
Influence of a fat-rich meal on the pharmacokinetics of a new oral formulation of cyclosporine in a crossover comparison with the market formulation.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh-hant
name
Influence of a fat-rich meal o ...... n with the market formulation.
@en
Influence of a fat-rich meal o ...... n with the market formulation.
@nl
type
label
Influence of a fat-rich meal o ...... n with the market formulation.
@en
Influence of a fat-rich meal o ...... n with the market formulation.
@nl
prefLabel
Influence of a fat-rich meal o ...... n with the market formulation.
@en
Influence of a fat-rich meal o ...... n with the market formulation.
@nl
P2093
P356
P1476
Influence of a fat-rich meal o ...... n with the market formulation.
@en
P2093
P304
P356
10.1023/A:1018922517162
P577
1994-01-01T00:00:00Z