pubmed-article:7674700 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0001554 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0031327 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0022635 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0178602 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0039225 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0005508 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0205345 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0037633 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C1382100 | lld:lifeskim |
pubmed-article:7674700 | lifeskim:mentions | umls-concept:C0205171 | lld:lifeskim |
pubmed-article:7674700 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:7674700 | pubmed:dateCreated | 1995-10-19 | lld:pubmed |
pubmed-article:7674700 | pubmed:abstractText | The relative bioavailability of ketoprofen from a liquid formulation as compared to a tablet formulation as reference after single oral dose administration was investigated in 16 healthy male subjects. The subjects received in a randomized, crossover design during one study period of 5 days 2.5 mg of ketoprofen as tablet or liquid formulation administered as single dose with a washout interval of 48 h. The plasma concentrations of S(+)- and R(-)-ketoprofen were determined before and up to 24 h post-administration. S(+)- and R(-)-ketoprofen in the collected plasma samples was determined using an internally standardized validated HPLC method. Regarding the geometric mean concentration-time courses there were no relevant differences between the two ketoprofen enantiomers for both formulations. Remarkable differences in the shape of concentration-time courses between the two formulations were found with higher Cmax (by about 70%) and earlier tmax (by 15 min) values for the ketoprofen solution. The treatments were widely equivalent with regard to AUC. The quotients of geometric means as well as 90% confidence intervals for AUC of R(-)-ketoprofen were 95.72% (92.55-99.00%) and for S(+)-ketoprofen 94.23% (89.91-98.76%). The administration of the ketoprofen solution resulted earlier in higher concentrations (by about 70%) for both enantiomers, whereas the extent of absorption expressed by AUC was nearly the same (about 95%) as compared to the equimolar tablet formulation. The differences between the two formulations for Cmax,norm and tmax were statistically significant. | lld:pubmed |
pubmed-article:7674700 | pubmed:language | eng | lld:pubmed |
pubmed-article:7674700 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7674700 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7674700 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7674700 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7674700 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7674700 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7674700 | pubmed:month | Mar | lld:pubmed |
pubmed-article:7674700 | pubmed:issn | 0379-0355 | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:LangeRR | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:LückerP WPW | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:JossUU | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:StieglerSS | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:Wetzelsberger... | lld:pubmed |
pubmed-article:7674700 | pubmed:author | pubmed-author:BirkesDD | lld:pubmed |
pubmed-article:7674700 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7674700 | pubmed:volume | 17 | lld:pubmed |
pubmed-article:7674700 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7674700 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7674700 | pubmed:pagination | 129-34 | lld:pubmed |
pubmed-article:7674700 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:7674700 | pubmed:meshHeading | pubmed-meshheading:7674700-... | lld:pubmed |
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pubmed-article:7674700 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:7674700 | pubmed:articleTitle | Pharmacokinetics and relative bioavailability after single dose administration of 25 mg ketoprofen solution as compared to tablets. | lld:pubmed |
pubmed-article:7674700 | pubmed:affiliation | Institut für klinische Pharmakologie Bobenheim, Prof. Dr. Lücker GmbH, Grünstadt, Germany. | lld:pubmed |
pubmed-article:7674700 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7674700 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:7674700 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:7674700 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |