Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1992-4-13
|
pubmed:abstractText |
[3H]Navelbine (NVB) was administered orally to two patients. Drug levels in biological fluids were monitored by radioimmunoassay (RIA) and direct radioactivity (RA) determinations. NVB absorption was rapid: maximum plasma concentrations appeared in the first 2 h after oral administrations. Pharmacokinetic parameters estimated from RIA data were in complete accordance with those obtained from i.v. injections. Bioavailability (i.v./po) estimated from RIA and RA data averaged 40.6 and 93.0%, respectively. NVB urine excretion was low. Fecal excretion remained its main elimination route. Moreover, large differences were observed in area under NVB plasma concentration-time curve (AUC) values obtained by the two methods, implying intense drug bio-transformations.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0959-4973
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
2
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
405-10
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1797198-Administration, Oral,
pubmed-meshheading:1797198-Aged,
pubmed-meshheading:1797198-Antineoplastic Agents,
pubmed-meshheading:1797198-Biological Availability,
pubmed-meshheading:1797198-Chromatography, High Pressure Liquid,
pubmed-meshheading:1797198-Feces,
pubmed-meshheading:1797198-Humans,
pubmed-meshheading:1797198-Intestinal Absorption,
pubmed-meshheading:1797198-Middle Aged,
pubmed-meshheading:1797198-Radioimmunoassay,
pubmed-meshheading:1797198-Tissue Distribution,
pubmed-meshheading:1797198-Vinblastine
|
pubmed:year |
1991
|
pubmed:articleTitle |
Oral administration of [3H]navelbine in patients: comparative pharmacokinetics using radioactive and radioimmunologic determination methods.
|
pubmed:affiliation |
Laboratoire de Pharmacocinétique et Toxicocinétique, INSERM U 278, Marseille, France.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|