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PMID: 856462 Published · ppublish English Journal Article

Plasma pharmacokinetics of adriamycin and its metabolites in humans with normal hepatic and renal function.

Cancer research ·Vol. 37 ·No. 5 ·1977-05-00 ·Pages 1416-20

Benjamin RS, Riggs CE, Bachur NR

Abstract

A new, nondestructive, plasma extraction technique ultilizing chloroform:isopropyl alcohol (1:1) and ammonium sulfate saturation has been devised to isolate adriamycin and its metabolites from human plasma. Adriamycin was the most prominent species in plasma. It disappeared according to a triphasic pattern with a mean half-life of 30 hr. Six metabolites have been clearly separated from adriamycin by thin-layer chromatography. Three were aglycones and three were polar metabolites, one of which has been identified as adriamycinol. All metabolites appeared rapidly in plasma and disappeared according to a biphasic or tri-phasic pattern. The polar metabolites in plasma were found in similar relative concentration to those in urine. In contrast to the small Quantities of aglycones in urine, however, significant concentrations of aglycones were found in plasma. The least prominent metabolite was adriamycin aglycone; the most prominent metabolite was a less polar aglycone, most likely deoxyadriamycin aglycone, and a more polar aglycone, presumably demethyl deoxyadriamycinol aglycone, was the only metabolite to show variable pharmacokinetics in different patients. The nondestructive plasma extraction technique has verified the presence of extensive human metabolism of adriamycin and demonstrated the presence of aglycone and polar metabolites.

MeSH Terms
Doxorubicin/blood,metabolism,therapeutic use Half-Life Humans Kidney/metabolism Liver/metabolism Neoplasms/drug therapy
Chemicals
Doxorubicin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Benjamin R S
Riggs C E
Bachur N R
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1977-05-00
Pages
1416-20
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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