Literature DB >> 1139436

Extrahpetic distribution of sulfobromophthalein.

C D Klaassen.   

Abstract

Plasma clearance of sulfobromophthalein (BSP) is widely used as a measure of hepatic function. Its validity depends upon its exclusive elimination from the body via bile. For example, in the present study, when BSP was administered intravenously (i.v.) to rats at four different doses (18.75, 37.5, 75, and 150 mg/kg), less than 0.5% of each dose was excreted into the urine and between 70 and 85% was excreted into the bile within 6 h after administration. It has been assumed that the distribution of BSP is limited to the blood and liver witith very little appearing in other tissues. When we measured the amount of BSP in the plasma, liver, and the bile 10 min after the i.v. administration of either a high (150 mg/kg) or a low (18.75 mg/kg) dose of BSP, only 60% of the dose was accounted for. The concentration of BSP and 12-I-labelled albumin (RISA) was measured in various tissue samples 10 min after administration of 17.5 or 150 mg of BSP or RISA per kilogram. More BSP was found in all tissues than was contained in the plasma entrapped therein. Thus, the distribution of BSP is not limited to the liver and plasma. During excretion BSP leaves other tissue (kidney, spleen, lung, etc.) and is ultimately excreted into the bile.

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Year:  1975        PMID: 1139436     DOI: 10.1139/y75-016

Source DB:  PubMed          Journal:  Can J Physiol Pharmacol        ISSN: 0008-4212            Impact factor:   2.273


  5 in total

1.  Pharmacokinetics, hepatic biotransformation and biliary and urinary excretion of bromosulfophthalein (BSP) in an experimental liver disease mimicking biliary cirrhosis.

Authors:  A Esteller; M D Torres; M Gomez-Bautista; E L Mariño; C Fernandez-Lastra; R Jimenez
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1990 Jan-Mar       Impact factor: 2.441

2.  Biliary excretion of sulfobromophthalein in isolated perfused livers from normal and spironolactone-treated rats.

Authors:  J M Pellegrino; A D Mottino; J V Rodriguez; E A Rodriguez Garay
Journal:  Experientia       Date:  1982-01-15

3.  Pharmacokinetics of the hepatic transport of organic anions: influence of extra- and intracellular binding on hepatic storage of dibromosulfophthalein and interactions with indocyanine green.

Authors:  D K Meijer; A Blom; J G Weitering; R Hornsveld
Journal:  J Pharmacokinet Biopharm       Date:  1984-02

4.  Drug elimination interactions: analysis using a mathematical model.

Authors:  R H Luecke; W D Wosilait
Journal:  J Pharmacokinet Biopharm       Date:  1979-12

5.  Pharmacokinetic aspects of sulfobromophthalein transport after diethyl maleate pretreatment in rats.

Authors:  J González; M J Aza; E Mariño; A Esteller
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1987 Jan-Mar       Impact factor: 2.441

  5 in total

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