Effect of induced hypoalbuminemia on distribution, total clearance and unbound clearance of Piroxicam in vivo in the rat

The influence of decreased albumin concentration on the pharmacokinetic behaviour of Piroxicam was studied in vivo in rats that had undergone plasmapheresis. Reductions of approximately 25% and 50% in the plasma albumin concentration were achieved, the former in rats not given plasma expander, the l...

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Veröffentlicht in:European journal of drug metabolism and pharmacokinetics 1993-04, Vol.18 (2), p.165-171
Hauptverfasser: TROCONIZ, J. I. F, LOPEZ-BUSTAMANTE, L. G, FOS, D
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container_end_page 171
container_issue 2
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container_title European journal of drug metabolism and pharmacokinetics
container_volume 18
creator TROCONIZ, J. I. F
LOPEZ-BUSTAMANTE, L. G
FOS, D
description The influence of decreased albumin concentration on the pharmacokinetic behaviour of Piroxicam was studied in vivo in rats that had undergone plasmapheresis. Reductions of approximately 25% and 50% in the plasma albumin concentration were achieved, the former in rats not given plasma expander, the latter in animals given Ficol-70 as a plasma expander. The unbound fraction of Piroxicam in plasma and the apparent volume of distribution at steady state experienced a statistically significant increase where the albumin concentration was reduced. The average total plasma clearance rose with the increase in fu, between the control (6.3 +/- 2.4 ml/h) and plasmapheretic groups (11.1 +/- 4 ml/h), in accordance with predictions of the 'well-stirred' and 'parallel-tube' models, but no statistically significant differences were found between the two groups, perhaps because of the great interindividual variability associated with this parameter. The total plasma clearance value of the Ficol group (5.4 +/- 2.2 ml/h) was close to that of the control group, despite the high increase in the unbound fraction in plasma. Alterations in the uptake process in the liver due to the high level of induced hypoalbuminemia may have occurred.
doi_str_mv 10.1007/BF03188792
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The average total plasma clearance rose with the increase in fu, between the control (6.3 +/- 2.4 ml/h) and plasmapheretic groups (11.1 +/- 4 ml/h), in accordance with predictions of the 'well-stirred' and 'parallel-tube' models, but no statistically significant differences were found between the two groups, perhaps because of the great interindividual variability associated with this parameter. The total plasma clearance value of the Ficol group (5.4 +/- 2.2 ml/h) was close to that of the control group, despite the high increase in the unbound fraction in plasma. 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Antiinflammatory agents</subject><subject>Hematocrit</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pharmacology. 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Antiinflammatory agents</topic><topic>Hematocrit</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Piroxicam - blood</topic><topic>Piroxicam - pharmacokinetics</topic><topic>Plasmapheresis</topic><topic>Protein Binding</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Serum Albumin - metabolism</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TROCONIZ, J. I. F</creatorcontrib><creatorcontrib>LOPEZ-BUSTAMANTE, L. 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Alterations in the uptake process in the liver due to the high level of induced hypoalbuminemia may have occurred.</abstract><cop>Genève</cop><pub>Médecine et hygiène</pub><pmid>8243500</pmid><doi>10.1007/BF03188792</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Animals
Biological and medical sciences
Blood Proteins - metabolism
Bones, joints and connective tissue. Antiinflammatory agents
Hematocrit
Male
Medical sciences
Pharmacology. Drug treatments
Piroxicam - blood
Piroxicam - pharmacokinetics
Plasmapheresis
Protein Binding
Rats
Rats, Wistar
Serum Albumin - metabolism
Tissue Distribution
title Effect of induced hypoalbuminemia on distribution, total clearance and unbound clearance of Piroxicam in vivo in the rat
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