THE RELATIONSHIP OF THE HUMAN PLASMA PROTEINS IN THE ACTION AND TRANSPORT OF PENICILLIN
1. A series of studies was carried out on the plasma obtained from normal human subjects after the administration of penicillin. 2. Bio-assays for penicillin were performed before and after the fractionation of the plasma into its component protein fractions. 3. It was observed that penicillin could...
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Published in | The Journal of pharmacology and experimental therapeutics Vol. 103; no. 2; pp. 202 - 208 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Pharmacology and Experimental Therapeutics
01.10.1951
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Subjects | |
Online Access | Get full text |
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Summary: | 1. A series of studies was carried out on the plasma obtained from normal human subjects after the administration of penicillin. 2. Bio-assays for penicillin were performed before and after the fractionation of the plasma into its component protein fractions. 3. It was observed that penicillin could be quantitatively recovered in Fraction VI, which in actuality represents the residue
left over after all other fractions have been precipitated. It contains only 2 per cent of the total plasma protein.
4. Dialysis experiments were set up in which identical penicillin concentrations in buffered saline were dialyzed against
3 per cent albumin and buffered saline controls. Bio- and chemical assays for penicillin within attainable blood level concentrations
indicated no combination of the penicillin with the protein fraction. Increasing the penicillin concentrations far beyond
attainable therapeutic blood levels resulted in binding of about two molecules of penicillin per molecule of albumin. The
data obtained indicate that statistical forces predominate.
5. It appears that though a protein-penicillin complex occurs it is of a nature or type which is readily dissociated when
the penicillin concentration is low. It therefore seems indicated that transport of penicillin G becomes a function of its
solubility in the plasma rather than a function of its protein interaction. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-3565 1521-0103 |