Displacement of Phenytoin from Serum Protein ... - Clinical Chemistry

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Such displacements of phenytoin from protein- binding sites increase the free fraction of phenytomn while decreasing the total concentration of phenytomn in.
WD, Swanson

CP, eds. Biostatistical

analysis.

Englewood Cliffs,

NJ: Prentice-Hall, Inc., 1974:79-85. 21. Valdes R, Graves SW. Protein binding of endogenous digoxinimmunoreactive factors in human serum and its variation with clinical condition. J Clin Endocrinol Metab 1985;60:1135-43. 22. Lightner DA, Wekoon WMD, Zhang M-H. Understanding bilirubin conformation and binding. J Biol Chem 1988263:16669-76.

23. da Fonseca-Wolihelin F, Heinze KG, Lomsky K, Schreiner H. Serum ultrafiltration for the elimination of endogenous interfering substances in creatinine determination. J Clin Chem Clin Biochem 1988;26:523-5. 24. TDx cardiac glycoside drug assays-Digoxin II. In: TDx system assay manual. Sydney, NSW: Abbott Laboratories Diagnostic Division. 1989:R-115;19.09.

CLIN. CHEM.37/1, 98-100 (1991)

Displacement of Phenytoin from Serum Protein Carriers by Antibiotics: Studies with Ceftriaxone, Nafcillin, and Sulfamethoxazole Amltava Dasgupta,1 David A. Dennen,1Roger Dean,2 and Ronald W. McLawhon1 Increased concentrations of free phenytoin in serum, attributable to the displacement of this anticonvulsant by other drugs, e.g., valproic acid and salicylic acid, have been reported. We observed in vitro and in vivo displace-

ment of phenytoin by the antibioticsceftriaxone, nafcillin, and sulfamethoxazole. In vitro studies demonstrated statistically significant (P