1976
DOI: 10.1016/s0003-2670(01)82852-x
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Enzymatic determination of acetazolamide in human plasma

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1977
1977
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Cited by 14 publications
(2 citation statements)
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“…The blood concentrations of inhibitors, calculated from known infusion rates and venous blood flows, were checked by assay in one experiment with each inhibitor. Concentrations of acetazolamide and benzolamide in venous plasma and saliva samples were measured by an enzyme inhibitor assay similar to that described by Yakatan, Martin & Smith (1976). Purified ovine erythrocyte carbonic anhydrase was inhibited by known concentrations of acetazolamide or benzolamide and a standard curve (% inhibition V8.…”
Section: Methodsmentioning
confidence: 99%
“…The blood concentrations of inhibitors, calculated from known infusion rates and venous blood flows, were checked by assay in one experiment with each inhibitor. Concentrations of acetazolamide and benzolamide in venous plasma and saliva samples were measured by an enzyme inhibitor assay similar to that described by Yakatan, Martin & Smith (1976). Purified ovine erythrocyte carbonic anhydrase was inhibited by known concentrations of acetazolamide or benzolamide and a standard curve (% inhibition V8.…”
Section: Methodsmentioning
confidence: 99%
“…Since the decrease in the catalytic rate is proportional to the chlorthalidone concentration, measurement of this decrease can be used to determine the chlorthalidone level in unknown samples. This principle was utilized previously for the assay of acetazolamide (5,6) and furosemide (7). Carbonic anhydrase catalyzes the hydration of carbon dioxide, and the activity of the enzyme toward the physiological substrate, carbon dioxide, is usually measured by determining the rate of increase that the enzyme causes in pH during bubbling of carbon dioxide through a slightly alkaline buffer (5).…”
mentioning
confidence: 99%