L Z Benet, D E Smith, E T Lin, F Vincenti, J G Gambertoglio
Index: Fed. Proc. 42(6) , 1695-8, (1983)
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A variety of furosemide assays and their application to biological samples have been described over the past 2 decades. We describe development of a specific, sensitive assay appropriate for efficient measurement of large numbers of biological samples. With development of this methodology we have demonstrated that the putative 2-amino-4-chloro-5-sulfamoylanthranilic acid metabolite is an artifact of sample preparation. In addition, some preparative techniques overestimate furosemide because they hydrolyze the glucuronide conjugate back to the parent compound. Applications of this assay to studies of normal subjects and patients who have received kidney transplants demonstrate a relatively constant amount of glucuronide formation and evidence that this conjugation occurs in the kidney. We also show that patients with renal transplants who are resistant to the effects of furosemide appear to have decreased secretion of the drug into the urinary site of action, the mechanism of which is unknown.
Structure | Name/CAS No. | Molecular Formula | Articles |
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4-Chloro-5-sulfamoylanthranilic Acid
CAS:3086-91-7 |
C7H7ClN2O4S |
The use of HPLC to elucidate the metabolism and urinary excr...
1981-09-01 [Acta Pharmacol. Toxicol. (Copenh.) 49(3) , 223-9, (1981)] |
The binding of furosemide to serum proteins in elderly patie...
1980-09-01 [Acta Pharmacol. Toxicol. (Copenh.) 47(3) , 202-7, (1980)] |
Furosemide accelerates gentamicin accumulation in cultured r...
1989-01-01 [Nephron 53(2) , 138-41, (1989)] |
Absorption and disposition of furosemide in healthy voluntee...
1980-01-01 [Drug Metab. Dispos. 8(5) , 337-42, (1980)] |
The urinary excretion of frusemide and its metabolites by ki...
1987-01-01 [Eur. J. Clin. Pharmacol. 32(3) , 313-5, (1987)] |
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