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March 1945


Author Affiliations

With the Technical Assistance of Kathleen O'Donnell, B.S. CHICAGO

From Cook County Hospital and Loyola University School of Medicine.

Arch Intern Med (Chic). 1945;75(3):168-174. doi:10.1001/archinte.1945.00210270025005

The search for the ideal sulfonamide compound has directed our attention to sulfamethazine, the latest of the sulfonamide compounds. Sulfamethazine (2-sulfanilamido-4, 6-dimethylpyrimidine) is the dimethyl homologue of sulfadiazine. The few reports now in the literature credit it with less toxicity than the sulfonamide drugs now in use. Rose, Martin and Bevan1 compared the solubility of this compound and its acetyl derivative with that of sulfapyridine, sulfadiazine and sulfathiazole. Sulfamethazine was found to be ten times more soluble in the free and five times more soluble in the acetylated form than sulfadiazine. Gilligan and Plummer2 showed it to be the most soluble of all the sulfonamide compounds in the varying range of urinary pH in both its free and its acetylated form. Clinical studies have been made by Macartney and his associates3 and others4 on the use of the drug in the treatment of pneumonia in

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