𝔖 Bobbio Scriptorium
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The bioavailability of cefpodoxime proxetil tablets relative to an oral solution

✍ Scribed by Marie T. Borin; Kristi K. Forbes; George S. Hughes


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
424 KB
Volume
16
Category
Article
ISSN
0142-2782

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✦ Synopsis


The bioavailability of cefpodoxime proxetil tablets relative to an oral solution of cefpodoxime proxetil in a sucrose/alcohol/citric acid vehicle was studied in 11 healthy volunteers in a randomized, crossover study. Fasted subjects took one cefpodoxime proxetil lOOmg tablet or 50mL of a 2mgmL-I cefpodoxime proxetil oral solution on two separate occasions. In a third study period, all subjects took a 100mg dose of the oral solution with a high-fat meal to investigate the effect of food on cefpodoxime proxetil absorption from the oral solution. Serial blood samples were obtained over a 24 h period, and urine was collected for 48 h after dosing. Cefpodoxime concentrations in plasma and in urine were determined using HPLC methods. The bioavailability of cefpodoxime proxetil tablets relative to the oral solution was 82%, as determined from AUC ratios. There was no difference in the rate of cefpodoxime absorption between dosage forms. Food had no effect on the extent of drug absorption from the oral solution but did result in delayed absorption. These results suggest that complete dissolution of cefpodoxime proxetil is critical for optimal bioavailability.


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## Abstract The bioavailability of quinidine sulfate after oral administration of a commercial sustained‐release quinidine tablet was compared with that of oral quinidine sulfate solution in 18 normal subjects. Three hundred milligrammes of each product was administered to each subject in standard