Bioavailability studies of acetaminophen and nitrofurantoin.
نویسندگان
چکیده
264 The Journal of Clinical Pharmacology T HE effects of dosage form variables on therapeutic efficacy and/or bioavailability of drugs are well documented.m Usually, these effects will be manifest principally in differences in rate of absorption and/or differences in efficiency of absorption. Since a formulation which releases a drug slowly over an extended time could have the same bioavailability as a formulation with a more rapid rate of absorption, it is important to commsider both rate and extent of absorption as criteria for assessing therapeutic equivalency. Uwilt et al.2 mmoted differences imm blood and plasma levels of aeetaminophen after administering 1 Gm of drug as whole tablets (eight different manufacturers), as crushed tablets (one manufacturer), and as a tablet containing sorbitol. However, his comparisons were made at a single sampling time (45 minutes after administration). McGilveray et al.3 compared efficiencies and rates of absorption of eight
منابع مشابه
High-performance liquid-chromatographic assay for nitrofurantoin in plasma and urine.
The high-performance liquid-chromatographic method described here for the quantitative analysis for nitrofurantoin in urine and plasma involves direct analysis of urine samples and analysis of plasma samples after protein precipitation by methanol. The assay, which requires only 0.2 ml of biological fluid and shows a linear relationship in the range 0.02 to 200 mg/liter, can be performed in 9 m...
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عنوان ژورنال:
- Journal of clinical pharmacology
دوره 14 5-6 شماره
صفحات -
تاریخ انتشار 1974