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Relative Bioavailability of Orally Administered Fosphenytoin Sodium Injection Compared with Phenytoin Sodium Injection in Healthy Volunteers
Study Objective To describe the pharmacokinetics of fosphenytoin (FPHT) sodium injection when administered orally, and to determine the relative oral bioavailability (FREL) of FPHT sodium injection compared with PHT sodium injection based on pharmacokinetic modeling in healthy volunteers. Design Ope...
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Published in: | Pharmacotherapy 2015-05, Vol.35 (5), p.482-488 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Study Objective
To describe the pharmacokinetics of fosphenytoin (FPHT) sodium injection when administered orally, and to determine the relative oral bioavailability (FREL) of FPHT sodium injection compared with PHT sodium injection based on pharmacokinetic modeling in healthy volunteers.
Design
Open‐label, randomized, single‐dose, two‐period, two‐sequence crossover study.
Setting
University‐affiliated clinical research center funded by the National Center of Research Resources.
Subjects
Ten healthy adult volunteers.
Intervention
Subjects were randomized to receive a single oral dose of either PHT sodium injection or FPHT sodium injection at a dose equivalent to 400 mg PHT acid. Blood samples were collected at baseline (just prior to administration) and at 0.5, 1, 2, 4, 6, 12, 24, 48, and 72 hours after dose administration. After a 7–14‐day washout period, the subjects underwent the same study procedures for administration of the other agent (PHT or FPHT).
Measurements and Main Results
The mean age and weight of the 10 subjects were 37 years and 72.5 kg, respectively, and the mean dose was 5.6 mg/kg based on PHT acid equivalence. The mean FREL of FPHT was 1.21 (95% confidence interval [CI] 1.07–1.35). Serum PHT concentrations were determined by fluorescence polarization immunoassay. The median (range) maximum serum concentration (Cmax) values were significantly higher after FPHT administration compared with PHT: 10.7 (9.0–19.4) mg/L versus 5.0 (3.2–8.9) mg/L (p=0.002). The PHT concentration after oral administration of FPHT displayed faster absorption compared with PHT, with a median (range) time to reach Cmax of 1.0 (0.5–2.0) hours versus 6.0 (2.0–24.0) hours (p=0.008). All subjects completed the study without any serious adverse events reported.
Conclusion
FPHT sodium injection given orally was absorbed more rapidly and to a significantly greater extent than PHT sodium injection given orally to healthy volunteers. Further evaluation of oral FPHT as an alternative in patients requiring enteral feedings is warranted. |
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ISSN: | 0277-0008 1875-9114 |
DOI: | 10.1002/phar.1589 |