Phenytoin, plasma or serum
Dilantin, Diphenylhydantoin
drug derivative is linked to a macromolecule. The kinetic interaction of microparticles in solutions, photometrically detected by turbidity measurements is induced by binding of drug‑conjugate to the antibody on the microparticles and is inhibited by the presence of phenytoin in the sample. A competitive reaction takes place between the drug conjugate and phenytoin in the serum sample for binding to the phenytoin antibody on the microparticles. The resulting turbidity is indirectly proportional to the amount of drug present in the sample.
Serum, Plasma Lithium Heparin
150 uL
4°C (transport with a cool pack if possible)
Trough 0-60 min before next dose.
Phenytoin is one of the most widely prescribed drugs for the treatment of seizure disorders. It is considered one of the drugs of choice for generalized major motor and focal seizures. Strong correlation has been observed between serum levels and both therapeutic and toxic effects. The primary pathway for phenytoin elimination (90%) involves a metabolic conversion to 5(4-hydroxyphenyl)-5-phenylhydantoin (HPPH) which is a saturable process that could lead to toxic serum levels with a small increase in dosage. Phenytoin toxicity primarily affects the centrol nervous sytem. Chromic treatment may lead to hyperplasia of the gums, anemia and osteomalacia. Because both metabolism and clearance are highly variable among individuals, a close monitoring of serum levels is appropriate for virtually every patient undergoing phenytoin therapy.
Anticonvulsant
Browse tests by laboratory
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200

