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Melatonin Pharmacokinetics Following Oral Administration in Preterm Neonates.


ABSTRACT: Melatonin possesses potential efficacy in perinatal brain injuries, and has been proposed as adjunctive pharmacological therapy in combination with hypothermia in the clinical setting. However, the pharmacokinetics of melatonin in preterm and term newborns is still unknown. The aim of this study was to analyze the pharmacokinetics of melatonin after intragastric administration in preterm infants. Preterm newborns were enrolled 24-72 h after birth, and randomly assigned to three groups receiving a single bolus of 0.5 mg·kg-1 melatonin, or 3 boluses of 1 or 5 mg·kg-1 of melatonin at 24-h intervals. Blood samples were collected before and at selective times after melatonin administration. The half-life of melatonin in plasma ranged from 7.98 to 10.94 h, and the area under the curve (AUC) from 10.48 to 118.17 µg·mL-1·h-1. Our results indicate a different pharmacokinetic profile in premature newborns, compared to adults and experimental animals. The high peak plasma concentrations and the long half-life indicate that in the neonatal clinical setting, it is possible to obtain and maintain high serum concentrations using a single administration of melatonin repeated every 12/24 h.

SUBMITTER: Carloni S 

PROVIDER: S-EPMC6149762 | biostudies-other | 2017 Dec

REPOSITORIES: biostudies-other

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Melatonin Pharmacokinetics Following Oral Administration in Preterm Neonates.

Carloni Silvia S   Proietti Fabrizio F   Rocchi Marco M   Longini Mariangela M   Marseglia Lucia L   D'Angelo Gabriella G   Balduini Walter W   Gitto Eloisa E   Buonocore Giuseppe G  

Molecules (Basel, Switzerland) 20171201 12


Melatonin possesses potential efficacy in perinatal brain injuries, and has been proposed as adjunctive pharmacological therapy in combination with hypothermia in the clinical setting. However, the pharmacokinetics of melatonin in preterm and term newborns is still unknown. The aim of this study was to analyze the pharmacokinetics of melatonin after intragastric administration in preterm infants. Preterm newborns were enrolled 24-72 h after birth, and randomly assigned to three groups receiving  ...[more]

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