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Updated: Mar 30, 2026

Intracerebroventricular and Intravascular Injection of Viral Particles and Fluorescent Microbeads into the Neonatal Brain
Published on: July 24, 2016
Pharmacokinetic considerations in the use of antivirals in neonates
Elena Yu Enioutina1,2, Jonathan E Constance1, Chris Stockmann1
1a Division of Clinical Pharmacology, Department of Pediatrics , University of Utah School of Medicine , 295 Chipeta Way, Salt Lake City , UT 84108 , USA.
Insights
Neonates are highly susceptible to viral infections due to immature immune systems. Reviewing antiviral drug pharmacokinetics in neonates is crucial for effective treatment and optimal dosing strategies.
Area of Science:
- Neonatal immunology
- Pharmacology
- Infectious diseases
Background:
- Neonates possess immature immune systems, increasing susceptibility to viral infections.
- Antiviral drugs, immunoglobulins, and monoclonal antibodies are used for prophylaxis and treatment in neonates.
- Neonatal drug pharmacokinetics (absorption, distribution, metabolism, excretion) differ significantly from adults.
Purpose of the Study:
- To review neonatal immune deficiencies predisposing to viral infections.
- To evaluate clinical manifestations and treatment of neonatal viral diseases.
- To analyze antiviral drug pharmacokinetics in neonates and provide dosing recommendations.
Main Methods:
- Literature review of studies on neonatal immune responses to microbial challenge.
- Focus on published studies detailing antiviral drug pharmacokinetics in neonates.
- Analysis of factors influencing drug pharmacokinetics in the neonatal population.
Main Results:
- Neonatal immune responses are deficient, increasing vulnerability to viral infections.
- Antiviral drug pharmacokinetics in neonates are influenced by gestational age, enzyme maturation, and renal clearance.
- Significant pharmacokinetic variability necessitates careful consideration for neonatal drug dosing.
Conclusions:
- Further research on antiviral drug pharmacokinetics and pharmacodynamics in neonates is essential.
- Gestational age, enzyme maturation, and renal function significantly impact antiviral drug pharmacokinetics in neonates.
- Tailored dosing strategies for antiviral drugs are critical for maximizing clinical benefits in neonates and infants.
Introduction:
Neonatal patients, because of the inability of their immune system to properly respond to microbial challenge, are highly susceptible to viral infections. Immunoglobulins, monoclonal antibody and antiviral drugs are used for prophylaxis and treatment of viral diseases in neonates. Neonates and, especially, preterm infants differ in drug absorption, distribution, metabolism and excretion from adults and older children.
Areas Covered:
This review will evaluate deficiencies of neonatal immune responses to microbial challenge that predispose newborns to viral infections, clinical manifestations and the treatment of viral diseases in neonates. We focus on published studies describing antiviral drug pharmacokinetics in neonates and make recommendations on the dosing of these drugs, allowing achievement of maximal clinical benefits in neonates.
Expert Opinion:
While some efforts were undertaken to study pharmacokinetics and pharmacodynamics of antiviral drugs, much more needs to be done. Current data indicate that the pharmacokinetics of antiviral drugs may vary significantly depending on gestational age, maturation processes of drug-metabolizing enzymes and renal clearance. Specifics of pharmacokinetics of antiviral drugs need to be taken into consideration when they are prescribed to neonates and infants.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Factors Affecting Drug Response: Overview
Pharmacokinetics: Drug–Food and Drug–Viral Interactions

