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Published on: April 11, 2014
Evidence for the safety of ascorbic acid administration to the premature infant
W T Bass1, N Malati, M C Castle
1Department of Pediatrics, Eastern Virginia Medical School, Norfolk, USA.
Insights
Early ascorbic acid (AA) administration in premature infants prevents a dangerous drop in AA levels post-birth. This study found AA supplementation safe, with no increased risk of hemolysis or other complications.
Area of Science:
- Neonatal Medicine
- Biochemistry
- Pediatric Nutrition
Background:
- Premature infants have high fetal blood ascorbic acid (AA) levels that drop rapidly after birth.
- This postnatal decline may increase risks of oxidant injury, including bronchopulmonary dysplasia and intraventricular hemorrhage.
- Concerns exist that AA administration could cause hemolysis in premature infants.
Purpose of the Study:
- To evaluate the safety and efficacy of early ascorbic acid (AA) administration in high-risk premature infants.
- To determine if AA prevents the immediate postnatal drop in AA levels.
- To assess the potential risks of AA, such as hemolysis and other complications.
Main Methods:
- Fifty-one high-risk premature infants were randomized into two groups: one receiving normal saline, the other receiving 100 mg/kg of ascorbic acid (AA) daily for the first week.
- A double-blind comparison assessed hemoglobin, hematocrit, erythrocyte morphology, bilirubin, blood transfusions, phototherapy, renal function, infection rates, bronchopulmonary dysplasia, and intraventricular hemorrhage.
- Outcomes were monitored during the first month of life.
Main Results:
- Ascorbic acid (AA) administration successfully prevented the immediate postnatal drop in AA levels.
- No evidence of increased hemolysis was observed in the AA group compared to the control group.
- There were no significant differences in renal function, infection rates, bronchopulmonary dysplasia, or intraventricular hemorrhage between the groups.
Conclusions:
- Early ascorbic acid (AA) administration appears safe for premature infants.
- AA supplementation effectively prevents the immediate postnatal decline in AA levels without causing significant adverse effects.
- Larger clinical studies are warranted to further investigate the antioxidant benefits of AA in premature infants.
Abstract:
Ascorbic acid (AA), a plasma antioxidant, is maintained at high levels in premature fetal blood and declines rapidly postpartum. The sudden reduction in blood AA levels secondary to premature delivery may increase the risk of oxidant injury, that is, bronchopulmonary dysplasia and intraventricular hemorrhage. There is concern that administration of AA to premature infants, in an effort to increase antioxidant capacity, may cause hemolysis. We felt that the benefits of early AA administration and prevention of the immediate postnatal drop in blood AA levels, might outweigh the risks of erthrocyte damage. Fifty one high-risk premature infants were randomized to receive either normal saline or 100 mg/kg of AA, daily for the first week of life. Double-blind comparisons were made of hemoglobin, hematocrit, erythrocyte morphology, bilirubin, number of blood transfusions and days of phototherapy, renal function tests, the incidence of infection, bronchopulmonary dysplasia, and intraventricular hemorrhage during the first month of life. The administration of AA prevented the immediate postnatal drop in AA and was not associated with evidence of increased hemolysis. No significant differences in renal function, rate of infection, bronchopulmonary dysplasia, or intraventricular hemorrhage were seen between the two groups. This study suggests that AA administration to the premature infant is safe and supports the designing and performance of larger clinical studies of the antioxidant properties of AA.
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