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Published on: December 9, 2010
Pharmacokinetics of dapsone administered daily and weekly in human immunodeficiency virus-infected children
M Mirochnick1, E Cooper, K McIntosh
1Boston Medical Center, Boston, Massachusetts, USA. markm@bu.edu
Insights
Dapsone liquid preparation is adequately absorbed in children for Pneumocystis pneumonia prophylaxis. Dosing of 2 mg/kg daily or 4 mg/kg weekly achieves adult-equivalent serum concentrations, with increased clearance in infants under two.
Area of Science:
- Pediatric pharmacology
- Infectious disease prophylaxis
Background:
- Dapsone is an alternative prophylaxis for Pneumocystis pneumonia in children intolerant to trimethoprim-sulfamethoxazole.
- Limited pharmacokinetic data exist for dapsone in pediatric populations.
Purpose of the Study:
- To evaluate dapsone pharmacokinetics in children using a new liquid preparation.
- To compare pediatric dapsone dosing regimens to adult standards.
Main Methods:
- Pharmacokinetic study of 30 children (0.3-12 years) on three dapsone liquid regimens (1 mg/kg daily, 2 mg/kg daily, 4 mg/kg weekly).
- Analysis of dapsone half-life, oral clearance, and apparent volume of distribution.
- Comparison of oral clearance between children <2 years and >2 years.
Main Results:
- Dosing of 2 mg/kg daily or 4 mg/kg weekly yielded peak concentrations comparable to adult daily 100-mg doses.
- Median half-life: 22.2 h; median oral clearance: 0.0365 L/kg/h; median apparent volume of distribution: 1.13 L/kg.
- Significantly higher median dapsone oral clearance in children <2 years (0.0484 L/kg/h) vs. >2 years (0.0278 L/kg/h), P=0.011.
Conclusions:
- The liquid dapsone preparation demonstrates adequate absorption in children.
- Pediatric dosing of 2 mg/kg daily or 4 mg/kg weekly achieves therapeutic serum concentrations similar to adults.
- Dapsone oral clearance is notably increased in children under two years of age.
Abstract:
Although dapsone is a commonly used alternative agent for prophylaxis against Pneumocystis carinii pneumonia in children intolerant to trimethoprim-sulfamethoxazole, there are few data that describe dapsone pharmacokinetics in children. We studied dapsone pharmacokinetics in 30 children (median age, 2.8 years; age range, 0. 3 to 12 years) receiving a new proprietary liquid preparation by three dosing regimens (1 mg/kg of body weight daily, 2 mg/kg daily, or 4 mg/kg weekly). Dosing of children with 2 mg/kg daily or 4 mg/kg weekly resulted in peak concentrations equivalent to those reached in adults receiving 100-mg tablets daily. For the entire population, the median half-life was 22.2 h (range, 7.1 to 40.3 h), the median oral clearance was 0.0365 liter/kg/h (range, 0.0104 to 0.1021 liter/kg/h), and the median oral apparent volume of distribution was 1.13 liters/kg (range, 0.50 to 2.32 liters/kg). The median dapsone oral clearance was significantly increased in those infants less than 2 years of age compared to the oral clearance in those over 2 years of age (0.0484 versus 0.0278 liter/kg/h; P = 0.011). These data suggest that absorption of this liquid preparation is adequate and that the concentrations in the sera of children receiving 2 mg/kg daily or 4 mg/kg weekly are equivalent to those seen in adults receiving standard dapsone dosing. Dapsone oral clearance appears to be increased in children under 2 years of age.
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