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Decreasing malathion application time for lice treatment reduces transdermal absorption.
Rhonda M Brand1, Anna R Charron, Randall E Brand
1Department of Internal Medicine, Evanston Northwestern Healthcare and Feinberg School of Medicine at Northwestern University, 1001 University Place, Evanston, IL 60201, USA. rhbrand@enh.org
International Journal of Pharmaceutics
|July 19, 2005
Summary
Reducing malathion application time for head lice treatment significantly lowers skin absorption. A 0.5-hour exposure is as effective as 8 hours, minimizing malathion exposure in children.
Area of Science:
- Dermatology
- Parasitology
- Toxicology
Background:
- Head lice infestations are common in the U.S., treated with topical pediculicides like Ovide (0.5% malathion).
- Current Ovide application requires 8-12 hours, despite malathion's rapid efficacy against lice and nits within 10 minutes.
- Concerns exist regarding excessive malathion exposure in children with prolonged application times.
Purpose of the Study:
- To investigate if reducing malathion application time decreases transdermal absorption.
- To compare malathion penetration and retention after 0.5-hour versus 8-hour topical application.
Main Methods:
- In vitro skin absorption studies were conducted using haired rat skin and human abdominal skin.
- Malathion penetration and residual amounts in the skin were quantified after washing post-application.
Main Results:
- A 0.5-hour malathion exposure resulted in significantly lower skin penetration (0.36%) and retention (2.1%) compared to an 8-hour exposure.
- The 8-hour application led to approximately three-fold greater penetration (1.02%) and retention (3.4%) in human skin (p<0.05).
- Similar absorption patterns were observed in rat skin, with absorption differences persisting for up to 72 hours.
Conclusions:
- A shortened 0.5-hour application of Ovide significantly reduces malathion skin penetration and retention compared to the standard 8-hour duration.
- This shorter duration appears to maintain efficacy, offering a potentially safer alternative for treating head lice.
- Further clinical trials in children are recommended to validate the efficacy of the reduced application time.