Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers

Transfer of piperaquine (PQ) into breast milk was examined in 27 Papua New Guinean women given a 3-day course of dihydro-artemisinin-PQ or sulfadoxine-pyrimethamine-PQ during the second/third trimester. Breast milk was sampled on days 1, 2, 3 to 5, 7 to 11, and 14 to 17 postdelivery, a median of 70...

Full description

Bibliographic Details
Main Authors: Moore, B., Salman, S., Benjamin, J., Page-Sharp, Madhu, Yadi, G., Batty, Kevin, Siba, P., Mueller, I., Davis, T.
Format: Journal Article
Published: American Society for Microbiology 2015
Online Access:http://hdl.handle.net/20.500.11937/14420
_version_ 1848748618331193344
author Moore, B.
Salman, S.
Benjamin, J.
Page-Sharp, Madhu
Yadi, G.
Batty, Kevin
Siba, P.
Mueller, I.
Davis, T.
author_facet Moore, B.
Salman, S.
Benjamin, J.
Page-Sharp, Madhu
Yadi, G.
Batty, Kevin
Siba, P.
Mueller, I.
Davis, T.
author_sort Moore, B.
building Curtin Institutional Repository
collection Online Access
description Transfer of piperaquine (PQ) into breast milk was examined in 27 Papua New Guinean women given a 3-day course of dihydro-artemisinin-PQ or sulfadoxine-pyrimethamine-PQ during the second/third trimester. Breast milk was sampled on days 1, 2, 3 to 5, 7 to 11, and 14 to 17 postdelivery, a median of 70 days postdose (range, 6 to 145 days). A blood sample was taken at delivery, and additional serial samples were available from 9 women who delivered within 42 days of dosing. Milk and plasma PQ were assayed by high-performance liquid chromatography. A population-based approach was used to model the log<inf>e</inf>(plasma) and milk concentration-time data. A sigmoid E<inf>max</inf> model best described PQ breast milk transfer. The population average milk: plasma PQ ratio was 0.58, with a peak of 2.5 at delivery. The model-derived maximum milk intake (148 ml/kg of body weight/day) was similar to the accepted value of 150 ml/kg/day. The median estimated absolute and relative cumulative infant PQ doses were 22 µg and 0.07%, respectively, corresponding to absolute and relative daily doses of 0.41 µg/kg and 0.004%. Model-based simulations for PQ treatment regimens given at birth, 1 week postdelivery, and 6 weeks postdelivery showed that the highest median estimated relative total infant dose (0.36%; median absolute total dose of 101 µg/kg) was seen after maternal PQ treatment 6 weeks postpartum. The maximum simulated relative total and daily doses from any scenario were 4.3% and 2.5%, respectively, which were lower than the recommended 10% upper limit. Piperaquine is transferred into breast milk after maternal treatment doses, but PQ exposure for suckling infants appears safe.
first_indexed 2025-11-14T07:07:54Z
format Journal Article
id curtin-20.500.11937-14420
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:07:54Z
publishDate 2015
publisher American Society for Microbiology
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-144202023-02-22T06:24:16Z Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers Moore, B. Salman, S. Benjamin, J. Page-Sharp, Madhu Yadi, G. Batty, Kevin Siba, P. Mueller, I. Davis, T. Transfer of piperaquine (PQ) into breast milk was examined in 27 Papua New Guinean women given a 3-day course of dihydro-artemisinin-PQ or sulfadoxine-pyrimethamine-PQ during the second/third trimester. Breast milk was sampled on days 1, 2, 3 to 5, 7 to 11, and 14 to 17 postdelivery, a median of 70 days postdose (range, 6 to 145 days). A blood sample was taken at delivery, and additional serial samples were available from 9 women who delivered within 42 days of dosing. Milk and plasma PQ were assayed by high-performance liquid chromatography. A population-based approach was used to model the log<inf>e</inf>(plasma) and milk concentration-time data. A sigmoid E<inf>max</inf> model best described PQ breast milk transfer. The population average milk: plasma PQ ratio was 0.58, with a peak of 2.5 at delivery. The model-derived maximum milk intake (148 ml/kg of body weight/day) was similar to the accepted value of 150 ml/kg/day. The median estimated absolute and relative cumulative infant PQ doses were 22 µg and 0.07%, respectively, corresponding to absolute and relative daily doses of 0.41 µg/kg and 0.004%. Model-based simulations for PQ treatment regimens given at birth, 1 week postdelivery, and 6 weeks postdelivery showed that the highest median estimated relative total infant dose (0.36%; median absolute total dose of 101 µg/kg) was seen after maternal PQ treatment 6 weeks postpartum. The maximum simulated relative total and daily doses from any scenario were 4.3% and 2.5%, respectively, which were lower than the recommended 10% upper limit. Piperaquine is transferred into breast milk after maternal treatment doses, but PQ exposure for suckling infants appears safe. 2015 Journal Article http://hdl.handle.net/20.500.11937/14420 10.1128/AAC.00327-15 American Society for Microbiology unknown
spellingShingle Moore, B.
Salman, S.
Benjamin, J.
Page-Sharp, Madhu
Yadi, G.
Batty, Kevin
Siba, P.
Mueller, I.
Davis, T.
Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title_full Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title_fullStr Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title_full_unstemmed Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title_short Pharmacokinetics of piperaquine transfer into the breast milk of Melanesian mothers
title_sort pharmacokinetics of piperaquine transfer into the breast milk of melanesian mothers
url http://hdl.handle.net/20.500.11937/14420