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Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model

We have previously reported 1,2,6,7-tetraoxaspiro [7.11]nonadecane (N-89) as a promising antimalarial compound. In this study, we evaluated the effect of transdermal therapy (tdt) of N-89 in combination (tdct) with other antimalarials as an application for children. We prepared ointment formulas con...

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Autores principales: Aly, Nagwa S. M., Matsumori, Hiroaki, Dinh, Thi Quyen, Sato, Akira, Miyoshi, Shin-Ichi, Chang, Kyung-Soo, Yu, Hak Sun, Cao, Duc Tuan, Kim, Hye-Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056811/
https://www.ncbi.nlm.nih.gov/pubmed/36986320
http://dx.doi.org/10.3390/pathogens12030398
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author Aly, Nagwa S. M.
Matsumori, Hiroaki
Dinh, Thi Quyen
Sato, Akira
Miyoshi, Shin-Ichi
Chang, Kyung-Soo
Yu, Hak Sun
Cao, Duc Tuan
Kim, Hye-Sook
author_facet Aly, Nagwa S. M.
Matsumori, Hiroaki
Dinh, Thi Quyen
Sato, Akira
Miyoshi, Shin-Ichi
Chang, Kyung-Soo
Yu, Hak Sun
Cao, Duc Tuan
Kim, Hye-Sook
author_sort Aly, Nagwa S. M.
collection PubMed
description We have previously reported 1,2,6,7-tetraoxaspiro [7.11]nonadecane (N-89) as a promising antimalarial compound. In this study, we evaluated the effect of transdermal therapy (tdt) of N-89 in combination (tdct) with other antimalarials as an application for children. We prepared ointment formulas containing N-89 plus another antimalarial drug, specifically, mefloquine, pyrimethamine, or chloroquine. In a 4-day suppressive test, the ED(50) values for N-89 alone or combined with either mefloquine, pyrimethamine, or chloroquine were 18, 3, 0.1, and 3 mg/kg, respectively. Interaction assays revealed that N-89 combination therapy showed a synergistic effect with mefloquine and pyrimethamine, but chloroquine provoked an antagonistic effect. Antimalarial activity and cure effect were compared for single-drug application and combination therapy. Low doses of tdct N-89 (35 mg/kg) combined with mefloquine (4 mg/kg) or pyrimethamine (1 mg/kg) gave an antimalarial effect but not a cure effect. In contrast, with high doses of N-89 (60 mg/kg) combined with mefloquine (8 mg/kg) or pyrimethamine (1 mg/kg), parasites disappeared on day 4 of treatment, and mice were completely cured without any parasite recurrence. Our results indicated that transdermal N-89 with mefloquine and pyrimethamine provides a promising antimalarial form for application to children.
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spelling pubmed-100568112023-03-30 Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model Aly, Nagwa S. M. Matsumori, Hiroaki Dinh, Thi Quyen Sato, Akira Miyoshi, Shin-Ichi Chang, Kyung-Soo Yu, Hak Sun Cao, Duc Tuan Kim, Hye-Sook Pathogens Article We have previously reported 1,2,6,7-tetraoxaspiro [7.11]nonadecane (N-89) as a promising antimalarial compound. In this study, we evaluated the effect of transdermal therapy (tdt) of N-89 in combination (tdct) with other antimalarials as an application for children. We prepared ointment formulas containing N-89 plus another antimalarial drug, specifically, mefloquine, pyrimethamine, or chloroquine. In a 4-day suppressive test, the ED(50) values for N-89 alone or combined with either mefloquine, pyrimethamine, or chloroquine were 18, 3, 0.1, and 3 mg/kg, respectively. Interaction assays revealed that N-89 combination therapy showed a synergistic effect with mefloquine and pyrimethamine, but chloroquine provoked an antagonistic effect. Antimalarial activity and cure effect were compared for single-drug application and combination therapy. Low doses of tdct N-89 (35 mg/kg) combined with mefloquine (4 mg/kg) or pyrimethamine (1 mg/kg) gave an antimalarial effect but not a cure effect. In contrast, with high doses of N-89 (60 mg/kg) combined with mefloquine (8 mg/kg) or pyrimethamine (1 mg/kg), parasites disappeared on day 4 of treatment, and mice were completely cured without any parasite recurrence. Our results indicated that transdermal N-89 with mefloquine and pyrimethamine provides a promising antimalarial form for application to children. MDPI 2023-03-01 /pmc/articles/PMC10056811/ /pubmed/36986320 http://dx.doi.org/10.3390/pathogens12030398 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aly, Nagwa S. M.
Matsumori, Hiroaki
Dinh, Thi Quyen
Sato, Akira
Miyoshi, Shin-Ichi
Chang, Kyung-Soo
Yu, Hak Sun
Cao, Duc Tuan
Kim, Hye-Sook
Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title_full Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title_fullStr Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title_full_unstemmed Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title_short Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model
title_sort pioneer use of antimalarial transdermal combination therapy in rodent malaria model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056811/
https://www.ncbi.nlm.nih.gov/pubmed/36986320
http://dx.doi.org/10.3390/pathogens12030398
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