Pathogens (Mar 2023)

Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model

  • Nagwa S. M. Aly,
  • Hiroaki Matsumori,
  • Thi Quyen Dinh,
  • Akira Sato,
  • Shin-Ichi Miyoshi,
  • Kyung-Soo Chang,
  • Hak Sun Yu,
  • Duc Tuan Cao,
  • Hye-Sook Kim

DOI
https://doi.org/10.3390/pathogens12030398
Journal volume & issue
Vol. 12, no. 3
p. 398

Abstract

Read online

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 ED50 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.

Keywords