Pioneer Use of Antimalarial Transdermal Combination Therapy in Rodent Malaria Model

Author:

Aly Nagwa S. M.12ORCID,Matsumori Hiroaki1,Dinh Thi Quyen1ORCID,Sato Akira13ORCID,Miyoshi Shin-Ichi4,Chang Kyung-Soo5,Yu Hak Sun6ORCID,Cao Duc Tuan7ORCID,Kim Hye-Sook1ORCID

Affiliation:

1. Division of International Infectious Disease Control, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama City 700-8530, Okayama, Japan

2. Department of Parasitology, Faculty of Medicine, Benha University, Benha 13511, Egypt

3. Department of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda 278-8530, Chiba, Japan

4. Department of Sanitary Microbiology, Faculty of Pharmaceutical Sciences, Okayama University, Tsushima-Naka, Kita-Ku, Okayama City 700-8530, Okayama, Japan

5. Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Republic of Korea

6. Department of Parasitology and Tropical Medicine, School of Medicine, Pusan National University, Yangsan-si 626-870, Republic of Korea

7. Department of Pharmaceutical Chemistry and Quality Control, Faculty of Pharmacy, Hai Phong University of Medicine and Pharmacy, Hai phong, Vietnam

Abstract

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.

Funder

Program of the Japan Initiative for Global Research Network on Infectious Diseases

Ministry of Education, Culture, Sports, Science, and Technology in Japan

Japan Agency for Medical Research and Development

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference30 articles.

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4. Dormoi, J., Amalvict, R., Gendrot, M., and Pradines, B. (2022). Methylene Blue-Based Combination Therapy with Amodiaquine Prevents Severe Malaria in an Experimental Rodent Model. Pharmaceutics, 14.

5. New neplanocin analogs 12. An alternative synthesis of (6′R)-6′-C- methylneplanocin A (RMNPA), a novel potent anti-malarial agent;Shuto;J. Med. Chem.,2002

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