Cited by 71Drug Solubulity and Delivery SystemsMalaria Research and ControlAdvancements in Transdermal Drug Delivery

Solid microemulsion preconcentrate (NanOsorb) of artemether for effective treatment of malaria

Joshi, Medha, Pathak, Sulabha, Sharma, Shobhona, Patravale, Vandana·2008·International Journal of Pharmaceutics

Abstract

A microemulsion preconcentrate was formulated on the basis of solubility of artemether (ARM) in the various oily phases and surfactants and phase diagrams. Various solid adsorbents were evaluated for their ability yield solid microemulsion preconcentrates (NanOsorb-ARM). NanOsorb-ARM on dilution yielded microemulsion with average globule size of 183 nm and polydispersity index of 0.498 when determined using photon correlation spectroscopy. The antimalarial activity of NanOsorb-ARM, ARM solution and marketed ARM formulation (Larither) was evaluated in Plasmodium berghei infected mice as per Peter's four day protocol. The acute lethal dose and the subacute toxicity of NanOsorb-ARM were determined as per the method suggested in Organization for Economic Cooperation and Development (OECD) guidelines. The NanOsorb-ARM exhibited significantly higher antimalarial activity (P<0.05) as compared to the marketed formulation of artemether (Larither). Surprisingly, placebo NanOsorb also showed significantly higher antimalarial activity as compared to Larither indicating that excipients used for the formulation of NanOsorb may have antimalarial activity. Subacute toxicity studies demonstrated that NanOsorb-ARM is comparatively safer than artemether oily solution with respect to survival, gross pathology, hematology and serum biochemistry in mice of both the genders.

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Crossref · 10.1016/j.ijpharm.2008.06.012

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  • NanoAbsorb is a solid microemulsion pre-concentrate formulation that can safely deliver artemether with higher antimalarial efficacy in vivo than the marketed formulation Larither.

    “NanoAbsorb is a solid microemulsion pre-concentrate formulation that can safely deliver the widely used drug artemether with higher antimalarial efficacy in vivo than the marketed formulation Larither 110 .”

    From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [110]

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Authors
Joshi, M., Pathak, S., Sharma, S., & Patravale, V.
Affiliations
  • Institute of Chemical Technology (IN)
  • Tata Institute of Fundamental Research (IN)
Corresponding author
Patravale, Vandana
Venue
International Journal of Pharmaceutics
Publisher
Elsevier BV
Published
2008-10
Volume
362
Issue
1-2
Pages
172-178
ISSN
0378-5173 (ISSN-L)
OpenAlex
W2128204697
Cited by
71
References
23
Citations by year
2025: 2 · 2024: 5 · 2023: 4 · 2022: 6 · 2021: 5 · 2020: 3 · 2019: 1 · 2018: 5 · 2017: 9 · 2016: 8 · 2015: 1 · 2014: 4 · 2013: 8 · 2012: 1
FWCI
2.10
Type
journal article
Language
en
Open access
closed
Locations
  • International Journal of Pharmaceutics (publishedVersion)
  • PubMed (publishedVersion)
Funders
University Grants Commission
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Drug Solubulity and Delivery Systems
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
Keywords
artemether, malaria treatment, antimalarial activity, Plasmodium berghei, toxicity, globule size
MeSH terms
Artemether, Animals, Antimalarials, Chromatography, High Pressure Liquid, Drug Carriers, Drug Compounding, Emulsions, Lethal Dose 50, Malaria, Male, Oils, Particle Size, Plasmodium berghei, Solubility, Surface-Active Agents, Toxicity Tests, Artemisinins, Mice

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