Solution Combustion Synthesis of Hierarchically Structured V2O5 Nanoflakes: Efficacy Against Plasmodium falciparum, Plasmodium berghei and the Malaria Vector Anopheles stephensi
The effective prevention and treatment of malaria still represent a major public health challenge. Here, the solution combustion method was used for the synthesis of hierarchically structured V 2 O 5 nanoflakes. The toxicity of V 2 O 5 nanoflakes was evaluated on the malaria vector Anopheles stephen...
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Veröffentlicht in: | Journal of cluster science 2017-07, Vol.28 (4), p.2337-2348 |
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Zusammenfassung: | The effective prevention and treatment of malaria still represent a major public health challenge. Here, the solution combustion method was used for the synthesis of hierarchically structured V
2
O
5
nanoflakes. The toxicity of V
2
O
5
nanoflakes was evaluated on the malaria vector
Anopheles stephensi
and on the malaria parasites
Plasmodium falciparum
and
P. berghei
, relying to in vitro and in vivo assays. V
2
O
5
nanoflakes were examined by various techniques, including powder X-ray diffraction, field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (XRD), and high resolution transmission electron microscopy (HR-TEM). LC
50
of V
2
O
5
nanoflakes against
A. stephensi
larvae and pupae were 1.936 ppm (larva I), 3.606 ppm (II), 4.750 ppm (III), 6.636 ppm (IV), and 8.876 ppm (pupae). Furthermore, the antiplasmodial activity of V
2
O
5
nanoflakes was evaluated against chloroquine-resistant (CQ-r) and CQ-sensitive (CQ-s) strains of
P. falciparum
. IC
50
of V
2
O
5
nanoflakes were 84.54 μg/ml (CQ-s) and 88.17 μg/ml (CQ-r). In vivo antiplasmodial experiments conducted on
P. berghei
infecting albino mice showed moderate activity of V
2
O
5
nanoflakes, if compared to chloroquine. Overall, our results highlighted the promising potential of the solution combustion method for the synthesis of hierarchically structured V
2
O
5
nanoflakes, which showed really high efficacy as mosquito larvicides and pupicides. |
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ISSN: | 1040-7278 1572-8862 |
DOI: | 10.1007/s10876-017-1228-7 |