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. 2011 Dec 12;205(2):333–336. doi: 10.1093/infdis/jir735

Table 1.

Results of In Vivo Efficacy Studies in Syrian Golden Hamsters

f-CNT-AmB
Miltefosine AmBisome
Drug, Route, and Dose 30 Days Postinfection (n = 7) Control (n = 8) IP 5 mg/kg (n = 11) OL 5 mg/kg (n = 8) OL 10 mg/kg (n = 7) OL 15 mg/kg (n = 8) OL 5 mg/kg (n = 8) IP 5 mg/kg (n = 11)
Amastigotes/500 nuclei 580.8 ± 26.6 615.5 ± 15.2 26.2 ± 7.3 57.7 ± 5.8 20.2 ± 2.2 10.8 ± 2.9 113.6 ±13.8 13.8 ± 5.3
% inhibition in spleen 95.5 ± 1.2 90.2 ± 0.2 96.6 ± 0.4 98.2 ± 0.5 80.6 ± 2.3 97.6 ± 0.9
% suppression in parasite replication 95.7 ± 1.2 99.9 ± 0.0 99.9 ± 0.0 99.9 ± 0.0 99.9 ± 0.0 97.7 ± 0.8
Parasite burden, LDUa 1225.3 ± 63.1 1583.5 ± 44.6 32.2 ± 9.2 71.1 ± 9.2 34.3 ± 7.1 14.9 ± 6.7 188.9 ± 88.9 16.4 ± 6.3

Data are expressed as mean ± standard deviation.

Abbreviations: AmB, amphotericin B; f-CNT, functionalized carbon nanotubes; IP, intraperitoneal; LDU, Leishman-Donovan unit; OL, oral.

a

LDU = number of amastigotes per 500 nuclei × tissue weight (mg).