Abstract:
Entamoeba histolytica and Entamoeba Bangladeshi both parasites are the member of
Entamoeba group. E. bangladeshi is a novel species which is identified very recently
and E. histolytica is a common parasite which is the main cause of amoebiasis. The
drugs of choice for invasive amoebiasis are tissue active agents, like metronidazole,
Ornidazole and chloroquine or the more toxic emetine derivatives, including
dehydroemetine. Ornidazole is derived from 5-nitroimdazole which kill the
trophozoites by alterations in the protoplasmic organelles of the amoeba. The aim of
the study is to determine the efficacy of Ornidazole against clinical isolates of E.
histolytica and E. bangladeshi. The clinical isolates of E. histolytica and E. bangladeshi
were treated with Ornidazole at different concentrations (0.96, 0.48, 0.24, 0.12, 0.06,
0.03 µg/ml). Drug sensitivity assay of the samples was carried out by using microtiter plates containing 100μl of parasite suspension (1×106 parasites/ml). Plates were incubated at 37ºC. After 4 hours the viable parasites were counted by haemocytometer under microscope. Viable counts of the E. histolytica and E.
bangladeshi in each concentration of drugs were compared with the control. Result
shows that after treatment with Ornidazole, the cell count of E. bangladeshi is higher
than E. histolytica when both parasites are compared with the control (p<0.05).
There is also a significant difference in percent cell inhibition between the two
clinical isolates. The percent cell inhibition of E. histolytica is 30% whereas only 18%
cell inhibiton is observed for E. bangladeshi. We conclude that Ornidazole is
sensitive against E. bangladeshi. However, the efficacy of Ornidazole to inhibit the
parasites is significant in E. histolytica than E. bangladeshi. In this study the parasite
inhibition was occurred in a dose dependent manner.
Description:
This thesis submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy (B.Pharm) in East West University, Dhaka, Bangladesh.