Abstract The exploration of natural materials for the production of nanoparticles against parasites is currently of particular interest due to its ecofriendly nature. In this study, we described the biosynthesis of silver nanoparticles derived from methanolic garlic extract. Infrared spectroscopy and GC-Mass spectrometry were used to screen the phytochemical composition of garlic and figure out how much of active components. In this study, Allium sativum extract (ASE) and ASE loaded in silver nanoparticles (Bio-AgNPs) were used to treat helminthiasis in vitro. Three doses of ASE (100, 50 and 25 mg/mL) and three doses of Bio-AgNPs (1, 0.5 and 0.25 mg/mL) were used to study the anthelmintic activity using the earthworm, Allolobophora caliginosa. Also, Albendazole was used as a reference drug. The Bio-AgNPs exhibits IC50 of 3.2 µg/mL which indicates their lower toxicity in normal cell lines. The phytochemical screening using GC mass showed the presence of many active compounds with medicinal activities. Both ASE and Bio-AgNPs posses’ anthelmintic activities by inducing paralysis and death in a time dependent manner when compared to the reference drug, Albendazole. Collectively, nanosilver manufactured from A. sativum extract properly functions as an anthelmintic agent and can quickly and dose-dependently kill worms.

Abstract Natural resources emerge as an essential and alternative tool for controlling parasitic agents. The present study was carried out to evaluate in vitro and in vivo effect of Persea americana fruit extract (PAFE) on helminthiasis and coccidiosis. In vitro, anthelmintic activity was performed using PAFE against Allolobophora caliginose. PAFE elicited significant anthelmintic activity comparable to mebendazole with the lesser time taken to paralysis and death for 200 mg/mL. In vitro anticoccidial activity of PAFE, amprolium, phenol, DettolTM, and formalin were studied after incubation with unsporulated oocysts. PAFE was able to significantly inhibit oocyst sporulation in a dose-dependent manner. A total 35 male mice were divided into seven groups. At day 0, all groups except first and second groups were infected with 1×103 E. papillata. Group 1 served as control. Group 2 served as uninfected-treated one. Group 3 was considered an infected-untreated group. After 60 min of infection, groups 4, 5, and 6 were treated with PAFE. Group 7 was treated with amprolium. However, not at par with amprolium, PAFE showed a good anticoccidial activity adjudged based on a significant change in body weight gain, feed intake, oocysts output, and content of carbohydrates and protein. Therefore, PAFE exhibits powerful anthelmintic and anticoccidial effects.

Abstract In every country in the globe, malaria is still regarded as a health risk. In terms of therapeutic medicines against parasites, medicinal plants are a promising source, although the types and concentrations of their active compounds can vary depending on the environment. In this study, the effect of Eucalyptus camaldulensis leaf extracts (ECE) collected from two different habitats (sandy and muddy) on the antioxidant and antimalarial activity was examined. Phytochemical analysis of ECE from muddy (ECEM) and sandy (ECES) habitats were compared. ECEM contained 13 expected compounds while ECES contained only 10 compounds. This was evidenced through infrared spectroscopy. Also, ECEM contained more phenolics and flavonoids than ECES as well as processes higher antioxidant activity that reached 55%. Plasmodium chabaudi-infected mice were treated with ECEM and ECES and the parasitemia was compared. ECEM could significantly suppress the parasitemia by approximately 84% and also was able to decrease the spleen index better than EXCS. Moreover, ECEM was better than ECES in ameliorating the induced decrease in erythrocyte number and hemoglobin content in mice infected with P. chabaudi. It is possible to use E. camaldulensis, which grows in muddy environments, as an antimalarial drug with the largest efficacy gradients.

Abstract Coccidiosis and helminthiasis are two parasitic diseases that harm both health and the economy. The present study aimed to assess the effect of Azadirachta indica leaf extracts (AILE) as an anti-parasitic modulator during murine coccidiosis as well as helminthic infection. Phytochemical analysis using FT-IR showed the presence of eleven compounds. A dose-dependent efficacy was observed in all experiments. At the highest concentration (200 mg/mL), time consumed to induce paralysis and death for worms was recorded at 9.329 ± 2.183 and 10.024 ± 1.542 min, respectively. Histological study revealed conspicuous deformity of surface architecture in all treated worms. SEM also revealed cuticular shrinkage of the body surface in all treated worms. In vitro study showed that incubation with AILE (100 mg/mL) for 96 hr inhibited sporulation by approximately 60%. AILE (50 and 25 mg/mL), amprolium, DettolTM, phenol, and formalin-induced variable inhibition levels at 96 hr of 28%, 44%, 37.33%, 81.33%, 89.33%, and 0% respectively. In addition, IC50 of AILE was obtained at 66.214 µg/mL with a percentage of antioxidant activity to be 74.76 ± 2.23. Our results indicate that AILE exhibits powerful anthelmintic and anticoccidial activities and it could be exploited further for the development of a novel therapeutic agent.