In vitro effect and scanning electron microscopic changes of Nigella sativa loaded chitosan nanoparticles on Schistosoma mansoni adult
Journal of Medicinal Plants Research • 2019
Publication Information
Authors
Shereen Magdy Kishik1*, Ahlam Farag Mohram1, Marwa Mohamed Nagib1, Hemat Salah Ali1
and Fatma Fawzi Hendawy2
Keywords
Schistosoma mansoni, Nigella sativa, chitosan nanoparticles, scanning electron microscope
Journal
Journal of Medicinal Plants Research
Publisher
academic journal
Volume
13
Issue
3
Pages
66-72
publication.type
International
Paper Link
Open Link
Supplementary Materials
Not Available
Abstract
Nanoparticles can act as drug carriers that can modulate pharmacokinetics, increase bioavailability and
target release with minimal toxic effects. The present work aimed to assess the therapeutic effect and
electron microscopic changes of Nigella sativa loaded Chitosan Nanoparticles (NSLCN) on adult
Schistosoma mansoni in vitro. Adult worms were removed from the portal and mesenteric veins of
infected mice after 90 days, and then three to five mature worms including both sexes were cultured.
Schistosoma adult was exposed to NSLCN at concentrations of (10, 20, 40, 60, 80, and 100 μg/ml) for 24,
and 48 h. Examination for worm viability was done after 24, and 48 h using a stereomicroscope
comparing with control negative and control positive groups. The mortality rate in worms reached
88.9% in the group treated with 100 μg and 80 and 84.6% in groups treated with 80 and 60 μg
respectively (p-value
target release with minimal toxic effects. The present work aimed to assess the therapeutic effect and
electron microscopic changes of Nigella sativa loaded Chitosan Nanoparticles (NSLCN) on adult
Schistosoma mansoni in vitro. Adult worms were removed from the portal and mesenteric veins of
infected mice after 90 days, and then three to five mature worms including both sexes were cultured.
Schistosoma adult was exposed to NSLCN at concentrations of (10, 20, 40, 60, 80, and 100 μg/ml) for 24,
and 48 h. Examination for worm viability was done after 24, and 48 h using a stereomicroscope
comparing with control negative and control positive groups. The mortality rate in worms reached
88.9% in the group treated with 100 μg and 80 and 84.6% in groups treated with 80 and 60 μg
respectively (p-value
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