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Preparation and in vitro evaluation of hydrogels with magnetic nanoparticles and Albendazole Sulfoxide and study its effectiveness on protoscoleces of hydatid cyst

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Date
2020
Author
Mehdizad Bakhtiar, Nayer
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Abstract
The chemotherapeutic failure of albendazole (ABZ) against cystic echinococcosis (CE) is resulted by its low aqueous solubility, poor absorption and its erratic bioavailability. A hydrogel is a three-dimensional network of hydrophilic polymers that can swell in water and hold a large amount of water .Also β-cyclodextrin polymers are cyclic oligosaccharide used for the delivery of poorly soluble drugs due to its suitable cavity size and loading capacity. Materials and Methodes: We evaluated the in vitro scolicidal and apoptotic effects of 100, 200, 400 and 800μg/mL of drugs by quantifying the expression of caspase‑3 mRNA. The enzymatic activity of caspase-3 was determined by fluorometric assay. To assess the efficacy of ABZ‑loaded β-CDPs against protoscoleces (PSCs), the mRNA expression of arginase (ARG) and thioredoxin peroxidase (TPx) were quantified by Real-time PCR. Results: Significant results were not obtained from scolicidal effects of albendazole sulfoxide and hydrogel with magnetic nanoparticles and albendazole sulfoxide in comparison to control groups. A statistically significant scolicidal activity of ABZ was observed only at a concentration of 800 μg/mL (100% PSCs mortality rate after 5 days of exposure), while the 200 and 400 μg/mL concentrations reached 100% PSCs mortality rate after 9 days of exposure. The 400 μg/mL ABZ-β-CDs had 100% PSCs mortality rate after 5 days of exposure. We found that ABZ-β-CDs induced higher caspase-3 activity and caspase-3 mRNA expression, suggesting a more potent apoptotic effect on the parasite. We also showed that ABZ-β-CDs can significantly down-regulate the EgArg and EgTPx respectively, indicating more potent interference against pathogenic process and impairment of growth of E. granulosus sensu stricto.
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http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/63345
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