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      International Journal of Nanomedicine (submit here)

      This international, peer-reviewed Open Access journal by Dove Medical Press focuses on the application of nanotechnology in diagnostics, therapeutics, and drug delivery systems throughout the biomedical field. Sign up for email alerts here.

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      Scolicidal Effects of Nanoparticles Against Hydatid Cyst Protoscolices in vitro

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          Abstract

          Background

          Echinococcus granulosus is causative agent of cystic echinococcosis (CE), which has a cosmopolitan distribution. The current methods for the treatment of human CE include surgery. Therefore, the development of new scolicidal agents with low side effects and more efficacies is an urgent need.

          Purpose

          The present study aimed to compare the scolicidal efficacies of silver, iron, copper, silica and zinc oxide nanoparticles (NPs) against hydatid cyst protoscolices in vitro.

          Methods

          Hydatid cysts of sheep liver and lung were collected. The cyst fluid containing protoscolices was aspirated aseptically. The scolicidal activities of the silver, iron, copper, silica and zinc nanoparticles (Ag-NP, Fe-NP, Cu-NP, Si-NP and Zn-NP) were tested at different concentrations of 0.25, 0.5 and 1 mg/mL following 10, 30 and 60 min of incubation in triplicate. Viability of protoscolices was confirmed by 0.1% eosin staining.

          Results

          Results showed that Ag-NPs at all concentrations tested had the highest scolicidal effect. Ag-NPs at 1 mg/mL concentration after 60 min of exposure time showed 80% mortality rate. Si-NPs had the high scolicidal activity at 1 mg/mL concentration (52.33%), Cu-NPs at 0.5 mg/mL concentration (41%), Fe-NPs at 1mg/mL concentration (28%) and Zn-NPs at concentration of 1mg/mL after 60 mins (15.67%).

          Conclusion

          The findings of the present study showed that Ag-NPs, Fe-NPs, Cu-NPs, Si-NPs and Zn-NPs had potent scolicidal effects and that Ag-NPs are recommended as effective scolicidal agents. However, further in vivo studies are required to evaluate the efficacy of these nanoparticles.

          Most cited references21

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          Biological, epidemiological, and clinical aspects of echinococcosis, a zoonosis of increasing concern.

          Echinococcosis in humans is a zoonotic infection caused by larval stages (metacestodes) of cestode species of the genus Echinococcus. Cystic echinococcosis (CE) is caused by Echinococcus granulosus, alveolar echinococcosis (AE) is caused by E. multilocularis, and polycystic forms are caused by either E. vogeli or E. oligarthrus. In untreated cases, AE has a high mortality rate. Although control is essentially feasible, CE remains a considerable health problem in many regions of the northern and southern hemispheres. AE is restricted to the northern hemisphere regions of North America and Eurasia. Recent studies have shown that E. multilocularis, the causative agent of AE, is more widely distributed than previously thought. There are also some hints of an increasing significance of polycystic forms of the disease, which are restricted to Central and South America. Various aspects of human echinococcosis are discussed in this review, including data on the infectivity of genetic variants of E. granulosus to humans, the increasing invasion of cities in Europe and Japan by red foxes, the main definitive hosts of E. multilocularis, and the first demonstration of urban cycles of the parasite. Examples of emergence or reemergence of CE are presented, and the question of potential spreading of E. multilocularis is critically assessed. Furthermore, information is presented on new and improved tools for diagnosing the infection in final hosts (dogs, foxes, and cats) by coproantigen or DNA detection and the application of molecular techniques to epidemiological studies. In the clinical field, the available methods for diagnosing human CE and AE are described and the treatment options are summarized. The development of new chemotherapeutic options for all forms of human echinococcosis remains an urgent requirement. A new option for the control of E. granulosus in the intermediate host population (mainly sheep and cattle) is vaccination. Attempts are made to reduce the prevalence of E. multilocualaris in fox populations by regular baiting with an anthelmintic (praziquantel). Recent data have shown that this control option may be used in restricted areas, for example in cities, with the aim of reducing the infection risk for humans.
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            Environmental behavior and ecotoxicity of engineered nanoparticles to algae, plants, and fungi.

            Developments in nanotechnology are leading to a rapid proliferation of new materials that are likely to become a source of engineered nanoparticles (ENPs) to the environment, where their possible ecotoxicological impacts remain unknown. The surface properties of ENPs are of essential importance for their aggregation behavior, and thus for their mobility in aquatic and terrestrial systems and for their interactions with algae, plants and, fungi. Interactions of ENPs with natural organic matter have to be considered as well, as those will alter the ENPs aggregation behavior in surface waters or in soils. Cells of plants, algae, and fungi possess cell walls that constitute a primary site for interaction and a barrier for the entrance of ENPs. Mechanisms allowing ENPs to pass through cell walls and membranes are as yet poorly understood. Inside cells, ENPs might directly provoke alterations of membranes and other cell structures and molecules, as well as protective mechanisms. Indirect effects of ENPs depend on their chemical and physical properties and may include physical restraints (clogging effects), solubilization of toxic ENP compounds, or production of reactive oxygen species. Many questions regarding the bioavailability of ENPs, their uptake by algae, plants, and fungi and the toxicity mechanisms remain to be elucidated.
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              From ecotoxicology to nanoecotoxicology.

              For hazard assessment of NPs quantitative nanoecotoxicological data are required. The objective of this review was to evaluate the currently existing literature data on toxicity (L(E)C50 values) of synthetic NPs in environmentally relevant species in order to: (i) identify tentatively most harmful NPs and most sensitive organism groups, and (ii) to provide relevant ecotoxicological information for further risk assessment. The focus was set on selected synthetic NPs (nano TiO(2), nano ZnO, nano CuO, nano Ag, SWCNTs, MWCNs and C60-fullerenes) and organism groups representing main food-chain levels (bacteria, algae, crustaceans, ciliates, fish, yeasts and nematodes). Altogether 77 effect values were found, mostly for nano TiO(2) (31%), C60 (18%), nano ZnO (17%), nano Ag (13%), SWCNTs and nano CuO (both 9%). Only 3% of the available quantitative ecotoxicological information concerned MWCNTs. Organism-wise, 33% of the data concerned crustaceans, 27% bacteria, 14% algae and 13% fish. For all organism groups studied, solubility of CuO- and ZnO-NPs was a key factor in their aquatic toxicity. On the basis of the 34 median L(E)C50 values derived from 77 individual values, NPs were ranked according to their lowest median L(E)C50 value for the above described organism groups: the most harmful were nano Ag and nano ZnO that were classified "extremely toxic", (L(E)C50<0.1mg/l), followed by C60 fullerenes and nano CuO that were classified "very toxic", (L(E)C50 0.1-1mg/l). SWCNTs and MWCNTs were classified "toxic" (L(E)C50 1-10mg/l). Nano TiO(2) was classified as "harmful", (L(E)C50 10-100mg/l). Throughout, algae and crustaceans (daphnids) were most sensitive and thus probably most vulnerable organism groups in aquatic exposure to NPs. Very low L(E)C50 values should deserve thorough attention of environmental risk assessors for evaluation of the potential adverse effects of synthetic NPs on ecosystems. As the quantitative nanoecotoxicological data are still rare, further studies are needed.
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                Author and article information

                Journal
                Int J Nanomedicine
                Int J Nanomedicine
                IJN
                intjnano
                International Journal of Nanomedicine
                Dove
                1176-9114
                1178-2013
                17 February 2020
                2020
                : 15
                : 1095-1100
                Affiliations
                [1 ]Department of Pathobiology, Faculty of Veterinary Medicine, University of Tabriz , Tabriz, Iran
                [2 ]Department of Basic Science, Faculty of Veterinary Medicine, University of Tabriz , Tabriz, Iran
                [3 ]Infectious Diseases and Anti-Infective Therapy Research Group, Sharjah Medical Research Institute and College of Pharmacy, University of Sharjah , Sharjah 27272, United Arab Emirates
                [4 ]Department of Medicine, School of Medicine, University of California Irvine , Irvine, CA, USA
                [5 ]Department of Pharmacy, City University College of Ajman , Ajman 18484, United Arab Emirates
                Author notes
                Correspondence: Roghayeh Norouzi Department of Pathobiology, Faculty of Veterinary Medicine, University of Tabriz , Tabriz, Iran Email roghayehnorouzi123@gmail.com
                Mohamed Ezzat El Zowalaty Department of Pharmacy, City University College of Ajman , Ajman18484, United Arab Emirates Email elzow005@gmail.com
                Author information
                http://orcid.org/0000-0003-4899-1168
                http://orcid.org/0000-0002-1056-4761
                Article
                228538
                10.2147/IJN.S228538
                7034968
                32110009
                00244700-0851-450f-9369-f5cfbe04d0e7
                © 2020 Norouzi et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 24 August 2019
                : 25 October 2019
                Page count
                Figures: 2, Tables: 1, References: 26, Pages: 6
                Categories
                Original Research

                Molecular medicine
                scolicidal,hydatid cyst,protoscolices,silver nanoparticle,iron nanoparticle,copper nanoparticle,silica nanoparticle,in vitro

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