Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/13885
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dc.contributor.authorPargoo, Esmaeel Mohammadi-
dc.contributor.authorAghasadegh, Mohammad Reza-
dc.contributor.authorParivar, Kazem-
dc.contributor.authorBolhassani, Azam-
dc.contributor.authorNikbin, Mehri-
dc.contributor.authorRahimi, Pooneh-
dc.contributor.authorArdestani, Mehdi Shafiee-
dc.date.accessioned2022-10-28T08:17:07Z-
dc.date.available2022-10-28T08:17:07Z-
dc.date.issued2020-03-16-
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13885-
dc.description.abstractHuman diseases like viral organisms for example, hepatitis, HIV and etc., attack the health and caused large mortality in populations by many years. So finding novel delivery vehicles based antiviral drugs employing nanomaterials is of high universal interest. In current approach a very biocompatible biodegradable nano-biopolymer anionic linear globular dendrimer second generation G2 was elaborately conjugated to a well-known anti-HIV drug Azidovudine and thereafter was characterized by different analytical techniques like AFM, Zeta sizer, 1HNMR, FTIR and LC-Mass spectroscopy. Then, Anionic Linear Globular DendrimerG2-Zidovudine Nano-Conjugate was assessed on human normal cells (toxicity assay by XTT test) and also HIV cell model and the results showed that Anionic Linear Globular DendrimerG2-Zidovudine Nano-Conjugate Significantly Decreased Retroviral Activity without any human cell toxicity respectively. Based on current experimental data such nano-compositions is proposed for further in vivo anti-HIV assays as well.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy & Pharmaceutical Sciecnes, University of Karachien_US
dc.subjectViral organismsen_US
dc.subjectHIVen_US
dc.subjectnano-biopolymer anionic linear globular dendrimer seconden_US
dc.subjectGeneration G2en_US
dc.titleNovel delivery based anionic linear globular dendrimerg2-zidovudine nano-conjugate significantly decreased retroviral activityen_US
dc.typeArticleen_US
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