نمایش مختصر رکورد

dc.contributor.authorAkbari, Azamen_US
dc.contributor.authorAkbarzadeh, Azimen_US
dc.contributor.authorRafiee Tehrani, Mortezaen_US
dc.contributor.authorCohan, Rezaen_US
dc.contributor.authorMozaffari, Alirezaen_US
dc.contributor.authorMemarzadeh, Mohammadrezaen_US
dc.date.accessioned1399-07-09T03:05:23Zfa_IR
dc.date.accessioned2020-09-30T03:05:23Z
dc.date.available1399-07-09T03:05:23Zfa_IR
dc.date.available2020-09-30T03:05:23Z
dc.date.issued2020-01-01en_US
dc.date.issued1398-10-11fa_IR
dc.date.submitted2019-04-15en_US
dc.date.submitted1398-01-26fa_IR
dc.identifier.citationAkbari, Azam, Akbarzadeh, Azim, Rafiee Tehrani, Morteza, Cohan, Reza, Mozaffari, Alireza, Memarzadeh, Mohammadreza. (2020). Preparation and Evaluation of a Liposome Drug Delivery System in Cancer Treatment in vitro. Journal of Nanostructures, 10(1), 140-147. doi: 10.22052/JNS.2020.01.015en_US
dc.identifier.issn2251-7871
dc.identifier.issn2251-788X
dc.identifier.urihttps://dx.doi.org/10.22052/JNS.2020.01.015
dc.identifier.urihttps://jns.kashanu.ac.ir/article_104454.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/233392
dc.description.abstractCancer is a fatal disease and relatively widespread in the world; Breast cancer is the most prevalent cancer among women. Hydroxyurea (HU) is a chemotherapy drug for the cure of cancer different types in patients, for example breast cancer, but has several defects, for to remove these problems in this study a nanoliposome (NL) suspension for Hydroxyurea (HU) delivery in breast cancer cell therapy was developed.HU was encapsulated into NLs. Size was measured by nanosizer. The release of the liposomal formulation was assessed during 36 h. FTIR analysis for liposomal Hydroxyurea and free Hydroxyurea was carried out. The uptake capacity of the formulation was determined by transfection of nanoliposomal hydroxyurea (NL-HU) in MDA-MB231 cells via flow cytometer and fluorescence microscopy studies, the cytotoxicity of NL-HU and free HU was evaluated in cells. Size of NL-HU was 174nm, HU encapsulation efficiencies in NLs was 81%. FTIR analysis showed the stability of HU in the liposome and no improper interaction between liposome and HU, release after 36h depicted sustained release behavior.NL-HU had suitable uptake in MDA-MB231 cells. Cytotoxicity of NL-HU on cells was considerable. We confirmed these nanoliposomes are potentially useful for delivery of Hydroxyurea in breast cancer cells treatment.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherUniversity of Kashanen_US
dc.relation.ispartofJournal of Nanostructuresen_US
dc.relation.isversionofhttps://dx.doi.org/10.22052/JNS.2020.01.015
dc.subjectNanoliposomeen_US
dc.subjectbreast canceren_US
dc.subjectHydroxyureaen_US
dc.subjectCytotoxicityen_US
dc.titlePreparation and Evaluation of a Liposome Drug Delivery System in Cancer Treatment in vitroen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentDepartment of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran | Department of Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iranen_US
dc.contributor.departmentDepartment of Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iranen_US
dc.contributor.departmentDepartment of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iranen_US
dc.contributor.departmentDepartment of Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iranen_US
dc.contributor.departmentResposible pharmacist office of Barij pharmaceutical company, Kashan, Iranen_US
dc.contributor.departmentMedicinal plant research center of Barij pharmaceutical company, Kashan, Iranen_US
dc.citation.volume10
dc.citation.issue1
dc.citation.spage140
dc.citation.epage147


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