نمایش مختصر رکورد

dc.contributor.authorMohammad-Beigi, Hosseinen_US
dc.contributor.authorShojaosadati, Seyed Abbasen_US
dc.contributor.authorMorshedi, Dinaen_US
dc.contributor.authorMirzazadeh, Negaren_US
dc.contributor.authorArpanaei, Ayyooben_US
dc.date.accessioned1399-07-08T20:19:19Zfa_IR
dc.date.accessioned2020-09-29T20:19:19Z
dc.date.available1399-07-08T20:19:19Zfa_IR
dc.date.available2020-09-29T20:19:19Z
dc.date.issued2016-03-01en_US
dc.date.issued1394-12-11fa_IR
dc.date.submitted2015-02-21en_US
dc.date.submitted1393-12-02fa_IR
dc.identifier.citationMohammad-Beigi, Hossein, Shojaosadati, Seyed Abbas, Morshedi, Dina, Mirzazadeh, Negar, Arpanaei, Ayyoob. (2016). The Effects of Organic Solvents on the Physicochemical Properties of Human Serum Albumin Nanoparticles. Iranian Journal of Biotechnology, 14(1), 45-50. doi: 10.15171/ijb.1168en_US
dc.identifier.issn1728-3043
dc.identifier.issn2322-2921
dc.identifier.urihttps://dx.doi.org/10.15171/ijb.1168
dc.identifier.urihttp://www.ijbiotech.com/article_13564.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/85813
dc.description.abstractBackground: Recently, applications of albumin nanoparticles as drug delivery carriers have increased. Most toxicology studies have shown that surface chemistry and size of nanoparticles play an important role in biocompatibility and toxicity. Objective: The effect of desolvating agents with different chemical properties on the size of synthesized HSA NPs was investigated. Materials and Methods: Acetone, ethanol, methanol, and acetonitrile were used to synthesize HSA NPs with controllable size by desolvation method. Scanning electron microscopy (SEM), dynamic light scattering (DLS), and circular dichroism (CD) were employed to characterize produced particles. Finally, the toxicity of HSA NPs synthesized under different conditions was evaluated on PC-12 cells. Results: The sizes of synthesized particles differed according to the different solvents used. The sizes were 275.3 nm, 155.3 nm, 100.11 nm, and 66.2 nm for acetonitrile, ethanol, acetone, and methanol, respectively. CD showed that larger NPs had more changes in the secondary structures. Finally, the toxicity monitored on the cultured PC-12 cells showed no significant toxic effect through treating with these NPs at different concentrations (0-500 mg.mL-1). Conclusions: The size of HSA NPs has a strong dependency on the desolvating agent. The mechanism in which the desolvating agent affects the size of HSA NPs is complex. Various factors such as dielectric constant, polarity, functional groups, and hydrogen bonding of the solvents have the potential to affect the size and structure of HSA NPs. CD analysis suggested that the solvent denaturing capability had a critical effect on the HSA particle size. The stronger denaturing capability of the solvent resulted in the larger HSA particle size.en_US
dc.format.extent146
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherNational Institute of Genetic Engineering and Biotechnologyen_US
dc.relation.ispartofIranian Journal of Biotechnologyen_US
dc.relation.isversionofhttps://dx.doi.org/10.15171/ijb.1168
dc.subjectDesolvating agentsen_US
dc.subjectHuman serum albumin nanoparticlesen_US
dc.subjectPhysicochemical propertiesen_US
dc.subjectNano Biotechnologyen_US
dc.titleThe Effects of Organic Solvents on the Physicochemical Properties of Human Serum Albumin Nanoparticlesen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentBiotechnology Group, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iranen_US
dc.contributor.departmentBiotechnology Group, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iranen_US
dc.contributor.departmentBiotechnology Group, Faculty of Chemical Engineering, Tarbiat Modares University, Tehran, Iranen_US
dc.contributor.departmentDepartment of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iranen_US
dc.citation.volume14
dc.citation.issue1
dc.citation.spage45
dc.citation.epage50


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