dc.creatorMessina, Paula Verónica
dc.creatorBesada Porto, Jose Miguel
dc.creatorRuso, Juan M.
dc.date2014
dc.identifierhttp://hdl.handle.net/11336/31561
dc.identifierRuso, Juan M.; Besada Porto, Jose Miguel; Messina, Paula Verónica; Self-Assembly Drugs: From Micelles to Nanomedicine ; Bentham Science Publishers; Current Topics in Medicinal Chemistry; 14; 5; 2014; 555-571
dc.identifier1568-0266
dc.identifierCONICET Digital
dc.identifierCONICET
dc.descriptionSelf-assembly has fascinated many scientists over the past few decades. Rapid advances and widespread interest in the study of this subject has led to the synthesis of an ever-increasing number of elegant and intricate functional structures with sizes that approach nano- and mesoscopic dimensions. Today, it has grown into a mature field of modern science whose interfaces with many disciplines have provided invaluable opportunities for crossing boundaries for scientists seeking to design novel molecular materials exhibiting unusual properties, and for researchers investigating the structure and function of biomolecules. Consequently, self-assembly transcends the traditional divisional boundaries of science and represents a highly interdisciplinary field including nanotechnology and nanomedicine. Basically, self-assembly focuses on a wide range of discrete molecules or molecular assemblies and uses physical transformations to achieve its goals. In this Review, we present a comprehensive overview of the advances in the field of drug self-assembly and discuss in detail the synthesis, self-assembly behavior, and physical properties as well as applications. We refer the reader to past reviews dealing with colloidal molecules and colloidal self-assembly. In the first part, we will discuss, compare, and link the various bioinformatic procedures: Molecular Dynamics and Quantitative Structure Activity Relationship. The second section deals with the self-assembly behavior in more detail, in which we focus on several experimental techniques, selected according to the depth of knowledge obtained. The last part will review the advances in drug-protein assembly. Nature provides many examples of proteins that form their substrate binding sites by bringing together the component pieces in a process of self-assembly. We will focus in the understanding of physical properties and applications developing thereof.
dc.descriptionFil: Messina, Paula Verónica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
dc.descriptionFil: Besada Porto, Jose Miguel. Universidad de Santiago de Compostela; España
dc.descriptionFil: Ruso, Juan M.. Universidad de Santiago de Compostela; España
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.languageeng
dc.publisherBentham Science Publishers
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/10.2174/1568026614666140121112118
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.eurekaselect.com/119817/article
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subjectSelf Assembly
dc.subjectDrugs
dc.subjectDrugs-Protein Complexation
dc.subjectDrug Delivery
dc.subjecthttps://purl.org/becyt/ford/2.10
dc.subjecthttps://purl.org/becyt/ford/2
dc.titleSelf-Assembly Drugs: From Micelles to Nanomedicine
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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