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      High-Resolution Imaging of Polyethylene Glycol Coated Dendrimers via Combined Atomic Force and Scanning Tunneling Microscopy

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          Abstract

          Dendrimers have shown great promise as drug delivery vehicles in recent years because they can be synthesized with designed size and functionalities for optimal transportation, targeting, and biocompatibility. One of the most well-known termini used for biocompatibility is polyethylene glycol (PEG), whose performance is affected by its actual conformation. However, the conformation of individual PEG bound to soft materials such as dendrimers has not been directly observed. Using atomic force microscopy (AFM) and scanning tunneling microscopy (STM), this work characterizes the structure adopted by PEGylated dendrimers with the highest resolution reported to date. AFM imaging enables visualization of the individual dendrimers, as well as the differentiation and characterization of the dendrimer core and PEG shell. STM provides direct imaging of the PEG extensions with high-resolution. Collectively, this investigation provides important insight into the structure of coated dendrimers, which is crucial for the design and development of better drug delivery vehicles.

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          Most cited references32

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          Dynamic atomic force microscopy methods

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            A nondestructive method for determining the spring constant of cantilevers for scanning force microscopy

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              Dendrimer-based drug and imaging conjugates: design considerations for nanomedical applications.

              Dendrimers are members of a versatile, fourth new class of polymer architecture (i.e. dendritic polymers after traditional linear, crosslinked and branched types). Typically, dendrimers are used as well-defined scaffolding or nanocontainers to conjugate, complex or encapsulate therapeutic drugs or imaging moieties. As a delivery vector, the dendrimer conjugate linker or spacer chemistry plays a crucial part in determining optimum drug delivery to disease sites by conserving active drug efficacy while influencing appropriate release patterns. This review focuses on several crucial issues related to those dendrimer features, namely the role of dendrimers as nanoscaffolding and nanocontainers, crucial principles that might be invoked for improving dendrimer cytotoxicity properties, understanding dendrimer cellular transport mechanisms and the exciting role of dendrimers as high-contrast MRI imaging agents. The review concludes with a brief survey of translational efforts from research and development phases to clinical trials that are actively emerging. 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                J Drug Deliv
                J Drug Deliv
                JDD
                Journal of Drug Delivery
                Hindawi Publishing Corporation
                2090-3014
                2090-3022
                2015
                1 January 2015
                : 2015
                : 535683
                Affiliations
                1Department of Chemistry, University of California, Davis, CA 95616, USA
                2Department of Chemical Engineering & Materials Science, Wayne State University, Detroit, MI 48202, USA
                Author notes

                Academic Editor: Kang Choon Lee

                Author information
                http://orcid.org/0000-0002-5713-5534
                Article
                10.1155/2015/535683
                4313004
                8db70ba4-59aa-42b6-a386-db1f875debf5
                Copyright © 2015 Shawn Riechers et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 10 September 2014
                : 11 December 2014
                Categories
                Research Article

                Pharmaceutical chemistry
                Pharmaceutical chemistry

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