Improving Cell Penetration of Gold Nanorods by Using an Amphipathic Arginine Rich Peptide
Received 8 November 2019
Accepted for publication 29 January 2020
Published 17 March 2020 Volume 2020:15 Pages 1837—1851
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Anderson Oliveira Lobo
Ana L Riveros,1,2 Cynthia Eggeling,3 Sebastián Riquelme,1 Carolina Adura,1 Carmen López-Iglesias,4 Fanny Guzmán,3 Eyleen Araya,5 Mario Almada,6 Josué Juárez,6 Miguel A Valdez,6 Ignacio A Fuentevilla,1,2,7 Olga López,8 Marcelo J Kogan1,2
1Departamento de Química Farmacológica y Toxicológica, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile; 2Advanced Center for Chronic Diseases (ACCDiS), Universidad de Chile, Santiago, Chile; 3Núcleo de Biotecnología Curauma (NBC), Universidad Católica de Valparaíso, Valparaíso, Chile; 4Microscopy CORE Lab, The Maastricht Multimodal Molecular Imaging Institute FHML, Maastricht University, Maastrich, Netherlands; 5Departamento de Ciencias Quimicas, Facultad de Ciencias Exactas, Universidad Andres Bello, Santiago, Chile; 6Departamento de Física, Universidad de Sonora, Hermosillo, Sonora, México; 7Laboratorio de Investigación en nutrición funcional (LINF), Instituto de Nutrición y Tecnología de los alimentos (INTA), Universidad de Chile, Santiago, Chile; 8Department Surfactants and Nanobiotechnology, Institute for advanced chemistry of Catalonia, Consejo Superior de Investigaciones Científicas (IQAC-CSIC), Barcelona, Spain
Correspondence: Marcelo J Kogan; Ana L Riveros
Department of Pharmacological and Toxicological Chemistry, University of Chile, Santos Dumont 964, Independencia, Santiago 8380494, Chile
Tel +56 2 29782897; +56 2 29782918
Email [email protected]; [email protected]
Introduction: Gold nanorods are highly reactive, have a large surface-to-volume ratio, and can be functionalized with biomolecules. Gold nanorods can absorb infrared electromagnetic radiation, which is subsequently dispersed as local heat. Gold nanoparticles can be used as powerful tools for the diagnosis and therapy of different diseases. To improve the biological barrier permeation of nanoparticles with low cytotoxicity, in this study, we conjugated gold nanorods with cell-penetrating peptides (oligoarginines) and with the amphipathic peptide CLPFFD.
Methods: We studied the interaction of the functionalized gold nanorods with biological membrane models (liposomes) by dynamic light scattering, transmission electron microscopy and the Langmuir balance. Furthermore, we evaluated the effects on cell viability and permeability with an MTS assay and TEM.
Results and Discussion: The interaction study by DLS, the Langmuir balance and cryo-TEM support that GNR-Arg7CLPFFD enhances the interactions between GNRs and biological membranes. In addition, cells treated with GNR-Arg7CLPFFD internalized 80% more nanoparticles than cells treated with GNR alone and did not induce cell damage.
Conclusion: Our results indicate that incorporation of an amphipathic sequence into oligoarginines for the functionalization of gold nanorods enhances biological membrane nanoparticle interactions and nanoparticle cell permeability with respect to nanorods functionalized with oligoarginine. Overall, functionalized gold nanorods with amphipathic arginine rich peptides might be candidates for improving drug delivery by facilitating biological barrier permeation.
Keywords: gold nanorods, cell-penetrating peptides, amphipathic arginine rich peptide, liposome, biological barrier permeation
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