Cargando…

Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells

BACKGROUND: The delivery of plasmonic particles, such as gold nanorods, to the tumor microenvironment has attracted much interest in biomedical optics for topical applications as the photoacoustic imaging and photothermal ablation of cancer. However, the systemic injection of free particles still cr...

Descripción completa

Detalles Bibliográficos
Autores principales: Borri, Claudia, Centi, Sonia, Ratto, Fulvio, Pini, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984317/
https://www.ncbi.nlm.nih.gov/pubmed/29855304
http://dx.doi.org/10.1186/s12951-018-0377-7
_version_ 1783328588706086912
author Borri, Claudia
Centi, Sonia
Ratto, Fulvio
Pini, Roberto
author_facet Borri, Claudia
Centi, Sonia
Ratto, Fulvio
Pini, Roberto
author_sort Borri, Claudia
collection PubMed
description BACKGROUND: The delivery of plasmonic particles, such as gold nanorods, to the tumor microenvironment has attracted much interest in biomedical optics for topical applications as the photoacoustic imaging and photothermal ablation of cancer. However, the systemic injection of free particles still crashes into a complexity of biological barriers, such as the reticuloendothelial system, that prevent their efficient biodistribution. In this context, the notion to exploit the inherent features of tumor-tropic cells for the creation of a Trojan horse is emerging as a plausible alternative. RESULTS: We report on a convenient approach to load cationic gold nanorods into murine macrophages that exhibit chemotactic sensitivity to track gradients of inflammatory stimuli. In particular, we compare a new model of poly-l-lysine-coated particles against two alternatives of cationic moieties that we have presented elsewhere, i.e. a small quaternary ammonium compound and an arginine-rich cell-penetrating peptide. Murine macrophages that are exposed to poly-l-lysine-coated gold nanorods at a dosage of 400 µM Au for 24 h undertake efficient uptake, i.e. around 3 pg Au per cell, retain the majority of their cargo until 24 h post-treatment and maintain around 90% of their pristine viability, chemotactic and pro-inflammatory functions. CONCLUSIONS: With respect to previous models of cationic coatings, poly-l-lysine is a competitive solution for the preparation of biological vehicles of gold nanorods, especially for applications that may require longer life span of the Trojan horse, say in the order of 24 h. This biopolymer combines the cost-effectiveness of small molecules and biocompatibility and efficiency of natural peptides and thus holds potential for translational developments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0377-7) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5984317
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-59843172018-06-07 Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells Borri, Claudia Centi, Sonia Ratto, Fulvio Pini, Roberto J Nanobiotechnology Research BACKGROUND: The delivery of plasmonic particles, such as gold nanorods, to the tumor microenvironment has attracted much interest in biomedical optics for topical applications as the photoacoustic imaging and photothermal ablation of cancer. However, the systemic injection of free particles still crashes into a complexity of biological barriers, such as the reticuloendothelial system, that prevent their efficient biodistribution. In this context, the notion to exploit the inherent features of tumor-tropic cells for the creation of a Trojan horse is emerging as a plausible alternative. RESULTS: We report on a convenient approach to load cationic gold nanorods into murine macrophages that exhibit chemotactic sensitivity to track gradients of inflammatory stimuli. In particular, we compare a new model of poly-l-lysine-coated particles against two alternatives of cationic moieties that we have presented elsewhere, i.e. a small quaternary ammonium compound and an arginine-rich cell-penetrating peptide. Murine macrophages that are exposed to poly-l-lysine-coated gold nanorods at a dosage of 400 µM Au for 24 h undertake efficient uptake, i.e. around 3 pg Au per cell, retain the majority of their cargo until 24 h post-treatment and maintain around 90% of their pristine viability, chemotactic and pro-inflammatory functions. CONCLUSIONS: With respect to previous models of cationic coatings, poly-l-lysine is a competitive solution for the preparation of biological vehicles of gold nanorods, especially for applications that may require longer life span of the Trojan horse, say in the order of 24 h. This biopolymer combines the cost-effectiveness of small molecules and biocompatibility and efficiency of natural peptides and thus holds potential for translational developments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0377-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-31 /pmc/articles/PMC5984317/ /pubmed/29855304 http://dx.doi.org/10.1186/s12951-018-0377-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Borri, Claudia
Centi, Sonia
Ratto, Fulvio
Pini, Roberto
Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title_full Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title_fullStr Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title_full_unstemmed Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title_short Polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
title_sort polylysine as a functional biopolymer to couple gold nanorods to tumor-tropic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984317/
https://www.ncbi.nlm.nih.gov/pubmed/29855304
http://dx.doi.org/10.1186/s12951-018-0377-7
work_keys_str_mv AT borriclaudia polylysineasafunctionalbiopolymertocouplegoldnanorodstotumortropiccells
AT centisonia polylysineasafunctionalbiopolymertocouplegoldnanorodstotumortropiccells
AT rattofulvio polylysineasafunctionalbiopolymertocouplegoldnanorodstotumortropiccells
AT piniroberto polylysineasafunctionalbiopolymertocouplegoldnanorodstotumortropiccells