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Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays

[Image: see text] Single-cell microarrays are emerging tools to unravel intrinsic diversity within complex cell populations, opening up new approaches for the in-depth understanding of highly relevant diseases. However, most of the current methods for their fabrication are based on cumbersome patter...

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Autores principales: Ferrara, Vittorio, Zito, Giovanni, Arrabito, Giuseppe, Cataldo, Sebastiano, Scopelliti, Michelangelo, Giordano, Carla, Vetri, Valeria, Pignataro, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997111/
https://www.ncbi.nlm.nih.gov/pubmed/33463257
http://dx.doi.org/10.1021/acsbiomaterials.9b01871
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author Ferrara, Vittorio
Zito, Giovanni
Arrabito, Giuseppe
Cataldo, Sebastiano
Scopelliti, Michelangelo
Giordano, Carla
Vetri, Valeria
Pignataro, Bruno
author_facet Ferrara, Vittorio
Zito, Giovanni
Arrabito, Giuseppe
Cataldo, Sebastiano
Scopelliti, Michelangelo
Giordano, Carla
Vetri, Valeria
Pignataro, Bruno
author_sort Ferrara, Vittorio
collection PubMed
description [Image: see text] Single-cell microarrays are emerging tools to unravel intrinsic diversity within complex cell populations, opening up new approaches for the in-depth understanding of highly relevant diseases. However, most of the current methods for their fabrication are based on cumbersome patterning approaches, employing organic solvents and/or expensive materials. Here, we demonstrate an unprecedented green-chemistry strategy to produce single-cell capture biochips onto glass surfaces by all-aqueous inkjet printing. At first, a chitosan film is easily inkjet printed and immobilized onto hydroxyl-rich glass surfaces by electrostatic immobilization. In turn, poly(ethylene glycol) diglycidyl ether is grafted on the chitosan film to expose reactive epoxy groups and induce antifouling properties. Subsequently, microscale collagen spots are printed onto the above surface to define the attachment area for single adherent human cancer cells harvesting with high yield. The reported inkjet printing approach enables one to modulate the collagen area available for cell attachment in order to control the number of captured cells per spot, from single-cells up to double- and multiple-cell arrays. Proof-of-principle of the approach includes pharmacological treatment of single-cells by the model drug doxorubicin. The herein presented strategy for single-cell array fabrication can constitute a first step toward an innovative and environmentally friendly generation of aqueous-based inkjet-printed cellular devices.
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spelling pubmed-79971112021-03-29 Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays Ferrara, Vittorio Zito, Giovanni Arrabito, Giuseppe Cataldo, Sebastiano Scopelliti, Michelangelo Giordano, Carla Vetri, Valeria Pignataro, Bruno ACS Biomater Sci Eng [Image: see text] Single-cell microarrays are emerging tools to unravel intrinsic diversity within complex cell populations, opening up new approaches for the in-depth understanding of highly relevant diseases. However, most of the current methods for their fabrication are based on cumbersome patterning approaches, employing organic solvents and/or expensive materials. Here, we demonstrate an unprecedented green-chemistry strategy to produce single-cell capture biochips onto glass surfaces by all-aqueous inkjet printing. At first, a chitosan film is easily inkjet printed and immobilized onto hydroxyl-rich glass surfaces by electrostatic immobilization. In turn, poly(ethylene glycol) diglycidyl ether is grafted on the chitosan film to expose reactive epoxy groups and induce antifouling properties. Subsequently, microscale collagen spots are printed onto the above surface to define the attachment area for single adherent human cancer cells harvesting with high yield. The reported inkjet printing approach enables one to modulate the collagen area available for cell attachment in order to control the number of captured cells per spot, from single-cells up to double- and multiple-cell arrays. Proof-of-principle of the approach includes pharmacological treatment of single-cells by the model drug doxorubicin. The herein presented strategy for single-cell array fabrication can constitute a first step toward an innovative and environmentally friendly generation of aqueous-based inkjet-printed cellular devices. American Chemical Society 2020-04-06 2020-05-11 /pmc/articles/PMC7997111/ /pubmed/33463257 http://dx.doi.org/10.1021/acsbiomaterials.9b01871 Text en Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Ferrara, Vittorio
Zito, Giovanni
Arrabito, Giuseppe
Cataldo, Sebastiano
Scopelliti, Michelangelo
Giordano, Carla
Vetri, Valeria
Pignataro, Bruno
Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title_full Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title_fullStr Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title_full_unstemmed Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title_short Aqueous Processed Biopolymer Interfaces for Single-Cell Microarrays
title_sort aqueous processed biopolymer interfaces for single-cell microarrays
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997111/
https://www.ncbi.nlm.nih.gov/pubmed/33463257
http://dx.doi.org/10.1021/acsbiomaterials.9b01871
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