Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion

Dip-pen nanolithography (DPN) and soft lithography are techniques suitable to modify the surface of biomaterials. Modified surfaces might play a role in modulating cells and reducing bacterial adhesion and biofilm formation. The main objective of this study was threefold: first, to create patterns a...

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Main Authors: Santiago Arango-Santander, Alejandro Pelaez-Vargas, Sidónio C. Freitas, Claudia García
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Nanotechnology
Online Access:http://dx.doi.org/10.1155/2018/8624735
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author Santiago Arango-Santander
Alejandro Pelaez-Vargas
Sidónio C. Freitas
Claudia García
author_facet Santiago Arango-Santander
Alejandro Pelaez-Vargas
Sidónio C. Freitas
Claudia García
author_sort Santiago Arango-Santander
collection DOAJ
description Dip-pen nanolithography (DPN) and soft lithography are techniques suitable to modify the surface of biomaterials. Modified surfaces might play a role in modulating cells and reducing bacterial adhesion and biofilm formation. The main objective of this study was threefold: first, to create patterns at microscale on model surfaces using DPN; second, to duplicate and transfer these patterns to a real biomaterial surface using a microstamping technique; and finally, to assess bacterial adhesion to these developed patterned surfaces using the cariogenic species Streptococcus mutans. DPN was used with a polymeric adhesive to create dot patterns on model surfaces. Elastomeric polydimethylsiloxane was used to duplicate the patterns and silica sol to transfer them to the medical grade stainless steel 316L surface by microstamping. Optical microscopy and atomic force microscopy (AFM) were used to characterize the patterns. S. mutans adhesion was assessed by colony-forming units (CFUs), MTT viability assay, and scanning electron microscopy (SEM). DPN allowed creating microarrays from 1 to 5 µm in diameter on model surfaces that were successfully transferred to the stainless steel 316L surface via microstamping. A significant reduction up to one order of magnitude in bacterial adhesion to micropatterned surfaces was observed. The presented experimental approach may be used to create patterns at microscale on a surface and transfer them to other surfaces of interest. A reduction in bacterial adhesion to patterned surfaces might have a major impact since adhesion is a key step in biofilm formation and development of biomaterial-related infections.
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spelling doaj-art-78885939e5f8471cb8e7f0f68af9c85a2025-02-03T01:28:04ZengWileyJournal of Nanotechnology1687-95031687-95112018-01-01201810.1155/2018/86247358624735Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial AdhesionSantiago Arango-Santander0Alejandro Pelaez-Vargas1Sidónio C. Freitas2Claudia García3GIOM Group, School of Dentistry, Universidad Cooperativa de Colombia, Carrera 47 # 37 sur 18, Envigado, ColombiaGIOM Group, School of Dentistry, Universidad Cooperativa de Colombia, Carrera 47 # 37 sur 18, Envigado, ColombiaGIOM Group, School of Dentistry, Universidad Cooperativa de Colombia, Carrera 47 # 37 sur 18, Envigado, ColombiaCerámicos y Vítreos Group, School of Physics, Universidad Nacional de Colombia, Calle 59 A # 63-20, Medellín, ColombiaDip-pen nanolithography (DPN) and soft lithography are techniques suitable to modify the surface of biomaterials. Modified surfaces might play a role in modulating cells and reducing bacterial adhesion and biofilm formation. The main objective of this study was threefold: first, to create patterns at microscale on model surfaces using DPN; second, to duplicate and transfer these patterns to a real biomaterial surface using a microstamping technique; and finally, to assess bacterial adhesion to these developed patterned surfaces using the cariogenic species Streptococcus mutans. DPN was used with a polymeric adhesive to create dot patterns on model surfaces. Elastomeric polydimethylsiloxane was used to duplicate the patterns and silica sol to transfer them to the medical grade stainless steel 316L surface by microstamping. Optical microscopy and atomic force microscopy (AFM) were used to characterize the patterns. S. mutans adhesion was assessed by colony-forming units (CFUs), MTT viability assay, and scanning electron microscopy (SEM). DPN allowed creating microarrays from 1 to 5 µm in diameter on model surfaces that were successfully transferred to the stainless steel 316L surface via microstamping. A significant reduction up to one order of magnitude in bacterial adhesion to micropatterned surfaces was observed. The presented experimental approach may be used to create patterns at microscale on a surface and transfer them to other surfaces of interest. A reduction in bacterial adhesion to patterned surfaces might have a major impact since adhesion is a key step in biofilm formation and development of biomaterial-related infections.http://dx.doi.org/10.1155/2018/8624735
spellingShingle Santiago Arango-Santander
Alejandro Pelaez-Vargas
Sidónio C. Freitas
Claudia García
Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
Journal of Nanotechnology
title Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
title_full Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
title_fullStr Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
title_full_unstemmed Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
title_short Surface Modification by Combination of Dip-Pen Nanolithography and Soft Lithography for Reduction of Bacterial Adhesion
title_sort surface modification by combination of dip pen nanolithography and soft lithography for reduction of bacterial adhesion
url http://dx.doi.org/10.1155/2018/8624735
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