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Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface

Investigating the interaction patterns at nano-bio interface is a key challenge for safe use of nanoparticles (NPs) to any biological system. The study intends to explore the role of interaction pattern at the iron oxide nanoparticle (IONP)-bacteria interface affecting antimicrobial propensity of IO...

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Autores principales: Arakha, Manoranjan, Pal, Sweta, Samantarrai, Devyani, Panigrahi, Tapan K., Mallick, Bairagi C., Pramanik, Krishna, Mallick, Bibekanand, Jha, Suman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594095/
https://www.ncbi.nlm.nih.gov/pubmed/26437582
http://dx.doi.org/10.1038/srep14813
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author Arakha, Manoranjan
Pal, Sweta
Samantarrai, Devyani
Panigrahi, Tapan K.
Mallick, Bairagi C.
Pramanik, Krishna
Mallick, Bibekanand
Jha, Suman
author_facet Arakha, Manoranjan
Pal, Sweta
Samantarrai, Devyani
Panigrahi, Tapan K.
Mallick, Bairagi C.
Pramanik, Krishna
Mallick, Bibekanand
Jha, Suman
author_sort Arakha, Manoranjan
collection PubMed
description Investigating the interaction patterns at nano-bio interface is a key challenge for safe use of nanoparticles (NPs) to any biological system. The study intends to explore the role of interaction pattern at the iron oxide nanoparticle (IONP)-bacteria interface affecting antimicrobial propensity of IONP. To this end, IONP with magnetite like atomic arrangement and negative surface potential (n-IONP) was synthesized by co-precipitation method. Positively charged chitosan molecule coating was used to reverse the surface potential of n-IONP, i.e. positive surface potential IONP (p-IONP). The comparative data from fourier transform infrared spectroscope, XRD, and zeta potential analyzer indicated the successful coating of IONP surface with chitosan molecule. Additionally, the nanocrystals obtained were found to have spherical size with 10–20 nm diameter. The BacLight fluorescence assay, bacterial growth kinetic and colony forming unit studies indicated that n-IONP (<50 μM) has insignificant antimicrobial activity against Bacillus subtilis and Escherichia coli. However, coating with chitosan molecule resulted significant increase in antimicrobial propensity of IONP. Additionally, the assay to study reactive oxygen species (ROS) indicated relatively higher ROS production upon p-IONP treatment of the bacteria. The data, altogether, indicated that the chitosan coating of IONP result in interface that enhances ROS production, hence the antimicrobial activity.
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spelling pubmed-45940952015-10-13 Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface Arakha, Manoranjan Pal, Sweta Samantarrai, Devyani Panigrahi, Tapan K. Mallick, Bairagi C. Pramanik, Krishna Mallick, Bibekanand Jha, Suman Sci Rep Article Investigating the interaction patterns at nano-bio interface is a key challenge for safe use of nanoparticles (NPs) to any biological system. The study intends to explore the role of interaction pattern at the iron oxide nanoparticle (IONP)-bacteria interface affecting antimicrobial propensity of IONP. To this end, IONP with magnetite like atomic arrangement and negative surface potential (n-IONP) was synthesized by co-precipitation method. Positively charged chitosan molecule coating was used to reverse the surface potential of n-IONP, i.e. positive surface potential IONP (p-IONP). The comparative data from fourier transform infrared spectroscope, XRD, and zeta potential analyzer indicated the successful coating of IONP surface with chitosan molecule. Additionally, the nanocrystals obtained were found to have spherical size with 10–20 nm diameter. The BacLight fluorescence assay, bacterial growth kinetic and colony forming unit studies indicated that n-IONP (<50 μM) has insignificant antimicrobial activity against Bacillus subtilis and Escherichia coli. However, coating with chitosan molecule resulted significant increase in antimicrobial propensity of IONP. Additionally, the assay to study reactive oxygen species (ROS) indicated relatively higher ROS production upon p-IONP treatment of the bacteria. The data, altogether, indicated that the chitosan coating of IONP result in interface that enhances ROS production, hence the antimicrobial activity. Nature Publishing Group 2015-10-06 /pmc/articles/PMC4594095/ /pubmed/26437582 http://dx.doi.org/10.1038/srep14813 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Arakha, Manoranjan
Pal, Sweta
Samantarrai, Devyani
Panigrahi, Tapan K.
Mallick, Bairagi C.
Pramanik, Krishna
Mallick, Bibekanand
Jha, Suman
Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title_full Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title_fullStr Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title_full_unstemmed Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title_short Antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
title_sort antimicrobial activity of iron oxide nanoparticle upon modulation of nanoparticle-bacteria interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594095/
https://www.ncbi.nlm.nih.gov/pubmed/26437582
http://dx.doi.org/10.1038/srep14813
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