Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells
This study aimed to address the significant problems of bacterial biofilms found in medical fields and many industries. It explores the potential of classic photoactive carbon dots (CDots), with 2,2′-(ethylenedioxy)bis (ethylamine) (EDA) for dot surface functionalization (thus, EDA-CDots) for their...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:59a68286620643329094da7002ef3d9c2021-11-18T07:26:36ZVisible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells2296-418510.3389/fbioe.2021.786077https://doaj.org/article/59a68286620643329094da7002ef3d9c2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fbioe.2021.786077/fullhttps://doaj.org/toc/2296-4185This study aimed to address the significant problems of bacterial biofilms found in medical fields and many industries. It explores the potential of classic photoactive carbon dots (CDots), with 2,2′-(ethylenedioxy)bis (ethylamine) (EDA) for dot surface functionalization (thus, EDA-CDots) for their inhibitory effect on B. subtilis biofilm formation and the inactivation of B. subtilis cells within established biofilm. The EDA-CDots were synthesized by chemical functionalization of selected small carbon nanoparticles with EDA molecules in amidation reactions. The inhibitory efficacy of CDots with visible light against biofilm formation was dependent significantly on the time point when CDots were added; the earlier the CDots were added, the better the inhibitory effect on the biofilm formation. The evaluation of antibacterial action of light-activated EDA-CDots against planktonic B. subtilis cells versus the cells in biofilm indicate that CDots are highly effective for inactivating planktonic cells but barely inactivate cells in established biofilms. However, when coupling with chelating agents (e.g., EDTA) to target the biofilm architecture by breaking or weakening the EPS protection, much enhanced photoinactivation of biofilm-associated cells by CDots was achieved. The study demonstrates the potential of CDots to prevent the initiation of biofilm formation and to inhibit biofilm growth at an early stage. Strategic combination treatment could enhance the effectiveness of photoinactivation by CDots to biofilm-associated cells.Xiuli DongChristopher M. OvertonYongan TangJasmine P. DarbyYa-Ping SunLiju YangFrontiers Media S.A.articlebiofilmcarbon dotsinactivationinhibitionphotoactiveBiotechnologyTP248.13-248.65ENFrontiers in Bioengineering and Biotechnology, Vol 9 (2021) |
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biofilm carbon dots inactivation inhibition photoactive Biotechnology TP248.13-248.65 |
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biofilm carbon dots inactivation inhibition photoactive Biotechnology TP248.13-248.65 Xiuli Dong Christopher M. Overton Yongan Tang Jasmine P. Darby Ya-Ping Sun Liju Yang Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
description |
This study aimed to address the significant problems of bacterial biofilms found in medical fields and many industries. It explores the potential of classic photoactive carbon dots (CDots), with 2,2′-(ethylenedioxy)bis (ethylamine) (EDA) for dot surface functionalization (thus, EDA-CDots) for their inhibitory effect on B. subtilis biofilm formation and the inactivation of B. subtilis cells within established biofilm. The EDA-CDots were synthesized by chemical functionalization of selected small carbon nanoparticles with EDA molecules in amidation reactions. The inhibitory efficacy of CDots with visible light against biofilm formation was dependent significantly on the time point when CDots were added; the earlier the CDots were added, the better the inhibitory effect on the biofilm formation. The evaluation of antibacterial action of light-activated EDA-CDots against planktonic B. subtilis cells versus the cells in biofilm indicate that CDots are highly effective for inactivating planktonic cells but barely inactivate cells in established biofilms. However, when coupling with chelating agents (e.g., EDTA) to target the biofilm architecture by breaking or weakening the EPS protection, much enhanced photoinactivation of biofilm-associated cells by CDots was achieved. The study demonstrates the potential of CDots to prevent the initiation of biofilm formation and to inhibit biofilm growth at an early stage. Strategic combination treatment could enhance the effectiveness of photoinactivation by CDots to biofilm-associated cells. |
format |
article |
author |
Xiuli Dong Christopher M. Overton Yongan Tang Jasmine P. Darby Ya-Ping Sun Liju Yang |
author_facet |
Xiuli Dong Christopher M. Overton Yongan Tang Jasmine P. Darby Ya-Ping Sun Liju Yang |
author_sort |
Xiuli Dong |
title |
Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
title_short |
Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
title_full |
Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
title_fullStr |
Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
title_full_unstemmed |
Visible Light-Activated Carbon Dots for Inhibiting Biofilm Formation and Inactivating Biofilm-Associated Bacterial Cells |
title_sort |
visible light-activated carbon dots for inhibiting biofilm formation and inactivating biofilm-associated bacterial cells |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/59a68286620643329094da7002ef3d9c |
work_keys_str_mv |
AT xiulidong visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells AT christophermoverton visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells AT yongantang visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells AT jasminepdarby visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells AT yapingsun visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells AT lijuyang visiblelightactivatedcarbondotsforinhibitingbiofilmformationandinactivatingbiofilmassociatedbacterialcells |
_version_ |
1718423409248960512 |