Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy

Up to 80% of all infections are biofilm-mediated and they are often challenging to treat as the underlying bacterial cells can become 100- to 1000-fold more tolerant toward antibiotics. Antibiotic-loaded nanoparticles have gained traction as a potential drug delivery system to treat biofilm infectio...

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Main Authors: Lee, Hiang Wee, Kharel, Sharad, Loo, Joachim Say Chye
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/164632
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1646322023-02-11T23:33:49Z Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy Lee, Hiang Wee Kharel, Sharad Loo, Joachim Say Chye School of Materials Science and Engineering Lee Kong Chian School of Medicine (LKCMedicine) Singapore Centre for Environmental Life Sciences and Engineering (SCELSE) Engineering::Materials Engineering::Bioengineering In-Vitro Vancomycin Up to 80% of all infections are biofilm-mediated and they are often challenging to treat as the underlying bacterial cells can become 100- to 1000-fold more tolerant toward antibiotics. Antibiotic-loaded nanoparticles have gained traction as a potential drug delivery system to treat biofilm infections. In particular, lipid-coated hybrid nanoparticles (LCHNPs) were investigated on their capability to deliver antibiotics into biofilms. In this study, LCHNPs composed of a poly(lactic-co-glycolic acid) (PLGA) core and dioleoyl-3-trimethylammonium propane (DOTAP) lipid shell were developed and loaded with vancomycin (Van). In vitro antibacterial and antibiofilm tests were performed to evaluate the antimicrobial efficacy of the LCHNPs. LCHNPs were successfully fabricated with high vancomycin encapsulation and loading efficiencies, and exhibited enhanced antibacterial effects against planktonic Staphylococcus aureus USA300 when compared against Free-Van and Van-PLGANPs. When used to treat USA300 biofilms, Van-LCHNPs eradicated up to 99.99% of the underlying biofilm cells, an effect which was not observed for Free-Van and Van-PLGANPs. Finally, we showed that by possessing a robust DOTAP shell, LCHNPs were able to penetrate deeply into the biofilms. Ministry of Education (MOE) Nanyang Technological University Singapore Food Agency Published version This project was supported by funding from the Singapore Centre of Environmental Life Sciences Engineering (SCELSE) (MOE/RCE: M4330019.C70), Ministry of Education AcRFTier 1 grant (RG19/18 and RT08/19), the Singapore National Biofilm Consortium (SNBC/2021/SF2/P04), and the Singapore Food Agency (SFS_RND_SUFP_001_06). 2023-02-07T02:02:38Z 2023-02-07T02:02:38Z 2022 Journal Article Lee, H. W., Kharel, S. & Loo, J. S. C. (2022). Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy. ACS Omega, 7(40), 35814-35824. https://dx.doi.org/10.1021/acsomega.2c04008 2470-1343 https://hdl.handle.net/10356/164632 10.1021/acsomega.2c04008 36249378 2-s2.0-85139216007 40 7 35814 35824 en MOE/RCE: M4330019.C70 RG19/18 RT08/19 SNBC/2021/SF2/P04 SFS_RND_SUFP_001_06 ACS Omega © 2022 The Authors. Published by American Chemical Society. This is an open-access article distributed under the terms of the Creative Commons Attribution License. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Engineering::Bioengineering
In-Vitro
Vancomycin
spellingShingle Engineering::Materials
Engineering::Bioengineering
In-Vitro
Vancomycin
Lee, Hiang Wee
Kharel, Sharad
Loo, Joachim Say Chye
Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
description Up to 80% of all infections are biofilm-mediated and they are often challenging to treat as the underlying bacterial cells can become 100- to 1000-fold more tolerant toward antibiotics. Antibiotic-loaded nanoparticles have gained traction as a potential drug delivery system to treat biofilm infections. In particular, lipid-coated hybrid nanoparticles (LCHNPs) were investigated on their capability to deliver antibiotics into biofilms. In this study, LCHNPs composed of a poly(lactic-co-glycolic acid) (PLGA) core and dioleoyl-3-trimethylammonium propane (DOTAP) lipid shell were developed and loaded with vancomycin (Van). In vitro antibacterial and antibiofilm tests were performed to evaluate the antimicrobial efficacy of the LCHNPs. LCHNPs were successfully fabricated with high vancomycin encapsulation and loading efficiencies, and exhibited enhanced antibacterial effects against planktonic Staphylococcus aureus USA300 when compared against Free-Van and Van-PLGANPs. When used to treat USA300 biofilms, Van-LCHNPs eradicated up to 99.99% of the underlying biofilm cells, an effect which was not observed for Free-Van and Van-PLGANPs. Finally, we showed that by possessing a robust DOTAP shell, LCHNPs were able to penetrate deeply into the biofilms.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Lee, Hiang Wee
Kharel, Sharad
Loo, Joachim Say Chye
format Article
author Lee, Hiang Wee
Kharel, Sharad
Loo, Joachim Say Chye
author_sort Lee, Hiang Wee
title Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
title_short Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
title_full Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
title_fullStr Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
title_full_unstemmed Lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
title_sort lipid-coated hybrid nanoparticles for enhanced bacterial biofilm penetration and antibiofilm efficacy
publishDate 2023
url https://hdl.handle.net/10356/164632
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