Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/151248
Title: Lipid-polymer hybrid nanoparticles enhance the potency of ampicillin against Enterococcus faecalis in a protozoa infection model
Authors: Tan, Chuan Hao
Jiang, Lai
Li, Wenrui
Chan, Siew Herng
Baek, Jong-Suep
Ng, Noele Kai Jing
Sailov, Talgat
Kharel, Sharad
Chong, Kelvin Kian Long
Loo, Joachim Say Chye
Keywords: Science::Biological sciences::Microbiology::Bacteria
Engineering::Materials::Biomaterials
Issue Date: 2021
Source: Tan, C. H., Jiang, L., Li, W., Chan, S. H., Baek, J., Ng, N. K. J., Sailov, T., Kharel, S., Chong, K. K. L. & Loo, J. S. C. (2021). Lipid-polymer hybrid nanoparticles enhance the potency of ampicillin against Enterococcus faecalis in a protozoa infection model. ACS Infectious Diseases, 7(6), 1607-1618. https://dx.doi.org/10.1021/acsinfecdis.0c00774
Project: Singapore Centre for Environmental Life Sciences Engineering (SCELSE) (MOE/RCE: M4330019.C70)
Ministry of Education AcRF-Tier 1 grant (RG19/18)
Agri-Food & Veterinary Authority of Singapore (APF LCK102)
Biomedical Research Council (BMRC) - Therapeutics Development Review (TDR-G-004-001)
NTU-HSPH grant (NTU-HSPH 17002)
Bill and Melinda Gates Foundation (OPP1199116)
Journal: ACS Infectious Diseases
Abstract: Enterococcus faecalis (E. faecalis) biofilms are implicated in endocarditis, urinary tract infections, and biliary tract infections. Coupled with E. faecalis internalization into host cells, this opportunistic pathogen poses great challenges to conventional antibiotic therapy. The inability of ampicillin (Amp) to eradicate bacteria hidden in biofilms and intracellular niches greatly reduces its efficacy against complicated E. faecalis infections. To enhance the potency of Amp against different forms of E. faecalis infections, Amp was loaded into Lipid-Polymer hybrid Nanoparticles (LPNs), a highly efficient nano delivery platform consisting of a unique combination of DOTAP lipid shell and PLGA polymeric core. The antibacterial activity of these nanoparticles (Amp-LPNs) was investigated in a protozoa infection model, achieving a much higher multiplicity of infection (MOI) compared with studies using animal phagocytes. A significant reduction of total E. faecalis was observed in all groups receiving 250 µg/mL Amp-LPNs compared with groups receiving the same concentration of free Amp during three different interventions, simulating acute and chronic infections and prophylaxis. In early intervention, no viable E. faecalis was observed after 3 h LPNs treatment whereas free Amp did not clear E. faecalis after 24 h treatment. Amp-LPNs also greatly enhanced the antibacterial activity of Amp at late intervention, and boosted the survival rate of protozoa approaching 400%, where no viable protozoa were identified in the free Amp groups at the 40 h post-infection treatment timepoint. Prophylactic effectiveness with Amp-LPNs at a concentration of 250 μg/mL was exhibited in both bacteria elimination and protozoa survival towards subsequent infections. Using protozoa as a surrogate model for animal phagocytes to study high MOI infections, this study suggests that LPN-formulated antibiotics hold the potential to significantly improve the therapeutic outcome in highly complicated bacterial infections.
URI: https://hdl.handle.net/10356/151248
ISSN: 2373-8227
DOI: 10.1021/acsinfecdis.0c00774
DOI (Related Dataset): https://doi.org/10.21979/N9/OIUE5O
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Infectious Diseases, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsinfecdis.0c00774
Fulltext Permission: embargo_20220421
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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