Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa

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Standard

Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa. / Zhang, Qicheng; Zhang, Ming; Huang, Zheng; Sun, Yi; Ye, Lei.

In: ACS Applied Polymer Materials, Vol. 5, No. 4, 2023, p. 3055–3064.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Zhang, Q, Zhang, M, Huang, Z, Sun, Y & Ye, L 2023, 'Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa', ACS Applied Polymer Materials, vol. 5, no. 4, pp. 3055–3064. https://doi.org/10.1021/acsapm.3c00204

APA

Zhang, Q., Zhang, M., Huang, Z., Sun, Y., & Ye, L. (2023). Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa. ACS Applied Polymer Materials, 5(4), 3055–3064. https://doi.org/10.1021/acsapm.3c00204

Vancouver

Zhang Q, Zhang M, Huang Z, Sun Y, Ye L. Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa. ACS Applied Polymer Materials. 2023;5(4):3055–3064. https://doi.org/10.1021/acsapm.3c00204

Author

Zhang, Qicheng ; Zhang, Ming ; Huang, Zheng ; Sun, Yi ; Ye, Lei. / Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa. In: ACS Applied Polymer Materials. 2023 ; Vol. 5, No. 4. pp. 3055–3064.

Bibtex

@article{1378b374960045fe941a7c65ad9ff175,
title = "Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa",
abstract = "Although photothermal therapy is of significance in therapeutic strategies for fighting bacterial infection, the precise target of photothermal agents to bacterial sites is still a challenge. In this work, lipopolysaccharide (LPS) imprinted photothermal molecularly imprinted polymers (PMIP) were prepared for the efficient capture and elimination of Pseudomonas aeruginosa. The LPS derived from Pseudomonas aeruginosa was selected as a template due to its cis-diol structure, which can provide active sites to direct the boronate affinity-mediated synthesis of molecularly imprinted polymers. Polydopamine with good biocompatibility and photothermal effect was used as an imprinting matrix to achieve good photothermal function and imprinting efficiency. The combination of bacteria-imprinting with photothermal ability allowed PMIP to deactivate target bacteria with enhanced precision and efficiency. Taken together, our study offers a promising strategy to design synthetic materials for targeting and treating pathogens for various infectious diseases and expands the application of molecular imprinting technology in the field of antimicrobials.",
keywords = "Bacteria, Boronate affinity, Lipopolysaccharide, Molecular imprinting, Photothermal agent",
author = "Qicheng Zhang and Ming Zhang and Zheng Huang and Yi Sun and Lei Ye",
note = "Funding Information: The authors are grateful for financial support from the Swedish Research Council VR (grant number 2019-04228) and the Novo Nordisk Foundation of Denmark (grant NNF21OC0066562). Q.Z. was awarded a Ph.D. fellowship by the China Scholarship Council. Publisher Copyright: {\textcopyright} 2023 The Authors. Published by American Chemical Society.",
year = "2023",
doi = "10.1021/acsapm.3c00204",
language = "English",
volume = "5",
pages = "3055–3064",
journal = "ACS Applied Polymer Materials",
issn = "2637-6105",
publisher = "American Chemical Society",
number = "4",

}

RIS

TY - JOUR

T1 - Molecularly Imprinted Polymers for Targeting Lipopolysaccharides and Photothermal Inactivation of Pseudomonas aeruginosa

AU - Zhang, Qicheng

AU - Zhang, Ming

AU - Huang, Zheng

AU - Sun, Yi

AU - Ye, Lei

N1 - Funding Information: The authors are grateful for financial support from the Swedish Research Council VR (grant number 2019-04228) and the Novo Nordisk Foundation of Denmark (grant NNF21OC0066562). Q.Z. was awarded a Ph.D. fellowship by the China Scholarship Council. Publisher Copyright: © 2023 The Authors. Published by American Chemical Society.

PY - 2023

Y1 - 2023

N2 - Although photothermal therapy is of significance in therapeutic strategies for fighting bacterial infection, the precise target of photothermal agents to bacterial sites is still a challenge. In this work, lipopolysaccharide (LPS) imprinted photothermal molecularly imprinted polymers (PMIP) were prepared for the efficient capture and elimination of Pseudomonas aeruginosa. The LPS derived from Pseudomonas aeruginosa was selected as a template due to its cis-diol structure, which can provide active sites to direct the boronate affinity-mediated synthesis of molecularly imprinted polymers. Polydopamine with good biocompatibility and photothermal effect was used as an imprinting matrix to achieve good photothermal function and imprinting efficiency. The combination of bacteria-imprinting with photothermal ability allowed PMIP to deactivate target bacteria with enhanced precision and efficiency. Taken together, our study offers a promising strategy to design synthetic materials for targeting and treating pathogens for various infectious diseases and expands the application of molecular imprinting technology in the field of antimicrobials.

AB - Although photothermal therapy is of significance in therapeutic strategies for fighting bacterial infection, the precise target of photothermal agents to bacterial sites is still a challenge. In this work, lipopolysaccharide (LPS) imprinted photothermal molecularly imprinted polymers (PMIP) were prepared for the efficient capture and elimination of Pseudomonas aeruginosa. The LPS derived from Pseudomonas aeruginosa was selected as a template due to its cis-diol structure, which can provide active sites to direct the boronate affinity-mediated synthesis of molecularly imprinted polymers. Polydopamine with good biocompatibility and photothermal effect was used as an imprinting matrix to achieve good photothermal function and imprinting efficiency. The combination of bacteria-imprinting with photothermal ability allowed PMIP to deactivate target bacteria with enhanced precision and efficiency. Taken together, our study offers a promising strategy to design synthetic materials for targeting and treating pathogens for various infectious diseases and expands the application of molecular imprinting technology in the field of antimicrobials.

KW - Bacteria

KW - Boronate affinity

KW - Lipopolysaccharide

KW - Molecular imprinting

KW - Photothermal agent

U2 - 10.1021/acsapm.3c00204

DO - 10.1021/acsapm.3c00204

M3 - Journal article

AN - SCOPUS:85152200521

VL - 5

SP - 3055

EP - 3064

JO - ACS Applied Polymer Materials

JF - ACS Applied Polymer Materials

SN - 2637-6105

IS - 4

ER -

ID: 344707980