Issue 39, 2024

Aggregation-induced emission silence-mediated pathogen detection using a rapidly degradable nanographene-embedded polymersome

Abstract

Typical pathogen detection processes are time-consuming and require expensive equipment and professional operators, limiting their practical applicability. Developing a rapid and easy-to-read method of accurately sensing pathogenic bacteria is critical for reducing the spread and risk of infection in high-risk areas. Herein, the synthesis of nanographene (nanoG) that exhibits aggregation-induced emission (AIE) is described. The nanoG was embedded into a hydrophobic shell of poly(lactic-co-glycolic acid) (PLGA) polymersome in a double-emulsion process, significantly enhancing the nanoG luminescence under irradiation at 330 nm due to the enrichment of nanoG between the inner and outer PLGA shells. Both Gram-positive and Gram-negative bacteria can rapidly degrade the PLGA vesicular structure, leading to dispersal of the nanoG inside the shell and silencing the AIE effect. A linear relationship between the bacterial concentration and emissivity was established, and the detection limit was identified. Moreover, the polymersome has excellent selectivity for methicillin-resistant Staphylococcus aureus (MRSA) detection after a screening pretreatment of a bacterial mixture with suitable antibiotics. The AIE silencing could be observed with the naked eye in an MRSA-infected wound treated with the polymersome after 1 h of incubation, demonstrating a high potential for clinical rapid screening applications.

Graphical abstract: Aggregation-induced emission silence-mediated pathogen detection using a rapidly degradable nanographene-embedded polymersome

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Article information

Article type
Paper
Submitted
25 Jun 2024
Accepted
02 Sep 2024
First published
04 Sep 2024

J. Mater. Chem. B, 2024,12, 10028-10040

Aggregation-induced emission silence-mediated pathogen detection using a rapidly degradable nanographene-embedded polymersome

C. Cheng, E. V. Varghese, W. Wang, C. Yao, C. Chen and W. Li, J. Mater. Chem. B, 2024, 12, 10028 DOI: 10.1039/D4TB01379D

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