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Jiayang Xie

Researcher at East China University of Science and Technology

Publications -  26
Citations -  667

Jiayang Xie is an academic researcher from East China University of Science and Technology. The author has contributed to research in topics: Antimicrobial & Chemistry. The author has an hindex of 7, co-authored 18 publications receiving 275 citations.

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Poly(2-Oxazoline)-Based Functional Peptide Mimics: Eradicating MRSA Infections and Persisters while Alleviating Antimicrobial Resistance.

TL;DR: This study demonstrated that poly(2-oxazoline) based glycine pseudopeptides can mimic host defense peptide and have potent in vitro and in vivo activities against methicillin-resistant Staphylococcus aureus that cause formidable infections.
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Host defense peptide mimicking poly-β-peptides with fast, potent and broad spectrum antibacterial activities

TL;DR: It is demonstrated that random copolymers of heterochiral poly-β-peptides, without the need for defined secondary structures, can mimic the antimicrobial HDP, implying the potential application of these poly- β-peptic as new antimicrobial agents to tackle drug resistant antimicrobial infections.
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Addressing MRSA infection and antibacterial resistance with peptoid polymers

TL;DR: In this paper, a ring-opening polymerization of N-substituted N-carboxyanhydrides (NNCA) was used to obtain peptoid polymers with variable C-terminal functional groups.
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Practical Preparation of Infection-Resistant Biomedical Surfaces from Antimicrobial β-Peptide Polymers.

TL;DR: In vivo study using methicillin-resistant Staphylococcus aureus-pre-incubated TPU-50:50 DM-Hex surfaces for subcutaneous implantation revealed a 3.4-log reduction of MRSA cells after the implantation for 11 days at the surrounding tissue of implanted TPU sheet and significant suppression of infection, compared to bare TPU control.
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Peptide polymer displaying potent activity against clinically isolated multidrug resistant Pseudomonas aeruginosa in vitro and in vivo

TL;DR: A 27-mer peptide polymer is reported, as a synthetic mimic of a host defense peptide, that displayed potent in vitro and in vivo activities against multiple strains of clinically isolated MDR Pseudomonas aeruginosa, performing even better than antibiotics within this study.