Immobilization of bacteriophage in wound-dressing nanostructure

被引:58
作者
Nogueira, Frederico [1 ,2 ]
Karumidze, Natia [3 ]
Kusradze, Ia [3 ]
Goderdzishvili, Marina [3 ]
Teixeira, Pilar [4 ]
Gouveia, Isabel C. [2 ]
机构
[1] Univ Beira Interior, CICS UBI Hlth Sci Res Ctr, Covilha, Portugal
[2] Univ Beira Interior, FibEnTech Fiber Mat & Environm Technol, Covilha, Portugal
[3] G Eliava Inst Bacteriophages Microbiol & Virol, Tbilisi, Georgia
[4] IBB, Lisbon, Portugal
关键词
Bacteriophages; Antimicrobial agents; Surface immobilization; Electrospinning; Pseudomonas aeruginosa; ATOPIC-DERMATITIS; PROTEIN-STRUCTURE; I-TASSER; SURFACES; ALTERNATIVES; COMBINATION; TEXTILES; EFFICACY; CHITOSAN; THERAPY;
D O I
10.1016/j.nano.2017.08.008
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Opportunistic bacteria that cause life-threatening infections are still a central problem associated with a healthcare setting. Bacteriophage capsid immobilization on nanostructured polymers maximizes its tail exposure and looks promising in applications toward skin-infections as alternative to antibiotics standardly used. The main goal of this work was to investigate the covalent immobilization of vB_Pae_Kakheti25 bacteriophage capsid on polycaprolactone (PCL) nanofibers (non-woven textile), as a potential effective antimicrobial, laundry resistant and non-toxic dressing for biomedical use. Surface analyses showed that the immobilization of vB_Pae_Kakheti25 bacteriophage capsid on PCL nanofibres oriented bacteriophage tails to interact with bacteria. Furthermore, antimicrobial assays showed a very effective 6 log bacterial reduction, which was equivalent to 99.9999%, after immediate and 2 hours of contact, even following 25 washing cycles (due to covalent bond). The activity of PCL-vB_Pae_Kakheti25 against P. aeruginosa was immediate and its reduction was complete. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:2475 / 2484
页数:10
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