2019
DOI: 10.1016/j.reactfunctpolym.2018.11.015
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Antimicrobial coating of textiles by laccase in situ polymerization of catechol and p-phenylenediamine

Abstract: A B S T R A C TTextile fabrics made up of cotton, wool, and polyethylene terephthalate (PET) were coated with poly(catechol) and poly(p-phenylenediamine) through the in situ enzymatic polymerization of catechol and p-phenylenediamine, assisted by laccase under high-pressure homogenization. All coated fabrics showed antimicrobial activity against both gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) strains and revealed antioxidant character, measured in terms of (ABTS •+ )-scavenging … Show more

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Cited by 30 publications
(18 citation statements)
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“…Numerous investigations of textile dye wastewater treatment by laccases were also reported, which is reflected in recent journal publications including immobilized [110][111][112] as well as non-immobilized laccases [60,113]. Apart from wastewater treatment applications, laccases were recently investigated in wool dyeing by the polymerization of syringic acid [114], the antimicrobial coating of textile fibers by polymerization of catechol and p-phenylenediamine [115], the pH-responsive and conducting coating of wool fabrics by the polymerization of diaminobenzenesulfonic acid [116], nylon and wool dyeing by laccase-catalyzed 1,4-dihydroxybenzene, 2,7-dihydroxynapthalene, and 2,5-diaminobenzenesulphonic acid coupling [117].…”
Section: Textiles and Fibersmentioning
confidence: 99%
See 1 more Smart Citation
“…Numerous investigations of textile dye wastewater treatment by laccases were also reported, which is reflected in recent journal publications including immobilized [110][111][112] as well as non-immobilized laccases [60,113]. Apart from wastewater treatment applications, laccases were recently investigated in wool dyeing by the polymerization of syringic acid [114], the antimicrobial coating of textile fibers by polymerization of catechol and p-phenylenediamine [115], the pH-responsive and conducting coating of wool fabrics by the polymerization of diaminobenzenesulfonic acid [116], nylon and wool dyeing by laccase-catalyzed 1,4-dihydroxybenzene, 2,7-dihydroxynapthalene, and 2,5-diaminobenzenesulphonic acid coupling [117].…”
Section: Textiles and Fibersmentioning
confidence: 99%
“…Since then, numerous studies were published, reporting the synthesis of hair dyes [63], phenoxazine derivatives [166], benzene-and naphthalene-derived non-toxic dyes [167], 2,5-diaminobenzenesulfonic acid (2,5-DABSA) and catechol [67] or resorcinol [168] coupling derivatives, several aminoindamine and indoaniline dyes for hair dyeing and cosmetics applications [169], and even a dye for protein gel staining [170]. Moreover, the dyeing of fabrics by the in situ polymerization of phenol and amine compounds has been reported [115,171]. These are also covered in patents dealing with the preparation of paper-based lacquer paintings (CN109627825A), oxygen scavenger coating composition (US2009226996A1), or thermal insulation coatings for exterior walls (CN109735175A)).…”
Section: Paints and Coatingsmentioning
confidence: 99%
“…The resulting colored fabrics presented high levels of coloration with additional conductive properties and good fastness behavior after washing. These fabrics also showed antimicrobial activity against gram‐positive ( Staphylococcus aureus ) and gram‐negative ( Escherichia coli ) microorganisms, and exhibited antioxidant properties in terms of ABTS scavenging activity …”
Section: Laccases As Versatile Enzymes: Traditional and New Industriamentioning
confidence: 99%
“…Applications of laccase-catalyzed in vitro reactions include the laccase/O 2 -mediated syntheses of polymeric (or oligomeric) products from methyl methacrylate or styrene (with acetylacetone as mediator, see Tsujimoto et al, 2001), acrylamide (Ikeda et al, 1998), phenols (Mita et al, 2003; Marjasvaara et al, 2006; Sun et al, 2013; Su et al, 2018a, 2019a), pyrrole (Song and Palmore, 2005; Junker et al, 2015), dopamine (Tan et al, 2010; Li et al, 2018), 3,4-ethylenedioxythiophene (Shumakovich et al, 2012b; Vasil'eva et al, 2018), or various arylamines (Ćirić-Marjanović et al, 2017; Zhang T. et al, 2018; Su et al, 2019a,b). With respect to the latter type of monomers, the focus often was—and still is—on the synthesis of oligo- or polyaniline (PANI) from aniline (Karamyshev et al, 2003; Vasil'eva et al, 2007, 2009; Streltsov et al, 2008, 2009; Shumakovich et al, 2010, 2012a, 2014; Leppänen et al, 2013; Zhang et al, 2014, 2016; Zhang Y. et al, 2018; Junker et al, 2014a; de Salas et al, 2016; Su et al, 2018b) or from p -aminodiphenylamine (PADPA), the linear para N-C-coupled aniline dimer Shumakovich et al, 2011; Junker et al, 2014b; Janoševic Ležaić et al, 2016; Luginbühl et al, 2016; Kashima et al, 2018;Kashima et al, 2019).…”
Section: The Use Of Laccases For In Vitro Oligo-and Polymerization Rementioning
confidence: 99%