EVALUATION OF ANTIMICROBIAL ACTIVITY OF A POLYHEXAMETHYLENE BIGUANIDE-COATED TEXTILE BY MONITORING BOTH BACTERIAL GROWTH (ISO 20743/2005 STANDARD) AND VIABILITY (LIVE/DEAD BACLIGHT KIT)

Antimicrobial textiles (65% cotton – 35% polyester) were functionalized using a patented technology that combines an antimicrobial molecule – polyhexamethylene biguanide (PHMB) and a precipitating agent – sodium laurylsulphate. Surface characterization was performed by x-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry, and both techniques made clear signatures of PHMB at the top surface of treated textiles. Washing led to a strong decrease of PHMB concentration at the surface. Comparison of textile surface analysis and antimicrobial tests indicated that the amount of PHMB at its extreme surface of textiles after five or 10 industrial washings was sufficient to inhibit Listeria innocua but not Pseudomonas aeruginosa growth. The viability of L. innocua cells after contact with PHMB-treated textile after one industrial washing was estimated using the Live/Dead BacLight kit (Molecular Probes, Eugene, OR): the combination of epifluorescence microscopy observations coupled with classic enumeration allowed detection of the presence of viable but nonculturable cells. PRACTICAL APPLICATIONS Protective clothing is required in the food-processing industry to protect products from being contaminated by microorganisms carried by workers' clothes or filtration systems. Consequently, there is an increasing interest in the use of antimicrobial functionalized textiles in the food industry to avoid that textiles could be vectors for pathogenic or food spoilage microorganisms. In the present study, the correlation between PHMB (the antimicrobial agent) at the surface of textiles (monitored by surface analysis characterization methods) and their antibacterial activity was assessed. After contact with antimicrobial textiles, the enumeration of bacteria was performed either by plate counting or by direct observation by epifluorescence microscopy in the presence of fluorescent viability markers in order to determine whether viable but nonculturable bacterial cells were present.