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Article

Development of Durable Antibacterial Textile Fabrics for Potential Application in Healthcare Environment

1
Institute of Textiles and Clothing, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China
2
Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China
*
Author to whom correspondence should be addressed.
Coatings 2020, 10(6), 520; https://doi.org/10.3390/coatings10060520
Submission received: 17 April 2020 / Revised: 20 May 2020 / Accepted: 27 May 2020 / Published: 29 May 2020
(This article belongs to the Special Issue Surface Treatment of Textiles)

Abstract

:
Recently, efforts at development of functional textiles with antibacterial effect have accelerated, the purpose being to provide protection against airborne bio-particles and micro-organisms. Growth of microbes on surface of textile materials can be inhibited by biocidal approach and biostatic approach. This paper describes the development of a healthcare textile with durable antibacterial properties by optimizing the conventional and commercialized antimicrobial agent polybiguanide derivative—poly(hexamethylenebiguanide) (PHMB). Pad-dry-cure method was used to coat PHMB on cotton fabrics. The durability to simulated healthcare laundering of the fabric samples was evaluated in detail. Specifically, effects of detergent and washing cycles were examined. It was found that the optimum finishing condition can impart to the fabrics excellent durability for simulated healthcare washing. The fabric samples showed 100% bactericidal effect after 52 washing cycles, and 104 washings slightly reduced the bactericidal activity. Nevertheless, both simulated healthcare washing and coating treatment were found to have slightly negative influence on the hand feel and tearing strength properties of cotton fabrics.

1. Introduction

Cotton is a green natural cellulosic fiber available abundantly. It has been widely used in daily life because of its favorable properties that include high strength, soft handle, affinity to skin, and bio-degradability [1,2]. However, due to the morphology and moisture affinity of natural origin, cotton fabrics provide a perfect environment for growth of microorganism on the surface [3]. Depending on moisture, nutrients, temperature and pH value, the bacterial growth can be very fast, which may cause some undesirable effects, such as unpleasant odor, reduction of mechanical strength, stains, and discoloration [1,4]. Even mild bacterial growth can lead to rotting and breakdown of the fibers, which may make the fabric unattractive due to the appearance of unwanted pigmentation. Moreover, the microorganism’s growth can accelerate the hydrolysis of cellulose and cause deterioration of the fabric.
Microorganisms that frequently contaminate surface of cotton fabrics include Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphylococcus aureus, and Acinetobacter baumannii. These can cause pathogenic effects on human beings due to user contamination and cross infection [5,6]. Therefore, it is of great concern for the textile industry to develop antibacterial textiles. The demand for antibacterial textiles has been gaining increasing attention in the past few decades [7,8]. In healthcare environment, textiles with antibacterial properties form a significant part of the hygienic regime of surgical procedures, preventing the spread of infectious pathogens to both patients and staff. Antibacterial finishing is thus typically carried out to give textiles improved resilience against microorganisms to prevent destruction of fibers and discoloration, and increased durability of the textiles with longer life, which plays an important role in addressing hygiene in clinical and sensitive environments by minimizing microbial colonization of textiles and the potential for transfer from fabric surfaces [9,10,11].
In this context, numerous methods have been developed to impart antibacterial properties to textiles to reduce the spread of microorganisms by killing or inhibiting their growth on the fabric surface, e.g., surface modification and finishing [3,12]. Gao and Cranston reviewed the application of various antibacterial agents to impart textiles with antimicrobial functions [3]. For examples, the conventional exhaust, pad-dry-cure processes, spraying and foam finishing method have been extensively studied for the antimicrobial finishing on textiles with triclosan and silicon-based quaternary agents [13,14]. Meanwhile, use of a wide variety of antibacterial agents in fabric finishing has been widely investigated, ranging from synthetic organic compounds, such as quaternary ammonium salt [9,15], polybiguanides [16,17], and N-halamines [18], through to TiO2, ZnO, and silver nanoparticles [6,10,19] and naturally derived antimicrobials, such as chitosan [20]. Recently, the combination of antibacterial and hydrophobicity for cotton fabric has attracted much interest for better antibacterial behavior. For example, Mohammad and colleagues developed such a dual-functional antibacterial textile by immobilizing silver nanoparticles as the antibacterial agent and then modified it with octyltriethoxysilane (OTES) to achieve the hydrophobic surface [21]. Thirumalaisamy et al. explored the method of bimetallic deposition to obtain superhydrophobic and antibacterial cotton fabric [22]. Recently, some novel methods of antibacterial finishing have been reported. In this regard, Poonam and coworkers fabricated a dual-functional cotton fabric with superhydrophobicity and antibacterial property by simply immersing cotton fabric in non-fluorinated hexadecyltrimethoxysilane solution [23]. The modified cotton fabric not only shows excellent antibacterial property, but also has outstanding oil-water separation efficiency. Another example is the environmentally friendly antibacterial cotton fabric reported by Chen et al. [24], which was finished with siloxane sulfopropylbetaine (SSPB). SSPB was found not to be leachable from the fabric and the coated fabric is nontoxic to skin. Rong et al. reported the method of heterogeneous transesterification to develop hydrophobic and antibacterial cotton fabric via constructing enamine bonds between acetoacetyl groups and cotton fiber [1]. The resulting material showed excellent and durable bacteria-resistance rates of over 99.99% against E. coli and S. aureus. Additionally, novel graphene oxide based antibacterial cotton fabric has also been reported and extensively investigated by Zhao and his colleagues [25]. However, although these attempts are highly meaningful and of importance for academia, there are still a long way from large-scale industrial production.
Polyhexamethylene biguanide (PHMB) is a widely used polymeric antibacterial agent due to its low toxicity and broad-spectrum biocide property, which has been commercially available in the market [15,26]. It is usually used as a biocide, and is also an important drug used in several topical applications. PHMB is composed of repeated basic biguanidine units connected by hexamethylene hydrocarbon chains, providing a cationic and amphipathic structure (Figure 1). The antibacterial activity of PHMB depends on the molecular structure, which increases with the level of polymerization, and the maximum biocidal efficiency is obtained when the hexamethylene group is employed as the spacer [16]. Biguanides in the PHMB molecules account for the inhibition and binding activities of PHMB.
However, a major concern for PHMB coating on fabric surface consists in the compromised tearing strength and hand feel values. The present study is thus focusing not only on the antibacterial behavior and durability, but also on the physical properties of cotton fiber after coating with PHMB formulation. The resulting cotton fabrics were subjected to detailed characterization by using a series of analytical techniques, including hand feel measurement and tearing strength.

2. Materials and Methods

2.1. Materials

One hundred percentwoven cotton fabric (fabric weight 272.8 g/cm2) was used in this study. Originally, the fabric was scoured in an aqueous solution containing 5 g/L sodium hydroxide (chemical grade, obtained from Sigma-Aldrich, St. Louis, MO, USA) to remove impurities at temperature of 60 °C for 30 min, after which it was thoroughly rinsed with tap water and dried at room temperature.
Antibacterial agent PHMB (20% w/v aqueous solution), PEG400 (400 g/mol in average) and polyurethane binder (20% w/v aqueous solution) were supplied by Breakthrough Textiles Co., LTD. (Taipei, Taiwan). The commercial detergent (Attack, concentrated liquid, 3 L, Kao (HK) Corp., Tokyo, Japan) was obtained from a local supermarket. Non-ionic detergent, C13 Oxoalcoholethoxylate (7EO), was obtained from SDC Enterprises Limited, Holmfirth, UK. Sodium hypochlorite (NaClO) and bromophenol blue (BPB) sodium were obtained from Sigma-Aldrich (St. Louis, MO, USA).

2.2. Pad-Dry-Cure Treatment

Finishing formulations were prepared by adding different amounts of PHMB, PEG400, and binder to deionized water, and the “pad-dry-cure” method was used to coat the antibacterial agent on the cotton fabric. Specifically, the fabric sample was first padded with finishing formulations with 80% wet pickup and then dried in thermal oven (Werner Mathis AG, Switzerland) at 90 °C for 5 min and cured in Mathis LabDryer (Werner Mathis AG, Switzerland) at 130 °C for 45 s with fan speed of 1600 rpm. After antibacterial finishing, fabric samples were stored under standard conditions at 20 ± 2 temperature and 65 ± 2% relative humidity for at least 24 h prior to subsequent testing.

2.3. Washing Test

Washing test was conducted to evaluate effects of simulated healthcare laundering on antibacterial property of coated fabric samples. Different washing conditions with three washing cycles (26/52/104) were used (Table 1). The test was conducted in a laboratory scale washing machine (Launder-Ometer, SDL Atlas, Rock Hill, SC, USA). After each washing cycle, the fabric sample was withdrawn and washed with tap water, and then the same volume of washing bath was added for the next cycle. Bleaching agent sodium hypochlorite (NaClO) was used in the washing solution.

2.4. Antibacterial Property

Antibacterial property of treated samples was qualitatively investigated against gram-positive S. aureus and gram-negative K. pneumoniae according to AATCC TM 147-2011, and the quantitative determination was performed in accordance with AATCC TM100-2019. The bacteria was grown in nutrient agar at 37 °C for 18 h. Fabric samples were cut into 20 mm × 20 mm pieces for the antibacterial test.

2.5. Scanning Electron Microscopy (SEM) Observation

Surface morphology of the fabric samples was observed by SEM (JEOL Model JSM-6490, JEOL USA, Inc., Peabody, MA, USA) with imaging up to 300,000× with a high resolution of 3 nm. The samples were treated by spray-gold prior to observation.

2.6. Qualitative Determination of PHMB by Dyeing with BPB

The anion of the aqueous sodium salt of BPB can be complexed with the cationic polymers on a substrate, leading to formation of a blue stable complex, which provides a standard method to determine cationic polymers [27,28]. The present study utilizes BPB to qualitatively determine the presence of PHMB coated on the fabrics.

2.7. Fourier Transform Infrared Spectroscopy Analysis

The physiochemical properties of PHMB-coated cotton fabric were analyzed via Fourier transform infrared spectroscopy (FTIR, Spectrum 100 FT-IR Spectrometer, Perkin Elmer, Waltham, MA, USA). The fabric samples were fastened on the sample stage and scanned from 400 cm−1 to 4000 cm−1 with a resolution of 4 cm−1.

2.8. Tearing Strength Analysis

Tearing strength of fabric samples before and after PHMB coating was measured by Elmendorf Tear Strength Tester according to American Society for Testing and Materials (ASTM) D2261 standard. Three specimens (200 mm × 75 mm) were measured for each sample.

2.9. Hand Feel Measurement

The hand feel value was analyzed by the PhabrOmeter instrument (Nu Cybertec, Inc., Davis, CA, USA) according to AATCC Test Method 202-2014. For the purpose of discussion, hand feel index (HFI) is defined as summation of resilience, softness, and smoothness, as shown in Equation (1).
HFI = Resilience + Softness + Smoothness.

3. Results

3.1. Surface Morphology

Optical photographs and SEM were performed to observe the change in surface morphology of the fabric samples after coating with PHMB formulation. Clearly, the surface of cotton fabric was smooth (Figure 2A). From Figure 2B, the coated PHMB was obviously observed, and BPB dyeing confirms that antibacterial agent PHMB was successfully coated on the surface of the cotton fabric (Figure 2D).

3.2. FTIR Measuremnt

FTIR analysis was conducted to confirm the presence of PHMB on the treated cotton fabric, as shown in Figure 3. A sharp and strong absorbance peak at 1550 cm−1 was observed in the spectrum of PHMB, characteristic of imine group. The broad double peaks at 3195 cm−1 and 3380 cm−1 are ascribed to stretching vibration of –NH- and –NH2- of PHMB molecule. Compared to PHMB, the absorption spectrum of cellulose is pretty weak, particularly for the untreated control cotton fabric. As shown in the insert, the characteristic peak of cellulose at 3330 cm−1 becomes stronger after coating with PHMB, which demonstrates that PHMB was successfully coated on the cotton fabric.

3.3. Effect of Concentration of PHMB on Antibacterial Activity

In order to explore effects of PHMB on the antibacterial activity, different concentrations were further studied (Figure 4). It can be clearly seen that all the samples treated with different amounts of PHMB show strong inhibition against S. aureus and K. pneumonia. Table 2 shows that the concentration of PHMB had a significantly positive relationship with antibacterial activity. It is noteworthy that the antibacterial activity for concentration of 2.5 and 5% was not significant. A significant antibacterial ability was seen for concentrations of 10 and 15%, however.

3.4. Effect of Detergent on Antibacterial Activity

In practical application, medical textiles are inevitably subjected to simulated healthcare laundering. Frequent laundering generally has a serious negative influence on the antibacterial activity of the treated fabric. Therefore, durability against laundering is of high importance for medical textiles. This study is thus focused on the effect of healthcare laundering washing on the antibacterial ability. Firstly, we studied the effect of commercial detergent on antibacterial activity against S. aureus of treated fabric samples. The fabric sample used in this experiment was not treated with PHMB, but was just subjected to the washing test. Table 3 shows the results of samples washed by detergent with and without bleaching agent sodium hypochlorite (300 ppm). It was found that addition of commercial detergent in the washing solution shows strong inhibition and disinfection against S. aureus, and this effect is irrespective of the number of washing cycles. Moreover, the fabric samples showed yellowing after being washed with the addition of the bleaching agent sodium hypochlorite.

3.5. Effect of Washing Cycles on Antibacterial Activity

Table 4 shows the effects of washing cycles on the antibacterial activity against S. aureus and K. pneumonia of PHMB coated fabric samples. As shown in Table 4, after 52 washing cycles, the fabric samples still showed strong inhibition and disinfection, against both S. aureus and K. pneumonia. However, a clear decrease was observed in the antibacterial ability for the samples after 104 washing cycles. This indicates that simulated healthcare laundering has a significant influence on antibacterial activity of treated fabrics, and the coated samples show excellent durability against washing.
The qualitative analysis of PHMB-coated fabric samples was also conducted via dyeing with BPB. As seen in Figure 5, it clearly shows that the blue complex salt was significantly formed on the treated samples, which demonstrates that PHMB still existed on the fabric samples after different washing cycles.

3.6. Tearing Strength Analysis

Figure 6 presents that the effects of scouring, coating and washing on tearing strength of the fabric substrate. Clearly, for the control sample, tearing strength in both warp and weft directions was found to be the highest compared to the other samples. There is an obvious reduction in tearing strength of fabric samples after scouring, indicating that scouring has a negative effect on tearing strength of fabrics. Likewise, after coating the scoured fabrics, tearing strength in the warp direction dropped from 28.44 to 24.07, whereas the weft direction saw a decrease from 28.89 to 24.45. Then, the coated fabric sample was washed 104 times and tearing strength sharply declined to 14.7 and 13.86, for warp and weft direction, respectively. The results demonstrate that scouring, coating and washing treatment have a significant negative influence on tearing strength, particularly washing.
Figure 7 shows that the effect of washing conditions on tearing strength. It can be clearly seen that there was no significant difference between washing temperature 65 °C and 75 °C. Compared with simulated healthcare washing, tearing strength of treated fabrics has an obvious decrease, but it is still higher than that of washed samples. This demonstrates that the strength loss for treated samples is acceptable.

3.7. Hand Feel Measurement

In the project, antibacterial finishing formulation was fully investigated to assess its effect on the hand feel property, as shown in Table 5.
After coating with above recipes, the samples were then assessed in terms of hand feel properties, such as resilience, softness, and smoothness, etc., as shown in Table 6. Clearly, compared to the control sample, hand feel properties show a significant decrease in terms of resilience, softness, and smoothness. This indicates that the antibacterial treatment has a negative impact on the hand feel of fabrics. Likewise, an obvious decline in whiteness was also observed after coating with PHMB recipe. This demonstrates that antibacterial treatment has a slightly negative influence on the performance of fabrics.
Next, the effect of washing on performance of textile fabrics was further investigated (Table 7). Compared to Table 6, HFI values of all the samples significantly decreased after washing, which indicates that washing has an obvious influence on the hand feel of textiles. Meanwhile, the whiteness also saw a sharp decrease from 80+ to 60+, particularly for the coated samples. This may be due to the loss of fluorescent whitening agent after washing because they are often used for textiles to improve the whiteness [29,30].

4. Discussion

PHMB is a cationic biocide marketed worldwide due to its excellent antibacterial activity, chemical stability, low toxicity, and reasonable cost, and has been extensively utilized in textile industry [3,7]. However, a common issue facing PHMB-coated fabrics is the durability against household laundering. The present study explored the effects of various parameters, such as washing cycles and household detergents, on the antibacterial activity of PHMB-coated fabric samples, as well as effects of PHMB formulation on the physical properties of cotton substrate, including tearing strength and hand feel value.
From SEM observation, the presence of PHMB was confirmed, and the stable blue complex was formed with BPB dyebath (Figure 2). The characteristic absorption peak of cellulose was also enhanced due to the coating of PHMB (Figure 3). The PHMB-coated fabric samples exhibit prominent inhibition activity against S. aureus and K. pneumonia (Figure 4). Moreover, the antibacterial behavior of PHMB was shown to a concentration dependent effect. However, there is no significant difference between the concentrations of 2.5% and 5% PHMB in the antibacterial behavior, while, for 10% and 15% PHMB, a significant antibacterial activity was observed (Table 3). The effectiveness against cellular organisms is due to the positively charged biguanide group attached to a flexible spacer. PHMB binds to the negatively charged phosphate head groups of phospholipids at bacteria cell wall or virus envelope, causing increased rigidity, sinking non-polar segments into hydrophobic domains, disrupting the membrane with subsequent cytoplasmic shedding, and culminating in cell death [16].
Durability against household laundering is an important property for medical textiles. Originally, we performed the washing tests with the commercial household detergent added to simulate the practical application scenario. However, it was found that the antibacterial properties of washed samples were seriously interfered by the commercial detergent, the possible reason of which may be the addition of some additives with microbicidal efficacy (Table 3). Therefore, a non-ionic surfactant 7EO was used for further experiments. The bleaching agent sodium hypochloride was abandoned due to the fabrics yellowing caused.
Next, we performed the antibacterial experiments on treated fabrics against two bacteria: S. aureus and K. pneumonia to pinpoint the effect of simulated healthcare laundering on the antibacterial ability. The fabric samples were shown strong bactericidal effect against both bacteria after 52 washing cycles (Table 4). The attenuated bactericidal activity was still observed in the samples with 104 washing cycles, which was further confirmed by BPB dyeing tests (Figure 5). This shows that frequent washing may negatively influence the antibacterial ability of PHMB-coated fabrics. In spite of this, the washing experiments demonstrate that the fabric samples treated with PHMB formulation possess satisfactory durability against washing. Similar results were also reported by Chen and coworkers [31]. In their study, PHMB was padded on the fabric and then dried at 120 °C for 5 min. PHMB-coated fabric samples still showed excellent antimicrobial property against S. aureus (99%) and K. pneumonia (94%) after 25 washing cycles. Gao et al. coated PHMB on the wool fabric by exhaustion method and studied the antibacterial behaviors against gram-negative bacteria E. coli [32]. They found that PHMB-coated wool fabric was durable to 5 accelerated washing cycles (ISO 5A cycle, equivalent to 40–50 wool washing cycles) and maintained 99% bacterial reduction for 8% PHMB treated samples. In the present study, the durability against laundering was dramatically increased to almost 104 washing cycles by optimizing the finish process. On the one hand, the underlying reason may be the electrostatic attraction between PHMB and cellulosic molecules [33], which is enhanced by the addition of polyurethane binder and high-temperature curing. On the other hand, polyurethane binder acts as a cross-linker and form hydrogen bond with PHMB and cellulosic molecules, which eventually enhance the durability property of PHMB treated fabrics [34].
Tearing strength of fabric is affected by many parameters, such as fiber structure and post-finishing process. The present study investigates the effects of scouring, coating, and washing on tearing strength of the fabric (Figure 6). Compared to the control sample, tearing strength of the fabrics were clearly debased after treatment, particularly after washing. In this study, the samples were firstly subjected to scouring treatment to remove the impurities, which slightly decrease the tearing strength of fabrics. And then, the scoured samples were coated with PHMB formulation via pad-dry-cure process, which further deteriorate the tearing strength. Accordingly, the tearing strength of the coated fabrics were gravely undermined after 104 washing cycles, the potential reason of which may be the hydrolysis of cellulosic fibers [35,36]. However, the effect of washing temperature on the tearing strength was not significant, even though a much strength loss was observed with a higher washing temperature (75 °C) (Figure 7).
Finishing treatment and regular washing generally have an obvious negative influence on the hand feel of a fabric [37,38], as confirmed in Table 6 and Table 7. For the samples of G1–G4, which were coated with different concentrations of PEG, there is an increase in the value of HFI, indicating that the reduction of PEG helps enhance the hand feel performance of fabrics. Looking at samples of G5–G8, concentration of the binder dropped from 5% to 3% and effects of PEG on the hand feel was further investigated. It can be found that HFI values increased, excluding the sample G5. Overall, HFI values of samples G5–G8 were higher than G1–G4 samples, which was due to the smaller amount of PHMB formulation used for the coating (Table 6). By contrast, HFI values of all the samples significantly decreased after washing, which indicates that washing has an obvious influence on the hand feel of textiles, and the whiteness also sharply decreased (Table 7).
In summary, the fabric samples coated with PHMB formulation show excellent antibacterial activity against S. aureus and K. pneumonia. Washing test shows that washing has a significantly negative influence on the antibacterial activity, tensile strength and hand values. However, the samples prepared by the optimum process exhibit satisfactory durability for simulated healthcare laundering.

5. Conclusions

Durability against simulated healthcare washing is an important property for medical textiles. The durability property can be achieved by optimizing the finishing process. It was found that the optimum finishing conditions can impart excellent durability to fabrics expected to undergo repeated simulated healthcare washing. After 104 washing cycles, the PHMB-coated fabric samples still show distinct inhibition activity, particularly against S. aureus. Additionally, the present study also shows that both simulated healthcare washing and coating treatment have negative influence on the hand feel behavior and tearing strength of cotton fabric. Therefore, the antibacterial finishing for textiles should not neglect the negative influence on the materials.

Author Contributions

Conceptualization, J.C., J.Y., K.-F.Y., and C.-W.K.; Data curation, W.-Y.W.; Formal analysis, W.-Y.W., J.-C.C., and C.-W.K.; Funding acquisition, C.-W.K.; Investigation, W.-Y.W.; Methodology, W.-Y.W., J.-C.C., and C.-W.K.; Project administration, C.-W.K.; Supervision, C.-W.K.; Validation, W.-Y.W.; Visualization, W.-Y.W.; Writing-original draft, W.-Y.W.; Writing-review & editing, C.-W.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by The Hong Kong Polytechnic University, grant numbers ZVNM and ZVQJ.

Acknowledgments

The authors would like to thank the financial support from The Hong Kong Polytechnic University for this work under the project of account codes: ZVNM and ZVQJ.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Chemical structure of poly(hexamethylenebiguanide) (PHMB).
Figure 1. Chemical structure of poly(hexamethylenebiguanide) (PHMB).
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Figure 2. Surface morphology of treated fabric observed by SEM: (A) untreated cotton fabric, (B) fabric treated with PHMB, and optical photographs: (C) untreated cotton fabric and (D) PHMB-coated fabric dyed with bromophenol blue (BPB).
Figure 2. Surface morphology of treated fabric observed by SEM: (A) untreated cotton fabric, (B) fabric treated with PHMB, and optical photographs: (C) untreated cotton fabric and (D) PHMB-coated fabric dyed with bromophenol blue (BPB).
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Figure 3. FTIR absorbance spectra of PHMB, untreated cotton fabric and PHMB-coated cotton fabric. The insert shows the spectrum of untreated cotton and treated counterpart.
Figure 3. FTIR absorbance spectra of PHMB, untreated cotton fabric and PHMB-coated cotton fabric. The insert shows the spectrum of untreated cotton and treated counterpart.
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Figure 4. Qualitative assay for the antibacterial activity of PHMB-coated fabrics against S. aureus and K. pneumonia.
Figure 4. Qualitative assay for the antibacterial activity of PHMB-coated fabrics against S. aureus and K. pneumonia.
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Figure 5. Qualitative test results of PHMB-coated fabric samples dyed with BPB: (A) pristine uncoated fabric; (B) no wash; (C) 26 washing cycles; (D) 52 washing cycles; and (E) 104 washing cycles.
Figure 5. Qualitative test results of PHMB-coated fabric samples dyed with BPB: (A) pristine uncoated fabric; (B) no wash; (C) 26 washing cycles; (D) 52 washing cycles; and (E) 104 washing cycles.
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Figure 6. Tearing strength of control sample, scoured, coated, and washed samples (104 washing cycles, 65 °C with nonionic detergent but without bleaching agent); warp (A) and weft (B).
Figure 6. Tearing strength of control sample, scoured, coated, and washed samples (104 washing cycles, 65 °C with nonionic detergent but without bleaching agent); warp (A) and weft (B).
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Figure 7. Tearing strength of control and treated samples after 52 washing cycles at 65 °C and 75 °C, warp.
Figure 7. Tearing strength of control and treated samples after 52 washing cycles at 65 °C and 75 °C, warp.
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Table 1. Washing test conditions 3.
Table 1. Washing test conditions 3.
No Detergent
0
With Detergent
1
Solution 1 1S10S11
Solution 2 2S20S21
1 Solution 1: 75 °C, 5 min, with or without detergent; 2 Solution 2: 65 °C, 10 min + NaClO (300 ppm), with or without detergent; 3 Washing cycles: 26/52/104.
Table 2. Effect of concentration of PHMB on antibacterial activity.
Table 2. Effect of concentration of PHMB on antibacterial activity.
SamplePHMB Conc./%Inhibition Zone/mm
S. aureusK. pneumoniae
Control000
12.54.53.5
254.55.5
3104.756.75
4156.757.25
Table 3. Antibacterial properties of untreated samples washed by detergent.
Table 3. Antibacterial properties of untreated samples washed by detergent.
Washing CyclesDetergent Detergent + NaClO
Inhibition/% 1Disinfection/% 2Inhibition/% 1Disinfection/% 2
Control, no wash0000
2601000100
5201000100
10401000100
1 Inhibitory % = [(control after 18 h) – (specimen after 18 h)]/[control after 18 h] × 100%. 2 Disinfectant % = [(control after 0 h] – [specimen after 18 h)]/[control after 0 h] × 100%.
Table 4. Antibacterial properties of treated samples washed by different cycles.
Table 4. Antibacterial properties of treated samples washed by different cycles.
Washing CyclesInhibition/% 1Disinfection/% 2
S. aureusK. pneumoniaeS. aureusK. pneumoniae
no wash100100100100
26100100100100
52100100100100
1049538.600
1 Inhibitory % = [(control after 18 h) − (specimen after 18 h)]/[control after 18 h] × 100%. 2 Disinfectant % = [(control after 0 h] − [specimen after 18 h)]/[control after 0 h] × 100%.
Table 5. The different antibacterial recipes for fabric samples antibacterial treatment.
Table 5. The different antibacterial recipes for fabric samples antibacterial treatment.
SamplePHMB (%, v/v)PEG (%, v/v)Binder (%, v/v)
G1555
G2535
G3515
G4505
G5553
G6533
G7513
G8503
Table 6. Hand feel properties of fabric samples coated with different antibacterial recipes.
Table 6. Hand feel properties of fabric samples coated with different antibacterial recipes.
SampleResilienceSoftnessSmoothnessHFIWhiteness
Control82.378.482.3243.084.6
G180.376.781.2238.283.9
G282.477.381.2240.983.5
G383.077.481.5241.982.4
G482.978.181.3242.384.2
G582.278.681.6242.483.2
G682.378.481.2241.984.2
G783.077.281.8242.082.5
G882.977.481.9242.283.2
Table 7. The hand feel properties of PHMB coated fabric samples after washing (104 cycles, 65 °C).
Table 7. The hand feel properties of PHMB coated fabric samples after washing (104 cycles, 65 °C).
SampleResilienceSoftnessSmoothnessHFIWhiteness
Control79.378.079.5236.882.7
G180.276.480.1236.761.1
G279.876.479.7235.963.5
G380.576.480.4237.363. 2
G480.376.678.0234.961.9
G580.876.880.6238.262.3
G679.677.279.2236.061.0
G780.076.780.0236.763.6
G881.376.980.4238.661.9

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MDPI and ACS Style

Wang, W.-Y.; Chiou, J.-C.; Yip, J.; Yung, K.-F.; Kan, C.-W. Development of Durable Antibacterial Textile Fabrics for Potential Application in Healthcare Environment. Coatings 2020, 10, 520. https://doi.org/10.3390/coatings10060520

AMA Style

Wang W-Y, Chiou J-C, Yip J, Yung K-F, Kan C-W. Development of Durable Antibacterial Textile Fabrics for Potential Application in Healthcare Environment. Coatings. 2020; 10(6):520. https://doi.org/10.3390/coatings10060520

Chicago/Turabian Style

Wang, Wen-Yi, Jia-Chi Chiou, Joanne Yip, Ka-Fu Yung, and Chi-Wai Kan. 2020. "Development of Durable Antibacterial Textile Fabrics for Potential Application in Healthcare Environment" Coatings 10, no. 6: 520. https://doi.org/10.3390/coatings10060520

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