Antimicrobial surface

Last updated

An antimicrobial surface is coated by an antimicrobial agent that inhibits the ability of microorganisms to grow [1] on the surface of a material. Such surfaces are becoming more widely investigated for possible use in various settings including clinics, industry, and even the home. The most common and most important use of antimicrobial coatings has been in the healthcare setting for sterilization of medical devices to prevent hospital associated infections, which have accounted for almost 100,000 deaths in the United States. [2] In addition to medical devices, linens and clothing can provide a suitable environment for many bacteria, fungi, and viruses to grow when in contact with the human body which allows for the transmission of infectious disease. [3]

Contents

Antimicrobial surfaces are functionalized in a variety of different processes. A coating may be applied to a surface that has a chemical compound which is toxic to microorganisms. In alternative, it is possible to functionalize a surface by adsorbing a polymer or polypeptide and/or by changing its micro and nanostructure. [4]

An innovation in antimicrobial surfaces is the discovery that copper and its alloys (brasses, bronzes, cupronickel, copper-nickel-zinc, and others) are natural antimicrobial materials that have intrinsic properties to destroy a wide range of microorganisms. An abundance of peer-reviewed antimicrobial efficacy studies have been published regarding copper’s efficacy to destroy E. coli O157:H7, methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus , Clostridium difficile , influenza A virus, adenovirus, and fungi. [5]

Apart from the health industry, antimicrobial surfaces have been utilized for their ability to keep surfaces cleaned. Either the physical nature of the surface, or the chemical make up can be manipulated to create an environment which cannot be inhabited by microorganisms for a variety of different reasons. Photocatalytic materials have been used for their ability to kill many microorganisms and therefore can be used for self-cleaning surfaces as well as air cleaning, water purification, and antitumor activity. [6]

Antimicrobial activity

Mechanisms

Silver

Silver ions have been shown to react with the thiol group in enzymes and inactivate them, leading to cell death. [7] These ions can inhibit oxidative enzymes such as yeast alcohol dehydrogenase. [8] Silver ions have also been shown to interact with DNA to enhance pyrimidine dimerization by the photodynamic reaction and possibly prevent DNA replication. [9]

The use of silver as an antimicrobial is well documented.

Copper

The antimicrobial mechanisms of copper have been studied for decades and are still under investigation. A summary of potential mechanisms is available here: Antimicrobial properties of copper#Mechanisms of antibacterial action of copper. Researchers today believe that the most important mechanisms include the following:

  • Elevated copper levels inside a cell causes oxidative stress and the generation of hydrogen peroxide. Under these conditions, copper participates in the so-called Fenton-type reaction — a chemical reaction causing oxidative damage to cells.
  • Excess copper causes a decline in the membrane integrity of microbes, leading to leakage of specific essential cell nutrients, such as potassium and glutamate. This leads to desiccation and subsequent cell death.
  • While copper is needed for many protein functions, in an excess situation (as on a copper alloy surface), copper binds to proteins that do not require copper for their function. This "inappropriate" binding leads to loss-of-function of the protein, and/or breakdown of the protein into nonfunctional portions.

Organosilanes

Organosilanes create a network of electrically charged molecules on the surface, which rupture the cell wall on contact. This is due to their structure which consists of a hydrophobic element, and a cationic element. While the hydrophobic element may prevent adherence in the first place, it may also intercalate with the cell wall, whose rupture is aided by the cationic component. [10]

Nutrient Uptake

The growth rate of E. coli and S. aureus was found to be independent of nutrient concentrations on non-antimicrobial surfaces. [11] It was also noted that antimicrobial agents such as Novaron AG 300 (Silver sodium hydrogen zirconium phosphate) do not inhibit the growth rate of E. coli or S. aureus when nutrient concentrations are high, but do as they are decreased. This result leads to the possible antimicrobial mechanism of limiting the cell's uptake, or use efficiency, of nutrients. [11]

Quaternary ammonium

The quaternary ammonium compound Dimethyloctadecyl (3-trimethoxysilyl propyl) ammonium chloride (Si-QAC) has been found to have antimicrobial activity when covalently bonded to a surface. [12] Many other quaternary ammonium compounds are known to have antimicrobial properties (e.g. alkyldimethylbenzylammonium chloride and didecyldimethylammonium chloride). These last two are membrane active compounds; against S. aureus the first forms a single monolayer coverage of the S. aureus cells on the outer membrane, while the second forms a double monolayer. [13] This leads to cell leakage and total release of the intracellular potassium and 260 nm-absorbing pools in this order. [13]

Selectivity

By definition, "antimicrobial" refers to something that is detrimental to a microbe. Because the definition of a microbe (or microorganism) is very general, something that is "antimicrobial" could have a detrimental effect against a range of organisms ranging from beneficial to harmful ones, and could include mammalian cells and cell types typically associated with disease such as bacteria, viruses, protozoans, and fungi.

Selectivity refers to the ability to combat a certain type or class of organism. Depending on the application, the ability to selectively combat certain microorganisms while having little detrimental effect against others dictates the usefulness of a particular antimicrobial surface in a given context.

Bactericides

A main way to combat the growth of bacterial cells on a surface is to prevent the initial adhesion of the cells to that surface. Some coatings which accomplish this include chlorhexidine incorporated hydroxyapatite coatings, chlorhexidine-containing polylactide coatings on an anodized surface, and polymer and calcium phosphate coatings with chlorhexidine. [14]

Antibiotic coatings provide another way of preventing the growth of bacteria. Gentamicin is an antibiotic which has a relatively broad antibacterial spectrum. Also, gentamicin is one of the rare kinds of thermo stable antibiotics and so it is one of the most widely used antibiotics for coating titanium implants. [14] Other antibiotics with broad antibacterial spectra are cephalothin, carbenicillin, amoxicillin, cefamandole, tobramycin, and vancomycin. [14]

Copper and copper alloy surfaces are an effective means for preventing the growth of bacteria. Extensive U.S. EPA-supervised antimicrobial efficacy tests on Staphylococcus aureus , Enterobacter aerogenes , Methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli 0157:H7, and Pseudomonas aeruginosa have determined that when cleaned regularly, some 355 different EPA-registered antimicrobial copper alloy surfaces:

See: Antimicrobial copper touch surfaces for main article.

Viral inhibitors

Influenza viruses are mainly spread from person to person through airborne droplets produced while coughing or sneezing. However, the viruses can also be transmitted when a person touches respiratory droplets settled on an object or surface. [15] It is during this stage that an antiviral surface could play the biggest role in cutting down on the spread of a virus. Glass slides painted with the hydrophobic long-chained polycation N,N dodecyl,methyl-polyethylenimine (N,N-dodecyl,methyl-PEI) are highly lethal to waterborne influenza A viruses, including not only wild-type human and avian strains but also their neuraminidase mutants resistant to anti-influenza drugs. [16]

Copper alloy surfaces have been investigated for their antiviral efficacies. After incubation for one hour on copper, active influenza A virus particles were reduced by 75%. After six hours, the particles were reduced on copper by 99.999%. [17] [18] Also, 75% of Adenovirus particles were inactivated on copper (C11000) within 1 hour. Within six hours, 99.999% of the adenovirus particles were inactivated. [19]

Fungal inhibitors

A chromogranin A-derived antifungal peptide (CGA 47–66, chromofungin) when embedded on a surface has been shown to have antifungal activity by interacting with the fungal membrane and thereby penetrating into the cell. [20] Additionally, in vitro studies have demonstrated that such an antifungal coating is able to inhibit the growth of yeast Candida albicans by 65% and completely stop the proliferation of filamentous fungus Neurospora crassa. [20]

Copper and copper alloy surfaces have demonstrated a die-off of Aspergillus spp., Fusarium spp., Penicillium chrysogenum , Aspergillus niger and Candida albicans fungal spores. [21] Hence, the potential to help prevent the spread of fungi that cause human infections by using copper alloys (instead of non-antifungal metals) in air conditioning systems is worthy of further investigation.

Surface modification

Physical modification

Surface roughness

The physical topology of a surface will determine the viable environment for bacteria. It may affect the ability for a microbe to adhere to its surface. Textile surfaces, tend to be very easy for microbes to adhere due to the abundance of interstitial spacing between fibers.

Figure 1: Wenzel model Wenzel.png
Figure 1: Wenzel model

Wenzel Model was developed to calculate the dependence that surface roughness has on the observed contact angle. Surfaces that are not atomically smooth will exhibit an observed contact angle that varies from the actual contact angle of the surface. The equation is expressed as:

where R is the ratio of the actual area of the surface to the observed area of a surface and θ is the Young's contact angle as defined for an ideal surface. [22] See Wetting. Based on physical modification of the surface, antiviral surface can be designed by decorating micropillars on the surface. [23]

Chemical modification

Grafting polymers onto and/or from surfaces

Antimicrobial activity can be imparted onto a surface through the grafting of functionalized polymers, for example those terminated with quaternary amine functional groups, through one of two principle methods. With these methods—“grafting to” and “grafting from”—polymers can be chemically bound to a solid surface and thus the properties of the surface (i.e. antimicrobial activity) can be controlled. [22] Quaternary ammonium ion-containing polymers (PQA) have been proven to effectively kill cells and spores through their interactions with cell membranes. [24] A wealth of nitrogenous monomers can be quaternized to be biologically active. These monomers, for example 2-dimethylaminoethyl methacrylate (DMAEMA) or 4-vinyl pyridine (4-VP) can be subsequently polymerized with ATRP. [24] Thus antimicrobial surfaces can be prepared via “grafting to” or “grafting from” mechanisms.

Grafting onto

Grafting to involves the strong adsorption or chemical bonding of a polymer molecule to a surface from solution. This process is typically achieved through a coupling agent that links a handle on the surface to a reactive group on either of the chain termini. Although simple, this approach suffers from the disadvantage of a relatively low grafting density as a result of steric hindrance from the already-attached polymer coils. After coupling, as in all cases, polymers attempt to maximize their entropy typically by assuming a brush or mushroom conformation. Thus, potential binding sites become inaccessible beneath this “mushroom domain”. [22]

Figure 2: Schematic of grafting density. Grafting Density.png
Figure 2: Schematic of grafting density.

Pre-synthesized polymers, like the PDMEAMA/PTMSPMA block copolymer, can be immobilized on a surface (i.e. glass) by simply immersing the surface in an aqueous solution containing the polymer. [24] For a process like this, grafting density depends on the concentration and molecular weight of the polymer as well as the amount time the surface was immersed in solution. [24] As expected, an inverse relationship exists between grafting density and molecular weight. [24] As the antimicrobial activity depends on the concentration of quaternary ammonium tethered to the surface, grafting density and molecular weight represent opposing factors that can be manipulated to achieve high efficacy.

Grafting from

This limitation can be overcome by polymerizing directly on the surface. This process is referred to as grafting from, or surface-initiated polymerization (SIP). As the name suggests, the initiator molecules must be immobilized on the solid surface. Like other polymerization methods, SIP can be tailored to follow radical, anionic, or cationic mechanisms and can be controlled utilizing reversible addition transfer polymerization (RAFT), atom transfer radical polymerization (ATRP), or nitroxide-mediated techniques. [22]

A controlled polymerization allows for the formation of stretched conformation polymer structures that maximize grafting density and thus biocidal efficiency. [24] This process also allows for high density grafting of high molecular weight polymer which further improves efficacy. [24]

Superhydrophobic surfaces

A superhydrophobic surface is a low energy, generally rough surface on which water has a contact angle of >150°. Nonpolar materials such as hydrocarbons traditionally have relatively low surface energies, however this property alone is not sufficient to achieve superhydrophobicity. Superhydrophobic surfaces can be created in a number of ways, however most of the synthesis strategies are inspired by natural designs. The Cassie-Baxter model provides an explanation for superhydropbicity—air trapped in microgrooves of a rough surface create a “composite” surface consisting of air and the tops of microprotrusions. [25] This structure is maintained as the scale of the features decreases, thus many approaches to the synthesis of superhydrophobic surfaces have focused on the fractal contribution. [25] Wax solidification, lithography, vapor deposition, template methods, polymer reconfirmation, sublimation, plasma, electrospinning, sol-gel processing, electrochemical methods, hydrothermal synthesis, layer-by-layer deposition, and one-pot reactions are approaches to the creation of superhydrophobic surfaces that have been suggested. [25]

Making a surface superhydrophobic represents an efficient means of imparting antimicrobial activity. A passive antibacterial effect results from the poor ability of microbes to adhere to the surface. The area of superhydropboic textiles takes advantage of this and could have potential applications as antimicrobial coatings.

Fluorocarbons

Fluorocarbons and especially perfluorocarbons are excellent substrate materials for the creation of superhydrophobic surfaces due to their extremely low surface energy. These types of materials are synthesized via the replacement of hydrogen atoms with fluorine atoms of a hydrocarbon.

Nanomaterials

Nanoparticles are used for a variety of different antimicrobial applications due to their extraordinary behavior. There are more studies being carried out on the ability for nanomaterials to be utilized for antimicrobial coatings due to their highly reactive nature. [3]

NanomaterialCharacteristicApplication
Titanium dioxide photo catalytic activity, low costUV protection, anti-bacterial, environmental purification, self-cleaning, solar cell efficiency
Organosilaneprevent adhesion by abrasive surface, low costantimicrobial coating with long-term effectiveness
Silver electrical Conductivity, low toxicityanti-microbial activity – bind and destroy cell membrane
Zinc oxide photo catalytic activityanti-microbial activity, used in textile industry
Copper electrical conductivityUV protection properties, anti-microbial additive
Magnetite superparamagnetic antimicrobial activity, generate radicals that cause protein damage
Magnesium oxide high specific surface areaantimicrobial activity, generate oxygen radicals that cause protein damage
Gold electrical conductivityanti-bacterial, acne curing agent
Gallium similar to Fe3+ (essential metabolic nutrient for bacteria)anti-bacterial against Clostridium difficile
Carbon nanotubes antistatic, electrical conductivity, absorptionCNT/TiO2 nanocomposits; antimicrobial surfaces, fire retardant, anti-static. [3]

There are quite a few physical characteristics that promote anti-microbial activity. However, most metal ions have the ability to create oxygen radicals, thus forming molecular oxygen which is highly toxic to bacteria. [3]

Coatings

Self-cleaning coatings

Photocatalytic coatings are those that include components (additives) that catalyze reactions, generally through a free radical mechanism, when excited by light. The photocatalytic activity (PCA) of a material provides a measure of its reactive potential, based on the ability of the material to create an electron hole pair when exposed to ultra-violet light. [26] Free radicals formed can oxidize and therefore breakdown organic materials, such as latex binders found in waterborne coatings. Antimicrobial coatings systems take advantage of this by including photocatalytically active compounds in their formulations (i.e. titanium dioxide) that cause the coating to “flake” off over time. [26] These flakes carry the microbes along with them, leaving a “clean” coating behind. Systems like this are often described to be self-cleaning.

Antimicrobial additives

Instead of doping a surface directly, antimicrobial activity can be imparted to a surface by applying a coating containing antimicrobial agents such as biocides or silver nanoparticles. In the case of the latter, the nanoparticles can have beneficial effects on the structural properties of the coating along with their antibacterial effect. [27]

Antimicrobial peptides

Antimicrobial Peptides (AMPs) have gained a lot of attention because they are much less susceptible to development of microbial resistance. [2] Other antibiotics may be susceptible to bacterial resistance, like multi-resistant staphylococcus aureus (MRSA) which is known as a common relic in the healthcare industry while other bacterial strains have become more of a concern for waste water treatment in local rivers or bays. [28] AMPs can be functionalized onto a surface by either chemical or physical attachment. AMPs can be physically attached by using oppositely charged polymeric layers and sandwiching the polypeptide between them. This may be repeated to achieve multiple layers of AMPs for the recurring antibacterial activity. [28] There are, however, a few drawbacks to this mechanism. Assembly thickness and polymer-peptide interactions can affect the diffusion of peptide to bacterial contact. [28] Further research should be carried out to determine the effectiveness of the adsorption technique. However, the chemical attachment of AMPs is also widely studied.

AMPs can be covalently bound to a surface, which minimizes the "leaching effect" of peptides. The peptide is typically attached by a very exergonic chemical reaction, thus forming a very stable antimicrobial surface. The surface can be functionalized first with a polymer resin such as polyethylene glycol (PEG). [28] Recent research has focused on producing synthetic polymers and nanomaterials with similar mechanisms of action to endogenous antimicrobial peptides. [29] [30]

Touch surfaces

Antimicrobial touch surfaces include all the various kinds of surfaces (such as door knobs, railings, tray tables, etc.) that are often touched by people at work or in everyday life, especially (for example) in hospitals and clinics.

Antimicrobial copper alloy touch surfaces are surfaces that are made from the metal copper or alloys of copper, such as brass and bronze. Copper and copper alloys have a natural ability to kill harmful microbes relatively rapidly – often within two hours or less (i.e. copper alloy surfaces are antimicrobial). Much of the antimicrobial efficacy work pertaining to copper has been or is currently being conducted at the University of Southampton and Northumbria University (United Kingdom), University of Stellenbosch (South Africa), Panjab University (India), University of Chile (Chile), Kitasato University (Japan), University of Coimbra (Portugal), and the University of Nebraska and Arizona State University (U.S.). Clinical trials evaluating the efficacy of copper alloys to reduce the incidence of nosocomial infections are on-going at hospitals in the UK, Chile, Japan, South Africa, and the U.S.

The United States Environmental Protection Agency (EPA) approved the registrations of 355 different copper alloys as “antimicrobial materials” with public health benefits. [31]

Characterization

Designing effective antimicrobial surfaces demands an in-depth understanding of the initial microbe-surface adhesion mechanisms. [32] Scanning electron microscopy (SEM) is used for nonliving samples. Bacterial colony forming unit (CFU) counting requires overnight incubation and detects bacteria that readily grow on solid media. Molecular dynamics (MD) simulation can be used to minimize the number of experiments with engineered substrates, with the quantification of time-lapse fluorescence microscopy images that can be processed in an hour. [33] Contact angle measurements can be used to characterize micro/nano-pillars use for rupturing cell walls. The analysis of the zeta potential by the streaming potential method of either an antimicrobial coating [34] or a self-disinfectant material [35] in contact with an aqueous environment, or by electrophoretic light scattering of nanoparticle dispersions of antibacterial additives [36] reveal information about surface and interfacial charge and let predict the electrostatic attraction or repulsion of microorganisms.

Application

Water Treatment

Antimicrobial Peptides and Chitosan

Naturally occurring chitin and certain peptides have been recognized for their antimicrobial properties in the past. Today, these materials are engineered into nanoparticles in order to produce low-cost disinfection applications. Natural peptides form nano-scale channels in the bacterial cell membranes, which causes osmotic collapse. [37] These peptides are now synthesized in order to tailor the antimicrobial nanostructures with respect to size, morphology, coatings, derivatization, and other properties allowing them to be used for specific antimicrobial properties as desired. Chitosan is a polymer obtained from chitin in arthropod shells, and has been used for its antibacterial properties for a while, but even more so since the polymer has been made into nanoparticles. Chitosan proves to be effective against bacteria, viruses, and fungi, however it is more effective against fungi and viruses than bacteria. The positively charged chitosan nanoparticles interact with the negatively charged cell membrane, which causes an increase in membrane permeability and eventually the intracellular components leak and rupture. [37]

Silver nanoparticles

Silver compounds and silver ions also have been known to show antimicrobial properties and have been used in a wide range of applications, including water treatment. It is shown that silver ions prevent DNA replication and affect the structure and permeability of the cell membrane. Silver also leads to UV inactivation of bacteria and viruses because silver ions are photoactive in the presence of UV-A and UV-C irradiation. Cysteine and silver ions form a complex that leads to the inactivation of Haemophilus influenzae phage and bacteriophage MS2. [37]

Medical and commercial applications

Surgical devices

Even with all the precautions taken by medical professionals, infection reportedly occurs in up to 13.9% of patients after stabilization of an open fracture, and in about 0.5-2% of patients who receive joint prostheses. [38] In order to reduce these numbers, the surfaces of the devices used in these procedures have been altered in hopes to prevent the growth of the bacteria that leads to these infections. This has been achieved by coating titanium devices with an antiseptic combination of chlorhexidine and chloroxylenol. This antiseptic combination successfully prevents the growth of the five main organisms that cause medical related infections, which include Staphylococcus epidermidis , Methicillin-resistant Staphylococcus aureus, Pseudomonas aeruginosa , Escherichia coli and Candida albicans . [38] Peptide-based gel coating with intrinsic antibacterial activity against Methicillin-resistant Staphylococcus aureus, was also shown to inhibit colonization of titanium implants in mice. [39]

Photocatalytic coatings

Photoactive pigments such as TiO2 and ZnO have been used on glass, ceramic, and steel substrates for self-cleaning and antimicrobial purposes. For photocatalytic bactericidal activity in water treatment applications, granular substrate materials have been used in the form of sands supporting mixed anatase/rutile TiO2 coatings. [40] Oxide semiconductor photocatalysts such as TiO2 react with incident irradiation exceeding the material's electronic band-gap resulting in the formation of electron-hole pairs (excitons) and the secondary generation of radical species through reaction with adsorbates at the photocatalyst surface yielding an oxidative or reductive effect that degrades living organisms. [41] [42] Titania has successfully be used as an antimicrobial coating on bathroom tiles, paving slabs, deodorizers, self-cleaning windows, and many more.

Copper touch surfaces

Copper alloy surfaces have intrinsic properties to destroy a wide range of microorganisms.

The US Environmental Protection Agency (EPA), which oversees the regulation of antimicrobial agents and materials in that country, found that copper alloys kill more than 99.9% of disease-causing bacteria within just two hours when cleaned regularly. [31] Copper and copper alloys are unique classes of solid materials as no other solid touch surfaces have permission in the U.S. to make human health claims (EPA public health registrations were previously restricted only to liquid and gaseous products). The EPA has granted antimicrobial registration status to 355 different copper alloy compositions. [31] In healthcare applications, EPA-approved antimicrobial copper products include bedrails, handrails, over-bed tables, sinks, faucets, door knobs, toilet hardware, intravenous poles, computer keyboards, etc. In public facility applications, EPA-approved antimicrobial copper products include health club equipment, elevator equipment, shopping cart handles, etc. In residential building applications, EPA-approved antimicrobial copper products include kitchen surfaces, bedrails, footboards, door push plates, towel bars, toilet hardware, wall tiles, etc. In mass transit facilities, EPA-approved antimicrobial copper products include handrails, stair rails grab bars, chairs, benches, etc. A comprehensive list of copper alloy surface products that have been granted antimicrobial registration status with public health claims by the EPA can be found here: Antimicrobial copper-alloy touch surfaces#Approved products.

Clinical trials are currently being conducted on microbial strains unique to individual healthcare facilities around the world to evaluate to what extent copper alloys can reduce the incidence of infection in hospital environments. Early results disclosed in 2011 from clinical studies funded by the U.S. Department of Defense that are taking place at intensive care units (ICUs) at Memorial Sloan-Kettering Cancer Center in New York City, the Medical University of South Carolina, and the Ralph H. Johnson VA Medical Center in Charleston, South Carolina, indicate that rooms where common touch surfaces were replaced with copper demonstrated a 97% reduction in surface pathogens versus the non-coppered rooms and that patients in the coppered ICU rooms had a 40.4% lower risk of contracting a hospital acquired infection versus patients in non-coppered ICU rooms. [43] [44] [45]

Anti-fouling coatings

Marine Biofouling is described as the undesirable buildup of microorganisms, plants, and animals on artificial surfaces immersed in water. [46] Significant buildup of biofouling on marine vessels can be problematic. Traditionally, biocides, a chemical substance or microorganism that can control the growth of harmful organisms by chemical or biological means, are used in order to prevent marine biofouling. Biocides can be either synthetic, such as tributyltin (TBT), or natural, which are derived from bacteria or plants. [46] TBT was historically the main biocide used for anti-fouling coatings, but more recently TBT compounds have been considered toxic chemicals which have negative effects on human and environment, and have been banned by the International Maritime Organization. [47] The early design of anti-fouling coatings consisted of the active ingredients (e.g. TBT) dispersed in the coating in which they "leached" into the sea water, killing any microbes or other marine life that had attached to the ship. The release rate for the biocide however tended to be uncontrolled and often rapid, leaving the coating only effective for 18 to 24 months before all the biocide leached out of the coating. [47]

Figure 3: Biocide release over time Biocide release.png
Figure 3: Biocide release over time

This problem however was resolved with the use of so-called self-polishing paints, in which the biocide was released at a slower rate as the seawater reacted with the surface layer of the paint. [47] More recently, copper-based anti-fouling paints have been used because they are less toxic than TBT in aquatic environment, but are only effective against marine animal life, and not so much weed growth. Non-stick coatings contain no biocide, but have extremely slippery surfaces which prevents most fouling and makes it easier to clean the little fouling that does occur. Natural biocides are found on marine organisms such as coral and sponges and also prevent fouling if applied to a vessel. Creating a difference in electrical charge between the hull and sea water is a common practice in the prevention of fouling. This technology has proven to be effective, but is easily damaged and can be expensive. Finally, microscopic prickles can be added to a coating, and depending on length and distribution have shown the ability to prevent the attachment of most biofouling. [47]

See also

Related Research Articles

<span class="mw-page-title-main">Biofilm</span> Aggregation of bacteria or cells on a surface

A biofilm comprises any syntrophic consortium of microorganisms in which cells stick to each other and often also to a surface. These adherent cells become embedded within a slimy extracellular matrix that is composed of extracellular polymeric substances (EPSs). The cells within the biofilm produce the EPS components, which are typically a polymeric conglomeration of extracellular polysaccharides, proteins, lipids and DNA. Because they have three-dimensional structure and represent a community lifestyle for microorganisms, they have been metaphorically described as "cities for microbes".

<span class="mw-page-title-main">Disinfectant</span> Antimicrobial agent that inactivates or destroys microbes

A disinfectant is a chemical substance or compound used to inactivate or destroy microorganisms on inert surfaces. Disinfection does not necessarily kill all microorganisms, especially resistant bacterial spores; it is less effective than sterilization, which is an extreme physical or chemical process that kills all types of life. Disinfectants are generally distinguished from other antimicrobial agents such as antibiotics, which destroy microorganisms within the body, and antiseptics, which destroy microorganisms on living tissue. Disinfectants are also different from biocides—the latter are intended to destroy all forms of life, not just microorganisms. Disinfectants work by destroying the cell wall of microbes or interfering with their metabolism. It is also a form of decontamination, and can be defined as the process whereby physical or chemical methods are used to reduce the amount of pathogenic microorganisms on a surface.

An antimicrobial is an agent that kills microorganisms (microbicide) or stops their growth. Antimicrobial medicines can be grouped according to the microorganisms they act primarily against. For example, antibiotics are used against bacteria, and antifungals are used against fungi. They can also be classified according to their function. The use of antimicrobial medicines to treat infection is known as antimicrobial chemotherapy, while the use of antimicrobial medicines to prevent infection is known as antimicrobial prophylaxis.

<span class="mw-page-title-main">Microbial ecology</span> Study of the relationship of microorganisms with their environment

Microbial ecology is the ecology of microorganisms: their relationship with one another and with their environment. It concerns the three major domains of life—Eukaryota, Archaea, and Bacteria—as well as viruses.

<span class="mw-page-title-main">Biofouling</span> Growth of marine organisms on surfaces

Biofouling or biological fouling is the accumulation of microorganisms, plants, algae, or small animals where it is not wanted on surfaces such as ship and submarine hulls, devices such as water inlets, pipework, grates, ponds, and rivers that cause degradation to the primary purpose of that item. Such accumulation is referred to as epibiosis when the host surface is another organism and the relationship is not parasitic. Since biofouling can occur almost anywhere water is present, biofouling poses risks to a wide variety of objects such as boat hulls and equipment, medical devices and membranes, as well as to entire industries, such as paper manufacturing, food processing, underwater construction, and desalination plants.

<span class="mw-page-title-main">Antimicrobial peptides</span> Class of peptides that have antimicrobial activity

Antimicrobial peptides (AMPs), also called host defence peptides (HDPs) are part of the innate immune response found among all classes of life. Fundamental differences exist between prokaryotic and eukaryotic cells that may represent targets for antimicrobial peptides. These peptides are potent, broad spectrum antimicrobials which demonstrate potential as novel therapeutic agents. Antimicrobial peptides have been demonstrated to kill Gram negative and Gram positive bacteria, enveloped viruses, fungi and even transformed or cancerous cells. Unlike the majority of conventional antibiotics it appears that antimicrobial peptides frequently destabilize biological membranes, can form transmembrane channels, and may also have the ability to enhance immunity by functioning as immunomodulators.

Virulence factors are cellular structures, molecules and regulatory systems that enable microbial pathogens to achieve the following:

In microbiology, the minimum inhibitory concentration (MIC) is the lowest concentration of a chemical, usually a drug, which prevents visible in vitro growth of bacteria or fungi. MIC testing is performed in both diagnostic and drug discovery laboratories.

<span class="mw-page-title-main">Skin flora</span> Microbiota that reside on the skin

Skin flora, also called skin microbiota, refers to microbiota that reside on the skin, typically human skin.

Lysostaphin is a Staphylococcus simulans metalloendopeptidase. It can function as a bacteriocin (antimicrobial) against Staphylococcus aureus.

<span class="mw-page-title-main">Contamination control</span> Activities aiming to reduce contamination

Contamination control is the generic term for all activities aiming to control the existence, growth and proliferation of contamination in certain areas. Contamination control may refer to the atmosphere as well as to surfaces, to particulate matter as well as to microbes and to contamination prevention as well as to decontamination.

Copper and its alloys are natural antimicrobial materials. Ancient civilizations exploited the antimicrobial properties of copper long before the concept of microbes became understood in the nineteenth century. In addition to several copper medicinal preparations, it was also observed centuries ago that water contained in copper vessels or transported in copper conveyance systems was of better quality than water contained or transported in other materials.

Polymers with the ability to kill or inhibit the growth of microorganisms such as bacteria, fungi, or viruses are classified as antimicrobial agents. This class of polymers consists of natural polymers with inherent antimicrobial activity and polymers modified to exhibit antimicrobial activity. Polymers are generally nonvolatile, chemically stable, and can be chemically and physically modified to display desired characteristics and antimicrobial activity. Antimicrobial polymers are a prime candidate for use in the food industry to prevent bacterial contamination and in water sanitation to inhibit the growth of microorganisms in drinking water.

Antimicrobial copper-alloy touch surfaces can prevent frequently touched surfaces from serving as reservoirs for the spread of pathogenic microbes. This is especially true in healthcare facilities, where harmful viruses, bacteria, and fungi colonize and persist on doorknobs, push plates, railings, tray tables, tap (faucet) handles, IV poles, HVAC systems, and other equipment. These microbes can sometimes survive on surfaces for more than 30 days.

Biofilm formation occurs when free floating microorganisms attach themselves to a surface. Although there are some beneficial uses of biofilms, they are generally considered undesirable, and means of biofilm prevention have been developed. Biofilms secrete extracellular polymeric substance that provides a structural matrix and facilitates adhesion for the microorganisms; the means of prevention have thus concentrated largely on two areas: killing the microbes that form the film, or preventing the adhesion of the microbes to a surface. Because biofilms protect the bacteria, they are often more resistant to traditional antimicrobial treatments, making them a serious health risk. For example, there are more than one million cases of catheter-associated urinary tract infections (CAUTI) reported each year, many of which can be attributed to bacterial biofilms. There is much research into the prevention of biofilms.

The lung microbiota is the pulmonary microbial community consisting of a complex variety of microorganisms found in the lower respiratory tract particularly on the mucous layer and the epithelial surfaces. These microorganisms include bacteria, fungi, viruses and bacteriophages. The bacterial part of the microbiota has been more closely studied. It consists of a core of nine genera: Prevotella, Sphingomonas, Pseudomonas, Acinetobacter, Fusobacterium, Megasphaera, Veillonella, Staphylococcus, and Streptococcus. They are aerobes as well as anaerobes and aerotolerant bacteria. The microbial communities are highly variable in particular individuals and compose of about 140 distinct families. The bronchial tree for instance contains a mean of 2000 bacterial genomes per cm2 surface. The harmful or potentially harmful bacteria are also detected routinely in respiratory specimens. The most significant are Moraxella catarrhalis, Haemophilus influenzae, and Streptococcus pneumoniae. They are known to cause respiratory disorders under particular conditions namely if the human immune system is impaired. The mechanism by which they persist in the lower airways in healthy individuals is unknown.

Microbes can be damaged or killed by elements of their physical environment such as temperature, radiation, or exposure to chemicals; these effects can be exploited in efforts to control pathogens, often for the purpose of food safety.

The host–pathogen interaction is defined as how microbes or viruses sustain themselves within host organisms on a molecular, cellular, organismal or population level. This term is most commonly used to refer to disease-causing microorganisms although they may not cause illness in all hosts. Because of this, the definition has been expanded to how known pathogens survive within their host, whether they cause disease or not.

Ultra-low fouling is a rating of a surface's ability to shed potential contamination. Surfaces are prone to contamination, which is a phenomenon known as fouling. Unwanted adsorbates caused by fouling change the properties of a surface, which is often counter-productive to the function of that surface. Consequently, a necessity for anti-fouling surfaces has arisen in many fields: blocked pipes inhibit factory productivity, biofouling increases fuel consumption on ships, medical devices must be kept sanitary, etc. Although chemical fouling inhibitors, metallic coatings, and cleaning processes can be used to reduce fouling, non-toxic surfaces with anti-fouling properties are ideal for fouling prevention. To be considered effective, an ultra-low fouling surface must be able to repel and withstand the accumulation of detrimental aggregates down to less than 5 ng/cm2. A recent surge of research has been conducted to create these surfaces in order to benefit the biological, nautical, mechanical, and medical fields.

Nanoparticles have been studied extensively for their antimicrobial properties in order to fight super bug bacteria. Several characteristics in particular make nanoparticles strong candidates as a traditional antibiotic drug alternative. Firstly, they have a high surface area to volume ratio, which increases contact area with target organisms. Secondly, they may be synthesized from polymers, lipids, and metals. Thirdly, a multitude of chemical structures, such as fullerenes and metal oxides, allow for a diverse set of chemical functionalities.

References

  1. "Dorlands Medical Dictionary:antibacterial". Archived from the original on 2010-11-18. Retrieved 2010-10-29.
  2. 1 2 Onaizi SA, Leong SS (2011). "Tethering antimicrobial peptides: current status and potential challenges". Biotechnology Advances. 29 (1): 67–74. doi:10.1016/j.biotechadv.2010.08.012. PMID   20817088.
  3. 1 2 3 4 Dastjerdi R, Montazer M (August 2010). "A review on the application of inorganic nano-structured materials in the modification of textiles: focus on anti-microbial properties". Colloids and Surfaces. B, Biointerfaces. 79 (1): 5–18. doi:10.1016/j.colsurfb.2010.03.029. PMID   20417070.
  4. Chen C, Enrico A, Pettersson T, Ek M, Herland A, Niklaus F, et al. (September 2020). "Bactericidal surfaces prepared by femtosecond laser patterning and layer-by-layer polyelectrolyte coating". Journal of Colloid and Interface Science. 575: 286–297. Bibcode:2020JCIS..575..286C. doi: 10.1016/j.jcis.2020.04.107 . PMID   32380320.
  5. "Copper Touch Surfaces". Archived from the original on 2012-07-23. Retrieved 2011-09-21.
  6. Fujishima A, Rao TN, Tryk DA (2000). "Titanium Dioxide Photocatalysis". J Photochem Photobiol C. 1: 1–21. doi:10.1016/S1389-5567(00)00002-2. S2CID   73665845.
  7. Liau SY, Read DC, Pugh WJ, Furr JR, Russell AD (October 1997). "Interaction of silver nitrate with readily identifiable groups: relationship to the antibacterial action of silver ions". Letters in Applied Microbiology. 25 (4): 279–283. doi: 10.1046/j.1472-765x.1997.00219.x . PMID   9351278.
  8. Snodgrass PJ, Vallee BL, Hoch FL (February 1960). "Effects of silver and mercurials on yeast alcohol dehydrogenase". The Journal of Biological Chemistry. 235 (2): 504–508. doi: 10.1016/S0021-9258(18)69555-9 . PMID   13832302.
  9. Russell AD, Hugo WB (1994). "Antimicrobial activity and action of silver". Prog. Med. Chem. Progress in Medicinal Chemistry. 31: 351–370. doi:10.1016/S0079-6468(08)70024-9. ISBN   9780444818072. PMID   8029478.
  10. "Biosafe - Organosilane Antimicrobials" (PDF). Gelest.
  11. 1 2 Yamada H, Takahashi N, Okuda S, Tsuchiya Y, Morisaki H (August 2010). "Direct observation and analysis of bacterial growth on an antimicrobial surface". Applied and Environmental Microbiology. 76 (16): 5409–5414. Bibcode:2010ApEnM..76.5409Y. doi:10.1128/aem.00576-10. PMC   2918969 . PMID   20562272.
  12. Isquith AJ, Abbott EA, Walters PA (December 1972). "Surface-bonded antimicrobial activity of an organosilicon quaternary ammonium chloride". Applied Microbiology. 24 (6): 859–863. doi: 10.1128/AEM.24.6.859-863.1972 . PMC   380687 . PMID   4650597.
  13. 1 2 Ioannou CJ, Hanlon GW, Denyer SP (January 2007). "Action of disinfectant quaternary ammonium compounds against Staphylococcus aureus". Antimicrobial Agents and Chemotherapy. 51 (1): 296–306. doi:10.1128/aac.00375-06. PMC   1797692 . PMID   17060529.
  14. 1 2 3 Zhao L, Chu PK, Zhang Y, Wu Z (October 2009). "Antibacterial coatings on titanium implants". Journal of Biomedical Materials Research Part B: Applied Biomaterials. 91 (1): 470–480. doi:10.1002/jbm.b.31463. PMID   19637369.
  15. Wright, P. F. and Webster, R.G. (2001) "Orthomyxoviruses". In: Fields, B.N. and Knipe, D.M. (eds.) Fields Virology, 4th Edition, Lippincott Williams & Wilkins, Philadelphia, pp. 1533–1579. ISBN   9780781718325
  16. Haldar J, Chen J, Tumpey TM, Gubareva LV, Klibanov AM (March 2008). "Hydrophobic polycationic coatings inactivate wild-type and zanamivir- and/or oseltamivir-resistant human and avian influenza viruses". Biotechnology Letters. 30 (3): 475–479. doi: 10.1007/s10529-007-9565-5 . PMID   17972018. S2CID   28291117.
  17. Noyce JO, Michels H, Keevil CW (April 2007). "Inactivation of influenza A virus on copper versus stainless steel surfaces". Applied and Environmental Microbiology. 73 (8): 2748–2750. Bibcode:2007ApEnM..73.2748N. doi:10.1128/AEM.01139-06. PMC   1855605 . PMID   17259354.
  18. "Viruses Influenza A". Archived from the original on 2009-10-18. Retrieved 2011-09-22.
  19. "Influenza A". coppertouchsurfaces.org. Archived from the original on 2011-08-14. Retrieved 2011-09-22.
  20. 1 2 Etienne O, Gasnier C, Taddei C, Voegel JC, Aunis D, Schaaf P, et al. (November 2005). "Antifungal coating by biofunctionalized polyelectrolyte multilayered films". Biomaterials. 26 (33): 6704–6712. doi:10.1016/j.biomaterials.2005.04.068. PMID   15992921.
  21. Weaver L, Michels HT, Keevil CW (January 2010). "Potential for preventing spread of fungi in air-conditioning systems constructed using copper instead of aluminium". Letters in Applied Microbiology. 50 (1): 18–23. doi:10.1111/j.1472-765X.2009.02753.x. PMID   19943884. S2CID   3912272.
  22. 1 2 3 4 Butt, H., Graf, K., Kappl, M. (2003) Physics and Chemistry of Interfaces. Wiley-VCH.
  23. S. Chatterjee, J S Murallidharan, A. Agrawal, R. Bhardwaj. Designing Antiviral surfaces to suppress the spread of COVID-19, Physics of Fluids, Vol. 33, pp 052101, 2021. doi.org/10.1063/5.0049404
  24. 1 2 3 4 5 6 7 Functional Biomaterials – Matyjaszewski Polymer Group. Carnegie Mellon University. Retrieved on 2020-09-07.
  25. 1 2 3 Xue CH, Jia ST, Zhang J, Ma JZ (June 2010). "Large-area fabrication of superhydrophobic surfaces for practical applications: an overview". Science and Technology of Advanced Materials. 11 (3): 033002. doi:10.1088/1468-6996/11/3/033002. PMC   5074297 . PMID   27877336.
  26. 1 2 Photocatalysis Applications of Titanium Dioxide Ti02. TitaniumArt.com. Retrieved on 2020-09-07.
  27. Leyland NS, Podporska-Carroll J, Browne J, Hinder SJ, Quilty B, Pillai SC (April 2016). "Highly Efficient F, Cu doped TiO2 anti-bacterial visible light active photocatalytic coatings to combat hospital-acquired infections". Scientific Reports. 6 (1): 24770. Bibcode:2016NatSR...624770L. doi:10.1038/srep24770. PMC   4838873 . PMID   27098010.
  28. 1 2 3 4 Huang JJ, Hu HY, Lu SQ, Li Y, Tang F, Lu Y, Wei B (July 2012). "Monitoring and evaluation of antibiotic-resistant bacteria at a municipal wastewater treatment plant in China". Environment International. 42: 31–36. doi:10.1016/j.envint.2011.03.001. PMID   21450343.
  29. Floros MC, Bortolatto JF, Oliveira OB, Salvador SL, Narine SS (March 2016). "Antimicrobial Activity of Amphiphilic Triazole-Linked Polymers Derived from Renewable Sources". ACS Biomaterials Science & Engineering. 2 (3): 336–343. doi:10.1021/acsbiomaterials.5b00412. PMID   33429537.
  30. Lam SJ, O'Brien-Simpson NM, Pantarat N, Sulistio A, Wong EH, Chen YY, et al. (September 2016). "Combating multidrug-resistant Gram-negative bacteria with structurally nanoengineered antimicrobial peptide polymers". Nature Microbiology. 1 (11): 16162. doi:10.1038/nmicrobiol.2016.162. PMID   27617798. S2CID   29908036.
  31. 1 2 3 EPA registers copper-containing alloy products, May 2008
  32. Wang C, Zolotarskaya O, Ashraf KM, Wen X, Ohman DE, Wynne KJ (June 2019). "Surface Characterization, Antimicrobial Effectiveness, and Human Cell Response for a Biomedical Grade Polyurethane Blended with a Mixed Soft Block PTMO-Quat/PEG Copolyoxetane Polyurethane". ACS Applied Materials & Interfaces. 11 (23): 20699–20714. doi:10.1021/acsami.9b04697. PMID   31117452. S2CID   162181434.
  33. Sibilo R, Mannelli I, Reigada R, Manzo C, Noyan MA, Mazumder P, Pruneri V (May 2020). "Direct and Fast Assessment of Antimicrobial Surface Activity Using Molecular Dynamics Simulation and Time-Lapse Imaging". Analytical Chemistry. 92 (10): 6795–6800. doi: 10.1021/acs.analchem.0c00367 . PMID   32295344.
  34. Zemljič, Lidija Fras; Plohl, Olivija; Vesel, Alenka; Luxbacher, Thomas; Potrč, Sanja (2020). "Physicochemical Characterization of Packaging Foils Coated by Chitosan and Polyphenols Colloidal Formulations". International Journal of Molecular Sciences. 21 (2): 495. doi: 10.3390/ijms21020495 . ISSN   1422-0067. PMC   7014365 . PMID   31941018.
  35. Kelly, Andrew M.; Kaltenhauser, Verena; Mühlbacher, Inge; Rametsteiner, Karl; Kren, Harald; Slugovc, Christian; Stelzer, Franz; Wiesbrock, Frank (2013). "Poly(2-oxazoline)-derived Contact Biocides: Contributions to the Understanding of Antimicrobial Activity: Poly(2-oxazoline)-derived Contact Biocides: Contributions to the Understanding …". Macromolecular Bioscience. 13 (1): 116–125. doi:10.1002/mabi.201200240. PMID   23208666.
  36. Masri, Abdulkader; Anwar, Ayaz; Khan, Naveed Ahmed; Shahbaz, Muhammad Saquib; Khan, Khalid Mohammed; Shahabuddin, Syed; Siddiqui, Ruqaiyyah (2019). "Antibacterial Effects of Quinazolin-4(3H)-One Functionalized-Conjugated Silver Nanoparticles". Antibiotics. 8 (4): 179. doi: 10.3390/antibiotics8040179 . ISSN   2079-6382. PMC   6963639 . PMID   31600971.
  37. 1 2 3 Li Q, Mahendra S, Lyon DY, Brunet L, Liga MV, Li D, Alvarez PJ (November 2008). "Antimicrobial nanomaterials for water disinfection and microbial control: potential applications and implications". Water Research. 42 (18): 4591–4602. Bibcode:2008WatRe..42.4591L. doi:10.1016/j.watres.2008.08.015. PMID   18804836.
  38. 1 2 Darouiche RO, Green G, Mansouri MD (April 1998). "Antimicrobial activity of antiseptic-coated orthopaedic devices". International Journal of Antimicrobial Agents. 10 (1): 83–86. doi:10.1016/s0924-8579(98)00017-x. PMID   9624548.
  39. Fichman G, Andrews C, Patel NL, Schneider JP (October 2021). "Antibacterial Gel Coatings Inspired by the Cryptic Function of a Mussel Byssal Peptide". Advanced Materials. 33 (40): e2103677. Bibcode:2021AdM....3303677F. doi:10.1002/adma.202103677. PMC   8492546 . PMID   34423482.
  40. Hanaor DA, Sorrell CC (2014). "Sand Supported Mixed-Phase TiO2 Photocatalysts for Water Decontamination Applications". Advanced Engineering Materials. 16 (2): 248–254. arXiv: 1404.2652 . Bibcode:2014arXiv1404.2652H. doi:10.1002/adem.201300259. S2CID   118571942.
  41. Cushnie TP, Robertson PK, Officer S, Pollard PM, Prabhu R, McCullagh C, Robertson JM (2010). "Photobactericidal effects of TiO2 thin films at low temperature". Journal of Photochemistry and Photobiology A: Chemistry. 216 (2–3): 290–294. doi:10.1016/j.jphotochem.2010.06.027.
  42. Hochmannova L, Vytrasova J (2010). "Photocatalytic and antimicrobial effects of interior paints". Progress in Organic Coatings. 67: 1–5. doi:10.1016/j.porgcoat.2009.09.016.
  43. Schmidt MG, et al. (Copper Touch Surface Initiative) (2011). "Copper surfaces in the ICU reduced the relative risk of acquiring an infection while hospitalized". BMC Proceedings. 5 (Suppl 6): O53. doi: 10.1186/1753-6561-5-S6-O53 . PMC   3239467 .
  44. "Research Proves Antimicrobial Copper Reduces the Risk of Infections by More Than 40%". coppertouchsurfaces.org. July 1, 2011. Archived from the original on 2011-07-25.
  45. World Health Organization’s 1st International Conference on Prevention and Infection Control (ICPIC) in Geneva, Switzerland on July 1st, 2011
  46. 1 2 Yebra DM, Kiil S, Dam-Johansen K (2004). "Antifouling technology – past, present and future steps towards efficient and environmentally friendly antifouling coatings". Progress in Organic Coatings. 50 (2): 75–104. doi:10.1016/j.porgcoat.2003.06.001.
  47. 1 2 3 4 "Focus on IMO - Anti-fouling systems". International Maritime Organisation.