Polymer Based Dentures: History
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Polymers remain an integral part of denture fabrication materials, specifically polymethyl methacrylate (PMMA). PMMA has been extensively used, particularly in construction as a denture base material. Nonetheless, various challenges, including microbial threats in the form of candidiasis occurrence, still remain a biological challenge to denture wearers. 

  • polymers
  • PMMA
  • denture
  • denture base
  • prosthodontics

1. Introduction

Dentures were developed thousands of years ago, starting in 3000 BC. They were developed in Egypt, known as the earliest country to develop medical and prosthetic devices. Research has found that the first dental prosthesis was registered in Egypt in 2500 BC [1]. The evolution of complete denture bases was found in the 16th century by the construction of a complete set of upper and lower dentures in Switzerland that was made from human bone, which are made from the curve-molded bone layouts, coarsely cut from a bull’s femur and intertwined at their furthest back points to frame a pivot. In the 18th century, dentures made from metals and other natural products were introduced, followed by the construction of porcelain in the late 18th century [2].
Polymer, particularly polymethyl methacrylate (PMMA) has been extensively used as a denture base material mainly due to its cost-effectiveness, simple fabrication and manipulation, easier maintenance and repair process, low density, satisfactory physical and mechanical properties, and optical properties almost similar to natural human gum. Initially, Rohm and Hass established the use of PMMA in sheet design, whereas Nemours pioneered the use of PMMA in powder structure. Dr. Walter Wright then utilized PMMA as a denture base material, which was employed as a prosthesis component for 10 years [3].
Nonetheless, various intraoral biological threats may occur to denture wearers. Denture stomatitis (DS), also known as chronic erythematous candidiasis, is an infection of oral mucosa that occurs conventionally beneath the dental prosthesis and most commonly in the palatal area [4]. The clinical manifestations of denture stomatitis can be seen as the appearance of mucosal inflammation, erythema and hyperplasia, a burning sensation of the affected site and discomfort and a change in taste perception.
The denture stomatitis is mainly caused by microbes and fungus on the denture. A prolonged period of denture wearing could promote the flourishing of the microbes and fungus. Ergo, it is essential that the dentures carry antibacterial properties to inhibit the growth of harmful microbes. Although PMMA has superior mechanical properties, its biological properties can still be improved. One of the ways that researchers have explored enhancing this material is through modifying its resin matrix by incorporating nanoparticles and micro filler into the material [5].

2. Polymethyl Methacrylate (PMMA)

PMMA is essentially an essence derived from an ester of methacrylic compound (CH2=C[CH3]CO2H), as in Figure 1, and it is a synthetic resin polymer produced by polymerization of methyl methacrylate (C5O2H8) to polymethylmethacrylate (C5O2H8)n. Polymerization is conventionally under the influence of an initiator and activated by free radicals, chemically or under other potential sources, such as light and heat. The denture base PMMA material fabrication and activation can be divided into other groups, as shown in Figure 2.
Figure 1. The structure of PMMA.
Figure 2. Denture base fabrication conventionally based on PMMA material.
The denture base polymers can be classified based on the polymerization activators, such as heat cure, light cure, or cold cure, which can differ in the type of polymerization activation and compositions. In the heat-cured type of PMMA, the polymerization reaction begins when the powder containing PMMA is mixed together with benzoyl peroxide initiator, a plasticizer (dibutyl phthalate) and liquid composed of methyl methacrylate (MMA) monomer, and ethylene glycol dimethacrylate that act as a cross-linking agent with hydroquinone as an inhibitor. Theoretically, the polymerization heat curing process is activated by heat as shown in Figure 3. The chemical reaction in this polymerization process of acrylic resin is when the process conversion of the monomer (MMA) to the polymer (PMMA) become a mixture of the two is subjected to heat by water bath to activate the initiator to dissociate into carbon dioxide (CO2) and generate free radicals when heated.
Meanwhile, for the light curing process, these components included a photo initiator system, an acrylic copolymer and microfine silica as fillers and a urethane dimethacrylate matrix for the light curing process. The photo initiator is also activated by the same visible light source that was used for cold curing light as activated composite. S unique high energy light source was employed to provide soft sheets that had already been combined for final polymerization. As a result, individuals who are allergic to methyl methacrylate monomer can use the light activated denture base materials as an alternative.
Figure 3. Chemical reaction of heat curing process [6].
Last but not least, in the cold cure PMMA type, the tertiary amine initiator, such as dimethyl para-toluidine, was added to the cold cure PMMA, which triggers benzoyl peroxide degradation, and this cold curing process does not require thermal energy. Figure 4 shows the chemistry of the resin has a conversion process from monomer (MMA) to polymer (PMMA) by activation of the tertiary amine of PMMA (polymer) + benzoyl peroxide (initiator) and MMA (monomer) + dimethyl-para-toludin. In the first step of MMA monomer suspension of polymerization, benzoyl peroxide acts as an initiator to interact with the monomer and is equal to two of the water. A soluble water-stabilizer is also helpful to obtain smooth and uniformly sized spherical microparticles.
This causes free radicals to be released, allowing polymerization to occur. Despite a high degree of polymerization resulting in solid physical features, incomplete polymerization and inadequate adaptability are still the key problems in the strength properties of this material. The limitations of the product yield through this polymerization technique are weak bond strength and expensive materials for equipment needed for inactivation [3].
Figure 4. Chemical reaction of PMMA by cold curing process [7].
The usage of PMMA as a denture has grown exponentially in recent decades due to its superior characteristics, as mentioned before. Nonetheless, the main concern for PMMA in constructing conventional dentures is the release of residual methyl methacrylate monomer, which is a free monomer when constructed by heat polymerization technique. Although recent studies show only minimal leaching (approximately 5.4 wt%) that occurs in PMMA monomer and is a rare occurrence, this monomer leaching [8] that is released from the PMMA material can also promote allergic reactions, such as denture stomatitis, oedema, and mucosal ulceration, which are made profound by the adhesion of microbes, such as Candida albicans and Staphylococcus aureus [4][9]. This material is also prone to change in dimensional stability due to error introduced during the manufacturing process within various procedures, such as separating media application, post-dewaxing operation, consistent polymer to monomer ratio, trial closure method, and curing cycle leads to the porosity of the denture. When porosity exceeds 11% from the initial composition of the material, the mechanical and aesthetic properties of the material deteriorated physically, thus providing irregular surfaces for the reservoir of microorganisms, such as Candida albicans [9].

3. Common Microbial Challenges Associated with PMMA in Conventional Denture

Denture Stomatitis

Denture stomatitis can be divided into three main types. Denture stomatitis Type 1 has localized areas of inflammation, possibly caused by trauma or the denture itself being too tight. Type 2 denture stomatitis, the most common presentation seen in long wearer dentures appears with generalized erythema covering the denture-bearing area (Figure 5) and Type 3 denture stomatitis, known as inflammatory papillary hyperplasia, will usually affect the hard palate or the alveolar ridges (Figure 6) [10].
There are various common causes of denture stomatitis. Candida albicans sp. has been one of the main factors in the aetiology of DS and is thought to be responsible for 90% of cases of denture stomatitis. A variety of bacteria, including Staphylococcus sp., Streptococcus sp., Fusobacterium sp., and Bacteroides sp. can be involved [11]. Candida’s position shifts when the immunological balance between the host and the fungus shifts from commensal to parasite and may also act as an opportunistic infection [12]Candida sp. must first adhere to diverse host cells, either directly with the aid of immobilized adhesins, such as integrins or cadherins, or indirectly with the help of other microbes [13]. Adherence proteins such as Amyotrophic Lateral Sclerosis type1-7 (ALS1-7), Amyotrophic Lateral Sclerosis type 9 (ALS9), and Hyphal Wall Protein (HWP1) aid in the adhesion of yeast cells to the host surface. The interaction of ALS proteins with abiotic materials is influenced by hydrophobicity, which contributes to biofilm development, for example, on prosthetic devices. Next, cells will penetrate the tissue via stimulated endocytosis and active penetration in the mouth cavity. C. albicans secretes a number of hydrolytic enzymes, including aspartic proteinases, a phospholipase, and a lipase, before penetrating the cellular barriers that will digest the invading cell’s membrane and surface molecules. Secreted aspartic proteinases were already investigated more extensively because they enable the host cell invasion and counteract the host immune system by degrading Immunoglobulin G (IgG) heavy chains, C3 protein, collagen, and fibronectin. Hence, these findings have proven the tissue irritation caused by the host’s weak defence mechanisms. The presence of perfect Candida growth circumstances thus resulting in the fungi being able to colonize the acrylic resin creating favourable conditions for adhesion and proliferation [11].
Moreover, the risk of developing this oral mucosal disease in patients who wear dentures ranges from 36.7% to 65% [14][15]. Continuous and repetitive denture use without periodic tissue rest, damage on the abutment and residual tooth, reduced salivary flow due to chronic diseases, such as Sjogren Syndrome or certain medication, denture age, immunocompromised patient with systemic chronic diseases, such as poorly controlled diabetes mellitus, and harmful habits, such as smoking, are all risk factors for this disease. Furthermore, the rough and hard denture’s fitting surface may also act as a reservoir and aid in the adhesion of microorganisms to the denture and enhancement of biofilm formation.
Poor denture hygiene encourages pathogenic germs to proliferate in dental plaque on denture fitting surfaces, and there is a definite correlation between poor denture hygiene and denture stomatitis lesions. If the denture is worn continually, especially at night, Candida can form a biofilm on the mucosa beneath it. A lower pH creates a relatively anaerobic environment, which encourages Candida growth. Saliva is unable to clean the denture-bearing area, allowing harmful bacteria to flourish. Poor denture hygiene also aided the growth of pathogenic germs in the dental plaque on the denture fitting surfaces. There is a definite correlation between poor denture hygiene and poor denture fit due to inflammation in the denture-bearing area [16].
There are many ways to treat denture stomatitis. One of them is by using antifungal medications that are available in various forms, such as topical application (Amphotericin B, Nystatin, Econazole) to minimize palatal irritation [17] and its benefit is enhanced if used with improved denture hygiene. Next, patient also should learn the correct denture hygiene technique. Effective active methods for cleaning dentures are thorough brushing of the denture in combination with a non-abrasive proprietary paste, which should be carried out after every meal. Moreover, it is also advisable to soak dentures in 0.1% aqueous chlorhexidine or warm soapy water every night to remove microbial plaque on the denture [18].
Figure 5. Clinical manifestation of Candida albicans sp. fungal infection characterized by the redness (erythema) on the denture base adaptation (saddle) area. In this case, the disease was precipitated by the Sjogren Syndrome due to the low quantity and quality of saliva.
Figure 6. Clinical manifestations of Candida albicans sp. fungal infection characterized by the redness (erythema) on the denture base adaptation (saddle) area. In this case, it was aggravated by poor oral hygiene, periodontal disease, and the presence of an untreated root stump.

4. Pathogens in Denture Stomatitis

4.1. Candida sp. (Candida albicans)

Candida albicans is a Candida species that may grow on various surfaces in many ways. Candida albicans is by far the most common isolated Candida species found in denture stomatitis presentation, followed by Candida glabrata [16]. Candida has the ability to bind with oral mucosa and is composed of key elements in resistance toward the oral cavity’s host clearance systems which function as protective reservoirs, preventing Candida from being washed away by saliva or dislodgement pressures. The capability of this yeast to adhere to mucosal cells, transform from single cell to filamentous form, secrete enzymes, such as aspartyl proteinase and phospholipase, and produce biofilms are all factors that contribute to its pathogenic action [19] C. albicans, on the other hand, has a strong desire to stick to the acrylic resin used to make dentures, and the acrylic resin has particular properties, such as hydrophobicity, that aid adherence as a key stage in biofilm development [20]

4.2. Staphylococcus aureus

Staphylococcus aureus is a Gram-positive bacteria with golden pigment characteristics based on its name ‘Aureus’. It also lives in a facultative anaerobe environment and can withstand high salt, extreme pH, and temperatures. Moreover, Staphylococcus aureus also produces many virulence factors and most of it is β–lactamase. Staphylococcus aureus can also adhere to a wide variety of oral surfaces, including dental prostheses, which is a non-shedding oral surface. These bacteria can also cause diseases by inducing pyogenic inflammation and producing toxins, such as exfoliative toxins A and B, which can dissolute the epidermal desmosome which causes fine sheets of skin to be peeled off and reveal the moist red skin beneath. Based on a few studies, they also found colonies of Staphylococcus aureus from the hard palate are arranged in small clusters obtained from the site of denture stomatitis. These colonies are identified as Staphylococcus aureus based on several tests and PCR amplification of Nuc and Coa genes, such as catalase-positive, Pastorex Staph Plus positive, and clumping factor-positive oxidase-negative. A delayed coagulase reaction was observed after a 23-h incubation in the tube coagulase test. Moreover, some studies found that Staphylococcus Aureus from denture wearers have caused greater activation of monocytes than from non-wearers but were less prone to phagocytosis, which suggests stronger virulence factors possessed by Staphylococcus aureus [21]. Furthermore, recent evidence suggests that Staphylococcus aureus strains are equally and frequently isolated from older persons presenting with denture stomatitis as asymptomatic denture wearers [22] Therefore, from these recent findings, it can be concluded that Staphylococcus aureus may also contribute to the occurrence of denture stomatitis due to its adherence ability to prosthetic materials and its strong virulence factor [18].

4.3. Streptococcus mutans

Streptococcus mutans is a common microorganism found on denture surfaces, and if incubated simultaneously with Candida albicans, it may occupy the binding sites and might be able to promote yeast adhesion. The in vitro adherence mechanisms of S. mutans and C. albicans can contribute to understanding these organisms’ behavior in the dental plaque. The interaction of these microorganisms is generally considered as mutual in a combined culture [23] Conventionally, the adherence and maturation of strep mutans is regarded as the initial step for oral biofilm formation and distinct adherence mechanisms, which can lead to candidiasis resistance to antifungal therapeutic agents. In complex biofilms, such as those found in the oral cavity, the ability of yeast to agglutinate with bacteria can be mediated by species interaction within the biofilm and external factors, such as saliva, oral hygiene, and exposure to antimicrobial agents. In-vitro evidence showed that despite the Candida–bacteria interaction, emerging studies have investigated that S. mutans species can also contribute to patients with candidiasis or yeast-related diseases [24].

4.4. Fusobacterium nucleatum

Fusobacterium nucleatum is a Gram-negative anaerobe that plays a role in producing plaque and biofilm in the oral cavity. F. nucleatum is a well-known “bridging” organism required for the sequential succession of colonization events in oral polymicrobial communities due to its capacity to develop physical contact with Gram-positive and Gram-negative species. It has the ability to link early commensal colonizers with late invaders, mainly composed of periodontal pathogens. As a result, it plays a critical role in the succession of genera in oral polymicrobial communities. Fusobacteria can form direct physical associations with eukaryotic microorganisms, such as fungus, and interact with bacteria. The coherence of F. nucleatum and Candida albicans has been widely established. It has been linked to the colonization of the oral cavity by Candida albicans, which was the main bacteria for the cause of denture stomatitis as stated by Jabra-Rizk et al. in 1999. Such inter-kingdom interactions could be crucial for C. albicans’ persistence as part of the microbes within the host and contribute to the advancement of polymicrobial infections under specific circumstances [25]. Therefore, a better understanding of the interacting cellular components should aid in developing new targeted therapies to block adherence. This mechanism could play a key role in polymicrobial pathogenesis involving these two organisms. 

5. Development of Digital Denture

Computer-aided design and manufacturing (CAD-CAM) systems are being widely used to design and to fabricate fixed, implant, and removable prostheses. Rapid technological advancement in artificial intelligence, data acquisition, rapid prototyping, and digital imaging such as cone beam computed tomography (CBCT) has supported the growth of digital manufacturing methods in dentistry. The manufacturing and fabrication process of dentures derived from the CAD-CAM system was found to be less porous, the most accurate, and with a fast-manufacturing time [26].
Digital dentistry using CAD-CAM technology and high precision 3D printers and scanners can improve dentures’ fit, aesthetics, and functional components, while reducing costs and labour and thus increasing efficiency and manufacturing outcomes. In digital dentures particularly, polymers would be of particular interest because of their ease of fabrication and desirable properties. The ability to design and produce dentures digitally opens the entire range of biomedical polymers for the utilization of material of choice in digital dentistry. The advent of new polymer materials with increased biocompatibility, durability, elasticity, and increased aesthetic appeal and cost-effectiveness offers significant advances for removable prosthetics [26][27].

6. Antimicrobial Properties on Digital Denture

One of the elements influencing microbial colonization on denture surfaces and the colour stability of the denture materials could be surface roughness [28] According to the current investigation, milled resins and quickly prototyped resins have comparable surface roughness. According to a study, conventional dentures have a rougher surface area than 3D-printed dentures. This surface substance is essential because it facilitates bacterial adhesions. Rough surfaces may encourage the growth of microorganisms [29].
They are frequently made of poly-methyl methacrylate (PMMA), a porous polymer that is more prone to the build-up of microbial biofilms than conventional dentures [30] The process of forming a biofilm starts with microbial adhesion. It is controlled by the pellicle adsorption of surface-bound salivary proteins and mucins [31].

7. Contemporary Modification on Denture Base Material

The summary of materials that have been introduced to improve the conventional and digital denture are compiled as tabulated in Table 1.
Some of the materials have been proven to help reduce bacterial colonization and also improve the overall mechanical properties of the materials. Materials that have helped to improve the denture, particularly biological properties, include Titanium Dioxide (TiO2), Graphene-Silver nanoparticles (G-Ag NP), Silver nanoparticles (NAg), graphene, 2-methacryloyloxyethyl phosphorylcholine (MPC) and dimethylaminohexadecyl methacrylate (DMAHDM), Surface Pre-reacted Glass-ionomer (S-PRG), food preservatives, including zinc oxide, potassium sorbate, sodium metabisulfite, nano-silver loaded zirconium phosphate, Phytoncide, Silicon Dioxide nanoparticles (SiO2 NP), quaternized N, N-dimethylaminoethyl methacrylate (DMAEMA), and also probiotics [32].
One of the nanoparticles that has been shown to increase the strength of dentures is Titanium Dioxide (TiO2). The composite mixture was created by successively adding 0.2 percent, 0.4 percent, 0.6 percent, 1 percent, and 2.5 percent weight-based amounts of TiO2 nanoparticles to PMMA. Gram-negative and positive bacteria, fungus, and other microbes are only a few of the microorganisms it has been shown to be active against. Additionally, the papers showed that there is antibacterial activity, and it is environmentally friendly. In addition, TiO2 has recently become more well-known because of its apparent high stability, catalytic function, availability, white colour, efficiency, and inexpensive cost. TiO2 is corrosion-resistant, non-toxic, and chemically inert. It also has a high refractive index. More research indicates that additional mechanical and biocompatibility tests should be carried out to extend the manufactured dentures for clinical usage [33].
Graphene-Ag nanoparticles are a substance that can be utilised to enhance 3D printed dentures (G-Ag NP). Radio-frequency Chemical Vapour Deposition (RF-CCVD) was used to create the composite of graphene silver nanoparticles (G-Ag Np). The physical and mechanical characteristics of PMMA were improved by the inclusion of graphene and silver nanoparticles. It has been demonstrated that silver fillings have an antibacterial effect. To ascertain whether the higher ratio of free monomers or the added fillers produce the antibacterial effect, additional investigation is required. With Candida albicans (the most common cause of prosthetic stomatitis) and other microorganisms that might cause oral infections, they intend to broaden the analysis by adding to the antibiotic spectrum [34].
A new kind of NAg solution (NS)/polymer methyl methacrylate denture base specimens (NS/PMMA) was created by synthesising silver nanoparticles (NAg) solution and combining it with acrylic acid and methyl methyacrylate (MMA) monomer. A widely used form of antimicrobial nanomaterial that has demonstrated a broad spectrum, high efficiency, strong antibacterial activity, and relatively good biocompatibility is easily accessible. Additionally, it is a simple, inexpensive method that has a great chance of developing into an antibacterial treatment for removable partial or complete dentures. It is unquestionably an appropriate material and can be utilised for the population of elderly individuals [35].
Nano-graphene (nGO) is another material that had been introduced to improve the properties of the denture. To clean and sterilize the nano-graphene nanoparticles (nGO) powder, 70% ethanol was used in the washing process. In order to prevent thermal damage to the nGO during heat-induced polymerization, chemically activated PMMA materials were chosen. nGO was added to PMMA powder at weight-relative doses of 0.25 g, 0.5 g, 1.0 g, or 2.0 g. It uses carbon-based nanoparticles to provide sustained, long-term antimicrobial-adhesive activities, without sacrificing mechanical qualities (nGO). Future studies should include novel approaches such functionalizing nGO with PEG, salinization, or carboxyl group to combat the inhomogeneous dispersion of nGO in composite [36].
Moreover, MPC (2-methacryloyloxyethyl phosphorylcholine), a protein repellent that hinders C. albicans from adhering to surfaces of denture, was added to other materials to improve the qualities of PMMA denture base materials. Dimethylaminohexadecyl methacrylate (DMAHDM) is also made up of antibacterial agents using the contact-killing method. When these positively charged substances come into contact with a negatively charged cell membrane, the result is a ruptured cell and cytoplasmic leakage. Less biofilm colony-forming units are produced when these ingredients are combined. This demonstrates that adding antibacterial properties and protein repelling chemicals will help conventional dentures to avoid developing denture stomatitis [37].
Next, The PMMA denture base can also be infused with food preservatives including sodium metabi-sulfite, potassium sorbate, and zinc oxide. By generating reactive oxygen species, ZnO promotes cell damage and apoptosis Reactive Oxygen Species (ROS). Two weak acid preservatives, Potassium Sorbate and Sodium Metabisulfite (PS and SM), can stop biological metabolism by accumulating protons inside of the microbial cells, however PS and SM also cause lipid peroxidation, which damages the cell membrane. Additionally, the release of sulphur dioxide molecules has been connected to the sulfur-containing compound SM. Disulfide bonds in protein structures can be broken by these substances, killing enzymes, and causing cellular damage. Therefore, it has been demonstrated that these effects of food preservatives on the denture base also have antibacterial capabilities on the denture base materials [38].
Phytoncide possessed antibacterial properties by weakening the cell wall, inducing bacterial self-degradation due to the disintegration of cell membranes, or interfering with the respiratory metabolism of bacteria. Therefore, the phytoncides that are generated from phenolic compounds may help to reduce microbial activity. Additionally, many of the secondary metabolites that plants generate stress different bacteria. Microorganisms will be impacted by this stress, and this occurrence is understood to be a plant defence mechanism. Allelopathy is a condition that influences ecological systems [39].
By inhibiting bacterial attachment to the denture base and having a self-cleaning effect, the extra layer of film created by SiO2 nanoparticles also aids in improving PMMA characteristics. The water molecules in micro-nano scale hierarchical structures are highly polar. It has a potent adsorption effect on dirt that is adhered to the surface, making it simple for the water to roll off the dirt from the sample surface. From a different angle, titanium dioxide further functions as a photocatalyst that would damage the bacterial cell membrane by creating reactive oxygen species, resulting in lipid peroxidation and cell death [40][41][42] As a result, the equilibrium of essential oils, such as K+, Na+, Ca2+, and Mg2+, will be disrupted [43].
Last but not least, lactobacillus produces antifungal peptides that might disrupt the fungus’ membrane or render its cytoplasm inactive after consumption, which enhances the qualities of denture materials. These probiotics inhibited and disrupted the Candida biofilm on the denture base resin. However, their used culture media had no impact on the denture base resin’s surface roughness. This will eventually aid in the prevention of denture stomatitis in people who wear dentures [44].
On the other hand, one of the remaining challenging aspects in modification of pure materials is to improve the fundamental properties without compromising other aspects of it. For example, although adding nanoparticles or fibers can improve the strength of PMMA, this may compromise the aesthetic, such as color or translucency, or increase biocompatibility issues via the leaching of degradation products in the oral cavity. Although the current laboratory modification of PMMA have resulted in encouraging outcomes, there is still needful careful interpretations and analysis prior using modified PMMA materials for clinical applications. The majority of biocompatibility and in vivo performance of modified materials are still questionable and require further clinical investigation and presumably human trials. Further research should focus on understanding the interactions of modified materials at the molecular level, the evaluation of various properties following American Dental Association specifications, and clinical performance in either simulated oral environments or in vivo clinical studies.
Table 1. Summary on modifications on conventional and digital denture to improve general characteristic properties of the material.

8. Conclusions

In conclusion, various materials and methods have been introduced to improve the biological properties, especially the biocompatibility and biofunctionalization of the denture base. Ideally, the incorporation of a specific substrate must improve the biological activity of the denture base, while improving the overall physical, mechanical, and optical properties. Nevertheless, the potential negative effect on mechanical properties upon improving the biological activities after incorporation of specific substrates, for an example incorporation of Quaternized N, N-dimethylaminoethyl methacrylate (DMAEMA), was carefully considered, as previously discussed in Table 1. Further research should mainly focus on improving the properties of the denture material, particularly the denture base material by incorporation of more inorganic and organic compounds, on a wider range of bacterial and fungal strains. A detailed investigation, particularly on characterization and mechanical properties, also needs to be emphasized together with future studies.

This entry is adapted from the peer-reviewed paper 10.3390/ijms231810426

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