Effects of Litsea cubeba Essential Oil Incorporated into Denture Soft Lining Materials

The antimicrobial properties, cell cytotoxicity and surface hardness of soft lining materials (GC soft liner, Viscogel and Coe comfort) incorporated with various concentrations of Litsea cubeba essential oil (LCEO) were evaluated. The minimum inhibitory concentrations of LCEO against Candida albicans and Streptococcus mutans were 1.25% v/v and 10% v/v, respectively. However, when LCEO was incorporated into the three soft lining materials (GC soft liner, Viscogel and Coe comfort), 10% v/v and 30% v/v of LCEO could inhibit the growth of C. albicans and S. mutans, respectively. The extracts of soft lining materials with 10% and 30% v/v LCEO, 2% chlorhexidine, 30% v/v nystatin and no additive were used for cytotoxicity tests on a human gingival fibroblast cell line. There was no significant difference in cell viability in all groups with additives compared to the no additive group (p > 0.05). Surface hardness increased significantly between 2 h and 7 day incubation times in all groups, including the controls (p < 0.05). A higher LCEO concentration had a dose-dependent effect on the surface hardness of all soft lining materials (p < 0.05). However, the surface hardness of materials with additive remained in accordance with ISO 10139-1. LCEO could be used as a natural product against oral pathogens, without having a negative impact on soft lining materials.


Introduction
Soft lining materials are used in various clinical treatments, such as relieving inflamed tissue, covering sharp atrophic ridges and improving denture fitting [1]. Soft lining materials are commonly used to relieve abused tissue and improve denture adaptation with antibiotic mouth rinse prescription in the case of denture stomatitis, a denture-induced oral infection among denture wearers [2]. Denture liners, on the other hand, are still prone to microbial accumulation, which typically includes Candida albicans, Staphyloccocus aureus and Streptococcus mutans [3]. Antimicrobial additives have been incorporated into soft lining materials as a drug delivery vehicle to improve the material properties and treatment effectiveness. Various substances, including nystatin, azole drugs, metallic oxide particles and natural products, have been chosen to combine into soft lining materials [4]. Due to the increase in antibiotic resistance and toxicity, alternative, naturally derived additives have become incredibly common.
Litsea cubeba, an evergreen tree from the Lauraceae family, is widely found in China, Japan and Southeast Asia. Litsea cubeba essential oil (LCEO) is extracted from various parts of the tree. It is reported that LCEO has the following pharmaceutical advantages: anti-inflammatory, anti-cancer and antimicrobial properties [5][6][7][8]. Chemical compounds vary depending on the part of tree; for example, citral, citronellal and limonene are the most common compounds in the roots and fruits, whilst β-phellandrene and β-terpinene are major compounds found in the stems and flowers [7,8]. In a previous study, a potent growth-inhibitory effect of L. cubeba on yeast and fungi (Saccharomyces cerevisiae, C. albicans and Aspergillus nigus) was revealed. In an agar disc diffusion assay, L. cubeba oil with citronellal as the main component completely inhibited this growth. The oil also affected the growth of Gram-positive bacteria (Bacillus subtilis and S. aureus), but it showed no effect on Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli) [8]. Another study showed that citral had broad antimicrobial effects against Gram-negative and Grampositive bacteria, fungi and protozoa. However, Gram-negative bacteria (P. aeruginosa and Klebsiella pneumoniae) are more resistant to citral than others [9].
Additionally, depending on the extraction procedure, traditional plants may have a variety of active chemical capabilities. In a previous work, the antioxidant capacity of Ephedra foeminea was changed by the use of various solvent extracts [10]. Another issue would be the drug form of an antibacterial agent. According to Khan et al., Cefuroxime axetil (CA), a semi-synthetic cephalosporin family of antibacterial antibiotics, has low oral bioavailability. To boost CA's solubility and cellular absorption capacity, a lipid-based self-nanoemulsifying drug delivery system was developed [11].
Nevertheless, adding substances into soft lining materials may adversely affect the mechanical properties of the materials. Therefore, it is crucial to maintain the most favorable condition in which antimicrobial activity is improved without compromising the other properties. Surface hardness is one of the required properties of soft lining materials for clinical use. Moreover, the cytotoxic effect on human gingival fibroblast cells is of concern, and the cytotoxicity of soft lining materials is attributed to leachable products [12].
Therefore, the aim of this study was to determine the optimum concentration of LCEO that could be used as an antimicrobial additive incorporated into soft lining materials while not significantly altering the surface hardness of the materials.

Antimicrobial Additives
LCEO (Thai-China Flavours and Fragrances Industry Co., Ltd., Nonthaburi, Thailand) containing citral as an active component was obtained by the steam distillation extraction technique from fruits. Nystatin oral suspension 100,000 IU/mL or 33.3 mg/mL (Continental Pharm Co., Ltd., Bangkok, Thailand) was selected to represent a conventional antifungal drug against C. albicans. Moreover, 2% chlorhexidine gluconate mouthwash (Faculty of Dentistry, Mahidol university, Bangkok, Thailand) was used as a positive control against S. mutans.

Soft Lining Material
GC soft liner (GC Dental Products Corp., Tokyo, Japan), Coe comfort (GC Dental Products Corp., Tokyo, Japan) and Viscogel (Dentsply Sirona Inc., Konstanz, Germany) were used in this study. The chemical compositions are listed in Table 1 [13]. and brain heart infusion agar (Becton, Dickinson and Company, Sparks, MD, USA), respectively. C. albicans and S. mutans were subcultured in Sabouraud dextrose media and brain heart infusion media, respectively, at 37 • C for 24 h before testing.

Antimicrobial Activity of LCEO
The antimicrobial activity of LCEO on C. albicans and S. mutans was assessed by using the agar disc diffusion assay. Inoculum suspensions were standardized by adjusting the turbidity to 1.0 and 0.5 McFarland standards using a McFarland densitometer (Biosan Medical-Biological Research & Technologies, GIBTHAI Co., Ltd., Bangkok, Thailand) for C. albicans and S. mutans, respectively. Then, 100 µL of diluted inoculum was used to form a lawn culture. LCEO was serially diluted in dimethyl sulfoxide (DMSO, Sigma-Aldrich, St. louis, MO, USA) to obtain a final concentration of 0.675, 1.25, 2.5, 5 and 10% v/v. The negative control was DMSO, and the positive control was nystatin oral suspension and 5% v/v of 2% chlorhexidine gluconate for C. albicans and S. mutans, respectively. Then, paper filter discs with a diameter of 6 mm were filled with 20 µL of the tested conditions. The plates were inoculated at 37 • C for 48 h. A digital caliper was used to measure the inhibition zone. The average inhibition zones were computed. Each experimental group (n = 5) was replicated five times independently.

Antimicrobial Activity of LCEO Incorporated into Soft Lining Materials
The antimicrobial activity of LCEO incorporated into GC soft liner, Coe comfort and Viscogel was assessed by using the agar well diffusion assay. Different concentrations of LCEO were added into the liquid components of soft lining materials before the powder was added and mixed. The final concentrations of the LCEO in the soft lining materials were 5%, 10%, 20% and 30% v/v. The final concentration of positive control in the materials against S. mutans was 5% v/v of 2% chlorhexidine gluconate (CHX), while soft lining materials with 30% v/v nystatin oral suspension (NYS) were used as a positive control against C. albicans. The negative control was soft lining materials without additives. All specimens were incubated at 37 • C for 48 h; the inhibition zone of each specimen was measured by using a digital veneer caliper, and the mean inhibition zones were calculated. Each experimental group (n = 5) was replicated five times independently.

Cytotoxicity Test
The test of the effects of different additives incorporated into GC soft liner, Coe comfort and Viscogel on a human gingival fibroblast (HGF) cell line (ATCC ® CRL-2014, Manassas, VA, USA) was adapted from ISO 10993-5 [14]. The specimens were fabricated in accordance with ISO 10993-12 [15]. A cuboidal sample, being 20 × 5 × 2 mm (3 cm 2 /mL extracted ratio), was created with a stainless-steel mold. Soft lining materials without additives and soft lining materials with 10%, 30% v/v LCEO, NYS and CHX were tested. All specimens were exposed to UV light for 15 min per side. Subsequently, each sample was immersed in a microcentrifuge tube containing 1.0 mL Dulbecco's modified Eagle's medium high-glucose (Hyclone TM , South logan, UT, USA) with 10% fetal bovine serum and 1% antibiotics penicillin-streptomycin. The samples were incubated in a shaking incubator at 37 • C for 24 h. Culture medium without sample was also incubated under the same conditions to serve as a negative control. HGF cells were cultured in DMEM supplemented with 10% v/v FBS and 1% v/v penicillin-streptomycin solution. HGF cells were plated into 96-well plates with the seeding density of 10,000 HGF cells/well/100 µL and incubated in a 5% CO 2 incubator at 37 • C. After 24 h, old medium was discarded, and 200 µL aliquots of prepared extracted solutions were subsequently added into the 96-well plate, and cells were incubated for 24 h. Cell viability was assessed by using the MTT assay (Sigma-Aldrich, St. louis, MO, USA). The absorbance was read at 570 nm using a microplate spectrophotometer (µQuant TM , Bio-Tek instruments Inc, Winooski, VT, USA). Each experimental group (n = 3) was replicated three times independently.

Shore AO Hardness Testing
Surface hardness was evaluated using a Shore durometer according to ISO 10139-1:2018 [16]. Cylindrical-shaped specimens were prepared from GC soft liner, Coe comfort and Viscogel in a stainless-steel mold with 55 mm diameter and 8.0 mm thickness [17]. Various concentrations of the additives were mixed into the soft lining materials to acquire final concentrations of 5%, 10%, 20%, 30% v/v LCEO, 5% v/v of 2% CHX and 30% v/v NYS. Soft ling materials without additive were used as controls. The mold was immersed into a 37 ± 1 • C water bath within 15 min after mixing for 2 h, and then the Shore AO hardness was measured. Each value was read after 5 s of loading at five different points and the mean hardness was calculated in each sample [17]. After this, the specimen was immersed in the water bath at 37 ± 1 • C for 7 days. The Shore AO hardness test was performed at the opposite site of the samples in the same manner. Five specimens in each group (n = 5) were tested.

Statistical Analysis
All statistical analyses were performed using PASW Statistics software (IBM Corp. Released 2019. IBM SPSS Statistics for Windows, Version 26.0, Armonk, NY, USA). The significance level was set at α = 0.05.
To assess the susceptibility of S. mutans and C. albicans towards LCEO incorporated in different soft lining materials, one-way ANOVA and Games-Howell multiple comparison were performed to analyze the significant differences in the agar well diffusion assay of LCEO.
To assess the HGF cell viability after 24 h exposure to the extracts, one-way ANOVA was performed for the GC soft liner and Coe comfort groups and Kruskal-Wallis analysis was used for Viscogel groups.
For the surface hardness testing, two-way repeated-measures ANOVA was applied.

Antimicrobial Activity of LCEO towards C. albicans and S. mutans
The antimicrobial activity of LCEO was demonstrated as the mean inhibition zone, as listed in Tables 2 and 3. The inhibitory zone against C. albicans was noticeably observed in the 1.25% v/v LCEO group, whereas the inhibitory zone against S. mutans was detected in the 10% v/v LCEO group ( Figure 1). Similar to the NYS group, the 5% v/v LCEO group showed a remarkable inhibitory effect against C. albicans. Table 2. Mean inhibition zone ± SD (n = 5) of different concentrations of LCEO against C. albicans. Inhibition zone less than 6 mm was defined as not detected (ND).

Candida albicans Mean Inhibition Zone ± SD (mm)
Negative control (DMSO) ND Nystatin oral suspension 12.74 ± 0.27 Table 3. Mean inhibition zone ± SD (n = 5) of different concentrations of LCEO against S. mutans. Inhibition zone less than 6 mm was defined as not detected (ND).

Streptococcus mutans
Polymers 2022, 14, x FOR PEER REVIEW 5 of 13 in the 10% v/v LCEO group (Figure 1). Similar to the NYS group, the 5% v/v LCEO group showed a remarkable inhibitory effect against C. albicans.  Table 2. Mean inhibition zone ± SD (n = 5) of different concentrations of LCEO against C. albicans. Inhibition zone less than 6 mm was defined as not detected (ND).

Candida albicans Mean Inhibition Zone ± SD (mm)
14.33 ± 0.52 Table 3. Mean inhibition zone ± SD (n = 5) of different concentrations of LCEO against S. mutans. Inhibition zone less than 6 mm was defined as not detected (ND).

Antimicrobial Activity of LCEO Incorporated into Different Soft Lining Materials against C. albicans and S. mutans
The antimicrobial activity of soft lining materials with various concentrations of LCEO is illustrated in Figure 2. The mean inhibition zones against C. albicans and S. mutans are shown in Tables 4 and 5, respectively. All three soft lining materials with 10% v/v LCEO displayed anti-candidal activity towards C. albicans. With a higher concentration of LCEO, the inhibition zones significantly increased in all materials (p < 0.05). Moreover, the inhibition zones of the groups of the three soft lining materials with 30% v/v LCEO demonstrated significantly larger values than the 30% v/v NYS groups (p < 0.05). Meanwhile, all three soft lining materials with 5-20% v/v of LCEO did not show any inhibitory effect against S. mutans. Only in the 30% v/v LCEO group, the inhibition zone could be detected around the samples. However, when compared to the CHX positive control groups, the inhibition zones of the 30% v/v LCEO groups were significantly smaller (p < 0.05).
LCEO displayed anti-candidal activity towards C. albicans. With a higher concentration of LCEO, the inhibition zones significantly increased in all materials (p < 0.05). Moreover, the inhibition zones of the groups of the three soft lining materials with 30% v/v LCEO demonstrated significantly larger values than the 30% v/v NYS groups (p < 0.05). Meanwhile, all three soft lining materials with 5-20% v/v of LCEO did not show any inhibitory effect against S. mutans. Only in the 30% v/v LCEO group, the inhibition zone could be detected around the samples. However, when compared to the CHX positive control groups, the inhibition zones of the 30% v/v LCEO groups were significantly smaller (p < 0.05).  Table 4. Mean inhibition zone ± SD (n = 5) of various additives incorporated into three soft lining materials (GC soft liner, Viscogel and Coe comfort) against C. albicans. Inhibition zone less than 6.0 mm was defined as not detected (ND). The statistical difference in various concentrations of LCEO and nystatin oral suspension is compared in the same row and the same capital letters indicate no significant difference in inhibition zone diameter (p > 0.05). No comparison among the three soft lining materials was performed.

Mean Inhibition Zone (Mean ± SD)
No Additive

Cell Viability of HGF Cell Line
As shown in Figure 3, the cell viability test was performed to obtain the percentages of cell viability of the HGF cell line after exposure to the three soft lining materials with additives (10%, 30% v/v LCEO, CHX and NYS) compared to their control materials (no additive). Within the same material, no cell cytotoxicity was detected when the groups of various additives were compared to the control group (p > 0.05).

Cell Viability of HGF Cell Line
As shown in Figure 3, the cell viability test was performed to obtain the percentages of cell viability of the HGF cell line after exposure to the three soft lining materials with additives (10%, 30% v/v LCEO, CHX and NYS) compared to their control materials (no additive). Within the same material, no cell cytotoxicity was detected when the groups of various additives were compared to the control group (p > 0.05).

Surface Hardness of Soft Lining Materials
The hardness results were illustrated in terms of Shore AO hardness values (Tables  6-8), with a higher value indicating greater hardness. Overall, both the aging process and the concentrations of LCEO could significantly affect the Shore AO hardness of these three soft lining materials (p < 0.05), as shown in Figure 4. In all groups, including controls, surface hardness increased from the initial stage (2 h) to the late stage (7 days). Furthermore, the Shore AO hardness of the material was shown to decrease with increasing LCEO concentration. Briefly, 10%, 20% and 30% v/v LCEO incorporated into soft lining materials markedly decreased hardness in both stages (p < 0.05).

Surface Hardness of Soft Lining Materials
The hardness results were illustrated in terms of Shore AO hardness values (Tables 6-8), with a higher value indicating greater hardness. Overall, both the aging process and the concentrations of LCEO could significantly affect the Shore AO hardness of these three soft lining materials (p < 0.05), as shown in Figure 4. In all groups, including controls, surface hardness increased from the initial stage (2 h) to the late stage (7 days). Furthermore, the Shore AO hardness of the material was shown to decrease with increasing LCEO concentration. Briefly, 10%, 20% and 30% v/v LCEO incorporated into soft lining materials markedly decreased hardness in both stages (p < 0.05).    Nevertheless, when various additives were added, the surface hardness of each soft lining material showed different results. In the case of the GC soft liner, all additives could lower the material's hardness at the 2 h initial stage. At the late stage, only 10% to 30% v/v of LCEO could significantly affect the hardness (p < 0.05) but no significant difference in surface hardness among control, NYS, CHX and 5% v/v LCEO was found (p > 0.05). Regarding Viscogel, in both the 2 h and 7 day incubation periods, there was no significant to 30% v/v of LCEO could significantly affect the hardness (p < 0.05) but no significant difference in surface hardness among control, NYS, CHX and 5% v/v LCEO was found (p > 0.05). Regarding Viscogel, in both the 2 h and 7 day incubation periods, there was no significant difference in surface hardness among the control, NYS, CHX and 5% v/v LCEO groups (p > 0.05). However, the higher concentrations from 10% to 30% v/v of LCEO could significantly reduce the hardness (p < 0.05) at 2 h and 7 days. Lastly, regarding Coe comfort, only CHX had no effect on the material's hardness at either incubation time, while NYS and all LCEO concentrations could reduce the surface hardness at both 2 h and 7 days.

Discussion
Citral, the main component of fruit-derived essential oil, is the active compound of LCEO and was used as an antimicrobial agent against C. albicans and S. mutans in the present study. In another study, citral showed antimicrobial properties against Gramnegative and Gram-positive bacteria, fungi and protozoa, and the authors found that Gramnegative bacteria were the most resistant strains, requiring a high minimum inhibitory concentration (MIC) of approximately 18,000 µg/mL to inhibit Pseudomonas aeruginosa growth. Meanwhile, a lower MIC of 750 µg/mL worked against Enterobacter species [9]. A previous study also found that the MIC of 0.05% v/v citral could inhibit the growth of S. aureus, E. coli, C. albicans and Microsporum gypseum [18]. Leite et al. revealed that citral had an MIC of 64 µg/mL in a test with all C. albicans strains, while the minimum fungicidal concentration (MFC) of citral ranged from 64 to 256 µg/mL depending on the candida strain [19]. In the present study, the MICs of LCEO against C. albicans and S. mutans were 1.25% v/v (11.1 mg/mL) and 10% v/v (89 mg/mL), respectively. The MIC of LCEO against C. albicans was in a range consistent with the results of Saikia et al. [20]. They used an agar disc diffusion experiment and found that the MIC of LCEO extracted from fruit against C. albicans ranged from 2.5 to 20 mg/mL. Conversely, Yang et al. reported that the minimum microbicidal concentration of LCEO from fruit against S. mutans was 0.75 mg/mL [21]. Therefore, variations in the type and amount of active ingredients extracted from different L. cubeba sources could affect LCEO's antimicrobial property.
When incorporating LCEO into all soft lining materials, the minimum concentration of LCEO against C. albicans and S. mutans was 10% and 30% v/v, respectively, indicating that LCEO incorporated into soft lining materials could inhibit C. albicans more effectively than S. mutans. However, higher concentrations of LCEO were required to inhibit these oral microbes when incorporated into soft lining materials. The findings are similar to a previous study that tested Melaleuca alternifolia oil loaded into various tissue conditioners against C. albicans. A higher concentration of M. alternifolia oil was required to inhibit the fungus [22]. This would be because denture soft lining materials are considered to be a drug delivery vehicle. The polymer network of the soft lining materials could release active ingredients into the environment in a sustainable manner [23].
As previously stated, the incorporation of LCEO into soft lining materials may affect the material properties or the gingival tissue surrounding them. The in vitro cytotoxicity of GC soft liner, Viscogel and Coe comfort that contained various additives towards HGF cell lines was evaluated using the MTT assay on 24 h eluate extracts. No significant cytotoxicity towards the HGF cell line was found in any additive group, including nystatin and chlorhexidine. Correspondingly, Luo et al. [24] investigated the acute and genetic toxicity of LCEO in the mouse and Sprague-Dawley (SD) rat, reporting a negative result for LCEO genetic toxicity both in vitro and in vivo. The oral LD 50 , dermal LD 50 and inhalation LC 50 were listed as 4000 mg/kg, 5000 mg/kg and 12,500 ppm, respectively. The essential oil was classified as Class 5 in the globally harmonized system of classification and labeling of chemicals (GHS), which is the least toxic class [24]. However, some studies have found that high concentrations of chlorhexidine, nystatin and LCEO may contribute to unfavorable cell viability. A previous study, for example, reported a less than 6% survival rate of human fibroblasts, myoblasts and osteoblasts when exposed to more than 0.02% chlorhexidine gluconate [25]. Furthermore, nystatin was shown to be cytotoxic in hamster buccal epithelial cells. The study found that cells exposed to 100-200 µg/mL (0.01-0.02%) nystatin solution had a lower survival rate. Cells exposed to nystatin suspension, on the other hand, had a higher survival rate. The difference in survival rate was due to nystatin's insolubility in water [26]. Moreover, vapor of LCEO induced apoptosis and cell cycle arrest in human non-small cell lung cancer cells (NSCLC cells, A549), according to a recent study [27].
In addition, incorporating substances into the polymer network chains of materials may affect their hardness. This present study revealed that when compared to the control groups, all additives incorporated into soft lining materials lowered Shore AO hardness. The higher concentration of LCEO resulted in lower Shore AO hardness both in 2 h and 7 day incubation periods, which indicates that adding LCEO also softened the materials in a dose-dependent manner. One possible factor associated with the hardness of materials would be a plasticizing effect. A plasticizer is an additive added to polymers to soften or make them more pliable. A good plasticizer is a compound that has a high degree of solvent power, is similar to the polymer chain in size and shape, as well as polarity, and can be retained within the polymer chain [28]. Therefore, the solubility parameter of polymers and additives is necessary to address the plasticizing property. The additives with a similar solubility parameter to the polymer chain have a better plasticizing effect. To evaluate the compatibility of polymers with plasticizers, Hansen's solubility parameter was used and these parameters of tested materials are listed in Table 9 [29][30][31][32]. Since citral has solubility parameters close to polymers, LCEO could potentially act as a plasticizer to reduce the hardness of soft lining materials. Furthermore, not only the plasticizer concentration but also the molecular weight could affect the plasticizer's efficiency [28]. A high-molecularweight plasticizer has lower solubility parameters, resulting in less plasticizer efficacy. For instance, comparing 30% v/v nystatin oral suspension to 30% v/v LCEO as plasticizers, nystatin has a higher molecular weight than LCEO, so the Shore AO hardness of the 30% v/v LCEO group was lower than that of the 30% NYS group (p < 0.05). The addition of the PMMA polymer to the powder also greatly influenced the plasticizer leachability of soft lining materials. Previous studies found that when the PMMA polymer concentration was less than 10% by weight, the leaching of the plasticizer decreased as the PMMA polymer concentration increased. The soft lining materials containing 10% by weight PMMA polymer had the lowest amount of plasticizer leaching. Meanwhile, PMMA concentrations greater than 15% by weight may result in increased plasticizer leaching out because PMMA may impede the penetration of external unreacted plasticizer [33]. According to our findings, the Viscogel powder composition contains PMMA, resulting in lower hardness changes than observed in GC soft liner and Coe comfort.
According to ISO:10139-1:2018, soft and extra-soft lining materials are classified by using Shore AO hardness after the aging process. After 2 h incubation, the hardness of a soft material should be between 30 and 50 units, and it should not exceed 60 units after 7 days. Meanwhile, the hardness of an extra-soft material should be less than 30 units after 2 h incubation and no more than 60 units after 7 days [16]. As a result, adding oil as an antimicrobial additive could lower the Shore AO hardness of the materials in the current study, but the hardness was still in accordance with ISO:10139-1.
However, the main limitation of this in vitro investigations was that, in the oral cavity, there are many other factors affecting the antimicrobial properties. Furthermore, in clinical situations, the biocompatibility of materials of significant concern. For example, saliva acts as a rinsing agent, and this may impact the release of compounds from materials, or the materials themselves may have adverse effects on the tissue underneath when using them for a period of time. Therefore, further research into the release profiles of leaching products over time and their cytotoxicity should be conducted, and a clinical study may be more beneficial.

Conclusions
Based on this in vitro study, LCEO could possibly be used as a novel antimicrobial additive incorporated into soft lining materials against oral pathogens, with an optimal concentration at 10% v/v for C. albicans and 30% v/v S. mutans. The soft lining materials with LCEO demonstrated no cytotoxicity towards the HGF cell line compared to materials without additives. The surface hardness of materials was dose-dependently related to the oil concentration; nonetheless, all investigated materials were classified as extra-soft types according to ISO 10139-1: 2018. Therefore, LCEO is a medicinal herb that has potential to treat denture stomatitis and reduce secondary caries, with no harmful effect when incorporated into denture soft lining materials.