The Formulation and Evaluation of Melaleuca alternifolia Cheel and Cymbopogon flexuosus Linn Essential Oils Emulgel for the Treatment of Vulvovaginal Candidiasis

The global concern regarding the occurrence of antifungal resistance to synthetic conventional azoles used for treating vulvovaginal candidiasis, along with the associated side effects, is significant. Consequently, the pursuit for substitutes such as natural therapies has ensued. Essential oils, derived from plants, have been extensively researched and found to possess antibacterial and antifungal properties. This study aimed to assess the antifungal efficacy of two essential oils, both alone and in combination, against Candida albicans. Essential oils were formulated into an emulgel separately and as combinations. The essential oils of Melaleuca alternifolia and Cymbopogon flexuosus were used in this study. The resulting emulgel formulations were characterized for their antifungal activity against Candida albicans. Physiochemical properties such as pH, viscosity, and appearance were also determined. The prepared emulgels were thereafter observed for stability over a period of 1 month. The MIC of Melaleuca alternifolia was seen to be 50 µL/mL while Cymbopogon flexuous was seen to be more potent at 25 µL/mL against C. albicans exhibiting strong synergistic effect at 0.4. The emulgel formed was white in color, smooth on skin, and had the odor of the essential oils, which is sweet to the nose. The pH of the formulations with the essential oils were acidic in the range of 3.70–3.83, making them suitable for vagina application. The emulgels had viscosities ranging from 4417.6 to 8968.7 mPas, owing to the thickness of the essential oils contained. The emulgel formulation with the combination of essential oils was more potent that the two with individual essential oils; furthermore, the one with Cymbopogon flexuous was more potent than the one with Melaleuca alternifolia. Based on the properties of the formulated emulgels and their activity against the test organism, the preparations have significant potential in the management of vulvovaginal candidiasis.


Introduction
A dosage form is a formulation that combines an active pharmaceutical ingredient (API) with excipients to facilitate the process of dosing, administering, and delivering the drug to patients.Various dosage forms exist, which vary based on the route of administration and the location where the active components take effect.Dosage forms encompass a variety of options, including solids (such as tablets, capsules, powders, and granules), semisolids (such as creams, ointments, pastes, and gels), liquids (including syrups, elixirs, decoctions, and lotions), and gases (such as aerosols) [1].The topical drug administration approach circumvents the first pass effect, a significant drawback of the oral route.However, its primary constraint lies in the difficulty of transferring hydrophobic chemical components through the skin [2].
Gels 2023, 9, 949 2 of 17 Emulgels are an innovative medication delivery technology that combine the properties of both emulsions and gels.They are utilized for the delivery of various pharmaceuticals, such as analgesics, anti-inflammatory meds, anti-acne medications, and anti-fungal compounds.Emulgels have characteristics such as easy removal, spreadability, thixotropy, lack of greasiness, extended shelf life, and transparency [3].Emulgels are gelled emulsions, which can be either water-in-oil or oil-in-water.This vehicle is highly suitable for hydrophobic medicines.Emulgels have the characteristics of both gels and emulsions, making them a dual-controlled release system capable of delivering both hydrophilic and lipophilic medicines.This is due to the presence of two distinct phases, namely aqueous and non-aqueous [4].Emulgels are created by employing oil-in-water systems for lipophilic medications and water-in-oil systems for hydrophilic pharmaceuticals.An emulgel is formed when a gelling ingredient is added to a standard emulsion.
The vagina serves as a pathway for the administration of medications by topical application.Vaginal formulations are exclusively employed for the administration of locally acting medications, such as antimicrobials, spermicidal agents, antimycotics, hormone therapy, contraceptives, and others.The vaginal route is chosen because of the profusion of blood vessels compared to systemic preparations [5].Drugs delivered vaginally can be absorbed through three primary mechanisms: transcellular, paracellular, and vesicular or receptor-mediated transport.The process of drug absorption from the vagina consists of two primary stages: drug breakdown in the vaginal lumen and penetration through the membrane [6].
Candidiasis is a prevalent opportunistic infection that can impact persons with weakened immune systems as well as those with normal immune function [7].Candida species are a component of the typical human microbiota.However, if the immune system of the host is weakened or if other circumstances disturb the equilibrium of bacteria, candida can proliferate excessively and lead to illness.Candidiasis is a mycotic infection resulting from the overgrowth of the yeast known as candida.Candida, a type of yeast, is typically found on the skin, mucous membranes, and in the gastrointestinal tract.However, it can proliferate and lead to infection in specific circumstances [8].Candidiasis can manifest in various forms, such as oral thrush, vaginal yeast infections, and invasive candidiasis.Vaginal yeast infections are a prevalent form of candidiasis, impacting around 75% of women at some stage in their lifetimes.Common symptoms include pruritus, stinging sensation, and discharge from the vaginal area [9].Invasive candidiasis occurs when the yeast infiltrates the bloodstream, potentially causing grave sickness or fatality.Invasive candidiasis is more likely to occur in individuals who have recently undergone surgery, have been using antibiotics for an extended period, or are undergoing immunosuppressive medication [10].Furthermore, candida can induce skin infections, including diaper rash, intertrigo, and nail infections [11].Inadequately managed candidiasis can lead to systemic candidiasis, a severe type of infection that can develop in critically ill patients in intensive care units and which is linked to high fatality rates [12].Vulvovaginal candidiasis (VVC) is characterized by inflammation of the vagina or vulva resulting from an infection caused by the candida yeast.It is the second most common cause of vaginitis, following bacterial vaginosis.The symptoms of VVC include pruritus in the vulva and vagina, white curd-like discharge, a sense of burning, erythema in the vulva and vagina, and dyspareunia [13].According to reports, a minimum of 70% of women globally will experience at least one occurrence of VVC during their reproductive years [14].
Vulvovaginal candidiasis (VVC) is peculiar because of the difficulties encountered in its pharmacological management.The golden standard for treatment involves the use of fluconazole in affected women [15].While this guideline of treatment has recorded notable successes over the years, recent trends in management have shown a pattern of resistance leading to inadequacy in therapeutic outcomes and reoccurrence of VVC after fluconazole therapy [16].This worrisome development underscores the need for the development of novel alternatives for a more efficient management of VVC in women.
Different approaches have been deployed to improve the management of VVC and minimise tendencies for resistance in therapy.Some of these approaches have leveraged on the growing applications of nanotechnologies to enhance drug delivery.One such effort was the development of low-intensity ultrasound-mediated drug-loaded nanoparticles to facilitate the intravaginal delivery of amphotericin B against VVC [17].Although this approach led to some improvement in the antifungal activity of the drug candidate (amphotericin B), the formulation technique (and required materials) can be characterized as quite sophisticated and may not be feasible for bulking-up and commercial development, especially in developing and underdeveloped regions of the world.As an improvement to nanotechnology-driven models in vulvovaginal drug delivery, interventions through phytomedicines are being sought.In line with this, Rusda et al. (2020) worked on the therapeutic effects of Nigella sativa plant extract on a female Wistar rats' VVC model and obtained evidence of the relevance of plant derivatives as useful remedies in VVC [18].Similarly, Córdoba et al. (2019) evaluated the activities of the essential oils of Laurus nobilis, Thymus vulgaris, Mentha piperita, Cymbopogon citratus, and Lippia junelliana against Candida species.In their submission, these essential oils showed significant levels of activity against the test fungi species [19].Building on these exploits, this research seeks to develop a novel dosage form of two essential oils towards the improved management of VVC.
Essential oils are intensely concentrated substances obtained from various parts of plants, such as leaves, stems, flowers, seeds, roots, fruit rinds, resins, or barks.Plant essential oils consist of intricate combinations of natural chemicals, encompassing both polar and non-polar molecules [20].They are a potential class of natural compounds that can suppress fungus.Terpenes and terpenoids included in essential oils can break the cell membranes of fungi, leading to their demise.The chitin structure present in the cell wall of fungus, which is absent in humans, makes it the primary focus for selectively harmful antifungal drugs [21].The existence of bioactive substances in Melaleuca alternifolia has been scientifically proved to possess numerous advantageous qualities [22].Due to its broad-spectrum anti-microbial characteristics, it has great potential for treating various illnesses.Similarly, Cymbopogon flexuosus exhibits efficacy against a wide range of pathogenic organisms.It has been employed for its antibacterial, antifungal, and antiviral properties [23].Based on these possibilities, the objective of this study is to develop an emulgel containing M. alternifolia and C. flexuosus to treat vulvovaginal candidiasis caused by Candida albicans.

Physicochemical Analysis of the Essential Oils of Melaleuca alternifolia and Cymbopogon flexuosus
Table 1 shows the physicochemical characteristics of essential oils of M. alternifolia and C. flexuosus.Both selected essential oils were colorless to pale yellow in color, clear, mobile liquids with their characteristic smell and highly soluble in 20% v/v Tween-80.

Distribution of Vagina Candidiasis among Collected Samples
Figure 1 shows the distribution of vagina candidiasis among samples collected.A total of 47 vagina swabs were collected and 40 (85.10%)vagina swabs yielded growth.The 40 vagina swabs that yielded growth were further identified based on the colonial morphology and Gram reactions as indicated in Table 2.
Figure 1 shows the distribution of vagina candidiasis among samples collected.A total of 47 vagina swabs were collected and 40 (85.10%)vagina swabs yielded growth.The 40 vagina swabs that yielded growth were further identified based on the colonial morphology and Gram reactions as indicated in Table 2.

S/No Identification Criteria Characteristics 1
Colonial Morphology White to cream colored, smooth, yeast-like appearance, and pasty concave colonies 2 Gram Reaction Gram positive, budded large oval cells

Antifungal Susceptibility Testing of Yeast Isolates
Figure 2 shows the anticandidal activity of M. alternifolia and C. flexuosus as indicated by the clear zones of inhibition at 100 µL/mL to 25 µL/mL.
Table 3 shows the means of zones of inhibition of different concentrations of M. alternifolia and C. flexuosus against selected strains of C. albicans.Isolates CA28 exhibited the highest mean zones of inhibition of 21 ± 0.00 and 22.33 ± 0.58 mm at 100 µL/mL for both essential oils, while the least was observed against CA42 and CA46 at 8.16 ± 0.35 and 8.00 ± 0.00 for M. alternifolia and C. flexuosus, respectively.All C. albicans were sensitive to nystatin at 300 µL/mL.cation Criteria Characteristics l Morphology White to cream colored, smooth, yeast-like appearance, and pasty concave colonies m Reaction Gram positive, budded large oval cells

Antifungal Susceptibility Testing of Yeast Isolates
Figure 2 shows the anticandidal activity of M. alternifolia and C. flexuosus as indicated by the clear zones of inhibition at 100 µL/mL to 25 µL/mL.
Table 3 shows the means of zones of inhibition of different concentrations of M. alternifolia and C. flexuosus against selected strains of C. albicans.Isolates CA28 exhibited the highest mean zones of inhibition of 21 ± 0.00 and 22.33 ± 0.58 mm at 100 µL/mL for both essential oils, while the least was observed against CA42 and CA46 at 8.16 ± 0.35 and 8.00 ± 0.00 for M. alternifolia and C. flexuosus, respectively.All C. albicans were sensitive to nystatin at 300 µL/mL.Table 3 shows the means of zones of inhibition of different concentrations of M. alternifolia and C. flexuosus against selected strains of C. albicans.Isolates CA28 exhibited the highest mean zones of inhibition of 21 ± 0.00 and 22.33 ± 0.58 mm at 100 µL/mL for both essential oils, while the least was observed against CA42 and CA46 at 8.16 ± 0.35 and 8.00 ± 0.00 for M. alternifolia and C. flexuosus, respectively.All C. albicans were sensitive to nystatin at 300 µL/mL.

Minimum Inhibitory Concentration (MIC) of Essential Oils
Table 4 shows the MIC of the M. alternifolia and C. flexuosus essential oils against C. albicans.The MIC ranges from 50 to 100 µL/mL and 25 to 100 µL/mL for M. alternifolia and C. flexuosus essential oils, respectively.

Synergistic Action of Melaleuca Alternifolia and Cymbopogon flexuosus Essential Oils in Combination
The results of the checkerboard bioassay at different mixing ratios are presented in Tables 5 and 6.They shows the combined synergy of C. flexuosus and M. alternifolia at ratios 50:50 and 75:25, respectively, at a concentration range of 6.25-100 µL.

Post-Formulation Antifungal Activity
Table 7 and Figure 3 show the zone of inhibition of the formulated emulgels against Candida albicans using 600, 900, and 1200 µL/mL.The highest inhibition (60 mm) was observed with C. flexuosus alone against C. albicans and in combination at 50 mm.Squatter colonies were observed with 500 mg/mL of 1% clotrimazole in DMSO with an approximate zone of inhibition of 20 mm.

Pseudo-Ternary Phase Diagram
The emulsion was optimized using the pseudo-ternary diagram.In this instance, a mixture of Smix (consisting of Tween 80 and Span 60) was included with coconut oil as  The zone of inhibition of 1% clotrimazole (positive control) was ~20 mm.

Pseudo-Ternary Phase Diagram
The emulsion was optimized using the pseudo-ternary diagram.In this instance, a mixture of Smix (consisting of Tween 80 and Span 60) was included with coconut oil as the dispersed phase, while water served as the dispersing medium.The shaded area represents the region of stable oil-in-water emulsion within the constructed pseudo-ternary phase as presented in Figure 4.Each corner of the phase diagram represents 100% concentration of a constituent; A: water, B: oil, C: Smix.

Pseudo-Ternary Phase Diagram
The emulsion was optimized using the pseudo-ternary diagram.In this instance, a mixture of Smix (consisting of Tween 80 and Span 60) was included with coconut oil as the dispersed phase, while water served as the dispersing medium.The shaded area represents the region of stable oil-in-water emulsion within the constructed pseudo-ternary phase as presented in Figure 4.Each corner of the phase diagram represents 100% concentration of a constituent; A: water, B: oil, C: Smix.

Physicochemical Properties of Emulgel Preparation
Physicochemical properties of five emulgel preparations are presented in Table 8.

Stability Testing of the Formulations
The five emulgel formulations were evaluated for their stability after one week, two weeks, and one month and the results are presented in Tables 9-11.

Viscosity Evaluation of the Formulations
The viscosities of the different emulgel formulations are presented in Table 12.Vulvovaginal candidiasis (VVC) is a prevalent health concern affecting women globally [24], including in Nigeria [25].The 85% prevalence of Candida albican caused the VVC observed in our study is.However, prevalence higher than the 49.7% [26] and 32.6% [27] reported in Lahore-Pakistan and North central Nigeria among women, respectively.This shows varying prevalence globally and maybe due to factors such as socio-demographic factors, sample size, and changes in the pattern of antibiotic resistance.The problem of antibiotic resistance has prompted the investigation of natural remedies, specifically plants that contain essential oils such as coriander oil, lemon grass essential oil, eucalyptus oil, and others [28].Candida albicans can switch morphology between yeast and filamentous growth, biofilm formation, and availability of enzymes such as lipases, phospholipases, and proteinase, thus increasing pathogenicity and the development of resistance [29].Azole medicines and their derivatives are the preferred antifungal treatment for VVC.These treatments can be taken orally or used topically.Fluconazole, an azole, is losing its efficiency against clinical isolates of C. albicans despite its initial efficacy.As a result, there is a quest for alternative medicinal remedies for yeast infections that have high effectiveness and minimum negative consequences [30].Compared to synthetic antimicrobials, natural compounds exhibit a wider range of activity, possess low toxicity, and have less adverse impacts on the environment [31], due to the integral role of plants in the ecosystem.
Emulgels, which are made by combining gel and emulsion, are a specific sort of topical drug delivery system [32].They are utilized for administering various medications, such as antimicrobials, antifungals, antimycotics, and analgesics [4].This study demonstrates the combined antifungal efficacy of two essential oils against vulvovaginal candidiasis, resulting in enhanced antifungal activity and reduced resistance.Previously, Melaleuca alternifolia has been investigated for its therapeutic applications, such as the treatment of VVC [33].While Cymbopogon flexuosus has been studied for its antifungal properties in treating oral candidiasis, there is currently little research available on its usage for vulvovaginal candidiasis, despite claims of its antifungal activities [34].This research enhances the presentation of essential oils from these plant species by producing an antifungal emulgel that is more appropriate for pharmaceutical applications, taking advantage of their therapeutic properties.
The essential oils assessment revealed antifungal activity against C. albicans with a minimum inhibitory concentration (MIC) of M. alternifolia was 50 µL, whereas the MIC of  2017) [34][35][36][37].Both species exhibited strong efficacy against several strains of Candida albicans.C. flexuosus showed more efficacy in suppressing the growth of C. albicans compared to Melaleuca alternifolia.The MIC was determined as the amount of essential oil required (increased per gram) to create an emulgel that exhibits antifungal properties against Candida albicans.The use of a combination of interaction between essential oils of M. alternifolia and C. flexuosus is probably a new area to enhance treatment, improve antimicrobial efficacy, and reduce dosage exposure and human burden.The combined effect of the essential oils of M. alternifolia and C. flexuosus exhibited the strongest synergism with FICI values of 0.4 and 0.5 against both selected C. albicans.Synergism in activity between these oils has also been confirmed in some other studies [35,37].
The emulgels were created by utilizing coconut oil as the primary emulsion oil.The gel was produced by combining xanthan gum and guar gum in different ratios of 3:2, 2:3, 4:1, and 1:4 to determine the optimal gel formulation.The pH range considered normal for the vagina is 3.80 ± 0.20 [38].The pH of the formulations including essential oils met the necessary pH range for vaginal use, rendering them compatible with the vaginal skin.The emulsion-only formulation had a pH of 3.16, while the emulgel without the essential oils had a pH range of 6.18-6.21.Consequently, it may be deduced that the essential oils decreased the pH of the emulgel system.The viscosity test conducted at a rotational speed of 60 revolutions per minute and a temperature of 30.4 • C yielded a viscosity of 4417.6 ± 8.2 mPas for the emulsion and 8694.1 ± 10.3 mPas for the unloaded emulgel.The emulgel, formulated with a blend of essential oils, exhibited a viscosity of 8946.3 ± 8.8 mPas at a temperature of 30.7 • C.These viscosities demonstrate how the thickness of the essential oils affects the internal friction of the final emulgel compositions.According to the reading, the viscosity of M. alternifolia essential oil is higher than that of C. flexuosus essential oil.Viscosity plays a crucial role in determining the extent to which an emulgel can spread; both temperature and storage time have an impact on it [39].An emulgel by its design possesses dual qualities, incorporating the attributes of both an emulsion and a gel.When applied against C. albicans in this study, the formulated emulgel acted by diffusion from the point of application into the surrounding regions containing the applied Candida strains.By diffusing and releasing its component essential oil principles, the emulgel was able to inhibit the growth of selected C. albicans around it, leading to the generation of an inhibition zone as presented in Figure 3.However, in Figure 3D, the positive control using 500 mg/mL of 1% clotrimazole in DMSO exhibited squatter colonies, probably indicating a resistant mutant against tested agent.This has also been documented among bacteria such as uropathogenic Escherichia coli [40], probably suggesting a high level of misuse due to an easy route of administration and readily available nature.
Stability studies showed that the prepared emulgel maintained a consistent look and qualities for a duration of one month.This demonstrates the high compatibility between the essential oils and the emulgel base, resulting in negligible deterioration during the measured one-month timeframe.This information is documented in Tables 9-11.The results of the antifungal action demonstrate the heightened antifungal effect of the essential oils when used together, as opposed to when used separately.This is evident in the reduction in the required concentration to hinder the proliferation of organisms.Furthermore, this demonstrates that C. flexuosus exhibits greater potency in comparison to M. alternifolia.
The investigation conducted in this research study has been able to demonstrate the activity of the test essential oils and the plant-based emulgel formulated from them against C. albicans; the organism implicated in VVC in women.The experiments at this level have been in vitro, indicating that further in vivo assessment would be required to enable the translation of the outcomes of these formulations into clinical applications.The observed in vitro activity patterns of both essential oils and manufactured emulgels suggest that they could potentially be used to treat VVC caused by C. albicans.
The mechanism of antifungal activity of C. flexuosus has been reported to be associated with the presence of the phytochemicals: geranyl acetate, β-citronellol, citronellal, limonene, and citral in its essential oil [41].These constituents act by depleting the plasma membrane of fungal organisms and inhibiting metabolic enzymes required for their functionality [41].On the other hand, the antifungal activity of M. alternifolia has been linked with presence of terpinene-4-ol and 1,8-cineole in its essential oil [42].These phytochemicals act on fungal organisms by inflicting damage on their cell membranes and other organelles, thereby leaving them vulnerable [42].While these described mechanisms and the corresponding phytochemicals responsible for their action have been determined to be true for fungal organisms, the precise mechanism of action of the essential oils utilized against C. albicans in this study needs to be further studied.
Taking cues from the outcomes obtained in this project and in the spirit of widening drug delivery possibilities, synthetic antifungal agents like fluconazole and nystatin can be co-formulated in an emulgel base with the essential oils of C. flexuosus and M. alternifolia in future studies.Combining plant derivatives with an established record of activity with synthetic molecules for the prospects of synergy can be deployed as a way of combating resistance in antifungal agents.As illustrated by Endo et al. (2010) in their research where they combined the extracts obtained from pomegranate peels with fluconazole against Candida albicans to obtain some synergism in antifungal activity [43], this approach can be considered as a follow-up to this research project.

Conclusions
The results obtained from this study show the anti-fungal activities of both M. alternifolia and C. flexuosus against vaginal strains of C. albicans individually.The best antifungal activity was seen when both essential oils were combined at the ratio of 75:25 C. flexuosus: M. alternifolia.The essential oils of C. flexuosus and M. alternifolia in combination are relatively stable within the emulgel made of xanthan and guar gum, showing very minimal degradation over a period of one month.The formulated emulgel showed satisfactory physicochemical characteristics and suitability for use in the vagina.This combination, delivered as an emulgel, can be considered in the future for the clinical management of vulvovaginal candidiasis.If successfully developed, this emulgel has tendencies to be superior to currently available synthetic counterparts as it adopts the advantages of plant-based

Ethical Considerations
Ethical clearance was obtained from the Ethical Review Committee of the State Ministry of Health (ERC/MOH/2023/06/120).In addition, oral consent was obtained from the women that met the study criteria.

Study Criteria (for Vaginal Swab Collection)
The inclusion criteria for this study included female patients who consented to participate in the study, registered in the selected health facility, and had symptoms suggesting vagina candidiasis as recommended by medical personnel.The exclusion criteria for this study included women on antibiotic therapy within 2 weeks before the study days and those who were not willing and not available at the time of study.

Physicochemical Analysis of Essential Oil
The physicochemical analysis of the essential oils of M. alternifolia and C. flexuosus was performed according to the protocol described by Zekri et al. (2023) [44].The solubility properties of the essential oils were determined using varying concentration of Tween-80.All obtained parameters were noted and recorded appropriately.

Determination of Organoleptic Properties of the Essential Oils
This involved the analysis of the odor, color, and texture.All obtained parameters were recorded appropriately.

Microbiological Analysis 4.6.1. Collection of Vaginal Swabs
A total of 47 high vagina swab (HVS) samples were collected with sterile cotton wool swabs according to the protocol described by Waikhom et al. (2020) [45].Samples were collected by the licensed nurse after consent was obtained.Swab samples were carefully labeled and transported in BHIB medium in cold chain to the Laboratory Unit, Pharmaceutical Microbiology and Biotechnology Laboratory, University of Ilorin, for immediate analysis.

Isolation and Identification of Candida albicans
Swabs were inoculated on prepared SDA plates and incubated aerobically at 37 • C for 24 h.Plates with no growth after 24 h were re-incubated for another 24 h to ensure their negativity, while those with colonial morphology on SDA plates were read and noted.Further identification was performed using Gram staining and germ tube test for large, budded yeast-like cells and filamentous extension of yeast cells after 3 h incubation in 500 µL human serum, respectively.All yeast isolates (40) were stored in BHIB with 25% glycerol at 4 • C for further analysis.

Determination of Inoculum Size
Yeast inocula were prepared using the McFarland turbidity standard as described by Cheesbrough (2006) [46].Freshly sub-cultured yeast isolates were inoculated into 2 mL normal saline and adjusted until their turbidity matched to 0.5 on the McFarland turbidity scale.This turbidity scale was prepared by adding 9.6 mL of 1% aqueous solution of barium chloride in 0.4 mL of 1% sulfuric acid, giving an approximate yeast density of 1.2 × 10 8 CFU/mL.The antimicrobial activity of individual essential oils were screened against selected yeast isolates using the agar well diffusion method as described by Katibi et al. (2022) [47].Standardized inocula were seeded into prepared MH agar.Using sterile corkborer no 6 (6 mm in diameter), wells were made in the seeded agar plates and bottom sealed using molten agar.A volume of 100 µL of solubilized essential oils in 20% Tween-80 at concentrations of 100, 200, and 300 µL/mL were added into each well and allowed to pre-diffuse for 45 min.Incubation was thereafter performed at 37 • C for 24 h.The degree of antifungal activity was evaluated by measuring the zones of inhibition diameter in millimeters (mm).All tests were carried out in triplicate for each isolate.

Determination of Minimum Inhibitory Concentrations (MIC) of the Essential Oils
The concentration of essential oils that yielded inhibitory effect in the agar well diffusion assay was used to determine the MIC using the microplate dilution method.Prepared MHB (100 µL) was placed in wells 2-9, then 200 µL of each of the essential oils solubilized in 20% Tween-80 was added to the wells 1.In well 2, 100 µL of 200 µL/mL essential oils was added to yield 200 µL/mL.From well 2, serial dilutions were performed up to well 9 and 100 µL removed from well 9 was discarded to yield a concentration range from 0.39 to 100 µL.Next, 50 µL of freshly prepared yeast turbidity was adjusted to approximately 0.5 McFarland turbidity standard to 1 × 10 8 cfu/mL.Wells 10, 11, and 12 were set as broth, organism, and test-agent sterility control and microtiter plates were incubated at 37 • C for 24 h.Post incubation, 40 µL of resazurin dye was added to each well as an indicator of microbial growth.Plates were incubated at 37 • C for another 24 h.The lowest concentration, where there was no color change from blue to pink, was regarded as the MIC.

Determination of Synergism of the Combination of the Essential Oils
This was performed using the broth microdilution checkerboard method as described by Satyajit et al. (2007) [44] with slight modification.A 96-well microtiter plate was used for this experiment.The plates were prepared under aseptic conditions.The MIC concentration was used as the stock solution.A volume of 100 µL of MHB was added into the rows from column 1-12.A volume of 100 µL each of the stock solutions of M. alternifolia essential oil was pipetted into row 1 from column 1-8.Then, a serial dilution was conducted in each column to give varying concentrations in a descending order.In column 8, 100 µL of stock solution of C. flexuosus essential oil was pipette into row 1-8.A serial dilution was conducted from column 8 down to column 1 to give varying concentrations and hence create a checkerboard sequence with varying combinations of both essential oils in each tube.A volume of 0.1 µL of 0.5 McFarland turbidity of the test organism was pipetted into each well from column 1-9.Columns 9-12 were the control tubes.Column 9 was for organism viability, column 10 for broth sterility, and columns 11 and 12 for essential oils sterility.The plates were incubated overnight at 37 • C and the MIC was read as the least dilution without any turbidity, as indicated after incubation with 40 µL of resazurin dye.A fractional inhibitory concentration index (FICI) was used to interpret the results [48].Synergy is more likely to be expressed when the ratio of the concentration of each antibiotic to the MIC of that antibiotic is the same for all components of the mixture.
The ΣFICs were calculated as follows: where: FIC A = The MIC of drug A in the combination/MIC of drug A alone.FIC B = The MIC of drug B in the combination/MIC of drug B alone.The combination is considered synergistic when the fractional inhibitory concentration (ΣFIC) index is ≤0.5.Indifference is indicated by an FIC index > 0.5 to ≤4, while antagonism is indicated when the ΣFIC is >4.

Pharmaceutical Analysis for Formulation of Emulgel 4.8.1. Drug-Excipient Compatibility Study
The drug-excipient compatibility study was conducted by physically mixing the drug and excipients in a 1:1 ratio and subjecting them to 40 • C/75% RH for one month.Finally, Tween-80 was selected as the surfactant and Span 60 as the co-surfactant.

Pseudo-Ternary Phase Diagrams for Emulsion
This was first conducted to obtain a formulation with a cloudy appearance, physical homogeneity, and easy flow ability.This was performed by varying the ratio of coconut oil as the oil phase to a mixture of Tween-80 as the surfactant and Span 60 as the co-surfactant to form a pseudo-ternary phase diagram.The surfactant and co-surfactant (Smix) were mixed at two different weight ratios (1:1 and 2:1).The coconut oil mixture and Smix were combined at different weight ratios from 1:9 to 9:1 in different glass vials for each phase diagram.The phase diagram was constructed using the template provided on ternaryplot.com.

Formulation of the Essential Oil Emulgel
In a bottle, a measured quantity of coconut oil, the surfactant and co-surfactant, and water were mixed thoroughly by shaking vigorously as shown in Table 13.A weighed quantity of guar gum was mixed with a weighed quantity of xanthan gum and the mixture was dispersed into a measured quantity of water in a beaker to form a gel as described in Table 14.The mixture was thoroughly mixed and set aside to swell.The essential oils were blended into prepared emulsion; the essential oil-loaded emulsion was blended with the gel (1:1 ratio) of emulsion: gum.This was homogenized to generate an emulgel with the composition described in Table 15.The physical appearances of the formulated emulgels were observed visually and then examined for their organoleptic properties such as color; odor; consistency; and grittiness, which were evaluated by application on the skin.

pH Measurement
The pH value was determined by using a standardized pH meter in a 1% aqueous solution of the sample formation.

Viscosity
Each sample was poured into a container (beaker).Viscosity of each sample was taken using an NDJ-5S Digital Display Viscometer (Rinch Industrial Co.Limited, Shanghai, China) at 60 rpm with a spindle size of 4.

Stability Test
The formulated emulgels were all subjected to stability studies to confirm their stability at room temperature (25 • C).Their appearance, color, spreadability and pH for each one was monitored after one week, two weeks, and one month post formulation [49].

Determination of Homogeneity
The emulgels were all tested for homogeneity by visual inspection in their containers.They were all tested for presence of any aggregates.

Post-Formulation Antifungal Analysis of Emulgels
The solutions of the formulated emulgels were prepared with dimethyl sulfoxide as the solvent.The antifungal activities of the emulgels were tested using the agar well diffusion method as described by Katibi et al. (2022) [47].A standardized inocula was used to flood plates of agar that had been prepared and labeled.On the inoculated plates, central holes were bored using a sterile corkborer no. 6.Then, the base of the holes was sealed using a few drops of molten agar.The emulgel solutions were then filled into the

Figure 1 .
Figure 1.Prevalence of vagina candidiasis among collected samples.

Figure 1 .
Figure 1.Prevalence of vagina candidiasis among collected samples.

Figure 2
Figure 2 shows the anticandidal activity of M. alternifolia and C. flexuosus as indicated by the clear zones of inhibition at 100 µL/mL to 25 µL/mL.

Figure 1 .
Figure 1.Prevalence of vagina candidiasis among collected samples.

Table 1 .
Physicochemical analysis of the selected essential oils (EO).

Table 2 .
Identification of yeast isolates.

Table 2 .
Identification of yeast isolates.
S/NoIdentification Criteria Characteristics 1 Colonial Morphology White to cream colored, smooth, yeast-like appearance, and pasty concave colonies 2 Gram Reaction Gram positive, budded large oval cells

Table 2 .
Identification of yeast isolates.

Table 3 .
Antifungal activity of essential oils against selected Candida albicans isolates.

Table 4 .
The MIC of essential oils against C. albicans.

Table 5 .
The checkerboard bioassay against Candida albicans at the ratio of 50:50.

Table 8 .
Physicochemical properties of the emulgel preparations.

Table 9 .
Physical evaluation after one week at 25 ± 5 • C.

Table 10 .
Physical evaluation after two weeks at 25 ± 5 • C.

Table 11 .
Physical evaluation after one month at 25 ± 5 • C.

Table 12 .
Viscosity measurements of the emulgel formulations.

Table 13 .
Composition of emulsion preparation.

Table 14 .
Composition of gel preparation.