ONLINE ONLY ARTICLES - ORIGINAL ARTICLE
|Year : 2020 | Volume
| Issue : 1 | Page : 188-189
Punica granatum as a salutiferous superfruit in the treatment of oral candidiasis – An in-vitro study
KS Prem Kumar, S Shiny Samlin, B Siva, R Sudharshan, A Vignesswary, K Divya
Department of Oral Medicine and Radiology, Best Dental Science College, Madurai, Tamil Nadu, India
|Date of Submission||04-Sep-2019|
|Date of Acceptance||27-Nov-2019|
|Date of Web Publication||08-May-2020|
S Shiny Samlin
Department of Oral Medicine and Radiology, Best Dental Science College, Ultra Nagar, Madurai.Chennai Highway, Madurai - 625 104, Tamil Nadu
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Context: The rise in the incidence of clinical resistance to antifungal therapy and failure to respond in recent years underscores the need for a time-honored approach to treat the disease using natural drugs instead of synthetic drugs, which have lesser adverse effects and good patient response. Punica granatum (pomegranate) is a fruit that has admirable medicinal value.
Aims: The study aimed to evaluate the in vitro antifungal efficacy of P. granatum peel extract against oral Candida compared with clotrimazole.
Settings and Design: The study design involves an in-vitro study.
Subjects and Methods: Saliva from candidiasis patients was inoculated and cultured on 60 separate Sabouraud dextrose agar plates and incubated at 37°C for 48 h from which Candida species were collected. Agar well-diffusion method was followed. Different concentrations of P. granatum peel extracts, ethanol solvent (control) and standard clotrimazole were added into the wells and allowed to diffuse at room temperature for 2 h. The plates were incubated at 37°C for 48 h. The antifungal potential of test compounds was determined based on the mean diameter of the zone of inhibition around the well in millimeters.
Statistical Analysis Used: Statistical analysis was performed using IBM software SPSS version 20 at one-way ANOVA.
Results: Antifungal efficacies of P. granatum peel extract and clotrimazole were statistically significant, and there was an increase in inhibitory efficacy with an increase in concentration. Minimum inhibitory concentration of P. granatum peel extract approximated with that of clotrimazole.
Conclusions: The results of this study indicate that P. granatum peel extract can be used as an effective natural substitute for synthetic antifungal agents.
Keywords: Candidiasis, clotrimazole, minimum inhibitory concentration, Punica granatum
|How to cite this article:|
Prem Kumar K S, Samlin S S, Siva B, Sudharshan R, Vignesswary A, Divya K. Punica granatum as a salutiferous superfruit in the treatment of oral candidiasis – An in-vitro study. J Oral Maxillofac Pathol 2020;24:188-9
|How to cite this URL:|
Prem Kumar K S, Samlin S S, Siva B, Sudharshan R, Vignesswary A, Divya K. Punica granatum as a salutiferous superfruit in the treatment of oral candidiasis – An in-vitro study. J Oral Maxillofac Pathol [serial online] 2020 [cited 2020 Jun 1];24:188-9. Available from: http://www.jomfp.in/text.asp?2020/24/1/188/283972
| Introduction|| |
“Nature itself is the best physician” stated Hippocrates. One such gift from nature is Punica granatum (pomegranate) with innate therapeutic properties, and the peel extract contains active antifungal compounds such as punicalagin, castacalagin, granatin, catechin, gallocatechin, kaempferol and quercetin.,,
Oral candidiasis is the most prevalent opportunistic infection affecting the oral mucosa caused by Candida albicans. The development of resistance to antifungal agents underscores the need to use natural drugs instead of synthetic drugs, which have lesser adverse effects. This study aims to evaluate the in vitro antifungal efficacy of P. granatum peel extract against oral Candida compared with clotrimazole.
| Subjects and Methods|| |
An in-vitro study was conducted in the department of oral medicine and radiology. A total of 60 patients who were diagnosed and confirmed by clinical and mycological examination as suffering from oral candidiasis were enrolled in the present study.
Determination of antimicrobial activity
The antimicrobial activity was performed by well diffusion method.,
Sabouraud dextrose agar
Sabouraud dextrose agar is recommended for the isolation of C. albicans.
Composition of media
Dextrose (Glucose) 40.000
Mycological peptone 10.000
Final pH (at 25°C) 5.6 ± 0.2
Preparation of the medium
Suspend 65.0 g in 1000 ml distilled water. Heat to boiling point to dissolve the medium completely. Sterilize the medium using autoclave at 15 lbs pressure (121°C) for 15 min. Cool to 45°C–50°C. Mix well and pour into sterile Petri plates.
Preparation of the extract
About 10 g of sample powder was soaked in 99.9% ethyl alcohol for 4 days and filtered using Whatman filter paper. The obtained filtrate was subjected to rotary evaporator at a temperature of 70°C and 120 rpm, and crude extract was obtained. The weight of crude extract was calculated by measuring the difference between the weights of beaker before and after the collection of extract. The final material (crude extract) was dissolved in ethanol and made into different concentrations of 10, 20, 30, 50, 100, 150 and 200 μl. Ethanol group was considered negative control in this study to investigate the presence of any antifungal property for ethanol because the crude extract was dissolved in ethanol. The final crude extract was subjected to antifungal susceptibility test.
The minimum inhibitory concentration (MIC) value is defined as the lowest concentration of plant extract in the medium that inhibited visible growth of the test fungal strains., The minimum fungicidal concentration (MFC) is defined as the concentration required to give 50% inhibition of hyphal growth.
Preparation of sample solutions for the experiment
The samples were weighed (10 mg/10 ml) and dissolved in sterile distilled water to prepare appropriate dilution to get required concentrations of about 10 μl (10 μg), 20 μl (20 μg), 30 μl (30 μg), 50 μl (50 μg), 100 μl (100 μg), 150 μl (150 μg) and 200 μl (200 μg). These solutions were refrigerated till they were used for the experiment.
The saliva samples were collected from Diamond Dental Clinic, Thanjavur. Saliva was collected by spitting method in graduated container from patients diagnosed as having candidiasis. The collected saliva was inoculated and cultured on 60 separate Sabouraud dextrose agar (SDA) plates. These plates were incubated at 37°C for 48 h from which Candida species were collected.
With the help of agar well diffusion method, antifungal property was evaluated. SDA plates were swabbed (sterile cotton swabs) with 8 h old broth culture of fungi. Wells (6 mm diameter and about 1 cm apart) were made in the plates using sterile cork borer. Different concentrations of plant extracts, ethanol solvent and standard clotrimazole were added using micropipette into the wells and allowed to diffuse at room temperature for 2 h. Later, these plates were incubated at a temperature of 37°C for a period of 48 h. The antimicrobial potential of test compounds was determined on the basis of mean diameter of zone of inhibition around the well in millimeters. The zones of inhibition of the tested microorganisms by the samples were measured using a millimeter scale.
Data were analyzed using IBM software SPSS version 20 at one-way ANOVA with a significance level 0.05.
| Results|| |
The results were obtained based on the zones of inhibition produced by P. granatum extract, ethanol and clotrimazole in the sixty samples. The widths of the zones of inhibition in each group have shown increase with increase in their concentrations, as tabulated in [Table 1]. The width of zones of inhibition of P. granatum approximated with that of clotrimazole at concentrations of 30 μl, 50 μl, 100 μl, 150 μl and 200 μl as depicted in [Figure 1] and [Figure 2]. This proves that P. granatum has almost equal antifungal efficacy as clotrimazole.
|Table 1: Zones of inhibition of Punica granatum, ethanol and clotrimazole group at different concentrations|
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|Figure 1: Zones of inhibition exhibited by Punica granatum, clotrimazole and ethanol at different concentrations|
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|Figure 2: Antifungal efficacy of Punica granatum, ethanol and clotrimazole against Candida species|
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| Discussion|| |
The Indian subcontinent is well known for its richness in the presence of numerous plants with medicinal properties. The reasons behind the need for the discovery of natural products with therapeutic properties are the adverse effects caused by synthetic drugs and the increasing resistance of microorganisms to the antimicrobials prescribed currently.
P. granatum is an antique, asomatous and novel fruit, which has therapeutic properties with the ability to heal various ailments of the human body. Plants have a natural capacity to synthesize phenols and tannins which provide defensive action against microorganisms.,P. granatum peel extract has high reserves of tannins and phenols as compared to the different parts of P. granatum plant in a study performed by Pai et al. Scalbert (1991) proposed different mechanisms to explain the antimicrobial activity of tannin. These include (i) inhibition of extracellular microbial enzymes, (ii) deprivation of substrates and metal ions required for microbial growth and (iii) direct action on microbial metabolism through the inhibition of oxidative phosphorylation. Shafighi et al. in an in vitro study proved that the MIC of peel extract is greater than that of flower, stem and leaf.
As observed by the scanning electron microscopy, the peel extracts showed morphological alterations along with cell aggregation and growth inhibition in the yeasts used for the trial. The appearance of the control sample was regular and homogeneous, with a normal budding profile at the cell and hyphae, whereas the treated cells presented an irregular cell wall, with viscous material on the surface along with the rupture of the hyphae and desquamation.
In the present study, the extract of P. granatum peel has the effect on C. albicans in all concentrations. This finding is in agreement with Duraipandian's study.P. granatum has proved to be effective against C. albicans, which is in accordance with the study conducted by Endo EH. It is also in accordance with the studies conducted by Vasconcelos et al. and Duraipandiyan et al. Vasconcelos et al. through a clinical trial showed that P. granatum peel extract was effective as a topical antifungal drug against C. albicans for treating two cases of denture stomatitis patients. According to Vasconcelos et al., in their in-vitro study, antimicrobial efficacy of P. granatum extract gel was proven to be higher than miconazole.
The MIC and MFC exhibited by P. granatum in this study were at concentrations of 30 μl/ml and 20 μl/ml, respectively, as tabulated in [Table 2], which is in close correlation with the results obtained by Madugula et al. in their study where the MIC and MFC were found to be 20 μl/ml and 10 μl/ml, respectively.
|Table 2: Determination of minimum inhibitory concentration and minimum fungicidal concentration for Candida species|
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In the present study, the P. granatum peel extract had MIC against C. albicans at all concentrations and the antifungal efficacy of P. granatum peel extract approximated with that of clotrimazole. P. granatum peel extract can be used as an antifungal agent in clinical trials. This study is limited as it is an in-vitro study. Further in-vivo studies should be carried out to confirm the results of this study.
| Conclusions|| |
Our results indicate that P. granatum peel extract is an effective antifungal agent against C. albicans and its antifungal efficacy approximates that of standard clotrimazole. The discovery of a natural antifungal agent with beneficial qualities of biosafety and efficacy will be a great boon in the therapy of fungal infections. Apart from providing treatment to drug-resistant patients, cost-effectiveness also plays a major role in the replacement of synthetic drugs with natural ones, especially in developing countries.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2]