Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, Trikaripur, Kasaragod, India, 671310
Salvadora persica (miswak) is a traditional medicinal plant widely used for oral hygiene. The roots of Salvadora persica possess strong antimicrobial and antioxidant properties, making them suitable for use in herbal oral care formulations. The aim of this study was to formulate and evaluate Salvadora persica root extract–based oral care products to improve dental hygiene and prevent common oral diseases. Roots of Salvadora persica were collected from Trikaripur, Kasaragod, and subjected to successive solvent extraction. Pharmacognostic and phytochemical evaluations were carried out to ensure the quality and presence of bioactive constituents. Antimicrobial activity of the extract was assessed against Lactobacillus using the agar well diffusion method, and the results were compared with an amoxicillin disc as the standard control. Antioxidant activity was evaluated using the DPPH free radical scavenging assay. Based on the results, herbal gel toothpaste, herbal chewable oral care tablets, and herbal tooth powder were formulated using the root extract. The prepared formulations were evaluated for quality, stability, and efficacy. The findings demonstrated satisfactory antimicrobial and antioxidant activities, confirming the effectiveness of the formulations. The study concludes that Salvadora persica is a promising natural ingredient for oral care products and provides a safe herbal alternative for maintaining oral hygiene and preventing dental disorders.
HERBAL FORMULATIONS
Herbal formulations are dosage forms prepared from one or more herbs or processed herbal substances in specified quantities to provide therapeutic, nutritional, or cosmetic benefits. These formulations are widely used to diagnose, prevent, and treat diseases, as well as to maintain overall health. They are prepared using various processes such as extraction, distillation, purification, and fermentation, and may include whole plants or their parts in fresh or dried forms. Herbal medicines are gaining increasing attention due to their natural origin, cost-effectiveness, and relatively fewer side effects compared to synthetic drugs. However, they also present certain limitations such as variability in composition, slower onset of action, and lack of standardization.
Advantages:
Disadvantages:
HERBAL COSMETICS
Herbal cosmetics are the product, which are formulated by using various herbal ingredients to form the base that are used to provide defined cosmetic benefits. Due to its purity, safety and efficacy herbal cosmetics are popular around the world. Herbal cosmetics are formulated using various herbal extracts containing a wide range of active principles such as glycosides, alkaloids, flavonoids, carotenoids, terpenoids, saponins, vitamins, amino acids, sugars, essential oil, enzyme etc.
HERBAL GEL TOOTHPASTE
Herbal gel toothpaste is a modern oral care formulation designed to promote dental health using plant-based ingredients. It typically contains natural extracts such as Salvadora persica (miswak), along with gelling agents and mild abrasives, providing gentle cleansing, antimicrobial action, and plaque control. Compared to conventional toothpaste, herbal gel formulations offer a safer and more eco-friendly alternative with minimal use of synthetic chemicals.
Advantages:
HERBAL CHEWABLE ORAL CARE TABLET
Herbal chewable oral care tablets are solid dosage forms designed to dissolve upon chewing. They releasing herbal extracts and bioactive compounds that help reduce oral bacteria, control odor, and maintain oral hygiene. Their pre-measured dosage ensures convenience, improved compliance, and suitability for individuals with swallowing difficulties. Additionally, they are portable, eco-friendly, and reduce plastic waste compared to conventional oral-care products.
Advantages:
HERBAL TOOTH POWDER
Herbal tooth powder is a natural oral hygiene formulation made from finely powdered herbs and minerals. It provides mechanical cleaning along with antimicrobial and antioxidant benefits. Ingredients such as Salvadora persica (miswak) help control plaque, reduce oral bacteria, and freshen breath. Due to their chemical-free composition, sustainability, and effectiveness, herbal tooth powders are increasingly popular as an alternative to conventional toothpaste.
Advantages:
MATERIALS AND METHODS
PLANT COLLECTION
The fresh root of Salvadora persica, were collected from Trikaripur, Kasaragod district, Kerala (India) in the month of October 2025. The herbarium was prepared by drying the specimens in the shade and then labeling them with the relevant information.
PLANT AUTHENTICATION
The plant material was identified and authenticated by Dr. Subrahmanya Prasad.K, Assistant professor, Department of botany, Nehru Arts and Science College, Kanhangad, Padannakkad.
PLANT PROFILE
Salvadora persica
Synonyms
Arak, Sewak, Peelu, Toothbrush tree
Scientific classification of Salvadora persica
|
Kingdom |
Plantae |
|
Subkingdom |
Tracheobionta |
|
Super division |
Spermatophyta |
|
Division |
Magnoliophyta |
|
Class |
Magnoliopsida |
|
Subclass |
Rosidae |
|
Order |
Brassicales |
|
Family |
Salvadoracea |
|
Genus |
Salvadora |
|
Species |
Salvadora persica |
Morphological characteristics
Salvadora persica is a small to medium sized tree, typically growing up to 3-6 meters tall. The root of Salvadora persica is a thick, deeply penetrating taproot with many spreading lateral roots. The outer part of the root is fibrous and light brown, while the inner part is soft and white, which is the portion used as miswak. The root is highly adapted to salinity and drought conditions. It contains antimicrobial compounds, silica, and fluoride, giving it medicinal properties. The stem is straight, with a smooth, grayish brown bark that peels off in thin layers. The branches are spreading, with a rounded crown. The leaves are elliptical or ovate, with a pointed tip, typically 2-5 cm long and 1-2 cm wide, and they are arranged oppositely on the stem. It produces small, greenish yellow flowers and are arranged in axillary clusters. The fruit is small, red or purple and are typically 1-2 cm in diameter.
Phytochemical constituents
Medicinal uses
Antibacterial, Antioxidant, Astringent, Oral hygiene (Natural toothbrush), gastrointestinal benefits, antidiabetics effect etc.
PREPARATION OF PLANT EXTRACT
Extraction of Salvadora persica was carried out by maceration. Maceration is an extraction technique used to extract bioactive compounds from plant material.
Procedure:
PHARMACOGNOSTIC STUDY
A. Determination of moisture content
B. Determination of ash value
C. Determination of Extractive value
PRELIMINARY PHYTOCHEMICAL SCREENING
The extract was subjected to preliminary phytochemical screening to detect the various phytoconstituents such as alkaloids, glycosides, carbohydrates, flavonoids, saponins, tannins and phenols.
INVITRO-ANTIMICROBIAL ACTIVITY
Antibacterial activity was determined by agar well diffusion method, activity of extract was tested against Lactobacillus.
Procedure:
Preparation of pre-inoculum: The bacteria Lactobacillus is prepared from curd. The curd is filtered and the broth is incubated at 25? for 24 hours.
Preparation of pour plates: A sabouraud dextrose agar (150 ml) is autoclaved and poured to the already autoclaved plate and cooled to room temperature and allowed to solidify. The culture was spread on the agar surface aseptically by using sterilized cotton.
Making wells on agar plates: Wells of 6mm in diameter were made aseptically on the agar plate by using a sterilized well digger. The extract is aseptically added in to the well by using a micropipette. The petri plates are kept in a refrigerator (1hr) for the diffusion of substances from well in to surrounding medium. During this time the growth of the organism is reduced: After 1 hour, the plates were incubated in inverted condition at 37? for 48 hours.
Measurement of the zone of inhibition: After 48 hours, the plates were observed for the presence of inhibition of bacterial growth, and it was indicated in the form of a clear zone of inhibition around each well containing the extract. The size of the inhibitory zone was measured in ‘mm’. The zone of inhibition obtained for the developed herbal extract was compared with the standard. Amoxicillin disc was used as standard.
ANTIOXIDANT ACTIVITY
Where,
RSA= Radical Scavenging Activity.
Abs control= absorbance of DPPH radical + methanol.
Abs sample= absorbance of DPPH radical + extract.
FORMULATION OF HERBAL GEL TOOTHPASTE
|
SR. NO |
INGREDIENTS |
F1 |
F2 |
F3 |
|
1 |
Salvadora persica extract |
3g |
2.5g |
2.5g |
|
2 |
Carbopol 940 |
1g |
1g |
1g |
|
3 |
Triethanolamine |
q.s |
q.s |
q.s |
|
4 |
Propylene glycol |
4ml |
5ml |
3.5ml |
|
5 |
Glycerin |
8ml |
8ml |
7.5ml |
|
6 |
Hydrated silica |
4.5g |
5g |
5g |
|
7 |
Methyl paraben |
0.15g |
0.15g |
0.15g |
|
8 |
Propyl paraben |
0.12g |
0.12g |
0.12g |
|
9 |
Sodium saccharin |
0.3g |
0.3g |
0.3g |
|
10 |
Peppermint oil |
0.5ml |
0.5ml |
0.5ml |
|
11 |
Distilled water |
Up to 100ml |
Up to 100ml |
Up to 100ml |
Procedure:
EVALUATION OF HERBAL GEL TOOTHPASTE
F1, F2, F3 was prepared and subjected to following evaluation method.
1. Physical Evaluation:
The colour, state, and appearance of the gel toothpaste were examined visually.
2. pH test:
Take 1gm of the herbal gel toothpaste in a 150ml beaker and add 10ml 0f freshly boiled and cooled water. Stir well to form a uniform suspension, and determine the pH of the suspension using pH meter.
3. Spreadability test:
Approximately 1–2 g of herbal gel toothpaste was placed between two glass slides (10 × 10 cm). A known weight was applied, and the slides were moved in opposite directions. After 3 minutes, the spread length was measured. The test was performed in triplicate, and spreadability (S) was calculated using the formula:
S = (M × L) / T
Where,
M is the applied weight, L is the length of spread, and T is the time required to separate the slides.
4. Extrudability:
The formulation was filled into collapsible aluminum tubes, sealed, and weighed. Tubes were placed between glass slides, clamped, and subjected to a 500 g load. The cap was removed, and the extruded paste was collected and weighed. Extrudability was expressed as the percentage of paste extruded.
5. Abrasiveness:
Approximately 15–20 cm of toothpaste was extruded from each of ten tubes onto butter paper. Samples were visually inspected and gently spread to detect the presence of coarse or sharp particles.
6. Fragrance Test:
A small quantity of each formulation was placed on a clean watch glass and evaluated organoleptically for odor type and intensity.
7. Shape retention:
The herbal gel toothpaste was dispensed onto a toothbrush and allowed to stand for 10 seconds. The shape retention was evaluated and graded as: (A) shape maintained, (B) shape mostly maintained, or (C) shape not maintained.
FORMULATION OF HERBAL CHEWABLE ORAL CARE TABLET
|
SR. NO |
INGREDIENTS |
F1 |
F2 |
F3 |
|
1 |
Salvadora persica extract |
2.5g |
2.5g |
2.5g |
|
2 |
Mannitol |
13g |
15g |
15g |
|
3 |
Sodium bicarbonate |
1.5g |
1.5g |
2g |
|
4 |
Acacia |
2.5g |
2g |
3g |
|
5 |
Magnesium stearate |
0.3g |
0.2g |
0.3g |
|
6 |
Talc |
0.2g |
0.2g |
0.3g |
|
7 |
Menthol |
0.1ml |
0.1ml |
0.1ml |
Procedure:
EVALUATION OF HERBAL CHEWABLE ORAL CARE TABLET
F1, F2, F3 was prepared and subjected to following evaluation method.
1. Physical Evaluation:
The colour, state, and appearance of the chewable oral care tablet were examined visually.
2. Pre-compression evaluation:
Angle of repose:
The angle of repose is the maximum angle formed between the surface of a powder pile and the horizontal plane. It is used to assess the flow properties of powders, where a lower angle indicates better flow. It is calculated using:
tan ???? = h / r
|
???? = tan-1 (h/r) |
Where,
θ is the angle of repose, h is the height of the pile, and r is the radius of its base.
Angle of repose as an indication of powder flow
Method:
A funnel was fixed at a constant height, and granules of the herbal chewable oral care tablet were allowed to flow freely to form a conical heap. The height and radius of the heap were measured, and the angle of repose was calculated. Care was taken to ensure smooth and uniform flow of particles.
Bulk density:
Bulk density was defined as the ratio of the mass of powder to its bulk volume. A known quantity of powder was introduced into a 100 mL graduated cylinder. The cylinder was dropped three times from a height of 1 inch at 2-second intervals, and the initial volume was recorded. Bulk density was calculated using:
|
Bulk density = mass / bulk volume |
Tap density:
Tap density was defined as the ratio of the mass of powder to its tapped volume. The same cylinder was tapped 100 times from a height of 1 inch at 2-second interval and the final volumewas recorded. Tap density was calculated using:
|
Tap density = mass / tap volume |
Hausner's Ratio:
Hausner's ratio is an indirect measure of powder flowability calculated using bulk and tapped densities. It was determined using the formula:
|
Hausner’s ratio = Tapped density / Bulk density |
Lower values indicate better flow properties.
Carr's Index:
Carr's index (compressibility index) is used to evaluate powder flow based on bulk and tapped densities. It was calculated using:
|
% Compressibility = ((tap density-bulk density) /tap density) × 100 |
Flow properties were interpreted using standard compressibility index ranges.
Carr’s index as an indication of powder flow
3. Post compression evaluation:
a) Weight variation:
Twenty tablets were individually weighed and the average weight was calculated. Individual weights were compared with the mean weight to ensure uniformity as per Indian Pharmacopoeia (IP) limits.
Weight variation specification as per I.P
b) Hardness:
Tablet hardness was evaluated using a Monsanto hardness tester. Ten tablets from each formulation were tested, and the force required to fracture each tablet was recorded.
c) Friability:
Friability was determined using a Roche friabilator. Twenty pre-weighed tablets were rotated at 25 rpm for 4 minutes. Tablets were dedusted and reweighed, and friability was calculated as:
|
% friability = ((initial weight – final weight) / initial weight) × 100 |
d) pH:
The pH was measured using a calibrated pH meter. Tablets were dissolved in 200 mL of distilled water in separate beakers, and the pH of each solution was recorded.
e) Disintegration time:
Disintegration test was performed to determine the time required for tablets to break into smaller particles. Six tablets (three with discs and three without) were tested using a standard disintegration apparatus in distilled water at room temperature. The average disintegration time was found to be approximately 2 minutes.
FORMULATION OF HERBAL TOOTH POWDER
|
SR. NO |
INGREDIENTS |
F1 |
F2 |
F3 |
|
1 |
Salvadora persica powder |
3g |
3g |
3g |
|
2 |
Sodium bentonite clay |
4.5g |
5g |
6g |
|
3 |
Himalayan rock salt |
3g |
3g |
3g |
|
4 |
Calcium carbonate |
6g |
6.5g |
8g |
|
5 |
Menthol crystals |
0.2g |
0.2g |
0.2g |
|
6 |
Xylitol |
2g |
2.5g |
3g |
|
7 |
Silica |
3.8g |
3.8g |
3.8g |
Procedure:
EVALUATION OF HERBAL TOOTH POWDER
F1, F2, F3 was prepared and subjected to following evaluation method.
1. Physical Evaluation:
The colour, state, and appearance of the powder were examined visually.
2. pH Determination:
About 5 g of the herbal tooth powder was dispersed in freshly boiled and cooled distilled water. The suspension was stirred thoroughly, and the pH was measured using a calibrated digital pH meter at room temperature.
3. Bulk Density:
Approximately 5 g of powder was accurately weighed and transferred into a dry 10 ml graduated measuring cylinder. The initial volume occupied by the powder was noted, and bulk density was calculated using the formula:
|
D = M / V |
D= Bulk density, M= Mass of particles, V = Total volume occupied
4. Tapped Density:
The same sample was subjected to mechanical tapping until no further change in volume was observed. The final tapped volume was recorded, and tapped density was calculated as:
|
Tapped density = Weight of powder (g) / Tapped density (ml) |
Angle of Repose:
The flow properties of the powder were determined by the funnel method. Approximately 25 g of powder was allowed to flow through a funnel fixed at a known height to form a conical heap. The height (h) and radius (r) of the heap were measured, and the angle of repose (θ) was calculated using:
|
θ= tan-1 (h/r) |
Where,
h – height of the powder cone
r – radius of the powder cone
5. Foaming power:
Foaming ability was evaluated by dispersing 2 g of powder in 50 ml of water in a measuring cylinder. The mixture was shaken ten times, and the increase in volume due to foam formation was recorded. Foaming power was calculated as:
|
Foaming power = V1 – V2 |
Where,
V1 = final volume (ml), V2 = initial volume (ml).
6. Spreadability Test:
About 0.6 g of powder was placed between two glass slides, and a load of 1.13 kg was applied for 30 minutes. The diameter of the spread sample was measured in centimeters and recorded as an index of spreadability.
7. Abrasiveness:
Abrasiveness was evaluated by rubbing 1 g of powder on a glass slide for 15 minutes. The surface was examined for scratches and recorded qualitatively as positive or negative, with higher scratch intensity indicating greater abrasiveness.
RESULTS AND DISCUSSION
Preparation of plant extract
Extraction of Salvadora persica was carried out by maceration, and the obtained extract was subsequently used for phytochemical studies.
Figure:2
Physico-chemical parameters
The following were the physico-chemical parameters evaluated,
|
SR. NO |
Parameters (%w/w) |
Salvadora persica |
|
1 |
Total ash |
6.6 ± 0.12 % |
|
2 |
Acid insoluble ash |
2.9 ± 0.05 % |
|
3 |
Water soluble ash |
3.4 ± 0.10 % |
|
4 |
Water soluble extractive value |
20.2 ± 0.35 % |
|
5 |
Alcohol soluble extractive value |
29.3 ± 0.42 % |
|
6 |
Moisture content |
13 ± 0.20 % |
Preliminary phytochemical screening
The extract was subjected to preliminary phytochemical screening to detect various phytochemical constituents. The preliminary phytochemical study revealed the presence and absence of certain phytochemicals in the extract of Salvadora persica.
|
SR. NO |
Chemical constituents |
Salvadora persica |
|
1 |
Alkaloids |
- |
|
2 |
Carbohydrates |
+ |
|
3 |
Flavonoids |
- |
|
4 |
Saponins |
+ |
|
5 |
Glycosides |
+ |
|
6 |
Tannins |
- |
|
7 |
Phenols |
+ |
Invitro-Antimicrobial activity
The antimicrobial activity of the extract was evaluated using the agar well diffusion method against Lactobacillus. The standard amoxicillin disc (positive control) produced a zone of inhibition of 10 mm, while the test extract showed a zone of 7 mm. These findings suggest that the extract exhibits moderate antimicrobial activity compared to the standard.
|
Sr. No |
Test samples |
Zone of inhibition (mm) |
|
1 |
Control |
10 |
|
2 |
Extract |
7 |
Antioxidant activity
The Antioxidant activity was expressed in terms of % inhibition, and the results are presented in the following table.
|
Concentration |
Absorbance |
% Inhibition |
|
10 |
0.590 |
15.7 |
|
20 |
0.515 |
26.4 |
|
30 |
0.440 |
37.1 |
|
40 |
0.360 |
48.5 |
|
50 |
0.290 |
58.5 |
Formulation of Herbal Gel Toothpaste
Salvadora persica herbal gel toothpaste was prepared and transferred into an aluminum collapsible tube.
|
SR. NO |
PARAMETERS |
F1 |
F2 |
F3 |
|
1 |
Colour |
Yellow |
Yellow |
Yellow |
|
2 |
Odour |
Characteristic |
Characteristic |
Characteristic |
|
3 |
Texture |
Smooth |
Smooth |
Smooth |
|
4 |
pH |
7.20 ± 0.01 |
7.45 ± 0.01 |
7.50 ± 0.02 |
|
5 |
Spreadability |
2.90 ± 0.10 |
3.10 ± 0.10 |
2.50 ± 0.10 |
|
6 |
Abrasiveness |
Slightly good |
Good |
Slightly good |
|
7 |
Fragrance |
Mildly aromatic with faint peppermint scent |
Fresh, pleasant, and characteristic Odour |
Strong, pungent, and medicinal odour |
|
8 |
Shape retention |
Moderate |
Good |
Poor |
Formulation of Herbal Chewable Oral Care Tablet
Salvadora persica herbal chewable oral care tablet was prepared and transferred into a dry, airtight container.
|
SR. NO |
PARAMETERS |
F1 |
F2 |
F3 |
|
1 |
Colour |
Light brown |
Light brown |
Light brown |
|
2 |
Shape |
Circular |
Circular |
Circular |
|
3 |
State |
Solid |
Solid |
Solid |
|
4 |
Texture |
Hard & Brittle |
Hard & Brittle |
Hard & Brittle |
|
5 |
Angle of repose (º) |
25.23 ± 0.11 |
23.21 ± 0.08 |
25.32 ± 0.14 |
|
6 |
Bulk density (g/ml) |
0.45 ± 0.01 |
0.50 ± 0.02 |
0.48 ± 0.01 |
|
7 |
Tapped density (g/ml) |
0.52 ± 0.02 |
0.56 ± 0.01 |
0.54 ± 0.02 |
|
8 |
Hausner’s ratio |
1.16 ± 0.02 |
1.12 ± 0.01 |
1.13 ± 0.01 |
|
9 |
Carr’s index (%) |
13.46 ± 0.15 |
10.71 ± 0.12 |
25.32 ± 0.14 |
|
10 |
Weight variation (mg) |
504.9 ± 1.72 |
499.3 ± 1.45 |
511.9 ± 1.60 |
|
11 |
Hardness (kg/cm²) |
3.41 ± 0.11 |
4.10 ± 0.10 |
3.85 ± 0.10 |
|
12 |
Friability (%) |
0.85 ± 0.01 |
0.65 ± 0.01 |
0.90 ± 0.01 |
|
13 |
pH |
7.20 ± 0.03 |
7.40 ± 0.02 |
7.00 ± 0.03 |
|
14 |
Disintegration time |
2.58 ± 0.08 |
1.0 ± 0.0 |
2.82 ± 0.08 |
Monsanto hardness tester Disintegration apparatus
Friabilator pH meter
Formulation of Herbal Tooth Powder
Salvadora persica herbal tooth powder was prepared and transferred into a suitable container
|
SR NO |
PARAMETERS |
F1 |
F2 |
F3 |
|
1 |
Colour |
Pale beige |
Pale beige |
Pale beige |
|
2 |
Odour |
Pleasant |
Pleasant |
Pleasant |
|
3 |
Taste |
Astringent |
Astringent |
Astringent |
|
4 |
Texture |
Fine |
Fine |
Fine |
|
5 |
Appearance |
Powder |
Powder |
Powder |
|
6 |
pH |
6.80 ± 0.05 |
7.00 ± 0.05 |
7.20 ± 0.05 |
|
7 |
Bulk density (g/ml) |
0.55 ± 0.01 |
0.53 ± 0.02 |
0.57 ± 0.01 |
|
8 |
Tapped density (g/ml) |
0.65 ± 0.02 |
0.64 ± 0.03 |
0.68 ± 0.01 |
|
9 |
Angle of repose (º) |
29.38 ± 0.35 |
30.11 ± 0.52 |
27.53 ± 0.38 |
|
10 |
Foaming power |
8.00 ± 0.35 |
7.50 ± 0.40 |
9.00 ± 0.25 |
|
11 |
Spreadability |
2.60 ± 0.10 |
2.90 ± 0.10 |
3.40 ± 0.10 |
|
12 |
Abrasiveness |
Slightly good |
Slightly good |
Good |
DISCUSSION
The present study evaluated the oral care potential of Salvadora persica through the formulation and assessment of herbal gel toothpaste, chewable oral care tablets, and tooth powder. The selection of Salvadora persica was based on its well-established traditional use as a natural oral hygiene agent and its reported antimicrobial and antioxidant properties.
The aqueous extract obtained by maceration revealed the presence of key phytoconstituents such as glycosides, saponins, carbohydrates, and phenolic compounds. These bioactive components are known to contribute to oral health by inhibiting pathogenic microorganisms, preventing plaque formation, and providing antioxidant protection to oral tissues. The use of aqueous extraction supports the retention of polar compounds, enhancing the biological activity of the extract.
Among the three herbal gel toothpaste formulations, F2 exhibited superior physicochemical characteristics, including optimal pH, good spreadability, appropriate abrasiveness, and better retention on tooth surfaces. These properties are essential for ensuring effective plaque removal and prolonged contact of active constituents with oral tissues. Similarly, the herbal chewable oral care tablet formulation F2 demonstrated acceptable weight variation, adequate hardness, low friability, and rapid disintegration, facilitating efficient release and action of the active components within the oral cavity.
In the case of herbal tooth powder formulations, F3 showed better performance with uniform particle size, good flow properties, and controlled abrasiveness. These attributes contribute to effective mechanical cleansing while minimizing potential damage to dental enamel.
The antioxidant activity of the extract, as demonstrated by the DPPH assay (58.5% inhibition), indicates its capacity to neutralize free radicals and reduce oxidative stress associated with oral diseases such as periodontitis. Furthermore, the antimicrobial activity against Lactobacillus species, although lower than the standard amoxicillin, confirms its potential as a natural antimicrobial agent. The comparatively moderate activity may be advantageous for long-term use by reducing the risk of antimicrobial resistance and adverse effects associated with synthetic agents.
Overall, the findings suggest that Salvadora persica extract can be effectively incorporated into various oral care formulations with satisfactory physicochemical and biological properties. The study supports its
traditional application and highlights its potential as a safe, natural, and effective alternative for modern oral hygiene products.
ACKNOWLEDGEMENT
We sincerely express our heartfelt gratitude to the Almighty for His abundant blessings and guidance throughout our academic journey and the successful completion of this research work. We would like to express our sincere thanks to Kerala University of Health Sciences, Thrissur, for providing us the opportunity to pursue our graduation and for their academic support.
We extend our deep gratitude to the Management of Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, Trikaripur, for their constant encouragement and support during the course of this study.
We are extremely grateful to Dr. M. Paridhavi, Principal, Rajiv Gandhi Institute of Pharmaceutical Sciences and Research, for his valuable guidance and support.
We express our sincere and heartfelt gratitude to our guide Mrs. Vyshnavy Devy D K, Associate Professor, for her continuous guidance, encouragement, patience, and valuable suggestions, which were instrumental in the successful completion of this research work.
We also sincerely thank Dr. Subrahmanya Prasad K, Assistant Professor, Department of Botany, Nehru Arts and Science College, Kanhangad, for his kind help in the authentication of the plant material used in this study.
We extend our thanks to all the teaching and non-teaching staff members of our institution for their cooperation and support throughout the study period.
Finally, we are deeply thankful to our friends and family members for their constant support, motivation, and encouragement throughout our academic journey.
REFERENCES
Jashira P, Darshana JK, Navyasree M Nair, Vismaya Vijayakumar, Varsha Vijayan K P, Vyshnavy Devy D K, Phytochemicals Enriched Herbal Oral Care Formulations for Enhanced Dental Health, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 5, 5583-5600. https://doi.org/10.5281/zenodo.20327797
10.5281/zenodo.20327797