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Abstract

The present study aimed to develop and evaluate an emulgel loaded with Pongamia pinnata seed oil and Wrightia tinctoria leaf extract for the treatment of skin disorders, with a particular focus on antimicrobial activity. Pongamia pinnata seed oil was extracted by mechanical pressing, while Wrightia tinctoria leaves were subjected to hot aqueous extraction. Four O/W type emulgel formulations (F1–F4) were prepared by incorporating a herbal emulsion into a gel base and evaluated for their physicochemical properties. All formulations exhibited good appearance, suitable pH, spreadability, extrudability, and stability without phase separation, with F4 showing the most favorable characteristics. Antimicrobial studies revealed that Wrightia tinctoria leaf extract showed strong antifungal activity with a MIC of 25 µl/ml against Candida albicans. In comparison, Pongamia pinnata seed oil and its combination showed moderate inhibition at 50 µl/ml. Against Staphylococcus aureus, both extracts were effective at 50 µl/ml, whereas the mixture showed reduced efficacy (MIC 100 µl/ml). The results suggest that topical emulgel formulations containing these extracts may offer dual antifungal and antibacterial effects, though further in vivo and extended antimicrobial studies are warranted to confirm therapeutic potential.

Keywords

Pongamia pinnata seed oil, Wrightia tinctoria leaf extract, Carbopol- 934, emulgel, skin disorder

Introduction

Skin disorders such as eczema, psoriasis, and dermatitis are common inflammatory conditions often requiring long-term management. Herbal drugs offer safe and effective alternatives, with Pongamia pinnata seed oil known for its anti-inflammatory, antimicrobial, and wound-healing properties, and Wrightia tinctoria traditionally used for treating psoriasis and other dermal ailments. However, conventional formulations face limitations in terms of penetration and stability.1

Pongamia pinnata seeds yield oil rich in bioactive compounds such as karanjin, pongamol, oleic acid, and linoleic acid, which exhibit diverse pharmacological properties including antioxidant and anti-inflammatory activities.2 Similarly, Wrightia tinctoria contains flavonoids, triterpenoids, and glycosides, which contribute to its therapeutic efficacy in treating skin diseases. To overcome formulation challenges and enhance delivery, emulgel serves as an effective drug carrier system by combining the advantages of emulsions and gels, offering improved Spreadability, stability, and controlled release 3

An emulgel is a dual-acting topical formulation in which an emulsion (O/W or W/O) is incorporated into a gel base using gelling agents such as Carbopol or HPMC. This system enables the delivery of both lipophilic and hydrophilic drugs, provides thermodynamic stability, reduces interfacial tension, and ensures controlled release of active ingredients through both emulsion and gel phases. Additionally, emulgel offer improved Spreadability, non-greasy texture, and patient compliance, making them highly suitable for dermatological applications.4, 5. Therefore, the present study aims to develop and evaluate an herbal emulgel containing Pongamia pinnata seed oil and Wrightia tinctoria leaf extract for the treatment of skin disorders, with emphasis on antimicrobial activity, stability, and therapeutic potential.

MATERIALS AND METHODS

Plant Collection and Authentication:

The seeds of Pongamia pinnata were collected from Tukkanatti, Belagavi district, Karnataka, India, while the leaves of Wrightia tinctoria were obtained from the medicinal garden of Rani Chennamma College of Pharmacy, Belagavi, Karnataka, India. The plant materials were authenticated by the Indian Council of Medical Research (ICMR) – National Institute of Traditional Medicine (NITM), Karnataka, India, and accession number of specimens were retained for future reference.

                 

 

Pongamia pinnata                                Wrightia tinctoria

Figure 1: Authentication letter

Method of Preparation of Plant Extracts: 6, 7

Wrightia tinctoria leaf extract: Healthy leaves of Wrightia tinctoria were collected and shade-dried at room temperature to prevent degradation of bioactive constituents. The dried leaves were then powdered using a mixer, sieved to obtain uniform particle size, and stored in a well-closed container in a dry place until use. A hot aqueous extract was prepared by mixing 10 g of the leaf powder with 100 mL of distilled water (10% w/v) and maintaining the mixture at a constant temperature of 60?°C. The extract was then filtered through Whatman filter paper to obtain a clear solution for further use.

Pongamia pinnata seed oil: Mature seeds of Pongamia pinnata were collected and thoroughly cleaned to remove dust, debris, and damaged seeds. The seeds were shade-dried (or sun-dried if necessary) to reduce moisture content. Further drying was performed, if required, to achieve an optimal moisture content of approximately 8–10%, which is ideal for efficient oil extraction. The dried kernels were then ground into a coarse powder or crushed to increase the surface area, thereby enhancing the extraction efficiency of the oil.

Figure 2: Extraction Process

Preliminary Phytochemical Screening of plant extracts:8, 11

Hot aqueous extract of Wrightia tinctoria leaves was subjected to preliminary phytochemical screening to detect the presence of various classes of phytoconstituents, including alkaloids, flavonoids, tannins, saponins, glycosides, and phenolic compounds, following standard qualitative procedures. The extracted oil from Pongamia pinnata seeds was similarly analyzed for the presence of phytoconstituents such as fatty acids, flavonoids, phenolic, terpenoids, and other bioactive compounds using standard phytochemical screening methods as given in table 1 and 2.

Table 1. Phytochemical Screening of Wrightia Tinctoria Leaf Extract

Phytochemical constituent

test

Inference

Flavonoids

Shinoda test

++

Alkaloids

Hager’s test

+++

Wagner’s test

+++

Tannins

Ferric Chloride Test

++

Lead Acetate

++

Phytochemical screening of Wrightia tinctoria leaf extract. The intensity of phytoconstituents is expressed as (+++) highly present, (++) moderately present

Table 2: Phytochemical screening of Pongamia pinnata seed oil

Phytochemical constituent

Test

Inference

Alkaloids

Wagner’s test

+++

Steroids

Liebermann–Burchard test

++

Tannins and Phenolics

Ferric chloride test

++

Fixed oil and fats

Spot test

+++

Flavonoids

Shinoda test

+++

Phytochemical screening of Pongamia pinnata seed oil. The intensity of phytoconstituents is expressed as (+++) highly present, (++) moderately present

Preparation of Emulgel loaded with Pongamia pinnata seed oil and Wrightia tinctoria leaf extract: The emulgel formulation was prepared using a two-phase system: an aqueous phase and an oil phase. The aqueous phase consisted of Carbopol 934, methyl paraben, and distilled water. Oil phase: Contained Pongamia pinnata seed oil, Wrightia tinctoria leaf extract, liquid paraffin, and isopropyl myristate. The aqueous and oil phases were separately prepared and then mixed. Triethanolamine was added to the mixture to neutralize Carbopol 934, resulting in the formation of a stable gel base.12-14

Table 3: Formulation of Emulgel loaded with plant extracts

Ingredients

F1

F2

F3

F4

Wrightia tinctoria extract (ml)

2.5

2.5

2.5

2.5

Pongamia pinnata seed oil (ml)

2.0

2.0

2.0

2.0

Carbopol 934 (gm)

1.0

1.0

1.0

1.0

Span 20 (ml)

1.75

1.75

1.75

1.75

Tween 80 (ml)

0.75

0.75

0.75

0.75

Propylene glycol (ml)

5.0

5.0

---

---

PEG 400 (ml)

---

---

5.0

5.0

Methyl paraben (ml)

0.01

0.01

0.01

0.01

Distilled water (q.s. to 50gm)

q.s.

q.s.

q.s.

q.s.

Formulation composition of emulgels (F1–F4) loaded with Wrightia tinctoria leaf extract and Pongamia pinnata seed oil. Propylene glycol serves as a co-solvent in F1 and F2, while PEG 400 is incorporated in F3 and F4. Distilled water is added q.s. to make up the final weight to 50 g.

Figure 3: Prepared formulation of Emulgel loaded with plant extracts (F1- F4)

Evaluation of Emulgel: 15- 19

Physical Appearance: The prepared emulgel formulations were inspected visually for color, consistency, and overall appearance.

Determination of pH: pH is a critical parameter for topical formulations to ensure compatibility with skin, which typically has a pH in the range of 5–7. A formulation with pH values outside this range may irritate. For evaluation, 1 g of the emulgel was dispersed in 100 mL of distilled water and allowed to stand for 2 hours. Measurements were carried out in triplicate using a calibrated pH meter and average values were recorded.

Spreadability: Spreadability determines the extent of area to which the emulgel spreads on application. A fixed amount of emulgel was placed between two glass slides (7.5 cm contact length). A 100 g weight was placed on the upper slide to allow uniform spreading, and excess gel was removed. The time taken by the upper slide to separate from the lower slide under a fixed weight was noted. The experiment was performed in triplicate, and the mean value was used for calculation.

The Spreadability was calculated using the formula:

???? = ????×????

       ????

Where;

  • S = Spreadability (g·cm/sec)
  • M = Weight tied to upper slide (10 g)
  • L = Length moved by the slide (6.8 cm)
  • T = Time taken (sec)

Extrudability: Extrudability was determined as the force required to extrude the emulgel from a collapsible tube. The formulation was filled into lacquered aluminum collapsible tubes, and the amount of gel extruded was noted. A greater extruded quantity indicated better Extrudability. The Extrudability was calculated using the formula:
Extrudability (%) = Weight extruded from tube (g) X 100

                                      Total weight loaded in the tube (g)

Homogeneity: The prepared emulgel formulations were evaluated visually for uniformity by observing them against light. The formulations were checked for the presence of aggregates, lumps, coarse particles, or phase separation. A homogeneous emulgel was identified by its smooth texture and uniform appearance.

Stability Studies: Stability studies were carried out on the optimized emulgel formulation for a period of 30 days in accordance with ICH guidelines. The formulations were stored at 25 ± 1 °C and samples were withdrawn at 0, 15, and 30 days and evaluated for physical appearance, color, phase separation, pH, homogeneity and Spreadability. Any changes in these parameters were recorded to assess the physical and chemical stability of the formulation.

Antimicrobial Activity using Minimum Inhibitory Concentration (MIC): The antimicrobial potential of the plant extracts in the emulgel was determined by MIC assay using Brain Heart Infusion (BHI) broth.

Procedure: Nine serial dilutions of each test sample were prepared. In the initial tube, 20 μL of extract was added to 380 μL of BHI broth. For subsequent dilutions, 200 μL of BHI broth was added into 9 test tubes separately. From the initial tube, 200 μL was transferred into the first tube containing 200 μL of BHI broth (10?¹ dilution). From the 10?¹ dilution, 200 μL was transferred into the second tube to make a 10?² dilution, and the process was continued up to 10?? dilution. From the stock culture of the required microorganisms, 5 μL was inoculated into 2 mL of BHI broth. In each serially diluted tube, 200 μL of the above culture suspension was added. The tubes were incubated at 37 °C for 24 hours and observed for turbidity. The lowest concentration of extract that inhibited visible growth was considered as the MIC. 20, 21

RESULTS AND DISCUSSION

Table 4. Results of prepared formulations

Sr. No.

Parameter

F1

F2

F3

F4

  1.  

Colour

Yellow

Yellow

Yellow

Yellow

  1.  

Appearance

Smooth

Smooth

Smooth

Smooth

  1.  

pH

6.6

6.5

6.5

6.7

  1.  

Spreadability (g.cm/sec)

11.22

8.5

9.8

13.8

  1.  

Extrudability (%)

89.6

91.6

88.1

92.6

  1.  

Stability test

Found to be stable

The results of the evaluation tests confirmed the stability and effectiveness of the developed emulgel. All the formulations were evaluated for their Colour and appearance. The physical appearances of all the formulations were found to be yellow in color, with a pleasant odor and smooth texture. The pH of all the formulations that is F1, F2, F3 and F4 were found to be in range of 6.5 to 6.7 which is good for skin pH. All the formulation of emulgel were shown pH nearer to skin required that is 5-7 pH. Spreadability study is one of the criteria for an emulgel to meet the ideal qualities that it should possess good Spreadability. If Spreadability value is more, it would be properly spread over the skin which is more beneficial as per patient compliance concern. All the formulations were checked for the Spreadability and Extrudability. The data were given in the table 4. Among all the formulations, F4 showed better Spreadability and Extrudability. The antimicrobial activity of Wrightia tinctoria leaf extract, Pongamia pinnata seed oil, and their combination was evaluated against Candida albicans and Staphylococcus aureus using the Minimum Inhibitory Concentration (MIC) method. The results are presented in Table 5.

Table 5: Antimicrobial activity of plant extracts by the MIC method

Sr. No.

Samples

100

μl/ml

50

μl/ml

25

μl/ml

12.5

μl/ml

6.25

μl/ml

3.12

μl/ml

1.6

μl/ml

0.8

μl/ml

0.4

μl/ml

0.2

μl/ml

B+C

B+O

 

Candida

albicans

 

 

 

 

 

 

 

 

 

 

 

 

01

Wrightia tinctoria

S

S

S

R

R

R

R

R

R

R

S

R

02

Pongamia pinnata

S

S

R

R

R

R

R

R

S

R

S

R

03

Mixture

S

S

R

R

R

R

R

R

R

R

S

R

 

Staph

aureus

 

 

 

 

 

 

 

 

 

 

 

 

01

Wrightia tinctoria

S

S

R

R

R

R

R

R

R

R

S

R

02

Pongamia pinnata

S

S

R

R

R

R

R

R

R

R

S

R

03

Mixture

S

R

R

R

R

R

R

R

R

R

S

R

Antimicrobial activity of Wrightia tinctoria leaf extract, Pongamia pinnata seed oil, and their mixture against Candida albicans and Staphylococcus aureus at different concentrations. “S” indicates sensitivity and “R” indicates resistance. B + C = Blank control, B + O = Blank ointment.

Table 6: MIC values of test samples against microorganisms

Sr. No.

Sample

MIC (µl/ml) –

Candida albicans

MIC (µl/ml) –

Staphylococcus aureus

01

Wrightia tinctoria leaf extract

25

50

02

Pongamia pinnata seed oil

50

50

03

Mixture (1:1)

50

100

The results indicate that Wrightia tinctoria leaf extract exhibited the highest antifungal activity with a MIC of 25 µl/ml against Candida albicans, while Pongamia pinnata seed oil and the mixture showed moderate inhibition at 50 µl/ml. Against Staphylococcus aureus, both Wrightia tinctoria leaf extract and Pongamia pinnata seed oil were effective at 50 µl/ml, whereas the mixture showed a higher MIC of 100 µl/ml, suggesting reduced antibacterial efficacy in combination. Since Wrightia tinctoria showed better antifungal activity and both extracts were moderately effective against Staphylococcus aureus, incorporating them into topical formulations such as gels or emulsions may provide dual action against fungal and bacterial skin infections. Further evaluation through time-kill assays, zone of inhibition, and in vivo studies will be necessary to confirm their therapeutic relevance.

     

 

Figure 4:  MIC dilution test of plant extracts against E. coli and C. albicans

CONCLUSION

The present study successfully developed and evaluated a stable and effective emulgel formulation incorporating Pongamia pinnata seed oil and Wrightia tinctoria leaf extract for potential topical application in the treatment of skin disorders. All prepared formulations (F1–F4) exhibited desirable physicochemical characteristics such as appropriate pH, smooth texture, good spreadability, and excellent extrudability without phase separation. Among them, formulation F4 demonstrated the most favorable performance in terms of spreadability and stability.

Phytochemical analysis confirmed the presence of bioactive constituents including flavonoids, alkaloids, tannins, and fatty acids, which are responsible for the antimicrobial and anti-inflammatory activities of the extracts. Antimicrobial studies revealed that Wrightia tinctoria exhibited strong antifungal activity against Candida albicans (MIC 25 µl/ml), while Pongamia pinnata oil showed moderate antifungal and antibacterial activity. The combination of both extracts provided a balanced spectrum of antimicrobial effects, supporting their synergistic therapeutic potential.

Overall, the findings indicate that the developed herbal emulgel is a promising formulation for managing fungal and bacterial skin infections with good patient acceptability. Further in vivo studies and clinical evaluations are recommended to establish its safety, efficacy, and mechanism of action for potential pharmaceutical application.

ACKNOWLEDGEMENT

The authors would like to thank KRET’s Rani Chennamma College of Pharmacy, Belagavi, for providing the necessary facilities and support for this research work. We would also like to acknowledge Dr. Harsha V. Hegde (ICMR-NITM, Belagavi) and Dr. Ulka Idate (Maratha Mandal’s Central Research Laboratory, Belagavi) for their valuable assistance during this work.

REFERENCES

  1. Shanu sharma . Shoven mcher, Shubham prasad tiwar, Shubha in-vitro anti-microbial activite and phyto chemical analysis of leaves scids bark flower of pongamia pinnata (linn pierre) as human pathogens: 2021:12(4):180-186
  2. Baker JT, Borris RP, Carté B, Cordell GA, Soejarto DD, Cragg GM, et al. Natural product drug discovery and development: New perspectives on international collaboration. J Nat Prod 1995; 58:1325-57.
  3. Patel et al. Emulgel Approach to Formulation Development: A Review. Biosci. Biotech. Res. Asia. 2021; 18(3): 459-465.
  4. Moorthy, K., Aravind, A., Punitha, T., Vinodhini, R., Suresh, M., & Thajuddin, N. (2012). In vitro screening of antimicrobial activity of Wrightia tinctoria (Roxb.) R. Br. Asian Journal of Pharmaceutical and Clinical Research, 5(5), 4.
  5. R. Parthasarathy et al. In vitro Antioxidant Activity of Bark and Leaf of Thespesia populnea. Research Journal of Pharmacognosy and Phytochemistry. 2016; 8(1): 1-4.
  6. Das S K, Khanum A, Ghosh A. Microemulsion based gel Technique- A Novel Approach for Sustained Delivery to Treat Fungal Infection. Indo American Journal of Pharmaceutical Research, 2019; 8(2): 1958.
  7. B. Ali Khan, S. Ullah, M.Khalid Khan et al. Formulation and evaluation of Ocimum basilicum-based emulgel for wound healing using animal model. Saudi Pharmaceutical Journal. 2020; 28(12): 1842–1850.
  8. Rashmi S, Neha S, Reshma S, Madhura B, Devraj Y, Vishal M, Rohit P, Isha S. The Effect of Surfactant on Polyherbal Liquid Shampoo and its Comparative Analysis.
  9. Bodake R, Belhekar A, Bochare V, Vidhate P, Kumbhar S. Formulation and evaluation of herbal mouth Wash. Int J Adv Res Sci Commun Technol. 2022;2(2):608-17.
  10. Manmode P D et al, Formulation and Evaluation of Flurbiprofen Emulgel by using natural permeation enhancers, 2021, 10 (1), 827-828.
  11. Afzal A et al. Preparation of Spilanthes acmella based emulgel: Antimicrobial study and evaluation. Pakistan Journal of Pharmaceutical Sciences. 2022; 35: 287-295.
  12. Redkar M R et al. Review on Optimization base Emulgel Formulation. Asian Journal of Pharmacy and Technology. 2019; 9(3): 228-237.
  13. Brijesh Mahesh Patil, Ashwin Bhanudas Kuchekar and Saish Rajendara Pawar, Emulgel approach to evaluation of BIOSCIENCES BIOTECHNOLOGY RESEARCH ASIA, September 2021. Vol. 18(3), P. 459-465.
  14. Mitkari BV, Korde SA, Mahadik KR, Kokare CR, Formulation and evaluation of topical liposomal gel for fluconazole. India journal of pharmaceutical education and research, 2010; 44(4): 324-329.
  15. Kabir A, biswas B, Rouf A. Design, Fabrication and evaluation of drug release kinetics from aceclofenanc matrix tablets using hydroxyl propyl methyl cellulose. Dhaka. Uni. J. Pharm. Sci 2009;8:23-30.
  16. Kaushal R., and G. D. Basarkar. "Formulation, development and in-vitro evaluation of terbinafine hydrochloride emulgel for topical fungal infection." Int. J. Pharm. Sci 21.2 (2013): 168-173.
  17. Rutuja Saurabh Shah. Formulation and Evaluation of Turmeric Emulgel. Asian Journal of Pharmacy and Technology. 2021; 11(3): 213-219.
  18. Vidya N. Dange et al. Formulation and Evaluation of Novel Herbal Gel by using Lemongrass Oil. Research Journal of Pharmaceutical Dosage Forms and Technology. 2019; 11(2): 67-70.
  19. Antimicrobial susceptibility testing protocols. Schwalve, Moore and Goodwin, Crc Press 2007.
  20. Vijayakumar S et al. Identification and isolation of antimicrobial compounds from the flower extract of Hibiscus rosa-sinensis L: In silico and in vitro approaches. Microb Pathog. 2018; 123: 527-535.
  21. L.T.M. Ngan et al. Antibacterial activity of Hibiscus rosa-sinensis L. red flower against antibiotic-resistant strains of Helicobacter pylori and identification of the flower constituents. Braz J Med Biol Res. 2021; 54(7): 1-10.

Reference

  1. Shanu sharma . Shoven mcher, Shubham prasad tiwar, Shubha in-vitro anti-microbial activite and phyto chemical analysis of leaves scids bark flower of pongamia pinnata (linn pierre) as human pathogens: 2021:12(4):180-186
  2. Baker JT, Borris RP, Carté B, Cordell GA, Soejarto DD, Cragg GM, et al. Natural product drug discovery and development: New perspectives on international collaboration. J Nat Prod 1995; 58:1325-57.
  3. Patel et al. Emulgel Approach to Formulation Development: A Review. Biosci. Biotech. Res. Asia. 2021; 18(3): 459-465.
  4. Moorthy, K., Aravind, A., Punitha, T., Vinodhini, R., Suresh, M., & Thajuddin, N. (2012). In vitro screening of antimicrobial activity of Wrightia tinctoria (Roxb.) R. Br. Asian Journal of Pharmaceutical and Clinical Research, 5(5), 4.
  5. R. Parthasarathy et al. In vitro Antioxidant Activity of Bark and Leaf of Thespesia populnea. Research Journal of Pharmacognosy and Phytochemistry. 2016; 8(1): 1-4.
  6. Das S K, Khanum A, Ghosh A. Microemulsion based gel Technique- A Novel Approach for Sustained Delivery to Treat Fungal Infection. Indo American Journal of Pharmaceutical Research, 2019; 8(2): 1958.
  7. B. Ali Khan, S. Ullah, M.Khalid Khan et al. Formulation and evaluation of Ocimum basilicum-based emulgel for wound healing using animal model. Saudi Pharmaceutical Journal. 2020; 28(12): 1842–1850.
  8. Rashmi S, Neha S, Reshma S, Madhura B, Devraj Y, Vishal M, Rohit P, Isha S. The Effect of Surfactant on Polyherbal Liquid Shampoo and its Comparative Analysis.
  9. Bodake R, Belhekar A, Bochare V, Vidhate P, Kumbhar S. Formulation and evaluation of herbal mouth Wash. Int J Adv Res Sci Commun Technol. 2022;2(2):608-17.
  10. Manmode P D et al, Formulation and Evaluation of Flurbiprofen Emulgel by using natural permeation enhancers, 2021, 10 (1), 827-828.
  11. Afzal A et al. Preparation of Spilanthes acmella based emulgel: Antimicrobial study and evaluation. Pakistan Journal of Pharmaceutical Sciences. 2022; 35: 287-295.
  12. Redkar M R et al. Review on Optimization base Emulgel Formulation. Asian Journal of Pharmacy and Technology. 2019; 9(3): 228-237.
  13. Brijesh Mahesh Patil, Ashwin Bhanudas Kuchekar and Saish Rajendara Pawar, Emulgel approach to evaluation of BIOSCIENCES BIOTECHNOLOGY RESEARCH ASIA, September 2021. Vol. 18(3), P. 459-465.
  14. Mitkari BV, Korde SA, Mahadik KR, Kokare CR, Formulation and evaluation of topical liposomal gel for fluconazole. India journal of pharmaceutical education and research, 2010; 44(4): 324-329.
  15. Kabir A, biswas B, Rouf A. Design, Fabrication and evaluation of drug release kinetics from aceclofenanc matrix tablets using hydroxyl propyl methyl cellulose. Dhaka. Uni. J. Pharm. Sci 2009;8:23-30.
  16. Kaushal R., and G. D. Basarkar. "Formulation, development and in-vitro evaluation of terbinafine hydrochloride emulgel for topical fungal infection." Int. J. Pharm. Sci 21.2 (2013): 168-173.
  17. Rutuja Saurabh Shah. Formulation and Evaluation of Turmeric Emulgel. Asian Journal of Pharmacy and Technology. 2021; 11(3): 213-219.
  18. Vidya N. Dange et al. Formulation and Evaluation of Novel Herbal Gel by using Lemongrass Oil. Research Journal of Pharmaceutical Dosage Forms and Technology. 2019; 11(2): 67-70.
  19. Antimicrobial susceptibility testing protocols. Schwalve, Moore and Goodwin, Crc Press 2007.
  20. Vijayakumar S et al. Identification and isolation of antimicrobial compounds from the flower extract of Hibiscus rosa-sinensis L: In silico and in vitro approaches. Microb Pathog. 2018; 123: 527-535.
  21. L.T.M. Ngan et al. Antibacterial activity of Hibiscus rosa-sinensis L. red flower against antibiotic-resistant strains of Helicobacter pylori and identification of the flower constituents. Braz J Med Biol Res. 2021; 54(7): 1-10.

Photo
Neha Shivathaya
Corresponding author

Pharmaceutics Department, Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Photo
Damodar Bhoote
Co-author

Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Photo
Abdulrahim Jamadar
Co-author

Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Photo
Ashwini Kotre
Co-author

Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Photo
Sanju Hirekurabar
Co-author

Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Photo
Jyoti Borade
Co-author

Rani Chennamma College of Pharmacy, Belagavi-10, Karnataka, India

Neha Shivathaya, Damodar Bhoote, Abdulrahim Jamadar, Ashwini Kotre, Sanju Hirekurabar, Jyoti Borade, Development and Evaluation of Emulgel Loaded with Pongamia pinnata Seed Oil and Wrightia tinctoria Leaf Extract for the Treatment of Skin Disorders, Int. J. of Pharm. Sci., 2025, Vol 3, Issue 10, 2077-2085. https://doi.org/10.5281/zenodo.17386677

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