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  • Formulation, Development And Evaluation Of Polyherbal Wound Healing Gel
  • 1Pharmacy. Student, Ashokraomane institute of Pharmacy, Ambap, Dist. Kolhapur Maharashtra India, 416112.
    2Assitant Professor. Ashokraomane institute of Pharmacy, Ambap, Dist. Kolhapur, Maharashtra India, 416112.
    3Professor.Ashokraomane institute of Pharmacy , Ambap , Dist . Kolhapur , Maharashtra India, 416112.

Abstract

The current study set out to create and assess a herbal gel with antibacterial and wound-healing properties that contained marigold, garlic, honey, cocoa powder, and aloe vera. The preparation included marigold, garlic, honey, cocoa powder, and aloe vera, all of which have excellent anti-inflammatory, antioxidant, and healing properties. Carbopol 934 was the gelling agent used in this study, and five formulations with various concentrations of honey and Carbopol were created and optimized for the study. A subset of the optimal formulations was chosen for additional research. The active medication was then added to the optimized gel. In order to assess toxicity or adverse effects, the formulations were first assessed using physicochemical criteria such as surface pH, spreadability, viscosity, and antimicrobial susceptibility test. The outcome showed that the skin's pH range was within the surface PH.When administered topically, the formulations did not cause any skin irritation, such as erythema or oedema, for around a month. They were stable under standard storage conditions.

Keywords

Marigold, Honey, Garlic, Aloe vera.

Introduction

A wound is just a break in the skin that occurs to humans frequently during regular activity. Skin tissue injury can result from a variety of reasons, including physical friction and high temperatures that can disturb the normal arrangement of mucosa or epithelial cells on the skin. The skin's ability to protect the body is crucial for wound healing, which allows for an instant restoration of that function. The process of healing a wound involves multiple stages, commencing with inflammation and progressing through proliferation, epithelialization, angiogenesis, and skin remodeling.Maintaining the wound's sterility, shielding it from contamination that could lead to infection, preventing dehydration (since moisture is vital for the new tissue arrangement), and absorbing or getting rid of wound exudate are all important during those intricate procedures. The Food and Drug Administration (FDA) classifies wound dressing preparations—also referred to as wound dressing combination with drugs—into three categories: solid wound dressings, semisolid wound dressing preparations (ointments, creams, gels), and wound cleaning fluid. To hasten the healing phase of wounds, the right dose forms and formulations must be applied in the wound therapy. A gel is one of the appropriate dose forms for this use. A gel is a stiff structure made of a three-dimensional cross-linking network that expands in the right solvent; hydrogels are those in which water is the solvent. The gel formula's high water content is appropriate for the environment required for wound healing. In order to speed up the healing process, it collects wound exudates and produces a moist environment. Additionally, when the gel is put to the wounded skin, it might produce a cooling feeling that helps lessen the patient's agony. In addition, it is simple to apply and remove from the skin. The market is flooded with topical wound healing solutions. The majority of them include active medicinal compounds, such Neomycin, that fall within the antiseptic and antibacterial categories. Bacitracin, Mupirocin, Hydrogen Peroxide, and Povidone Lodine. Because of the high potential of bacterial resistance, the use of antimicrobials in medicine has recently become a topic of discussion. It sets off a variety of studies aimed at discovering novel pharmacological compounds with potential as medicines for wound healing. Utilizing natural wealth is one area of the searches. Many plants that are found in nature have the ability to heal wounds. The African marigold, or yellow marigold (Tagetes erecta), is one of the plants. In the past, Tageteserecta leaves were chewed or diced and applied to wounds to promote healing until the area healed. The pharmacological effects of Tagetes erecta leaf include antibacterial and anti-inflammatory properties that are related to the healing of wounds. Numerous investigations have demonstrated this plant's efficacy in the healing of wounds. Tagetes erecta leaf ethanol extract has demonstrated the capacity to quicken wound healing.

TOPICAL DRUG DELIVERY SYSTEM

The goal of any drug delivery system is to provide a therapeutic amount of drug to the proper site in the body to promptly achieve and then maintain the desired drug concentrations. The route of administration has a significant impact on the therapeutic outcome of a drug. One of the human body's easiest organs to administer topically is the skin, which serves as the primary route for topical medication delivery systems. Topical delivery is the process of applying a drug formulation topically to treat cutaneous conditions directly or the skin-related symptoms of a general illness (like psoriasis) with the goal of limiting the drug's pharmacological or other effects to the skin's surface or inside the skin.The most common topical delivery method is semi-solid formulation in all its forms, although foams, sprays, medicated powders, solutions, and medicated adhesive systems are also in use.External topicals are applied to the cutaneous tissues by spreading, spraying, or in some other way to cover the diseased area.Internal topicals are administered orally, vaginally, or on the tissues of the anorectum to provide local action on the mucosal membrane.

MATERIALS AND METHODS

Plant material

Plant material used includes marigold leaves, aloevera leaves, cocoa powder, and garlic.

Preparation of extract

Preparation of ethanolic extract of  Marigold , aloevera ,Cocoa powder, Garlic etc.by using Soxhlet extraction method.

Preformulation studies

Incompatibility study

It is important to detect any possible chemical or physical interactions since they can affect the bioavailability and stability of the drug.

Physicochemical Properties

Assess the physicochemical properties of individual herbal extracts and the gel formulation. This includes solubility, pH, viscosity, and compatibility of herbal extracts with gel base components.

Safety Evaluation

 Evaluate the safety profile of herbal extracts. Ensure they do not cause irritation, sensitization, or toxicity when applied topically. Perform skin irritation tests if necessary.

Formulation Optimization

Adjust the formulation based on pre-formulation study results to enhance stability, efficacy, and safety. Optimize the concentration of herbal extracts and gel base ingredients to achieve desired therapeutic effects.

Preparation of gel

Accurately weighed 0.6gm Carbopol 934 was taken in a beaker and dispersed in 25 ml of distilled water. Kept the beaker aside to swell the Carbopol for half an hour and then stirring should bedone using mechanical/lab stirrer at 1200 rpm for 30 min.

Take required quantity of Extract. Stirr continuously while you add 1ml of honey and 4 drops of coconut oil. Add 4 drops of clove oil and with constantly stirring and Add a 1ml rose water.

Evaluation

The gel has been evaluated using the following criteria.

Homogeneity

All developed gels were tested for homogeneity by visual inspection after the gels have been set in the container for their appearance and presence of any aggregates.

PH of the gel

 

The pH of various gel formulations were determined by using digital pH meter. 2.5gm of gel was accurately weighed and dispersed in 25ml of distilled water and stored for two hours. The measurement of pH of each formulation was carried out in triplicate and the average values are represented. The pH of dispersions was measured using pH meter.

Spreadibility

Spreadibility was determined by the apparatus which consists of a wooden block, which was provided by a pulley at one end. By this method spreadibility was measured on the basis of slipand drag characteristics of gels. An excess of gel (about 2 g) under study was placed on this ground slide. The gel was then sandwiched between this slide and another glass slide having the dimension of fixed ground slide and provided with the hook. Excess of the gel was scrapped off from the edges. The top plate was then subjected to pull of 80 g.With the help of strring attached to the hook and the time (in seconds) required by the top slide to cover a distance of 7.5 cm be noted. A shorter interval indicates better spreadibility. Spreadibility was calculated using the following formula: SMXL/T Where, S Spreadibility, M-Weight in the pan (tied to the upper slide),1,Length moved by the glass slide and T-Time (in sec.) taken to separate the slide completely each other.

Viscosity

Viscosity of herbal gel was determined by using Brookfield viscometer at 5, 10 20, 30 and 50rpm using spindle no.64. Each reading was taken after equilibrium of the sample at the end of two minutes. The viscosity determination of samples was repeated three times.

Grittiness

All the formulations were evaluated microscopically for the presence of any appreciable particulate matter which was seen under light microscope

Stability Study

Accelerated stability studies indicated that the physical appearance, theological properties, spreadability in the prepared gel remained unchanged upon storage for 1 month.

Antimicrobial study

This parameter evaluates the ability of the gel to prevent or control the growth of microorganism in the wound area.

Stability Study

Accelerated stability studies indicated that the physical appearance, rheological properties, spreadability in the prepared gel remained unchanged upon storage for 1 month.

Wound healing rate

This parameter measures the speed at which the wound heals with the use of the gel.

Wound closure

The wound closure parameter measures the extent to which the gel helps to close the wound.

Tissue regeneration

This parameter evaluates the ability of the gel to promote the regeneration of new tissue in the wound area.

RESULT AND DISCUSSION

The present work aimed to increase stability of gel formulation with Carbopol 934. The prepared formulations were characterized for physical appearance, pH, spreadability, viscosity.greasiness, homogeneity, etc.

Table No 1. .Data of Calibration curve


       
            Data of Calibration curve.png
       

    

Table No.2. Result of Calibration


       
            Result of Calibration.png
       

    


       
            Calibration curve.png
       

    

Calibration curve

Table No.3. Formulation of Gel


       
            Formulation of Gel .png
       


       
            Gel Formulation.jpg
       

        

Fig No.1. Gel Formulation

Table 4: Data showing physicochemical


       
            Data showing physicochemical.png
       

    

All values are expressed as mean±SD++= fair,+++=good

 

Stability Studies:

Accelerated stability studies indicated that the pshysical appearance, theological properties, spreadability in the prepared gel remained unchanged upon storage for I motth. The pH observed of prepared gel through I month storage was in between 6-7. Rheological propertiesand spreadability was obtained uniformly. Gel formulation was maintaining drug level after Imonth of accelerated stability.


       
            Evaluation.png
       

    

 

Wound closure

The wound healing capabilities of the Samples: gel was assayed by performing in vitro cell migration studies on 1929 cells by a previously described method. Briefly, 2105 cells/ml, were seeded in 6-well plates and were cultured overnight. Cells were then washed with Delbucco's Phosphate Buffered Saline (DPBS) and a scratch was made with a sterile 200µl. tip. The detached cells and other cellular debris were removed by washing the cells with DPBS. The cells were treated with 1000 µg/ml. of sample code F8 and 5 µg/mL, of positive control, Cipladine and incubated for 24 h. Cipladine is a standard drug that is used in wound healing. Untreated cells were negative control. The cell migration and morphological changes of cells were observed in the images taken by inverted microscope, equipped with digital camera. The experiments were performed in triplicate (n % 3). The width of the scratch and wound closure at different time intervals (0, 48hrs) was analyzed by SAGLO software.

Table no.1 Percentage (%) of cells migrated towards the wound and involved in wound closure.

 


       
            Table no.1 Percentage (%) of cells migrated towards the wound and involved in wound closure..png
       

    

 

 

Microscopical images representing the In vitro wound healing nature of Samples:

Cream: L929 cells were incubated in presence or absence of Samples: Cream and standard drug Cipladine and images were captured at 0 and 48 hrs.


       
            Control or Untreated.jpg
       

    Control or Untreated

 


       
            Standard(Cipladine).jpg
       

    

Standard(Cipladine)


       
            Sample Gel (1000 µg per mL).jpg
       

    

Sample Gel (1000 µg/mL)

At the concentration (1000mu*g / m * L) Samples: Gel: showed the Good wound healing activity as compared to standard.

CONCLUSION

From the above observations, it can be concluded that all the monographic parameters of the selected herbs were within in the Pharmacopeial  limit  indicates the good quality of raw materials. The microbiological studies indicated that the formulations possess wound healing activity. The wound contraction studies revealed that the wound contraction increases on increasing the concentration of herbal extract. The study also reveals the better activity of polyherbal formulation may be due to the synergistic action of the plant's constituents present in the formulation. Thus, the prepared topical gels possess a multifaceted approach in healing the wound.

REFERENCE

  1. Ampai P, Kiattisin K, Pensak J, Chansakaow S, Vejabhikul S, Leelapornpisid P (2013). Appraisal of biological activities and identification of phenolic compound of African marigold flower extract, Pakistan Journal of Pharmaceutical Science. 26, 1071-1076.
  2. Chatterjee S, Rajaranjan S, Sharma UR, Ramesh K (2009), Evaluation of anti- nociceptive and anti-inflammatory activities of Tagetes erecta. Archives of Pharmaceutical Science and Research, 1, 207-211.
  3. Chivde BV, Kumar VK, Shiramane R5 (2011). Evaluation of Hepatoprotective Activity of Flowers of Tagetes erecta Linn. International Journal of Pharmaceutical & Biological Archives, 2, 692-695.
  4. Dixit P. Tripathi S, Verma NK (2013). A brief study on marigold. International Research Journal of Pharmacy, 4, 43-48.
  5. Giri K, Bose A, Mishra KS (2011). Hepatoprotective activity of Tagetes erecta against carbon tetrachloride-induced hepatic damage in rats. Acta Poloniae Pharmaceutica and Drug Research, 68, 999-1003.
  6. Ibrahim M. Kazim SM, Kiranmai M (2011). Combined wound healing activity of Gymnema sylvestere and Tagetes erecta Linn. International Journal of Pharmaceutical Applications, 2, 135-140.
  7. Khulbe A. Pandey S, Sah PS (2013). Antidepressant like action of the hydromethanolic flower extract of Tagetes erecta in mice and its possible mechanism of action. Indian Journal of Pharmacology, 45, 386-390.
  8. Kishore N, Dwivedi RS (2006). Fungi-toxicity of the essential oil of Tagetes erecta against Pythium aphanidermatum fitz. the damping of the pathogen. Flavour and Fragrance Journal, 6, 291-294.
  9. Li-Wei X, Jang C, Huan-Yang Q. Yan-Ping S (2011). Chemical constituents from Tagetes erecta flowers. Chemistry of Natural Compounds, 47,281-283.
  10. Majumder J. Rai P, Perinban S, Singh B (2014). Guidelines for production of marigoldin North Indian condition. Directorate of Floricultural Research, 11-13.
  11. Martha R. Gutierrez P, Luna HH (2006). Antioxidant activity of Tagetes erecta essential oil. Journal of the Journal of Pharmacy Research. 2. 1035-1038.
  12. Shinde NV, Kanase KG, Shilimkar VC (2009) Antincelceptive and anti- inflammatory effects of solvent extracts of Tagetes erectus Linn (Asteraceae).Tropical Journal of Pharmaceutical Research, 8, 325-329
  13. The Plant List (2013). Version 1.1. Published on the Internet. http://www.theplantlist.org/ (accessed 1st January)
  14. Vallisuta O, Nukoolkarn V. Mitrevej A, Sarisota N, Pimporm L Phrutivorapongkul P, Sinchaipanid N (2014). In vitro studies on the cytotoxicity. and elastase and tyrosinase inhibitory activities of marigold (Tagetes erecta L.) flower extracts. Experimental and Therapeutic Medicine, 7, 246-250.
  15. Shelton MR. Aloe vera - its chemical and therapeutic properties. Int J Dermatol 1991: 30:679-83.
  16. Tyler VE, Brady LR, Robbers JE. Pharmacognosy. Philadelphia: Les and Febiger, 1976:81-83.
  17. Chithra P, Sajithlal GB, Chandrakasan G. Influence of aloe vera on the glycosaminoglycans in the matrix of healing dermal wounds in rats. J Ethnopharmacol 1998; 59(3):179-86.
  18. Zhang L, Tizard IR. Activation of mouse macrophage cell line by Acemannan: the major carbohydrate fraction of aloe vera, Immunopharmacology 1996; 35(2):119-28.
  19. Mortan JF. Folk uses and commercial exploitation of aloe vera leaf pulp. Econ Bot 1961; 15 (4): 311-19.6. Rubin MB. Vitamins and wound healing. Plast Surg Nurs 1984:4:16-19.
  20. Davis RH, Leitner MG, Russo JM. Byrne ME. Wound healing. Oral and topical activity of aloe vera. J Am Podiatr Med Assoc 1989; 79(11):559-62.
  21. Chithra P, Sajithlal GB, Chandrakasan G. Influence of Aloe very on collagen characteristics in healing of dermal wounds in rats. Mol Cell Biochem 1998; 181(1-2):71-6.
  22. Stone N. Meistar A. Function of ascorbic in the conversion of proline to collagen, bydroxyproline, Nature 1965: 194:555-57.
  23. Wynn RL. Aloe vera gel: update for dentistry. Gen Dent 2005:53(1)6-9.
  24. Hayes SM. Lichen planus - report of successful treatment with aloe vera. Gen Dent 1999; 47(3):268-72.
  25. Leigh GC. Dental irrigators. Research letters. Dr Dent 2005; 198(12):756-7.

Reference

  1. Ampai P, Kiattisin K, Pensak J, Chansakaow S, Vejabhikul S, Leelapornpisid P (2013). Appraisal of biological activities and identification of phenolic compound of African marigold flower extract, Pakistan Journal of Pharmaceutical Science. 26, 1071-1076.
  2. Chatterjee S, Rajaranjan S, Sharma UR, Ramesh K (2009), Evaluation of anti- nociceptive and anti-inflammatory activities of Tagetes erecta. Archives of Pharmaceutical Science and Research, 1, 207-211.
  3. Chivde BV, Kumar VK, Shiramane R5 (2011). Evaluation of Hepatoprotective Activity of Flowers of Tagetes erecta Linn. International Journal of Pharmaceutical & Biological Archives, 2, 692-695.
  4. Dixit P. Tripathi S, Verma NK (2013). A brief study on marigold. International Research Journal of Pharmacy, 4, 43-48.
  5. Giri K, Bose A, Mishra KS (2011). Hepatoprotective activity of Tagetes erecta against carbon tetrachloride-induced hepatic damage in rats. Acta Poloniae Pharmaceutica and Drug Research, 68, 999-1003.
  6. Ibrahim M. Kazim SM, Kiranmai M (2011). Combined wound healing activity of Gymnema sylvestere and Tagetes erecta Linn. International Journal of Pharmaceutical Applications, 2, 135-140.
  7. Khulbe A. Pandey S, Sah PS (2013). Antidepressant like action of the hydromethanolic flower extract of Tagetes erecta in mice and its possible mechanism of action. Indian Journal of Pharmacology, 45, 386-390.
  8. Kishore N, Dwivedi RS (2006). Fungi-toxicity of the essential oil of Tagetes erecta against Pythium aphanidermatum fitz. the damping of the pathogen. Flavour and Fragrance Journal, 6, 291-294.
  9. Li-Wei X, Jang C, Huan-Yang Q. Yan-Ping S (2011). Chemical constituents from Tagetes erecta flowers. Chemistry of Natural Compounds, 47,281-283.
  10. Majumder J. Rai P, Perinban S, Singh B (2014). Guidelines for production of marigoldin North Indian condition. Directorate of Floricultural Research, 11-13.
  11. Martha R. Gutierrez P, Luna HH (2006). Antioxidant activity of Tagetes erecta essential oil. Journal of the Journal of Pharmacy Research. 2. 1035-1038.
  12. Shinde NV, Kanase KG, Shilimkar VC (2009) Antincelceptive and anti- inflammatory effects of solvent extracts of Tagetes erectus Linn (Asteraceae).Tropical Journal of Pharmaceutical Research, 8, 325-329
  13. The Plant List (2013). Version 1.1. Published on the Internet. http://www.theplantlist.org/ (accessed 1st January)
  14. Vallisuta O, Nukoolkarn V. Mitrevej A, Sarisota N, Pimporm L Phrutivorapongkul P, Sinchaipanid N (2014). In vitro studies on the cytotoxicity. and elastase and tyrosinase inhibitory activities of marigold (Tagetes erecta L.) flower extracts. Experimental and Therapeutic Medicine, 7, 246-250.
  15. Shelton MR. Aloe vera - its chemical and therapeutic properties. Int J Dermatol 1991: 30:679-83.
  16. Tyler VE, Brady LR, Robbers JE. Pharmacognosy. Philadelphia: Les and Febiger, 1976:81-83.
  17. Chithra P, Sajithlal GB, Chandrakasan G. Influence of aloe vera on the glycosaminoglycans in the matrix of healing dermal wounds in rats. J Ethnopharmacol 1998; 59(3):179-86.
  18. Zhang L, Tizard IR. Activation of mouse macrophage cell line by Acemannan: the major carbohydrate fraction of aloe vera, Immunopharmacology 1996; 35(2):119-28.
  19. Mortan JF. Folk uses and commercial exploitation of aloe vera leaf pulp. Econ Bot 1961; 15 (4): 311-19.6. Rubin MB. Vitamins and wound healing. Plast Surg Nurs 1984:4:16-19.
  20. Davis RH, Leitner MG, Russo JM. Byrne ME. Wound healing. Oral and topical activity of aloe vera. J Am Podiatr Med Assoc 1989; 79(11):559-62.
  21. Chithra P, Sajithlal GB, Chandrakasan G. Influence of Aloe very on collagen characteristics in healing of dermal wounds in rats. Mol Cell Biochem 1998; 181(1-2):71-6.
  22. Stone N. Meistar A. Function of ascorbic in the conversion of proline to collagen, bydroxyproline, Nature 1965: 194:555-57.
  23. Wynn RL. Aloe vera gel: update for dentistry. Gen Dent 2005:53(1)6-9.
  24. Hayes SM. Lichen planus - report of successful treatment with aloe vera. Gen Dent 1999; 47(3):268-72.
  25. Leigh GC. Dental irrigators. Research letters. Dr Dent 2005; 198(12):756-7.

Photo
Omkar Salunkhe
Corresponding author

Student of Ashokrao Mane Institute of Pharmacy,Ambap

Photo
Pranjal Chougule
Co-author

Assistant Professor of Ashokrao Mane Institute of Pharmacy, Ambap

Photo
Nilesh Chougule
Co-author

Professor of Ashokrao Mane Institute of Pharmacy, Ambap

Omkar Salunkhe, Pranjal Chougule, Nilesh Chougule, Formulation, Development And Evaluation Of Polyherbal Wound Healing Gel, Int. J. of Pharm. Sci., 2024, Vol 2, Issue 7, 2341-2348. https://doi.org/10.5281/zenodo.13144255

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