Wound healing efficacy of novel ayurveda formulation- Pentabark Kashaya: In wistar rats using excision wound model- an in vivo study.

KLE Ayurveda Pharmacy, Khasbag , Belagavi.

Sighting Study - No Mortality, no changes in behavior pattern, normal food and water intake, normal urine and stool frequency and no signs of toxicity were observed in experimental animals throughout the study tim period. No abnormal change in the body weight was observed and there was a normal increase in the body weight, i.e. 5-7 grams over 14 days duration. Limit test Study – Four animals observed in limit test study did not exhibit any signs of toxicity and there was no mortality, rest of the parameters were normal throughout the study. 1. Wound contraction rate - The percentage of wound contraction rate in the test group was significant on 4 th day (36.03%), 8 th day (83.87%), 12 th day (91.60%), and 16 th day (97.50%) when compared to the standard group on 4 th day (30.20%), 8 th day (73.78%), 12 th day (86.70%), 16 th day (92.93%) and control group on 4 th day (25.03%), 8 th day (60.92%), 12 th day (80.95%), 16 th day (88.07%) ( Table 2 , Fig. 1 , Fig. 2 ). Table 2 Showing Comparison of three groups (Control, Standard and Test)with respect to mean area of wound (cm) and percentage of wound contraction at different time points. Table 2 Groups (n = 6 in each) Summary Area of wound(cm) % of Wound contraction 4th 8th 12th 16th 4–8th 4–12th 4–16th 8–12th 8–16th 12–16th Control Mean 25.03 60.92 80.95 88.07 47.90 74.67 84.67 36.83 64.67 36.33 ±S.D 6.415 4.196 4.878 5.000 7.831 6.919 5.785 2.317 3.386 2.254 Test Mean 36.03 83.87 91.60 97.50 75.17 87.17 96.33 56.00 83.50 59.00 ±S.D 5.003 1.832 2.156 0.5291 2.787 3.189 0.8165 2.280 3.987 2.280 Standard Mean 30.20 73.78 86.70 92.93 64.33 81.00 90.33 47.33 72.50 45.33 ±S.D 3.379 3.974 3.065 2.938 7.474 4.648 3.983 2.803 3.584 2.803 F Value 14.26 48.01 17.15 16.61 24.61 12.84 20.93 11.83 9.146 5.005 P Value 0.0065∗ <0.0001∗ 0.0020∗ 0.0042∗ 0.0009∗ 0.0025∗ 0.0011∗ 0.0021∗ 0.0155∗ 0.0382∗ (Note: ∗p < 0.05 C- control, S-standard, T-test). Wound contraction rate - The percentage of wound contraction rate in the test group was significant on 4 th day (36.03%), 8 th day (83.87%), 12 th day (91.60%), and 16 th day (97.50%) when compared to the standard group on 4 th day (30.20%), 8 th day (73.78%), 12 th day (86.70%), 16 th day (92.93%) and control group on 4 th day (25.03%), 8 th day (60.92%), 12 th day (80.95%), 16 th day (88.07%) ( Table 2 , Fig. 1 , Fig. 2 ). Table 2 Showing Comparison of three groups (Control, Standard and Test)with respect to mean area of wound (cm) and percentage of wound contraction at different time points. Table 2 Groups (n = 6 in each) Summary Area of wound(cm) % of Wound contraction 4th 8th 12th 16th 4–8th 4–12th 4–16th 8–12th 8–16th 12–16th Control Mean 25.03 60.92 80.95 88.07 47.90 74.67 84.67 36.83 64.67 36.33 ±S.D 6.415 4.196 4.878 5.000 7.831 6.919 5.785 2.317 3.386 2.254 Test Mean 36.03 83.87 91.60 97.50 75.17 87.17 96.33 56.00 83.50 59.00 ±S.D 5.003 1.832 2.156 0.5291 2.787 3.189 0.8165 2.280 3.987 2.280 Standard Mean 30.20 73.78 86.70 92.93 64.33 81.00 90.33 47.33 72.50 45.33 ±S.D 3.379 3.974 3.065 2.938 7.474 4.648 3.983 2.803 3.584 2.803 F Value 14.26 48.01 17.15 16.61 24.61 12.84 20.93 11.83 9.146 5.005 P Value 0.0065∗ <0.0001∗ 0.0020∗ 0.0042∗ 0.0009∗ 0.0025∗ 0.0011∗ 0.0021∗ 0.0155∗ 0.0382∗ (Note: ∗p < 0.05 C- control, S-standard, T-test). Showing Comparison of three groups (Control, Standard and Test)with respect to mean area of wound (cm) and percentage of wound contraction at different time points. (Note: ∗p < 0.05 C- control, S-standard, T-test). The percentage of wound contraction rate in the test group was significant from 4 th to 8 th day (75.17%), 4 th to 12 th day (87.17%) and 4 th to 16 th day (96.33%) when compared to the standard group on 4 th to 8 th day (64.33%), 4 th to 12 th day (81.00%), 4 th to 16 th day (90.33%) and control group on 4 th to 8 th day (47.90%), 4 th to 12 th day (74.67%), 4 th to 16 th day (84.67%) ( Table 2 ). 2. Epithelialization Time (in days)- Significant results were seen in test group i.e. p = 0.0006 and Mean ± SD (7.500 ± 1.049) when compared with control group (12.83 ± 1.329) and standard group (11.50 ± 1.049) ( Table 3 ). Table 3 Showing Comparison of three groups with respect to Epithelialization Time and Wound closure day. Table 3 Groups Summary Epithelialization time(days) Wound closure day Control Mean ± SD 12.83 ± 1.329 11.17 ± 0.9832 Test Mean ± SD 7.500 ± 1.049 5.667 ± 0.8165 Standard Mean ± SD 11.50 ± 1.049 9.000 ± 1.265 F- value 45.22 36.68 P –value 0.0006 <0.0001 3. Wound Closure Day (WCD) - Significant results were seen in test group i.e. (p < 0.0001) and Mean ± SD (5.667 ± 0.8165) when compared with control (11.17 ± 0.9832) and standard group (9.000 ± 1.265) ( Table 3 ). Total microbial load of wound: There was a reduction in total fungal count on 1 st day, 3 rd day and 12 th day in the test group(14 cfu/ml, 14 cfu/ml, 07 cfu/ml) and standard group (16 cfu/ml, 12 cfu/ml, 05 cfu/ml) when compared to control group (13 cfu/ml, 24 cfu/ml, 27 cfu/ml). Reduction in the total bacterial count was seen on 1 st day, 3 rd day and 12 th day in the test group (66 cfu/ml, 12 cfu/ml, 11 cfu/ml) and standard group (58 cfu/ml, 10 cfu/ml, 0 cfu/ml) when compared to control group (64 cfu/ml, 34 cfu/ml, 30 cfu/ml) ( Table 4 ). Table 4 Showing Total microbial load of wound and Histopathology of healed skin. Table 4 Total Microbial Load Sl.no Group Total fungal count Total bacterial count 1 st day 3 rd day 12 th day 1 st day 3 rd day 12 th day 1. Control 13 cfu/ml 24 cfu/ml 27 cfu/ml 64 cfu/ml 34 cfu/ml 30 cfu/ml 2. Test 14 cfu/ml 14 cfu/ml 07 cfu/ml 66 cfu/ml 12 cfu/ml 11 cfu/ml 3. Standard 16 cfu/ml 12 cfu/ml 05 cfu/ml 58 cfu/ml 10 cfu/ml 08 cfu/ml Histopathology of Healed skin 1. MICROPSCOPY Control group Standard Group Test Group 2. Re-epithelialization – +++ ++++ 3. Dermal edema ++ _ _ 4. Dermal Congestion ++ + + 5. Dermal Inflammatory Infiltration ++ + + 6. Neutrophocytic Infiltration ++ _ _ 7. Lymphocytic Infiltration + + + 8. Macrophages + _ _ 9. Dermal Granulation Tissue ++ _ _ 10. Dermal Fibroblasts + ++ ++ 11. Dermal Fibrocytes + ++ +++ 12. Dermal Collagen/Fibrosis + +++ ++++ 13. Overall grade of healing Poor Good Very Good 4. Histopathology of healed skin: The healed skin of animals in all the three groups was excised (1 × 1cm) and specimens were collected in formalin solution. Staining of specimens were done with hematoxylin and eosin reagents. 40× magnified images were obtained through microscope and readings were analyzed with the help of Microbiologist. Marked increase in the re-epithelialization, dermal fibroblast, dermal fibrocytes were seen in test group when compared to control group ( Table 4 ). Epithelialization Time (in days)- Significant results were seen in test group i.e. p = 0.0006 and Mean ± SD (7.500 ± 1.049) when compared with control group (12.83 ± 1.329) and standard group (11.50 ± 1.049) ( Table 3 ). Table 3 Showing Comparison of three groups with respect to Epithelialization Time and Wound closure day. Table 3 Groups Summary Epithelialization time(days) Wound closure day Control Mean ± SD 12.83 ± 1.329 11.17 ± 0.9832 Test Mean ± SD 7.500 ± 1.049 5.667 ± 0.8165 Standard Mean ± SD 11.50 ± 1.049 9.000 ± 1.265 F- value 45.22 36.68 P –value 0.0006 <0.0001 Showing Comparison of three groups with respect to Epithelialization Time and Wound closure day. Wound Closure Day (WCD) - Significant results were seen in test group i.e. (p < 0.0001) and Mean ± SD (5.667 ± 0.8165) when compared with control (11.17 ± 0.9832) and standard group (9.000 ± 1.265) ( Table 3 ). Total microbial load of wound: There was a reduction in total fungal count on 1 st day, 3 rd day and 12 th day in the test group(14 cfu/ml, 14 cfu/ml, 07 cfu/ml) and standard group (16 cfu/ml, 12 cfu/ml, 05 cfu/ml) when compared to control group (13 cfu/ml, 24 cfu/ml, 27 cfu/ml). Reduction in the total bacterial count was seen on 1 st day, 3 rd day and 12 th day in the test group (66 cfu/ml, 12 cfu/ml, 11 cfu/ml) and standard group (58 cfu/ml, 10 cfu/ml, 0 cfu/ml) when compared to control group (64 cfu/ml, 34 cfu/ml, 30 cfu/ml) ( Table 4 ). Table 4 Showing Total microbial load of wound and Histopathology of healed skin. Table 4 Total Microbial Load Sl.no Group Total fungal count Total bacterial count 1 st day 3 rd day 12 th day 1 st day 3 rd day 12 th day 1. Control 13 cfu/ml 24 cfu/ml 27 cfu/ml 64 cfu/ml 34 cfu/ml 30 cfu/ml 2. Test 14 cfu/ml 14 cfu/ml 07 cfu/ml 66 cfu/ml 12 cfu/ml 11 cfu/ml 3. Standard 16 cfu/ml 12 cfu/ml 05 cfu/ml 58 cfu/ml 10 cfu/ml 08 cfu/ml Histopathology of Healed skin 1. MICROPSCOPY Control group Standard Group Test Group 2. Re-epithelialization – +++ ++++ 3. Dermal edema ++ _ _ 4. Dermal Congestion ++ + + 5. Dermal Inflammatory Infiltration ++ + + 6. Neutrophocytic Infiltration ++ _ _ 7. Lymphocytic Infiltration + + + 8. Macrophages + _ _ 9. Dermal Granulation Tissue ++ _ _ 10. Dermal Fibroblasts + ++ ++ 11. Dermal Fibrocytes + ++ +++ 12. Dermal Collagen/Fibrosis + +++ ++++ 13. Overall grade of healing Poor Good Very Good Showing Total microbial load of wound and Histopathology of healed skin. Histopathology of healed skin: The healed skin of animals in all the three groups was excised (1 × 1cm) and specimens were collected in formalin solution. Staining of specimens were done with hematoxylin and eosin reagents. 40× magnified images were obtained through microscope and readings were analyzed with the help of Microbiologist. Marked increase in the re-epithelialization, dermal fibroblast, dermal fibrocytes were seen in test group when compared to control group ( Table 4 ).

The present study was conducted in the Animal house of Shri B.M.K Ayurveda Mahavidhyalaya, KAHER, Shahapur, Belagavi. This study was approved by the Animal Ethics Committee of the institution (IAEC letter number BMK/IAEC/Res No 06/2014 dated on 21st April 2014). Vata (Ficus bengalensis Linn), Udumbara (Ficus racemosa Linn), Ashwatha (Ficus religiosa Linn) , Parish (Thesposia populnea Soland.), Plaksha (Ficus infectoria Roxb), Kasisa ( Ferrous Sulphate (FeSO 4 7H 2 O)), Tuttha ( Copper Sulphate (CuSO 4 7H 2 O)), and Spatika ( Potash Alum (K 2 SO 4 Al 2 SO 4 ) 3 24H 2 O) were procured from the GMP certified KLE Ayurved Pharmacy, Belagavi. Authentication and quality control analysis of all raw drugs were done at AYUSH approved Drug testing laboratory, KAHER's B.M.K Ayurveda Mahavidyalaya, Belagavi. Ingredients required ( Table 1 ) were taken in quantity as listed in the table. Panchavalkala (Stem barks of 5 plant) Kashaya (Decoction) 100 ml was prepared as per standard operative procedure [ 12 ]. Prepared Kashaya was taken in a steel vessel and it was mixed with Shodhita Kasisa, Shodhita Tuttha and Shodhita Sphatika as per the mentioned quantity. Preservatives, Sodium benzoate and Methyl paraben were added individually and stirred well till they were completely dissolved and was filtered and stored in a 100ml plastic bottle. Table 1 Showing ingredients of 100 ml Pentabark Kashaya . Table 1 Sl.No Name of Drug Latin Name Part used Quantity 1 Vata Ficus bengalensis Linn Bark 10 gm 2 Udumbara Ficus racemosa Linn Bark 10 gm 3 Ashwatha Ficus religiosa Linn Bark 10 gm 4 Parisha Thesposia populnea Soland. Bark 10 gm 5 Plaksha Ficus infectoria Roxb Bark 10 gm 6 ShodhitaKasisa Ferrous Sulphate (FeSO 4 7H 2 O) 1 gm a 7 ShodhitaTutta Copper Sulphate (CuSO 4 7H 2 O) 25 mg a 8 ShodhitaSpatika Potash Alum (K 2 SO 4 Al 2 SO 4 ) 3 24H 2 O) 2.75 mg a 9 Sodium benzoate 10 mg 10 Methyl paraben 100 mg a Note - Selection of quantity of Shodhita Tutta (0.012%), Kasisa (0.5–1%) and Spatika (1–10%) was made on the basis of text book inorganic pharmaceutical Chemistry by Bently and Indian pharmacopoeia. Showing ingredients of 100 ml Pentabark Kashaya . Note - Selection of quantity of Shodhita Tutta (0.012%), Kasisa (0.5–1%) and Spatika (1–10%) was made on the basis of text book inorganic pharmaceutical Chemistry by Bently and Indian pharmacopoeia. Experimental animals were procured from Animal House of KAHER's Shri J.N. Medical College, Belagavi. Animals were acclimatized to the laboratory conditions for seven days prior to the start of the study. They were housed in colony cages at an ambient temperature of 22±3 °C and relative humidity of 30%. Artificial lighting was arranged with the sequence of 12 hour light and dark, hygienic condition was maintained by replacing the floor bed every day. Animals were provided with free excess of standard pellet diet (Amrut feeds, VRK scientists choice Laboratory animals feed, Saidurga feeds and foods, Bangalore) and fresh water ad libitum . Five female Wistar rats of 150–200 g were selected for the study. 10% of the total body surface area was shaved from the dorsal area of the trunk, 24 hours before the application of the test drug. The study includes two steps,i.e Sighting and Limit test study to assess the dermal toxicity. a. Sighting study : Test drug 2000 mg/kg body weight was applied to exposed skin of one rat through dropper and it was maintained in contact with the skin with a porous gauze dressing and non-irritating tape throughout 24 hour exposure period. After 24 hours, the skin was washed with luke warm water and wiped with gauze. Rat was observed for every hour up to 24 hours for any signs of toxicity. b. Limit test study :The test substance 2000 mg/kg body weight was applied to exposed skin of next four female rats, after 24 hours the skin was washed with lukewarm water and wiped with gauze. Observations were done for every 24 hours up to 14 days for any signs of toxicity. Sighting study : Test drug 2000 mg/kg body weight was applied to exposed skin of one rat through dropper and it was maintained in contact with the skin with a porous gauze dressing and non-irritating tape throughout 24 hour exposure period. After 24 hours, the skin was washed with luke warm water and wiped with gauze. Rat was observed for every hour up to 24 hours for any signs of toxicity. Limit test study :The test substance 2000 mg/kg body weight was applied to exposed skin of next four female rats, after 24 hours the skin was washed with lukewarm water and wiped with gauze. Observations were done for every 24 hours up to 14 days for any signs of toxicity. Healthy Male Wistar rats weighing between 150 and 200gm were divided into three groups containing six rats in each group. Group 1 was control group, Group 2 was the test group applied with PK and Group 3 was Standard group applied with 5% Povidone iodine solution. Creating excision wound : The excised wounds were created in the animals as per reference of Morton and Malone Excision wound model. The dorsal fur of the rats was shaved with an electric clipper. Under light ether anesthesia, an impression of 2.5 cm was made on the dorsal inter scapular region using a circular seal.Full thickness skin of 2 mm depth and circular area 2.5cm x 2.5 cm was excised along the impression. The wound was traced on the polythene sheet and the animals were housed in individual cages. Assessment of quantity of Kashaya required for application: Gauze piece weighed about 400 mg was taken, and with the help of dropper Kashaya was dropped on the gauze piece. 6 drops were sufficient for complete soakage of gauze. Wound Swab collection – Aseptic precautions were followed by wearing the sterile gloves and samples of wound swab from the three groups were collected by identifying a small area(1 cm) of clean viable tissue and the swab was rotated for 5 s while applying enough pressure. Swab was carefully inserted into a sterile container and samples were immediately sent for microbial study [ 15 , 16 ]. Method of Application : The Kashaya was externally applied over raw surfaces of wound once daily after cleaning the previous application with the help of gauze piece. The study was conducted for the duration of 21 days. The assessment of wound closure was done by charting the raw wound surface area on every alternate day by transparent paper until complete wound healing. These wound tracings were retraced on a millimeterscale graph paper, to determine the wound area. Calculation of Wound contraction (WC) was done as per following formula [ 17 ]. i.e. Percentage of Wound Closure = Initial wound size - specific day wound size Initial Wound size × 100 Epithelialization period was monitored by noting the number of days required for Escher to fall away, leaving no raw wound behind. Average Wound Closure Day was assessed by measurement and pictogram. The raw surface of the wound comes to the level of skin with scab on the upper surface was considered as wound closure day.The total microbial load was evaluated by taking woundswabs on the 1 st , 3 rd , and 12 th day. Excisional biopsy of healed skin was sent for histopathological study to assess the quality wound healing. Statistical analysis –The obtained results were stated in the form of mean ± SD. One way ANOVA and Tukeys HSD test were used to assess changes in between three groups at each time point. All p-value< 0.05 was considered to be statistically significant.

Pentabark Kashaya did not exhibit any signs of dermal toxicity on topical application. PK showed a significant improvement in the assessment parameters like wound contraction rate, epithelialization time, wound infection, wound closure day and histo-pathological changes. The study proves that Pentabark Kashaya is safe for application, effective in wound healing and readily available compound for the wound healing.

Wound healing is a natural process, which mainly depends on tissue regeneration [ 18 ]. Wound management always aims to enhance the wound healing process and reduce the risk factor like infection which directly impacts on the wound healing process. Researches are carried out in this direction with usage of various medicinal plants which has wound healing properties [ 19 ]. Pentabark Kashaya is a poly herbo-mineral new formulation, to ensure its safety acute dermal toxicity study was carried out prior to the wound healing effect on experimental animals. There were no changes related to fur, skin, eyes, salivation, and central nervous system in all the animals of sighting and limit test study group till the end of study probable reason may be non-irritating nature of the drug which was absorbed through the dermal route but did not show any signs of toxicity. The overall effect of acute dermal toxicity study was drawn at the end of study based on all parameters. The drug did not show any dermal toxicity and is safe for external application. Wound healing is a complex multi factorial process that results in the contraction and closure of the wound and restoration of a functional barrier [ 20 ]. An injured tissue always heals in three phases which consists of inflammation, proliferation, and remodelling [ 20 ]. There is an extensive loss of cells and tissues in an excised wound, and this makes the repair process more complicated [ 21 ]. a) Wound contraction : Reduction of the wound size is an attempt to cover the raw surface area by the activity of myofibroblast which exerts centripetal force on wound margins thus increasing contractility. It is the process of mobilizing the healthy skin surrounding the wound to cover the denuded area [ 22 ]. In the present study test drug group showed a significant wound contraction rate (p < 0.0065) from the 4th day (Mean −36.03) itself compared to control (Mean - 25.03) and standard (Mean - 30.20) group. Panchavalkala kashaya is proved to possess antimicrobial, anti-inflammatory and wound healing properties. Panchvalakala contains Tannins, phytosterols and flavonoids which are proved to possess anti-inflammatory actions, antioxidant and blood purifying properties. Phytochemicals of Panchavalkala helps to prevent the prolongation of the initial phase by reducing infection there by promotes wound contraction, increases the collagen content and neoangiogenesis in the later phases ( Fig. 1 and Fig. 2 ) [ 23 ]. Shodhita Tutta (CuSO 4 ) is one of the ingredients; it clearly promotes angiogenic responses in wounds in both in vitro in vivo models [ 24 ]. Several copper-dependent enzymes, mainly amine oxidases, are known to be increased during wound healing. These copper-dependent enzymes are important in the remodeling and healing of the wounds [ 25 ]. Sphatika (Potash Alum) possess astringent and hemostatic properties and helps in the tissue contraction and reduces inflammation there by enhances wound healing [ 26 ]. Shodhitakasisa is known to possess krimighna (Antimicrobial) and vranaghna (wound healing) properties [ 27 ]. Recent researches showed similar wound contraction rate of polyherbal fractions of Clinacanthus nutans and Elephanto pusscaber when compared to PK [ 28 ]. A study conducted on polyherbal formulation showed similar results on excision wound healing model [ [17] , [29] , [30] ]. This emphasizes that, the test drug has started showing the wound healing effect from the initial day of the wound. Fig. 1 Wound of Control group 4 th day (19/3/2015) and 16 th day (31/3/2015). Fig. 1 Fig. 2 Wound of Standard group 4 th day (19/3/2015) and 16 th day (31/3/2015). Fig. 2 b) Epithelialization time : Test group (Mean - 7.5) showed significant reduction (p < 0.05) in the epithelialization time compared to standard (Mean - 11.50) and control group (Mean - 12.83) ( Fig. 1 and Fig. 2 ). Aqueous extract of Ashwatha ( Ficus religiosa), Vata (Ficus benghalensis) Udumbar ( Ficus racemosa ), Parisha ( Thespesia populnea) showed high rate of wound contraction, decrease in the period of epithelialization by collagen synthesis, high skin breaking strength in excision and incision wound models [ 29 , [31] , [32] , [33] ]. Previous researches on excision wound model using Laghu panchamula extract showed epithelialization time of 8.5 day but PK has showed at 7.5 days [ 34 ]. A study conducted on wound healing with roots of Ficus racemosa L. and other studies has showed similar results [ [29] , [35] , [36] ]. c) Wound infection : Infection of the wound is the major factor which hinders the normal healing process of wounds. Infection in the wound is due to the presence of necrotic tissue and disruption of protective barrier to microorganisms. Swab test performed on 1st day (14 cfu/ml), 3rd day (14 cfu/ml) and 12th day (7 cfu/ml) to see the microbial load of the wound showed progressive decrease in total bacterial load and total fungal count compared to control group (13 cfu/ml, 24 cfu/ml, 27 cfu/ml). This may be due to the antibacterial activity of the PK which forms the protective barrier on the wound [ 37 ]. PK showed progressive reduction in the microbial load with time, during the course of treatment, indicating the efficacy of the formulation in reducing the microbial load and thus controlling infection, facilitating wound healing [ 23 ]. Aqueous extract of Panchavalkala is known to possess antimicrobial activity thus reducing discharge, malodour and slough in the wound [ 23 ]. PK has shown antibacterial activity against selected gram positive and gram-negative bacteria like Staphylococcus aureus at the concentration of 50 μg/ml in disc diffusion method and MIC 0.8 μg/ml , E. coli 25 μg/ml in disc diffusion method and MIC 3.12 μg/ml and Pseudomonas aeruginosa 25 μg/ml in disc diffusion method and MIC 50 μg/ml [ 37 ] . Tuttha (Copper sulfate) has antibacterial activity against multi drug resistant bacteria [ 38 ]. d) Wound closure day : Test group (Mean – 5.667) showed a significant reduction (p < 0.0001) in the wound closure day compared to standard (Mean – 9.0) and the control group (Mean – 11.17). Wound closure is a combination of wound contraction, mediated by myo fibroblasts, and re-epithelialization, which is caused by the penetration of the new epithelium into the granulation tissue [ 39 ]. Promotion of collagen synthesis by fibroblast, neoangiogenesis, increases amount of granulation tissue is due to presence of saponins, alkaloids, tannins in the panchavalakala which speeds up the regeneration process [ 23 ]. Recent studies on the Jatyadi taila application on the excision wound model showed wound healing on 9 th day, but PK showed on the 8 th day from post wounding [ 40 ] (see Fig. 3 ). Wound contraction : Reduction of the wound size is an attempt to cover the raw surface area by the activity of myofibroblast which exerts centripetal force on wound margins thus increasing contractility. It is the process of mobilizing the healthy skin surrounding the wound to cover the denuded area [ 22 ]. In the present study test drug group showed a significant wound contraction rate (p < 0.0065) from the 4th day (Mean −36.03) itself compared to control (Mean - 25.03) and standard (Mean - 30.20) group. Panchavalkala kashaya is proved to possess antimicrobial, anti-inflammatory and wound healing properties. Panchvalakala contains Tannins, phytosterols and flavonoids which are proved to possess anti-inflammatory actions, antioxidant and blood purifying properties. Phytochemicals of Panchavalkala helps to prevent the prolongation of the initial phase by reducing infection there by promotes wound contraction, increases the collagen content and neoangiogenesis in the later phases ( Fig. 1 and Fig. 2 ) [ 23 ]. Shodhita Tutta (CuSO 4 ) is one of the ingredients; it clearly promotes angiogenic responses in wounds in both in vitro in vivo models [ 24 ]. Several copper-dependent enzymes, mainly amine oxidases, are known to be increased during wound healing. These copper-dependent enzymes are important in the remodeling and healing of the wounds [ 25 ]. Sphatika (Potash Alum) possess astringent and hemostatic properties and helps in the tissue contraction and reduces inflammation there by enhances wound healing [ 26 ]. Shodhitakasisa is known to possess krimighna (Antimicrobial) and vranaghna (wound healing) properties [ 27 ]. Recent researches showed similar wound contraction rate of polyherbal fractions of Clinacanthus nutans and Elephanto pusscaber when compared to PK [ 28 ]. A study conducted on polyherbal formulation showed similar results on excision wound healing model [ [17] , [29] , [30] ]. This emphasizes that, the test drug has started showing the wound healing effect from the initial day of the wound. Fig. 1 Wound of Control group 4 th day (19/3/2015) and 16 th day (31/3/2015). Fig. 1 Fig. 2 Wound of Standard group 4 th day (19/3/2015) and 16 th day (31/3/2015). Fig. 2 Wound of Control group 4 th day (19/3/2015) and 16 th day (31/3/2015). Wound of Standard group 4 th day (19/3/2015) and 16 th day (31/3/2015). Epithelialization time : Test group (Mean - 7.5) showed significant reduction (p < 0.05) in the epithelialization time compared to standard (Mean - 11.50) and control group (Mean - 12.83) ( Fig. 1 and Fig. 2 ). Aqueous extract of Ashwatha ( Ficus religiosa), Vata (Ficus benghalensis) Udumbar ( Ficus racemosa ), Parisha ( Thespesia populnea) showed high rate of wound contraction, decrease in the period of epithelialization by collagen synthesis, high skin breaking strength in excision and incision wound models [ 29 , [31] , [32] , [33] ]. Previous researches on excision wound model using Laghu panchamula extract showed epithelialization time of 8.5 day but PK has showed at 7.5 days [ 34 ]. A study conducted on wound healing with roots of Ficus racemosa L. and other studies has showed similar results [ [29] , [35] , [36] ]. Wound infection : Infection of the wound is the major factor which hinders the normal healing process of wounds. Infection in the wound is due to the presence of necrotic tissue and disruption of protective barrier to microorganisms. Swab test performed on 1st day (14 cfu/ml), 3rd day (14 cfu/ml) and 12th day (7 cfu/ml) to see the microbial load of the wound showed progressive decrease in total bacterial load and total fungal count compared to control group (13 cfu/ml, 24 cfu/ml, 27 cfu/ml). This may be due to the antibacterial activity of the PK which forms the protective barrier on the wound [ 37 ]. PK showed progressive reduction in the microbial load with time, during the course of treatment, indicating the efficacy of the formulation in reducing the microbial load and thus controlling infection, facilitating wound healing [ 23 ]. Aqueous extract of Panchavalkala is known to possess antimicrobial activity thus reducing discharge, malodour and slough in the wound [ 23 ]. PK has shown antibacterial activity against selected gram positive and gram-negative bacteria like Staphylococcus aureus at the concentration of 50 μg/ml in disc diffusion method and MIC 0.8 μg/ml , E. coli 25 μg/ml in disc diffusion method and MIC 3.12 μg/ml and Pseudomonas aeruginosa 25 μg/ml in disc diffusion method and MIC 50 μg/ml [ 37 ] . Tuttha (Copper sulfate) has antibacterial activity against multi drug resistant bacteria [ 38 ]. Wound closure day : Test group (Mean – 5.667) showed a significant reduction (p < 0.0001) in the wound closure day compared to standard (Mean – 9.0) and the control group (Mean – 11.17). Wound closure is a combination of wound contraction, mediated by myo fibroblasts, and re-epithelialization, which is caused by the penetration of the new epithelium into the granulation tissue [ 39 ]. Promotion of collagen synthesis by fibroblast, neoangiogenesis, increases amount of granulation tissue is due to presence of saponins, alkaloids, tannins in the panchavalakala which speeds up the regeneration process [ 23 ]. Recent studies on the Jatyadi taila application on the excision wound model showed wound healing on 9 th day, but PK showed on the 8 th day from post wounding [ 40 ] (see Fig. 3 ). A marked increase in the re-epithelialization dermal fibroblast, dermal fibrocytes was seen in test group ( Fig. 4 ) when compared to control group which shows that the drug has promoted collagen synthesis, neoangiogenesis and matrix modelling. The dermal collagen/fibrosis were increased in test group when compared to the standard and a control group which shows the minimal scar tissue formation. Fig. 3 Wound of Test group 4 th day (19/3/2015) and 16 th day (31/3/2015). Fig. 3 Fig. 4 Histopathology of healed skin of Control, Standard and Test group (1/4/2015). Fig. 4 Wound of Test group 4 th day (19/3/2015) and 16 th day (31/3/2015). Histopathology of healed skin of Control, Standard and Test group (1/4/2015). Similar study conducted on wound healing activity showed the improvement of dermal collagen, neoangiogenesis and re epithelialization which was assessed by histopathology of skin [ [18] , [29] ]. PK contains panchavalkala which contains Tannins, Alkaloids, Saponins, Glycosides, Flavonoids, Phytosterols, which possesses antimicrobial, antioxidant, antiseptic, anti-inflammatory, wound purifying, healing, astringent properties [ 23 ] . Tuttha, sphatika and kasisa are known to possess astringent, angiogenic, antimicrobial, haemostatic and wound healing activities [ [24] , [25] , [26] , [27] ]. Thus PK helped in all stages of wound healing like inflammatory, epithelialization, angiogenesis, granulation tissue formation and collagen deposition.

Wounds are a significant cause of morbidity worldwide and studies proved that, for every million patients around 10,000 would die due to microbial infections [ 1 ]. A “wound” is defined as the disruption of normal anatomic structures and function [ 2 ]. Studies estimated that 5million patients get affected every year due to traumatic wounds [ 3 ]. Acharya sushruta has given utmost importance to Vrana (wound) and defines vrana (wound) as one which does the disruption of shareeradhatu (body tissues), leaves the vranavastu (scar) after ropana (healing) and remains till the end of life. He has described the classification of vrana , sadya - asadyata (prognosis) and its management in detail, which emphasizes the importance of wound care [ 4 ]. The major aim of the wound management is prevention of the infection and accelerating the healing process, which is achieved by use of topical antimicrobial dressing such as povidone iodine, soframycin and silver containing products. Numerous antiseptic agents support to prevent contamination, infection of the wound but have no role in accelerating the natural healing process [ 5 , 6 ]. There is a necessity to develop such a preparation possessing Antibacterial, Anti-inflammatory and wound healing properties. In this regard an innovative polyherbomineral formulation i.e. Pentabark Kashaya was formulated by combining the drugs like Panchavalkala kashaya, Shodhita Kasisa, Tuttha , and Sphatika , so that an effective wound cleansing and healing agent can be brought into practice. Panchavalkala Kashaya is having the Vrana Shodhana and Ropana properties and being frequently used in every specialty of Ayurveda [ 7 ]. Recent researches proved that Panchavalkala Kashaya is effective in conditions like vaginitis, leucorrhoea, endometriosis, infected wounds and also possess anti-inflammatory, analgesic, antimicrobial and, anticancer activity [ 8 ]. The lacuna of using Kashaya is that it should be readily prepared and used immediately or else it loses its property (both in terms of efficacy and stability) [ 9 ]. It is a need of hour to enhance its efficacy, increase stability and make readily available compound for the usage so we have added Shodhita Kasisa, Tuttha, and Sphatika to the Panchavalkala Kashaya as these drugs possess property of Krimighna, Vranashodhana and Vrnaropana [ 10 , 11 ]. Published research works in relaton to Panchavalkala usage is available in the form of kashaya , powder and ointment in the management of wounds, but studies with additions of other herbal or mineral drugs to panchavalkala are not available [ 7 ]. Hence the present study was planned to prepare a novel formulation by combining panchavalkala kashaya with other mineral drugs followed with dermal toxicity and wound healing efficacy in excision wound model was undertaken.

None.