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Year : 2013  |  Volume : 45  |  Issue : 5  |  Page : 474--478

Wound healing activity of Sida cordifolia Linn. in rats

Rajesh S Pawar1, Pradeep K Chaurasiya1, Harish Rajak2, Pradeep K Singour1, Fedelic Ashish Toppo1, Ankit Jain1,  
1 Pharmacognosy and Phytochemistry Laboratory, Faculty of Pharmacy, VNS Group of Institutions, Neelbud, Bhopal, Madhya Pradesh, India
2 Department of Pharmacy, Guru Ghasidas Vishwavidyalaya, Bilaspur, C.G., India

Correspondence Address:
Rajesh S Pawar
Pharmacognosy and Phytochemistry Laboratory, Faculty of Pharmacy, VNS Group of Institutions, Neelbud, Bhopal, Madhya Pradesh


Introduction: The present study provides a scientific evaluation for the wound healing potential of ethanolic (EtOH) extract of Sida cordifolia Linn. (SCL) plant. Materials and Methods: Excision, incision and burn wounds were inflicted upon three groups of six rats each. Group I was assigned as control (ointment base). Group II was treated with 10% EtOH extract ointment. Group III was treated with standard silver sulfadiazine (0.01%) cream. The parameters observed were percentage of wound contraction, epithelialization period, hydroxyproline content, tensile strength including histopathological studies. Result: It was noted that the effect produced by the ethanolic extract of SCL ointment showed significant (P < 0.01) healing in all wound models when compared with the control group. All parameters such as wound contraction, epithelialization period, hydroxyproline content, tensile strength and histopathological studies showed significant (P < 0.01) changes when compared with the control. Conclusion: The ethanolic extract ointment of SCL effectively stimulates wound contraction; increases tensile strength of excision, incision and burn wounds.

How to cite this article:
Pawar RS, Chaurasiya PK, Rajak H, Singour PK, Toppo FA, Jain A. Wound healing activity of Sida cordifolia Linn. in rats.Indian J Pharmacol 2013;45:474-478

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Pawar RS, Chaurasiya PK, Rajak H, Singour PK, Toppo FA, Jain A. Wound healing activity of Sida cordifolia Linn. in rats. Indian J Pharmacol [serial online] 2013 [cited 2022 Jul 1 ];45:474-478
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Healing is a complex and intricate process initiated in response to injury that restores the function and integrity of damaged tissues. Healing process can be broadly categorized into three stages; inflammatory phase consisting the establishment of homeostasis and inflammation; proliferate phase (consisting of granulation, contraction and epithelization) a finally the remodeling phase, which ultimately determines the strength and appearance of the healed area. [1] Several natural products, [2] plant products, which are composed of active principles, such as alkaloids and flavonoids [3] and biomolecules [4] have been reported to promote the process of wound healing.

Sida cordifolia Linn. (SCL) (Malvaceae) syn. Country Mallow is a small, erect, downy shrub. [5] It is almost odorless with slightly bitter taste. [6] In Ayurveda practices, S. cordifolia had three common applications: Mashabaladi Kvatha, where the plant seeds were mixed with other ingredients to relieve muscular pain; Balataila, a process for the treatment of the nervous system complaints, stomach problems and as a cardiac tonic; and the crushed leaves of the plant as an astringent for the treatment and dressing of wounds or skin injuries. Traditionally, root juice is also used to promote the healing of wounds. [7] In view of these cited activities, observations and traditional uses of plant, the present study was undertaken to explore the wound healing potential of ethanolic extract of SCL in excision, incision and burn experimental models.

 Materials and Methods

Plant Material

The whole plant of S. cordifolia were identified, and collected in the month of October from the forest of Pachmarhi region, dist. Hoshangabad. A voucher specimen no. No./HD/CHPY825 has been deposited in the Department of Botany, Jawaharlal Krishi Vishwavidhyala, Jabalpur. The plants were washed, shade dried, pulverized into moderately coarse powder, passed through a 40 mesh sieve and stored in an air tight container for further use.

 Plant Drug Extraction

The powdered plant (60 g) of S. cordifolia was extracted with ethanol using the Soxhlet apparatus for 24 h until the extraction was completed. The solvent was removed under reduced pressure. The dried extract was weighed and percentage yield was obtained with respect to dry powdered material.

 Preliminary Phytochemical Screening

The different identification tests were performed to detect the presence of metabolites in ethanolic extract of SCL. [8],[9]

 Preparation of Formulation and Standard Used

Simple ointment was prepared from the 10% ethanolic extract of SCL by trituration method in a ceramic pestle and mortar using White soft paraffin obtained from S.D. Fine Chemical, India. [10] About 10 g of semisolid extract was incorporated into the 100 g of simple ointment base B.P. [11] Simple ointment base was used as the control group and was applied twice per day. Extract ointment was used twice per day to treat different groups of animals. Silver sulfadiazine (0.01%) obtained from Rexin Pharmaceutical Pvt. Ltd. was used as standard drug for comparing the wound healing potential of extract in different animal models and was applied twice per day.


Wistar albino rats (150-180 g) of either sex were selected for the experiment. They were housed individually in standard laboratory environment for 7 days of period, fed with commercial pellets and water ad libitum. Animal study was performed in Division of Pharmacology, VNS Institute of Pharmacy, Bhopal. The procedures were reviewed and approved by the Institutional Animal Ethics Committee (Registration No.778/03/c/CPCSEA).

 Wound Healing Activities

Grouping of Animals

For excision, incision and burn wound model, animals were divided into three groups in each model consisting of six animals as follows: group I-simple ointment base; Group II-10% ethanolic extract ointment of SCL and Group III-silver sulfadiazine (0.01%) cream was used as standard.

Excision wound model

Excision wound model as per the method described [12] was used. Three groups of animals containing six rats in each group were anesthetized by open mask method with anesthetic ether. The rats were depilated on the back and a predetermined area of 500 mm 2 full thickness skins was excised in the dorsal interscapular region. Rats were left undressed to the open environment. The formulation ointment and standard drug were applied daily until the complete healing. In this model, wound contraction and epithelialization period was monitored. Wound contraction was measured as percent contraction in each 2 days after wound formation. From the healed wound, a specimen sample of tissue was collected from each rat for histopathological examination. [13],[14]

Incision wound model

In incision wound model, 6 cm long paravertebral incision were made through the full thickness of the skin on either side of the vertebral column of the rats, after all the animals of each group were anesthetized under light ether anesthesia. [15] No local or systemic antimicrobials were used throughout the experiment. All groups were treated same as in excision model, the both edges kept together and stitched with Black silk surgical thread (no. 000) and a curved needle (no. 11) was used for stitching. The continuous threads on both wound edges were tightened for good closure of the wound. After stitching, wound was left undressed then ointment base, standard ointment and extracts ointment were applied daily until 10 days; when wounds were cured thoroughly the sutures were removed on the day 10 and tensile strength of cured wound skin was measured using tensiometer. [16]

Burn wound model

Burn wounds were created on dorsal part of shaved rat's skin surface using concentrate sulfuric acid, exposed for 10 s. After 24 h, dead tissues were excised using sterile surgical blade through a template designed to produce a third degree burn. [17] All groups were treated same as in excision model. In this model, wound contraction and epithelialization period was monitored. A specimen sample from the healed wound of tissue was collected from each rat for histopathological examination. [18]

 Wound Healing Evaluation Parameters

Measurement of Wound Contraction

An excision wound margin was traced after wound creation by using transparent paper and area measured by graph paper. Wound contraction was measured in each 2 days interval, until complete wound healing and expressed in percentage of healed wound area. [19] The evaluated surface area was then employed to calculate the percentage of wound contraction, taking initial size of wound, 300 mm 2 , as 100%, by using the following formula as:


Epithelialization period

It was evaluated by noting the number of days required for the Escher to fall off from the wound surface exclusive of leaving a raw wound behind. [20]

Measurement of tensile strength

The tensile strength of a wound represents the degree of wound healing. It indicates how much the repaired tissue resists to breaking under tension and may indicate in part the quality of repaired tissue. The sutures were removed on the 9 th day after wounding and the tensile strength of removed tissue was measured on the 10 th day with the help of tensiometer. [21] In this method, wound breaking strength was measured as the weight of water at the time of wound breaking per area of the specimen.

Hydroxyproline estimation

Wound tissues were analyzed for hydroxyproline content, a basic constituent of collagen. Tissues were dried in a hot air oven at 60-70°C to constant weight and hydrolyzed in 6 N HCl at 130°C for 4 h in sealed tubes. The hydrolysate was neutralized to pH 7 then subjected to chloramine-T oxidation for 20 min. [22] The reaction was terminated by the addition of 0.4 M perchloric acid and developed color with Ehlrich reagent at 60°C was read at 557 nm in ultraviolet (Cintra) spectrophotometer.

Histopathological studies

Wound tissue specimens from control, test and standard groups were taken after complete healing of excision, incision and dead burn wound and after usual processing 6-mm thick sections were cut and stained with hematoxylin and eosin. [23] Sections were qualitatively assessed under the light microscope and observed in respect of fibroblast proliferation, collagen formation, angiogenesis and epithelialization.

 Statistical Analysis

All treated groups were compared with the control groups. The results were analyzed statistically using one-way analysis of variance (ANOVA). The result were found to be significantly at P < 0.01. All tests were conducted using Graph Pad Software, Inc., a privately held California corporation.


Percentage yield was found to be 4.91 g (w/w). Preliminary phytochemical screening of ethanolic extract of SCL showed the presence of alkaloids, flavonoids and tannins.

 Wound Contraction

A better healing pattern with complete wound closure was observed in standard and treated group of all models within 10 and 14 days respectively while it was about 22 days in control rats as shown in [Table 1] and [Table 2].{Table 1}{Table 2}

 Epithelialization Period

The epithelialization time was measured from the 1 st day. The epithelialization time was found to be significantly (P < 0.01) reduced in Groups II and III as depicted in [Table 3] and [Table 4] for incision and burn models. The treatments with ethanolic extract as well as conventional wound treatment cream were superior to control groups, which received ointment base.{Table 3}{Table 4}

 Tensile Strength of Incision and Burn Wound Model

Tensile strength for the treated group on day 20 was found to be significant (P < 0.01) than the control group as shown in [Table 2] and [Table 4].

 Hydroxyproline Estimation

Treated group showed significant increased hydroxyproline level when compared with the control group (P < 0.01) [Table 2] and [Table 4].

 Histopathological Studies

The histopathological studies of the tissue of the excision, incision and burn wound area was performed and histopathological characters of incision wound treated group with control, standard and extract ointment are shown in [Figure 1]a-c. Group I (control) showed reduced fibroblast cells, collagen fibers and blood vessels, while Group II (standard) showed increased in fibroblast cells, collagen fibers and blood vessels in both incision and burn wound models. Group III (extract ointment) also showed increased in fibroblast cells, collagen fibers and blood vessels, but not more than Group II in both incision and burn wound models. The histopathology examination showed that the original tissue regeneration was much greater on ethanolic extract and standard. Fibroblast cells, collagen fibers and blood vessels are prominently present in standard and extract treated group as compared with the control. While in control rats wounds have shown incomplete healing [Figure 1]a.{Figure 1}

The results showed that ethanolic extract ointment possesses a definite prohealing action. This was demonstrated by a significant increase in the rate of wound contraction and by enhanced epithelialization. Significant increase (P < 0.01) in tensile strength and hydroxyproline content were observed, which was further supported by histopathological studies. Since incisional wound treated with ethanolic extract of SCL showed greater tensile strength, it might be inferred that the ethanolic extract of SCL not only increased collagen synthesis per cell, but also aided in cross-linking of the protein.


The chemical constituents of SCL plants and their medicinal values have been reviewed. Its chemical constituents mainly consist of oils and fats, org. acids, flavonoids, triterpenes, steroids, sterols and proteins. [24] Biological activities in the skin are due to its interaction with various binding protein. In this tissue repair process inflammatory cells promote the migration and proliferation of endothelial cells, which synthesize extracellular matrices including collagen and of keratinocytes resulting to re-epithelialization of the wounded tissue. The wound healing action of SCL may probably be due to the phytoconstituents present in the plant or could be a function of either the individual or the additive effects of the phytoconstituents. The present result also indicated a significant decrease in wound area from day 8 onward indicating early healing. In incision wound, an increase in tensile strength of treated wounds was observed and this may be due to the increase in collagen concentration and stabilization of the fibers. [25]

The ethanolic extract of SCL increased cellular proliferation and collagen synthesis at the wound site as evidenced by the increase in total protein and total collagen contents reflected by hydroxyproline content of granulation tissues. In our study, hydroxyproline content was significantly increased (P < 0.01) when compared with the control. Since SCL extract has increased levels of these compounds considerably it is likely that the observed increase in tensile strength was not only due to increased collagen synthesis but also due to its proper deposition and alignment.

Collagen is the predominant extracellular protein in the granulation tissue of healing wound and there is a rapid granulation tissue of healing wound and there is wound rapid increase in the synthesis of this protein in the wound area soon after an injury which provides strength and integrity to tissue matrix. Measurement of this hydroxyproline, which comes from the breakdown of collagen, has been used as an index of collagen turnover. The hydroxyproline content of the granulation tissue indicates the presence of higher collagen content and its turnover leading to rapid healing with a concurrent increase in the tensile strength of the treated wounds.


The results of the study showed that the ethanolic extract ointment of SCL effectively stimulates wound contraction; increases tensile strength of excision, incision and burn wound as compared with the control group. These finding could justify the inclusion of this plant in the management of wound healing.


1Evans P. The healing process at the cellular level. Physiotherapy 1983;20:256.
2Suguna L, Chandrakasan G, Joseph KT. Influence of honey on biochemical and biophysical parameters of wounds in rats. J Clin Biochem Nutr 1999;14:91.
3Sharma SP, Aithal KS, Srinivasn KK, Udupa AL, Kumar V, Kulkarni DR. Anti-inflammatory and wound healing activities of the crude alcoholic extracts and flavonoids of Vitex leucoxylon. Fitoterapia 1990;61:263.
4Chitra P, Suguna L, Chandrakasan G. Influence of arginine wound healing in rats. J Clin Biochem Nutr 1995;18:111.
5Nadkarni AK. The Indian materia medica. Vol. I, 3 rd ed. Popular Prakshan, Bombay. 2000;3:1134-7.
6Rangari VD. Pharmacogn Phytochem 2008;2:274-5.
7Kirtikar KR, Basu BD. Indian Medicinal Plants. 2 nd ed. Dehradun: Bishen Singh Mahendra Pal Singh; 1980. p. 312.
8Kokate CK. Practical Pharmacognosy. New Delhi: Vallabh Prakashan; 1994. p. 107-13.
9Harborne JB. Phytochemical Methods. London: Chapman & Hall; 1998. p. 60-6.
10Cooper. Gunn's Dispensing for pharmaceutical students. In: Carter, S.L. (Ed.), 12 th ed., CBS Publisher and Distributors, Delhi 1987;199-200.
11Anonymous, "British Pharmacopoeia", London: General Medical Council, The Pharmaceutical Press, 17 Bloomsbury Square London, .1953, WCI 396.
12Mukherjee PK, Verpoorte R, Suresh B. Evaluation of in-vivo wound healing activity of Hypericum patulum (Family: Hypericaceae) leaf extract on different wound model in rats. J Ethnopharmacol 2000;70:315-21.
13Taranalli AD, Tipare SV, Kumar S, Torgal SS. Wound healing activity of Oxalis corniculata whole plant extract in rats. Indian J Pharm Sci 2004;66:444-6.
14Anderson JE. Muirs Text Book of Pathology. 11 th ed. ELBS; 1980:77-85.
15Ehrlich HP, Hunt TK. The effect of cortisone and anabolic steroids on the tensile strength of healing wounds. Ann Surg 1968;57:117.
16Hemalata S, Subramanian N, Ravichandran V, Chinnaswamy K. Wound healing activity of Indigofera ennaphylla Linn. Indian J Pharm Sci 2001;63:331-3.
17Nakae H, Inaba H. Effectiveness of electrolyzed oxidized water irrigation in a burn-wound infection model. J Trauma 2000;49:511-4.
18Mcmanus JF, Mowry RW. Staining Methods: Histologic and Histochemical. New York, Evanston/London: Harper and Row; 1965.
19Sadaf F, Saleem R, Ahmed M, Ahmad SI, Navaid-ul-Zafar. Healing potential of cream containing extract of Sphaeranthus indicus on dermal wounds in Guinea pigs. J Ethnopharmacol 2006;107:161-3.
20Rashed AN, Afifi FU, Disi AM. Simple evaluation of the wound healing activity of a crude extract of Portulaca oleracea L. (growing in Jordan) in Mus musculus JVI-1. J Ethnopharmacol 2003;88:131-6.
21Kuwano H, Yano K, Ohno S, Ikebe M, Kitamura K, Toh Y, et al. Dipyridamole inhibits early wound healing in rat skin incisions. J Surg Res 1994;56:267-70.
22Woessner JF Jr. The determination of hydroxyproline in tissue and protein samples containing small proportions of this imino acid. Arch Biochem Biophys 1961;93:440-7.
23Ranajit, K., Sutradhar, A.K.M., Matior, R., Mesbah, UA, Sitesh CB. Bioactive flavones of Sida cordifolia. Phytochemistry Lett. 2008;1:179-82.
24Clark, RAF. Wound repair: Overview and general considerations. In: Clark, R.A., Henson, P.M. (Eds.), the Molecular and Cellular Biology of Wound Repair. Plenum Press, New York, 1996:3.
25Udupa AL, Kulkarni DR, Udupa SL. Effect of Tridax procumbans extracts on wound healing. Int J Pharmacogn 1995;33:37.