Pharmacological and Therapeutic Potential of Calotropis gigantea and Aerva lanata: A Review
Akashdeep Tyagi1*, Preeti Chaudhary2, Vipin Kumar Garg1
1Department of Pharmaceutical Technology, Meerut Institute of Engineering and Technology,
Meerut, Uttar Pradesh, India.
2Department of Pharmacy, NCRD’s Sterling Institute of Pharmacy, Nerul, Navi Mumbai, Maharashtra, India.
*Corresponding Author E-mail: akash.at009@gmail.com
ABSTRACT:
Calotropis giganteabelongs to the Asclepiadaceae family is commonly known as Arka and Ruvi and it is found throughout India. The Aerva lanata plant is a member of Amaranthaceae family and its usually known as mountain knot grass and gorakhabooti and their role in disease cure has been documented. Different part of these plants contains numerous types of chemical constituents such as flavonoids, alkaloids, quercetin, kaempferol, sterols, cynogenic glycoside, with diverse pharmacological activities. Moreover, these plants show, anti-microbial activity, analgesic, wound healing, anti-inflammatory, hepatoprotective, anti-diuretic and anti-diabetic activities. Hence this review representsan overview of medicinal uses of Calotropis gigantea and Aerva lanata plant which is used in many formulations.
KEYWORDS: Aerva lanata, Calotropis gigantea, anti-diuretic, anti-inflammatory, kaempferol, quercetin.
INTRODUCTION:
Nature has long provided a rich source of therapies in the form of medicinal plants for a wide range of ailments, dating back to ancient times. Plants have long been used for therapeutic purposes, both in the traditional and modern eras. Herbs have a variety of phytoconstituents, which contribute to their wide range of pharmacological activity, resulting in positive effects. According to the latest data from the WHO (World Health Organization) herbal medicines are used by 80% of people throughout the world for portion of their basic healthcare31. Cheaper remedies have surpassed traditional drugs in popularity because to their lower risk of unwanted effects and efficacy in treating chronic diseases.
Calotropis gigantea, also known as'madar'is a milky shrub that grows up to 1-3 metres tall and may be foundthroughout India. It belongs to the Asclepiadaceae family1,2. According to a phytochemical analysis, Calotropis gigantea leaves include a resin-mudarine, as well as glycosides such as calotropin, uscharin, and calotoxin3. Calotropis is a genus with around six species including sister species. Calotropis gigantea and Calotropis procera being prevalent in India’s wastelands4. It has been demonstrated by earlier studies that the hydroalcoholic extract of flowers possesses hepatoprotective activity5. The aerial component of calotropis gigantea has already been found to have anti-diarrheal effects in castor oil-induced diarrhoea6. An analgesic effect of an alcoholic extract of the flowers was recently discovered7. C. gigantea flowers have traditionally been used to treat inflammation, ulcers, and asthma-like conditions8. C.gigantea roots are used in the Indian system of traditional medicine for the treatment of leprosy, dermatitis, syphilis, elephantiasis, ulceration, antidiarrheal, and cough. Calotropis gigantea's milky juice has been used to induce abortion and has been described as a strong purgative and gastrointestinal irritant9.
Figure: Calotropis gigantea Leaves
Taxonomical hierarchy of Calotropis gigantea:
Kingdom: Plantae
Subkingdom: Tracheobionta
Order: Gentianales
Division: Magnoliophyta
Super division: Spermatophyta
Class: Magnoliopsida
Subclass: Asteridae
Family: Asclepiadoideae
Genus: Calotropis
Species: Calotropis gigantea
Geographic Distribution:
All the species of Calotropis are drought-resistant, drought-tolerant and salt-tolerant. Air pollination is common, as is pollination by animals. As a result, such species can easily be found in the wild weed along the roadside, at the lagoon's edge, and in native meadows that have been overgrazed. It also thrives in sandy soil and low-rainfall locations. Calotropis species have been reported in Nepal, India, Iran, Pakistan, Iraq, Omen, Yemen, Afghanistan and Zimbabwe10,11.
Chemical Constituent and its Structure:
Alkaloids, cyanogenic glycosides, phenolic tannins, cardenolides12,13, flavonoids14,15,16,sterols17 proteinases, calotropain-FI and calotropain-FII18, calotropin-DI and calotropin-DII19 and non-protein amino acid Giganticine20 are all reported to be present in Calotropis gigantea.
Alkaloid Cardenolides
Sterol Flavonoids
Traditional Uses of Calotropis gigantea:
|
Plant Part |
Uses |
Reference |
|
Whole Plant |
Used in the treatment of Leprosy |
Lyengar et al.,1986 |
|
Used in the treatment of Rheumatism |
Subaramaniam,1999; Katiyar and Kolhe 2000-2001 |
|
|
Used in the treatment of Bronchial Asthma |
Shankara.,1979 |
|
|
Used in the treatment of Pneumonia |
Jain and Tarafder,1970 |
|
|
Used as Purgative |
Deka et al.,1984 |
|
|
Used in treatment of Fever |
Pal et al.,1999; Kumar et al.,2003 |
|
|
Fruit |
Used in the treatment of Leucoderma |
Lyengar et al.,1986 |
|
Leave |
Used in the treatment of Pneumonia |
Girach et al.,1997 |
|
Used as Vermicide |
Tarafder,1984 |
|
|
Seed |
Used in the treatment of Malaria |
MaiKhuri and Gangwar,1993 |
|
Used in the treatment of Blood Clots |
Chelvan,1998 |
|
|
Flower |
Used in the treatment of T.B |
Topno and Ghosh,1999 |
|
Used as Wound Healer |
Reddy et al.,1988;Rao et al.,2000 |
Pharmacological Activities:
Antimicrobial Activity:
The anti-candida activity of aqueous, methanol, and petroleum etherextract of Calotropis gigantea leaves was discovered towards clinical isolates of candidakrusei, and candida albicans21. An aqueous extract of Calotropis gigantea was found to exhibit antibacterial activity against S. aureus, E. coli, P. aeruginosa, and klebsella pneumonia22. Aqueous extract of Calotropis gigantea latex was reported to substantially inhibits S.aureus, E.coli and C.krusei23.
Analgesics Activity:
In thermal and chemical models in mice, an alcoholic extract of C.gigantea flowers was reported to have analgesic activity. The HPM and the acetic acid induced writhing test were used to assess analgesic activity. A single oral dose of ethanolic extract of the flower of C.gigantea reduced writhings and delayed paw licking time significantly24. Albino rats were used to test the analgesic activity of an alcoholic extract of peeled roots of Calotropis gigantea. Eddie's hot plate method and acetic acid-induced writhings were both shown to be analgesic. The extract of root was given orally in doses of 250 and 500mg/kg, which significantly reduced the number of writhings and delayed paw licking time25.
Anti-inflammatory Activity:
Ethanolic extract of Calotropis gigantea leaves was found to have anti-inflammatory activity against carrageena-induced paw edema in wistar albino rats. The anti -inflammatory effect of 400mg/kg after oral treatment of C.gigantea was shown to be more potent than 100mg/kg ibuprofen26.
Wound Healing Activity:
The wound healing abilities of a C.gigantea root bark extract was investigated inwistar albino rats.For excision wound healing models, the rats were administered extract in the form of an ointment topically, while for incision wound healing models, Extract was given orally 100, 200, and 400mg/kg. According to the findings extract therapy hastens wound healing in rats27.
Antipyretic Activity:
Chitme et al., discovered that a water ethanol (50:50) extract of Calotropis gigantea has antipyretic efficacy. The efficiency of antipyretics in albino rats and rabbits was investigated using yeast and TAB vaccine - induced pyrexia. Extract reduced fever and also controlled body temperature at dosage of 200 and 400mg/kg28.
Hepatoprotective Activity:
In male Wistar rats, an ethanol extract of Calotropis gigantea stems was found to have hepatoprotective effects towards carbon tetrachloride induced liver damage. The extract dramatically reduced AST, ALT, and lipid peroxide levels, as well as providing efficient liver protection. Additionally, the extract protects the rats from oxidative damage29.
Insecticidal Activity:
A methanol extract of Calotropis gigantea root bark as well as its petroleum ether fraction and chloroform, were tasted for residual film toxicity fumigant and repellent efficacy against numerous strains of tribolium castaneum larvae and adults. Methanolic extract outperformed chloroform fraction and petroleum ether fraction in terms of insecticidal activity against T.castaneum. There was no evidence of fumiganttoxicity in any of the samples30.
Aerva lanata:
Aerva lanata belongs to Amaranthaceae family32. It is atype oftropical plant which grows in Africa, India, Sri Lanka, Java and Philippines. Aerva lanata is a weed that may be found all across India, especially in hot and humid areas.
Aerva lanata is used to treat diabetes, helminthic infection inflammation, skin disorders, cough, cholera, dysentery, kidney stone, headache, and diarrhea in traditional medicinal systems.A. lanata has been intensively examined for its therapeutic characteristics utilising advanced scientific procedures over the last two decades, and has been reported to have diuretic action33, urolithiasis activity34, anti-inflammatory activity35, antimicrobial activity36, anti-diabetic activity37, nephroprotective activity38, hepatoprotective activity39,40, anthelmintic activity41, and antidiarrhoeal activity42.
Figure: Calotropis gigantea Leaves
Common Names:
Acaranthes lanata, Aerva elegans mog43. It is known as Kapurijadi or Gorakhabooti and in English, it is known as Mountain knot grass44.
Taxonomical hierarchy of Aerva lanata:45
Kingdom: Plantae
Order: Caryophyllales
Phylum: Mangoliophyta46
Class: Magnoliopsida
Subclass: Caryophyllidae47
Division: Tracheophyta
Sub-division: Spermatophytina
Family: Amaranthaceae
Genes: Aerva
Species: Lanta
Botanical Name: Aerva Lanata
Cultivation:
Seed propagation is used to cultivate Aerva lanata. Each plant is placed in a row with a 30cm spacing between them. Sunlight is required for the plant's growth. These plants are grown during the month of September. It will flower in the first year of growing. To protect against external elements such as microorganisms, weeds, insects, and so on, Inorganic, organic, and synthetic fertilizers are employed during the cultivation process.Cow-dung, animal manure and plant waste are also utilized as organic fertilizers. Although it has little nutritional value, peat increases the plant’s absorption qualities.
Morphology:
The plant Aerva lanata is dioecious prostrate herb with a cylindrical branching root 7-12cm long, and 2-8mm thick, mildly twisted with humerous thin. Roots are externally pale yellowish brown and internally white. Leaves are simple alternating with complete obovate or suborbicular lamina border and have short petiole and exstipulate. Flowers are tiny, bisexual and greenish white and their stamens are attached to five lobed ovoid ovaries. The fruits are spherical in shape and compressed membranous utricle capsule with a single seed that is greenish in colour. Reinform, lustrous black coriaceous testa48,49,50.
Chemical Constituents:
Canthin-6-one alkaloids, 10 - methoxy canthin, 6-methoxy beta carbolin -1- propionic acid, Beta -D- glucopyranosyloxycanthin -6- one, aervoside, 6- methoy beta - carbolin, ervolanine and propionic acid are among the physiologically active alkaloids, sugar, saponins and minerals are also present. Aerva lanata contain flavonoids, such as quercetin, galactoside, kaempferol, isohamnetic, flavonone glucoside pernisol and persinoside A and B.
Among the chemical ingredients are, benzoic acid, lupeol acetate, methyl grevullate, beta sitosteryl acetate, 24 different types of tannic acid, and 27 different types of terpenoids.51,52,53,54
Flavonoid Quercetin
Isohamnetin Kaempferol
Beta sitosteryl acetate Lupeol acetate
Benzoic acid
Pharmacological Activities:
Anti-Urolithiasis and Diuretic:
An alcoholic extract of Aerva lanata was studied for itsdiureticproperties. At dosage of 800mg/kg, the alcoholic extract worked better as a diuretic than the control group. Aerva lanata aqueous solution (2g/kg body wt./ dose/for 28 days) reduced OSE and markers of crystal deposition in CaO2 urolithic rats. The study’s findings indicated that Aerva lanata can be used to treat urolithiasis55,56.
Anti-Inflammatory Activity:
Carrageenan-induced rat paw edema was suppressed by benzene and alcoholic extract of Aerva lanata shoots (800mg/kg), indicating anti-inflammatory effect57.
Anti-Diabetic Activity:
Methanol extract of Aerva lanata indicated that the methanol extract (400mg/kg) hadgreaterantidiabetic effect than the standard medicineglibenclamidein streptozotocin-induced diabetic rats58.
Hepatoprotective Activity:
A petroleumether extractable fraction of the entire plant Aerva lanata was examined in Sprague Dawley rats for its potential to protect against liver damage caused by CCL4(carbon tetra chloride). Aerva lanata dramatically increased serum total protein and albumin/globulin ratios and reduced histopathological changes, and reduced hepatic lipid peroxidation59.
CONCLUSION:
Calotropis gigantea and Aerva lanata are potential plant with many curative principles and economic values. They are used as a traditional medicinal plant with unique properties. The present review paper shows that both plants are popular remedies in Ayurvedic and traditional practitioners for the treatment of a range of ailments. Though Calotropisgigantea and Aerva lanata have various medicinal applications, but still the phytochemicals of these plantsneed to be standardized to explore its medicinal values with the help of various methods. Further research is necessary to elucidate the phytochemical and pharmacological aspects of these plants. Both the plants are potential source for the development of new drugs to pharmaceutical industry due to the presence of a number of phytoconstituents and their wide variety of pharmacological actions.
ACKNOWLEDGMENTS:
I wish to express my gratitude to Dr. Preeti Chaudhary, Assistant Professor at NCRD’s Sterling Institute of Pharmacy, Navi Mumbai for providing encouragement and helping me for carrying out this work and I am also thankful to Dr. Vipin Kumar Garg for his assistance for this paper.
REFERENCES:
1. Kirtikar KR and Basu BD: Indian Medicinal Plants. International Book Distributors and Publishers, Dehradun, India, Edition 2, Vol. 1, 2008: 1607-1609
2. Nadkarni KM and Nadkarni AK: Indian Materia Medica. Popular Prakashan Pvt. Ltd, Edition 3, Vol. 1, 1976: 237-241.
3. Chaudhuri RHN: Pharmacognostic studies on the roots of Calotropis gigantea R.Br.exAit. Bull Bot Surv India 1961; 3: 171- 173.
4. Nadkarni KM. (2002) The Indian Materia Medica, Bombay Popular Prakashan: Vol I: 231-241.
5. Patel RB, Raval JD, Gandhi TP. (1998) Indian Drug. 26:224-225.
6. Chitme HR, Chandra R, Kaushik S. (2004) J. Pharm. Pharmaceutical. Sci. 7:70-75.
7. Pathak AK, Agral A. (2007) Fitoterapia, 78:40- 42
8. Kirtikar KR, Basu BD. (1980) Indian Medicinal Plants, II Edn. Vol3, Lalit Mohan Basu: Allahabad: 1606-166.
9. Srivastava SR, Keshri G, Bhargavana B, Singh C, Singh MM. Original research article: Pregnancy interceptive activity of the roots of Calotropis gigantea Linn. in rats. Contraception 2007;75:318-22
10. Sharma AK, Kharb R, Kaur R. Pharmacognostical aspects of Calotropis procera (Ait.) R. Br. International Journal of Pharma and Bio Sciences. 2011;2(3):480–8
11. Parihar G, Sharma A, Ghule S, Sharma P, Deshmukh P, Srivastava DN. Anti inflammatory effect of Calotropis procera root bark extract. Asian Journal of Pharmacy and Life Science. 2011;1(1):29–44.
12. Lhinhatrakool T, Satthivaiyakit S. 19-Norand 18, 20-Epoxy cardenolides from the leaves of Calotropis gigantea. Journal of Natural Product 2006; 69(8):1249-1251.
13. Seeka C, Satthivaiyakit S. Cytotoxic cardenolides from the leaves of Calotropis gigantea. Chemical and Pharmaceutical Bulletin 2010; 58(5):725-728.
14. Sen S, Sahu NP, Mahato SB. Flavonolglycosuides from Calotropis gigantea. Phytochemistry 1992; 31 (8):2919-2921.
15. Gupta J, Ali M. Rare Chemical Constituents from Calotropis gigantea roots. Indian Journal of Pharmaceutical Sciences 2000; 62(1):29-32.
16. Anjaneyulu V, Row LR. The triterpenoids of Calotropis gigantea Linn. Current Science 1968; 37(6):156-157.
17. Habib MR, Nikkon F, Rahman M, Haque ME, Karim MR. Isolation of Stigmasterol and βsitosterol from methanolic extract of root bark of Calotropis gigantea. Pakistan Journal of Biological Sciences 2007; 10(22):4174-4176.
18. Abraham KI, Joshi PN. Studies on proteinases from Calotropis gigantea latex. Purification and some properties of two proteinases containing carbohydrate. Biochimica et Biophysica Acta 1979; 568(1):111-119
19. Pal G, Sinha NK. Isolation, crystallization and properties of calotropin D-I and D-II from Calotropis gigantea. Archives of Biochemistry and Biophysics 1980; 202(20):321-329.
20. Pari K, Rao PJ, Devakumar C, Rastogi JN. A Novel Insect antifungal nonprotein amino acid from Calotropis gigantea. Journal of Natural Product 1998; 61(91):102-104.
21. Kumar G, Karthik L, Bhaskara Rao KV, In vitro anti-Candida activity of Calotropis gigantea against clinical isolates of Candida. Journal of Pharmacy Research 2010;3(3):539-
22. Kumar G, Karthik L, Bhaskara Rao KV, Antibacterial activity of aqueous extract of Calotropis gigantea leaves – an in vitro study. International Journal of Pharmaceutical Sciences Review and Research 2010;4(2):141-144.
23. Singh N, Jain NK, Kannojia P, Garud N, Pathak AK, Mehta SC, In vitro antioxidant activity of Calotropis gigantea hydroalcohlic leaves extract. Der Pharmacia Lettre 2010;2(3):95-
24. Pathak AK, Argal A, Analgesic activity of Calotropis gigantea flower. Fitoterapia 2007; 78(1):40-42.
25. Argal A, Pathak AK, CNS activity of Calotropis gigantea roots. J. Ethnopharmacol. 2006; 106(1):142-145.
26. Das S, Das S, Das MK, Basu SP, Evaluation of anti-inflammatory effect of Calotropis gigantea and Tridax procumbens on Wistar albino rats. J. Pharm. Sci. and Res.2009; 1(4):123-126.
27. Deshmukh PT, Fernandes J, Aarte A, Toppo E, Wound healing activity of Calotropis gigantea root bark in rats. J. Ethnopharmacol. 2009; 125(1):178-181.
28. Chitme HR, Chandra R, Kaushik S, Evaluation of antipyretic activity of Calotropis gigantea (Asclepiadaceae) in experimental animals. Phototherapy Research 2005;19(5):454-456.
29. Lodhi G, Singh HK, Pant KK, Hussain Z, Hepatoprotective effects of Calotropis gigantea extract against carbon tetrachloride induced liver injury in rats. Acta. Pharm. 2009; 59:89-96.
30. Alam MA, Habib MR, Nikkon F, Khalequzzaman M, Karim MR, Insecticidal activity of root bark of Calotropis gigantea L. against Tribolium castaneum (Herbst). World Journal of Zoology 2009;4(2):90-95.
31. Adepu A, Narala S, Ganji A, Chilvalvar S. A Review on natural plant: Aerva lanata. Int J Pharma Sci. 2013; 3:398-402.
32. Goyal M, Pareek A, Nagori BP, Sasmal D. Aerva lanata: a review on phytochemistry and pharmacological aspects. Phcog Rev 2011; 5:195-198.
33. Sharma A, Sharma SC, Vaghela JS. Phytopharmacological investigation of Aerva lanata flowers with special emphasis on diuretic activity. Pharmacogn J 2010; 2(17): 59-62
34. Soundararajan P, Mahesh R, Ramesh T, Begum VH. Effect of Aerva lanata on calcium oxalate urolithiasis in rats. Indian J Exp Biol 2006; 44(12): 981-986
35. Sharma A Tarachand, Tanwar M, Nagar N, Sharma AK. Analgesic and anti-inflammatory activity of flowers extract of Aerva lanata. Adv Pharmacol Toxicol 2011; 12(3): 13-18.
36. Chowdhury D, Sayeed A, Islam A, Shah Alam Bhuiyan M, AstaqMohal Khan GR. Antimicrobial activity and cytotoxicity of Aerva lanata. Fitoterapia 2002; 73(1): 92-94.
37. Deshmukh TA, Yadav BV, Badole SL, Bodhankar SL, Dhaneshwar SR. Antihyperglycaemic activity of alcoholic extract of Aerva lanata (L.) A.L. Juss. Ex. J.A. Schultes leaves in alloxan induced diabetic mice. J Appl Biomed 2008; 6(2): 81-87
38. Shirwaikar A, Issac D, Malini S. Effect of Aerva lanata on cisplatin and gentamycin models of acute renal failure. J Ethnopharmacol 2004; 90(1): 81-86.
39. Ramachandra YL, Shilali K, Ahmed M, Sudeep HV, Kavitha BT, Gurumurthy H, et al. Hepatoprotective properties of Boerhaaviadiffusa and Aerva lanata against carbon tetra chloride induced hepatic damage in rats. Pharmacologyonline 2011; 3: 435-441
40. Manokaran S, Jaswanth A, Sengottuvelu S, Nandhakumar J, Duraisamy R, Karthikeyan D, et al. Hepatoprotective activity of Aerva lanata Linn. against paracetamol induced hepatotoxicity in rats. Research J Pharm and Tech 2008; 1(4): 398- 400.
41. Rajesh R, Chitra K, Paarakh PM. In vitro anthelmintic activity of aerial parts of Aerva lanata Linn Juss. Int J Pharm Sci Drug Res 2010; 2(4): 269-271.
42. Singh S, Rai AK, Sharma P, Singh PA. Antidiarrhoeal activity of Aerva lanata in experimentally induced diarrhoea in rats. Pharmacologyonline 2011; 2:921-928
43. India biodiversity. http://indiabiodiversity.org/species/show/32892. 8 Sep, 2014.
44. Nagaratna A, Prakash LH, Harini A. A pharmacological review on Gorakha ganja (Aerva lanata (Linn) Juss. Ex. Schult). Journal of Pharmacognosy and Phytochemistry. 2014; 3:253-257.
45. ITISReport.http://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN and search_value=506581. 8 September, 2014.
46. GBIF Organization. http://www.gbif.org/species/ 3085014/classification. 8 September, 2014.
47. NCBI Resources. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263055/ 8 September, 2014
48. Chunekar KC, Pandey GS. Editor, Bhavapraksha Nighantu of Bhavamishra. Chaukhambha Bharathi Academy, Varanasi, 2010, 103-104
49. Kirtikar KR, Basu BD. Indian Medicinal plants. Edn 2, Vol 3, International Book Distributors, Dehradun, 2065.
50. Guptha AK, Neeraj T, Sharma M. Quality standards of Indian Medicinal Plants. Vol 3, ICMR, New Delhi, 2005, 9-19.
51. Manoj Goyal, Anil Pareek, B.P Nagori and D. Samal, Aerva lanata: a review on phytochemistry and pharmacological aspects, Pharmacognosy Review 2011 July Dec;5,195-198
52. Arunaadepu, Sagarnarala, Ashokganji and Sapnilchilvalvar, A review on natural plant: aerva lanata, International Journal of Pharmascience, 3,2013,398-402
53. Dr. Gopi Krishnamaddikera, Benefits of Aerva lanata
54. Mandallbitachandras, Sastrym. S, Chemical constituents of aerva lanata, Fitoterapia,61,1990,188sta
55. Vetrichelvan T, Jegadeesan M, Senthil Palaniappan M, Murali NP, Sasikumar K. Diuretic and antiinflammatory activities of aervaIanata in rats. Indian J Pharm Sci 2000;62:300-2.
56. Soundararajan P, Mahesh R, Ramesh T, Begum VH. Effect of Aerva lanata on calcium oxalate urolithiasis in rats. Indian J Exp Biol 2006;44:981-6
57. Vetrichelvan T, Jegadeesan M, Senthil P, Murali NP, Sasikumar K. Diuretic and Anti-inflammatory activity of Aerva lanata in rats. Indian Journal of Pharmaceutical Sciences 2000, 300-302.
58. Rajesh R, Chitra K, Paarakh PM. Anti-diabetic and histopathological studies of aerial parts of Aerva lanata linnjuss on streptozotocin induced diabetic rats. World Journal of Pharmacy and Pharmaceutical Sciences 2014; 3(8): 455-471.
59. Nevin KG, Vijayammal PL. Effect of Aerva lanata against hepatotoxicity of carbon tetrachloride in rats. Environ Toxicol Pharmacol 2005; 20:471-7.
Received on 23.07.2022 Modified on 19.11.2022
Accepted on 20.01.2023 ©A&V Publications All right reserved
Res. J. Pharmacology and Pharmacodynamics.2023;15(1):19-23.
DOI: 10.52711/2321-5836.2023.00005