Open Access Open Access  Restricted Access Subscription Access

Formulation, Standardization, and Preclinical Evaluation of Polyherbal Suspension against Inflammatory Bowel Disease


Affiliations
1 QVIA RDS (India) Private Limited, Bangalore – 560103, Karnataka, India
2 Department of Pharmacology, SRM College of Pharmacy, SRMIST, Kattankulathur, Chengalpattu – 603203, Tamil Nadu, India
3 Labcorp Scientific Services and Solutions Private Limited, Mumbai – 400093, Maharashtra, India
 

The pharmacological healing for inflammatory bowel diseases continues to be uncertain and requires immediate therapeutic interventions. A poly-herbal formulation obtained from a traditional and authentic classic text of Ayurveda was assessed for its effect against IBD (inflammatory bowel disease) in this study. The formulated poly-herbal suspension comprises three different drugs namely, Burma dhaniya (Eryngium foetidum), Sapota (Manilkara zapota), and Curry leaves (Murraya koenigii). The formulated suspension was evaluated for certain standard parameters like organoleptic and accelerated stability studies at various temperatures. It was checked for its efficacy by oral route in acetic acid-induced colitis affected Balb/c mice. Mice were orally administered with formulated suspension (275 mg/kg, 550 mg/kg,), every 24 hours for 10 days. Histopathology, macroscopic damage score, myeloperoxidase (MPO) activity, and red blood cell parameters were evaluated after treatment. Reduction in the MPO activity, decrease in the macroscopic damage scores, and an increase in RBC cell count were seen distinctly at a high dose of 550 mg/Kg. The results obtained, established the effectiveness of the poly-herbal suspension against inflammatory bowel disease by treating the mice from acetic acid-induced colitis by reducing inflammation and oxidative damage to the colon. The maximum therapeutic effective activity was found to be 550 mg/kg for IBD mice.


Keywords

Acetic Acid, Inflammatory Bowel Disease, Myeloperoxidase, Polyherbal Suspension, Ulcerative Colitis.
Font Size

User

Notifications
JOURNAL COVERS
  

  • Salminen S, Bouley C, Boutron MC, Cummings JH, Franck A, Gibson GR, et al. Functional food science and gas- trointestinal physiology and function. Br J Nutr. 1998; 80(S1):S147–71. https://doi.org/10.1079/BJN19980108. PMid:9849357
  • Riddle MS, Tribble DR, Cachafiero SP, Putnam SD, Hooper TI. Development of a travelers’ diarrhea vaccine for the mil- itary: How much is an ounce of prevention really worth?. Vaccine. 2008; 26(20):2490–502. https://doi.org/10.1016/j. vaccine.2008.03.008. PMid:18417259
  • Loddo I, Romano C. Inflammatory bowel disease: genet- ics, epigenetics, and pathogenesis. Front Immunol. 2015; 6:551. https://doi.org/10.3389/fimmu.2015.00551. PMid:26579126. PMCid:PMC4629465
  • Schicho R, Shaykhutdinov R, Ngo J, Nazyrova A, Schneider C, Panaccione R, et al. Quantitative metabolomic profil- ing of serum, plasma, and urine by 1H NMR spectroscopy discriminates between patients with inflammatory bowel disease and healthy individuals. J. Proteome Res. 2012; 11(6):3344–57. https://doi.org/10.1021/pr300139q. PMid:22574726. PMCid:PMC3558013
  • Mu L, Liu L, Niu R, Zhao B, Shi J, Li Y, et al. Indoor air pollution and risk of lung cancer among Chinese female non-smokers. Cancer Causes and Control. 2013; 24(3):439–50. https://doi.org/10.1007/s10552-012-0130-8. PMid:23314675. PMCid:PMC3574203
  • Vojinovic J. Vitamin D receptor agonists’ anti‐inflammatory properties. Ann N Y Acad Sci. 2014; 1317(1):47–56. https:// doi.org/10.1111/nyas.12429. PMid:24754474
  • Yamamoto T, Nakahigashi M, Saniabadi AR. Review arti- cle: diet and inflammatory bowel disease-epidemiology and treatment. Aliment Pharmacol Ther. 2009; 30(2):99– 112. https://doi.org/10.1111/j.1365-2036.2009.04035.x. PMid:19438426
  • Kaufmann WE, Worley PF, Pegg J, Bremer M, Isakson P. COX-2, a synaptically induced enzyme, is expressed by excitatory neurons at postsynaptic sites in rat cerebral cortex. Proc Natl Acad Sci U.S.A. 1996; 93(6):2317–21. https://doi.org/10.1073/pnas.93.6.2317. PMid:8637870. PMCid:PMC39793
  • Ricciotti E, FitzGerald GA. Prostaglandins and inflamma- tion. Arterioscler Thromb Vasc Biol. 2011; 31(5):986–1000. https://doi.org/10.1161/ATVBAHA.110.207449. PMid:21508345. PMCid:PMC3081099
  • Izard CE. Four systems for emotion activation: Cognitive and noncognitive processes. Psychol Rev. 1993; 100(1):68. https://doi.org/10.1037/0033-295X.100.1.68. PMid:8426882
  • Miller GE, Chen E, Zhou ES. If it goes up, must it come down? Chronic stress and the hypothalamic-pituitary-adrenocor- tical axis in humans. Psychol Bull. 2007; 133(1):25. https:// doi.org/10.1037/0033-2909.133.1.25. PMid:17201569
  • Gowri SS, Vasantha K. Phytochemical screening and anti- bacterial activity of Syzygium cumini (L.)(Myrtaceae) leaves extracts. Int J Pharm Tech Res. 2010; 2(2):1569–73.
  • Farnsworth NR. Biological and phytochemical screening of plants. J Pharm Sci. 1966; 55(3):225–76. https://doi. org/10.1002/jps.2600550302. PMid:5335471
  • Niu X, Fan T, Li W, Huang H, Zhang Y, Xing W. Protective effect of sanguinarine against acetic acid-induced ulcer- ative colitis in mice. Toxicol Appl Pharmacol. 2013; 267(3):256–65. https://doi.org/10.1016/j.taap.2013.01.009. PMid:23352506
  • Krawisz JE, Sharon P, Stenson WF. Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity: Assessment of inflammation in rat and hamster models. Gastroenterology. 1984; 87(6):1344–50. https://doi. org/10.1016/0016-5085(84)90202-6
  • Tsikas D. Analysis of nitrite and nitrate i biological flu- ids by assays based on the Griess reaction: Appraisal of the Griess reaction in the l-arginine/nitric oxide area of research. J Chromatogr B. 2007; 851(1–2):51–70. https:// doi.org/10.1016/j.jchromb.2006.07.054. PMid:16950667
  • Masoodi I, Kochhar R, Dutta U, Vaishnavi C, Prasad KK, Vaiphei K, et al. Fecal lactoferrin, myeloperoxidase and serum C-reactive are effective biomarkers in the assess- ment of disease activity and severity in patients with idiopathic ulcerative colitis. J Gastroenterol Hepatol. 2009; 24(11):1768–74. https://doi.org/10.1111/j.1440- 1746.2009.06048.x. PMid:20136960
  • Lih-Brody L, Powell SR, Collier KP, Reddy GM, Cerchia R, Kahn E, et al. Increased oxidative stress and decreased anti- oxidant defenses in mucosa of inflammatory bowel disease. Dig Dis Sci. 1996; 41:2078–86. https://doi.org/10.1007/ BF02093613. PMid:8888724
  • Krawisz JE, Sharon P, Stenson WF. Qualitative assay for acute intestinal inflammation based on myeloperoxidase activity. Gastroenterology. 1984; 87:1344–50. https://doi.org/10.1016/0016-5085(84)90202-6
  • Arnhold J. Properties, functions and secretion of human myeloperoxidase. Biochemistry. 2004; 69:4–9. https://doi.org/10.1023/B:BIRY.0000016344.59411.ee. PMid:14972011
  • Elson CO, Sartor RB, Tennyson GS, Riddell RH. Experimental models of inflammatory bowel disease. Gastroenterology. 1995; 109:1344–67. https://doi.org/10.1016/0016-5085(95)90599-5
  • Sharon P, Stenson WF. Metabolism of arachidonic acid in acetic acid colitis in rats. Gastroenterology. 1985; 88:55–63.https://doi.org/10.1016/S0016-5085(85)80132-3
  • McQuaid KR. Drug used in treatment of gastrointestinal disease. In: Katzung BG, Master SB, Trever AJ, editors. Basic and Clinical Pharmacology. 12th ed. New York: McGraw Hill- Lange; 2012. p. 1081–108.
  • Billerey- Larmonier C, Uno JK, Larmonier N, Midura AJ, Timmermann B, Ghishan FK, et al. Protective effects of dietary curcumin in mouse model of chemically induced colitis are strain dependent. Inflamm Bowel Dis. 2008; 14(6):780–93. https://doi.org/10.1002/ibd.20348 PMid:18200517. PMCid:PMC4427520
  • Calixto JB. Efficacy, safety, quality control, marketing and regulatory guidelines for herbal medicines (phytothera- peutic agents). Braz J Med Biol Res. 2000; 33(2):179–89. https://doi.org/10.1590/S0100-879X2000000200004. PMid:10657057
  • Rodrigues TLM, Castro GLS, Viana RG et al. Physiological performance and chemical compositions of the Eryngium foetidumL.(Apiaceae)essentialoilcultivatedwithdifferent fertilizer sources. Nat Prod Res. 2021; 35:5544–8. https:// doi.org/10.1080/14786419.2020.1795653. PMid:32691619
  • Fayek NM, Monem AR, Mossa MY, Meselhy MR, Shazly AH. Chemical and biological study of Manilkara zapota (L.) van Royen leaves (Sapotaceae) cultivated in Egypt. Pharmacognosy Res. 2012; 4:85–91. https:// doi.org/10.4103/0974-8490.94723. PMid:22518080. PMCid:PMC3326762
  • Srinivasan K. Role of spices beyond food flavoring: Nutraceuticals with multiple health effects. Food Rev Int. 200; 21:167–88. https://doi.org/10.1081/FRI-200051872

Abstract Views: 149

PDF Views: 91




  • Formulation, Standardization, and Preclinical Evaluation of Polyherbal Suspension against Inflammatory Bowel Disease

Abstract Views: 149  |  PDF Views: 91

Authors

Prerna Dubey
QVIA RDS (India) Private Limited, Bangalore – 560103, Karnataka, India
Rukaiah Fatma Begum
Department of Pharmacology, SRM College of Pharmacy, SRMIST, Kattankulathur, Chengalpattu – 603203, Tamil Nadu, India
V. Chitra
Department of Pharmacology, SRM College of Pharmacy, SRMIST, Kattankulathur, Chengalpattu – 603203, Tamil Nadu, India
R. Mrinalini
Department of Pharmacology, SRM College of Pharmacy, SRMIST, Kattankulathur, Chengalpattu – 603203, Tamil Nadu, India
Harini Gunasekaran
Labcorp Scientific Services and Solutions Private Limited, Mumbai – 400093, Maharashtra, India
M. Sumithra
Department of Pharmacology, SRM College of Pharmacy, SRMIST, Kattankulathur, Chengalpattu – 603203, Tamil Nadu, India

Abstract


The pharmacological healing for inflammatory bowel diseases continues to be uncertain and requires immediate therapeutic interventions. A poly-herbal formulation obtained from a traditional and authentic classic text of Ayurveda was assessed for its effect against IBD (inflammatory bowel disease) in this study. The formulated poly-herbal suspension comprises three different drugs namely, Burma dhaniya (Eryngium foetidum), Sapota (Manilkara zapota), and Curry leaves (Murraya koenigii). The formulated suspension was evaluated for certain standard parameters like organoleptic and accelerated stability studies at various temperatures. It was checked for its efficacy by oral route in acetic acid-induced colitis affected Balb/c mice. Mice were orally administered with formulated suspension (275 mg/kg, 550 mg/kg,), every 24 hours for 10 days. Histopathology, macroscopic damage score, myeloperoxidase (MPO) activity, and red blood cell parameters were evaluated after treatment. Reduction in the MPO activity, decrease in the macroscopic damage scores, and an increase in RBC cell count were seen distinctly at a high dose of 550 mg/Kg. The results obtained, established the effectiveness of the poly-herbal suspension against inflammatory bowel disease by treating the mice from acetic acid-induced colitis by reducing inflammation and oxidative damage to the colon. The maximum therapeutic effective activity was found to be 550 mg/kg for IBD mice.


Keywords


Acetic Acid, Inflammatory Bowel Disease, Myeloperoxidase, Polyherbal Suspension, Ulcerative Colitis.

References





DOI: https://doi.org/10.18311/jnr%2F2022%2F29781