3 research outputs found

    DEVELOPMENT OF TLC FINGERPRINTING PROFILE OF SHADANGA PANIYA – AN AYURVEDIC FORMULATION TO TREAT SYMPTOMS OF COVID-19

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    BACKGROUND: Shadanga Paniya is a compound Ayurvedic formulation that contains six ingredients. Ayurvedic Physicians have been using Shadanga Paniya to treat fever for ages. Symptoms of COVID-19 are also being treated by Shadanga Paniya. However, the Shadanga Paniya has not reported standardisation. AIMS: To prepare Shadanga Paniya as per the standard classical protocol. To carry out qualitative tests, standardisation and TLC profile development for Shadanga Paniya. MATERIALS AND METHODS: All the ingredients of Shadanga Paniya wiz. Nagarmotha, Pittapapada, Khasa, Lal Chandana, Sugandhbala and Sunthi were taken in equal amounts. All these ingredients are heated over mild heat with water. The filtration of liquid Shadanga Paniya is carried out after completing proper deduction. Shadanga Paniya was subjected to organoleptic tests. Qualitative tests, physicochemical parameters and thin layer chromatography studies were also carried out. The comparative TLC studies of Shadanga Paniya was carried out with its ingredients. RESULTS: Organoleptic tests of Shadanga Paniya showed that the colour of the liquid was reddish-brown, and the liquid was clear. It has a characteristic odour with an astringent taste. Qualitative analysis showed the presence of flavonoids, carbohydrates, saponin, phenols and glycosides. Test sample parameters revealed a total solids content (0.812 % w/v) and specific gravity (1.0083). The test sample has a Refractive index (1.334) and pH (4.2). The Thin Layer Chromatography study exhibited 3 bands at 254 nm and 366 nm. After spray, it showed 7 bands under 254 nm and 366 nm. The comparative TLC studies showed the similarities between Shadanga Paniya and its ingredients. CONCLUSION: The typical type of solvent system [Toluene: Ethyl acetate: Formic acid: Methanol (6:3:0.1:1)] is shows the proper separation in Shadanga Paniya. Therefore, the findings of the present study may be found helpful to standardise Shadanga Paniya

    ANTI-INFLAMMATORY ACTIVITY OF WILD AND CULTIVATED VARIETIES OF ERANDA (RICINUS COMMUNIS LINN.) ROOT

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    In Ayurveda, Eranda (Ricinus communis Linn; Euphorbiaceae) root is highlighted for its anti-inflammatory and analgesic action and used as one of the ingredient in many compound formulations. Ricinus communis L. is available both in wild as well as cultivated state. Due to its high demand and less supply of wild variety root, its cultivated variety is fulfilling the market demand. Hence, the present study is carried to evaluate the anti-inflammatory activity of both the varieties of Eranda root. Decoction of both wild and cultivated varieties of Eranda root (10.8 ml/kg) were taken as test drugs, Phenyl butazone (100 mg/kg) as reference standard and experiment was carried out on Wistar strain albino rats following carrageenan induced paw edema model. Students unpaired t test was applied for analyzing the obtained data, after one, three and five hours. Wild variety root decoction, at studied dose (10.8 ml/kg) level, showed marked decrease in paw edema, in comparison to normal control rats, after one hour (25.25%) and five hours (27.79%) of carrageenan injection. The wild variety root provides additional anti-inflammatory effect, in comparison to reference standard (in percentage form), after one hour (13.63%) and five hours (22.18%) whereas the cultivated variety decreased the inflammation after one hour (15.15%) and increase the inflammation after five hours (02.50%). Decoction of wild variety, of Ricinus communis L. root provided considerable suppression of carrageenan induced paw edema compared to its cultivated variety

    Drug utilization pattern of antiseizure drugs and their adverse effects in the pediatric population, in a tertiary care hospital attached to a medical college

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    Background: Epilepsy is “a condition characterized by recurrent (two or more) seizure, unprovoked by any immediate identified cause.” The desired outcome of antiseizure drug (ASD) therapy is to be seizure-free throughout the rest of life. The objective was to study the utilization pattern and adverse drug reactions (ADRs) associated with the use of ASDs in pediatric outpatients in epilepsy clinic.Methods: This cross-sectional, observational and single center study was carried out over a period of 1 year in 430 pediatric patients. Analyzed data included demographic details and drugs prescribed in respective seizure types along with ADRs due to ASDs. Results: In a total 430 patients analyzed, seizure were most commonly observed in boys (69.8%) in 6-10 year of age (45.3%), with a positive family history in (16%), with no specific cause of seizure in (71.6%), with most common type was focal seizure in (62.3%), which was mainly treated with carbamazepine (73.8%). Most common ADR was irritability (32.2%) with Valproate being main drug. 87.3% ADRs were in “ possible” as per World Health Organization causality assessment scale, 94.9% ADRs were “mild” as per Hartwig and Siegel severity assessment scale and 98.3% ADRs were “preventable” as per Schumock and Thornton preventability scale.Conclusion: Focal seizure was most common type of seizure observed mainly in boys of 6-10 year with carbamazepine as mainly prescribed drug. Use of appropriate ASDs in the majority of patients as per guidelines, has decreased number of ADRs in our study. Prescribing drugs were mainly from essential drug list and by generic names
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