Littérature scientifique sur le sujet « Raththa kothippu »

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Articles de revues sur le sujet "Raththa kothippu"

1

Sivalathajini, Dr S., Dr A. Manoharan, and Dr S. Umakalyani. "Physicochemical and Phytochemical Evaluation of Siddha formulation Saaranai chooranam." Middle East Journal of Applied Science & Technology 06, no. 02 (2023): 76–84. http://dx.doi.org/10.46431/mejast.2023.6209.

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Background: Siddha system of medicine depends largely on herbal for the treatment of diseases which was practiced at village levels and now becomes an important medicine in worldwide, According to the Akasthiyar -2000-Part– III textbook, Saaranai Chooranam is a herbal drug that is indicated for Raththa kothippu (Systemic Hypertension) Saaranai is the Tamil name for Trianthema portulacastrum, which belongs to the family Aizoaceae. Aim & Objective: This study primarily aims to evaluate the Physicochemical and Phytochemical evaluation of Saaranai Chooranam, Preliminary Phytochemical analysis such as High Performed Thin Layered Chromatography and Powder Microscopy of Saaranai Chooranam. Methodology: The Physicochemical analysis of Saaranai Chooranam is carried out using standard procedures. Results: Preliminary Phytochemical screening found, the presence of phytochemicals such as Proteins, Terpenoids, Alkaloids, Carbohydrates, and Tannins. High-performance thin-layer chromatography fingerprinting revealed the presence of many phytochemicals with different Rf values and densitometric scans of the plates showed numerous bands and peaks. The Powder Microscopy reveals the presence ofTracheidal fibre, Vessel with bordered pits, Calcium oxalate crystal, Stone cell, Group of sclereids with brownish content, Paracytic stomata and surrounding subsidiary cells, Rosette Calcium oxalate crystal, Sclereid with narrow lumen, Thick walled cells, Tracheidal fibre and Trichome. Physicochemical analysis revealed the values of total ash (17.86%), acid-insoluble ash (1.34%), water-soluble ash (13.62), sulphated ash (25.72%), pH (6.05 in 4% alcohol solution), volatile oil (0.5%), foaming index (111.11%) and swelling index (4ml). Conclusion: This study is an effort to explore the different Physico and Phytochemical compounds of Saaranai Chooranam effective in the management of Raththa kothippu (Systemic hypertension).
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Sivalathajini, S. "Hypolipidemic Activity of Saaranai Chooranam Against Atherogenic Diet Induced Hyperlipidemia in Experimental Rats in the Management of Raththa Kothippu (Systemic Hypertension)." Galore International Journal of Applied Sciences and Humanities 9, no. 1 (2025): 1–9. https://doi.org/10.52403/gijash.20250101.

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In worldwide Siddha system of medicine nowadays become most important medicine, it has fewer side effects in chronic usage. Therefore, in medicines of Siddha system should emphasis their Indications, Contraindications and cautions. The trial drug Saaranai chooranam has been mentioned in siddha literature of “Agasthiyar erandayiram – Part-III” for the management of Raththa kothippu (Systemic hypertension). Primary objective of study to evaluate the Hypolipidemic activity of saaranai chooranamagainst atherogenic diet induced hyperlipidemia in experimental rats. This Observational in vivo study carried out Arulmigu Kalasalingam College of Pharmacy, Tamil Nadu, India. The trial drug contains equal ratio of Saaranai Root and Inthuppu, with adjuvant Ghee or Jagarry. All animals starved for 18 hours and provided water ad libitumbefore the experiment. The animals were divided into five groups of six rats each. Group I served as normal control administered with 2% Carboxy Methyl Cellulose only, Group II served as hyperlipidemic control rats received atherogenic diet, Group III and IV served as test groups received Saaranai Chooranam 200mg/kg and Saaranai Chooranam 400mg/kg respectively. Group V served as Atorvastatin (10mg/kg/day) considered as standard. All the groups except the normal control group administered received atherogenic diet After inducing the hyperlipidemia, the respective treatment was continued for 7 days. Animals were given standard pellet diet and water ad libitum. The next day after the completion of experimental study, the blood was taken from the rats, Liver lipid extraction, Biochemical analysis, Histopathology. The data were statistically analyzed by one-way ANOVA followed by Dennett’s t-test, and value P < 0.05 was considered to be significant. The results obtained from the pharmacological screening have led to the conclusions that, Saaranai chooranam has significant antihyperlipidemic activity. Hence it can be exploited as antihyperlipidemic therapeutic agent or adjuvant in existing therapy for the treatment of hyperlipidemia. Keywords: Saaranai chooranam, Raththa kothippu, Hyperlipidemia, Akasthiyar erandayirum.
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Dr., S. Sivalathajini*. "Vasodilation Activity of Saaranai Chooranam in Experimental Rats (In Vivo) In the Management of Raththa Kothippu (Systemic Hypertension)." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 4423–27. https://doi.org/10.5281/zenodo.15521204.

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Siddha Medicine is a one of the most popular medicines in nowadays, it has so many drugs using complete cure of the particular diseases. The trial drug <em>Saaranai chooranam</em> has been mentioned in siddha literature of <em>&ldquo;Agasthiyar erandayiram &ndash; Part-III&rdquo;</em> for the management of <em>Raththa kothippu</em> (Systemic hypertension). Primary objective of study to evaluate the Vaso dialation activity of <em>Saaranai chooranam </em>in experimental rats. This Observational in vivo study carried out Arulmigu Kalasalingam College of Pharmacy, Tamil Nadu, India. The trial drug contains equal ratio of <em>Saaranai </em>Root and <em>Inthuppu,</em> with adjuvant Ghee or Jagarry. Vasodilation drugs frequently used to treat Systemic Hypertension. A decrease in both diastolic and systolic pressures was observed after <em>Saaranai Chooranam</em> at doses of 200 and 400 mg/kg. The hypotensive response to <em>Saaranai Chooranam</em> could be mediated not only by a central effect but also by a direct effect on the vessels. Effects of <em>Saaranai Chooranam</em> on blood pressure investigated whether it would interfere with the arterial blood pressure of Wistar rats. Rapid and transitory reductions of systolic and diastolic pressures were observed in at doses higher than 100 mg/kg, shows a typical recording of arterial blood pressure before and after treatment of drugs 200 and 400 mg/kg of <em>Saaranai Chooranam</em>. Systolic and diastolic pressures were significantly reduced respectively. Our results suggest that <em>Saaranai Chooranam</em> probably is responsible for the vasodilator activity.
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Sivalathajini, Dr S., Dr A. Manoharan, and Dr S. Umakalyani. "Evaluation of Herbal Formulation of Saaranai Chooranam Through Fourier Transform Infrared Spectroscopic Study." Asian Journal of Basic Science & Research 05, no. 02 (2023): 40–45. http://dx.doi.org/10.38177/ajbsr.2023.5204.

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Background: The Siddha system of medicine is purely scientific and the peculiar complex system of science and philosophy. Fourier Transform Infrared Spectroscopy (FTIR) is certainly one of the most important analytical techniques for herbal medicine. FTIR can be implemented during herbal drug development in production for process monitoring or in quality control laboratories. Aim &amp; Objective: The aim of study is to evaluate the morphology and elemental characterization of the Saaranai chooranam. The functional groups of their formulations are analysed through FTIR spectroscopy and the biological roles of the functional groups are discussed in this study. Materials and methods: The raw drugs is collected and purified as per Siddha literature. Drug Saaranai chooranam, which has been illustrated in the text Dr.S.Venkattarajan, Akasthiyar-2000, Part – III, Page: 102, for the management of Raththa Kothippu (Systemic Hypertension). Results: The Fourier Transform Infrared Spectroscopy compounds showed the presence of functional groups O-H Stretching (Alcohol), C-H Stretching (Alkane), O=C=O Stretching (Carbon dioxide), C-C bending (Alkene), O-H bending (Carboxylic acid), C-O Stretching (Aromatic ester), C-O Stretching (Tertiary alcohol), S=O Stretching (Sulfoxide), C-H bending (1,2-disubstituted) and C-1 Stretching (Halo compound) which ensures the therapeutic effect of the drug. Conclusion: The instrumental analysis FT-IRS study of Saaranai chooranam is the presence of functional groups through the stretch and bends which is responsible for its functional activity. The functional groups in Saaranai chooranam have diuretic and nervin tonic activities. This will ensure the efficacy and therapeutic effect of the drug.
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Preyadarsheni K and Komalavalli T. "Standardization of Siddha Herbal Formulation - Vaasathi Kashayam According to PLIM Guidelines." International Journal of Ayurveda and Pharma Research, November 20, 2024, 26–40. https://doi.org/10.47070/ijapr.v12i10.3404.

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Despite the fact that the global market for herbal and traditional medicines has surged, the rise in demand has brought about a threat for adulteration/substitution of raw drugs, clamoring consumers' faith into skepticism with the ensuing implications. To evaluate and avoid substandard herbal medicine manufacture, the Indian government has taken stringent measures, notably the establishment of PLIM (Pharmacopeial Laboratory of Indian Medicine - Protocol for testing AYUSH pharmaceuticals). The purpose of this research is the standardization of Siddha herbal decoction formulation 'Vaasathi kashyam' encompassing the leaves of Justicia adhatoda.L (Acanthaceae) and dry fruits of Vitis vinifera.L (Vitaceae) procured from the classic Siddha text 'Agathiyar 2000' specifically indicated for systemic hypertension (Raththa kothippu noi). The physicochemical parameters, phytochemical analysis, and powder microscopy of Vaasathi kashayam revealed an acidic pH and demonstrated the presence of phytochemicals such as tannins, phenols, terpenoids, alkaloids, flavonoids, and carbohydrates. HPTLC fingerprinting illustrates phytochemical spikes. Furthermore, the number of heavy metals, pesticide residues (organochlorine, organophosphorus and pyrethroids) and aflatoxins in VK was trace (BQL) or nonexistent, indicating its safety for therapeutic use. The total aerobic bacterial count and yeast/mold growth reported no growth/colonies, implying that the sample is free of aerobic microorganisms. Standardization of VK entailed authenticating along with evaluating the safety and quality of the prepared VK sample. These standardized characteristics could be deployed as a reference standard to guide subsequent VK qc evaluations.
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