Standardization of Siddha poly herbal formulation Siringipaerathi Chooranam through a scientific method FTIR (Fourier Transform Infrared Spectroscopy)

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INTERNATIONAL JOURNAL OF CURRENT RESEARCH IN CHEMISTRY AND PHARMACEUTICAL SCIENCES (p-issn: 2348-5213: e-issn: 2348-5221) www.ijcrcps.com DOI: 10.22192/ijcrcps Coden: IJCROO(USA) Volume 6, Issue 2-2019 Research Article DOI: http://dx.doi.org/10.22192/ijcrcps.2019.06.02.001 Standardization of Siddha poly herbal formulation Siringipaerathi Chooranam through a scientific method FTIR (Fourier Transform Infrared Spectroscopy) Vijaya Nirmala R 1., Abinaya R 1., Punithavalli V 1., Velpandian V 2. 1 Post Graduate, Department of Gunapadam (Pharmacology), Govt. Siddha Medical College, Chennai. 2 Head of the Department, Department of Gunapadam (Pharmacology), Govt. Siddha Medical College, Chennai. E-mail: drvijiguna@gmail.com Abstract Aim and objective: The aim of the study is to standardize the Siddha poly herbal drug Siringipaerathi Chooranam through the scientific method FTIR. Materials and methods: Siddha system of medicines plays an important role in treating acute and chronic diseases through the herbal preparation. Siringipaerathi Chooranam is the herbal formulation which has been indicated for Jaundice in Siddha classical literature. Thus this trail drug was standardize through FTIR and the results were noted. Results: The instrumental analysis of Siringipaerathi Chooranam through FTIR shows the presence of Alcohol, Amine,, Acid, Alkene, Aromatic, Alkyl Halide, Nitro groups, Ether, Esters. Conclusion: The functional group analysis of Siddha drug Siringipaerathi Chooranam will provide the good information for the biological activity. Keywords: Standardization, Herbs, Siringipaerathi Chooranam, FTIR. Introduction Among the traditional system of medicine Siddha system was explored by the Siddhars in South India that is based on Herbs, metals, and minerals for treating various diseases [1]. Siringipaerathi Chooranam is one of the Siddha poly herbal drug which have the potency of treating Jaundice as mentioned in classical Siddha literature. Characterization of the drug plays a major role in determining the durg for its various aspects. Now a days scientific validation of traditional medicines were important for its safety and efficacy before going to administer in human population. Standardization of poly herbal formulation for characterization is important for the quality of drugs [2].There has been noted that there was a increasing use of traditional medicines in recent decades [3]. 2019, IJCRCPS. All Rights Reserved 1

Materials and Methods Drug selection: for Hepatoprotective activity from the Siddha literature Sarabendra Vaidhiya Muraigal. Soolai, Moola, Kusta, Pitharoga Muraigal, page no: 194-195. In this research paper purified and prepared Siringipaerathi Chooranam was taken as a trial drug Table: 1. Ingredients: Name of drugs Botanical name Quantity Inji Zingiber officinalis 560 gm (16 palam) Milagu Piper nigrum 50.4gm (12 varahan) Thippili Piper longum 33.6gm(8 varahan) Thipili moolam Piper longum 16.8gm(4 varahan) Lavanga pathiri Cinnamomum tamala 35gm(1 palam) Elam Elettaria cardamomum 42gm (10 varahan) Kodiveli ver Plumbago zeylanica 42gm (10 varahan) Lavanga pattai Cinnamomum zeylanicum 35gm (1 palam) Moongil uppu Bambusa arundinaceae 35gm (1 palam) Sandhana thool Santalum album 35gm (1 palam) Vilamichu-ver Plectranthus vettiveroides 35gm (1 palam) Sathikkai Myristica fragrans 35gm (1 palam) Seeragam Cuminum cyminum 35gm (1 palam) Kirambu Syzygium aromaticum 35gm (1 palam) Sugar Saccharum officinarum Equal quantity Nei English Name : Ghee 30ml Collection of the Plant materials: All the raw materials were bought from the Ramasamy Mudhaliyar Store, Parry s corner, Chennai. Identification and Authentication of the drug: All the plant materials were identified and authenticated by the Botanists and Gunapadam experts in Government Siddha Medical College, Arumbakkam, and Chennai-106. Purification of the drugs All the drugs mentioned here were purified as per the Siddha literature [4]. Inji Milagu Thippili Thippilimoolam Lavangapathiri Elam Kodiveli-ver Lavangapattai Sandhana kattai Vilamichu-ver Sathikkai Seeragam Kirambu Outer skin of ginger was peeled off. It was soaked in sour buttermilk for 3 hours and allowed to dry Soaked in lemon juice and allowed to dry. Remove the nodules and dried. Dried in sun light. Roasted in the pan and outer skin was removed. The root was cleaned with a white cloth. Dried in sun light. The skin was peeled off to get purified and powdered The root was cleaned with a white cloth. Cleaned and cut into small pieces and dried. Clean the dust particles and allowed it to dry. Flower buds were removed. Preparation of the Drug: Procedure: In order to obtain the purified form of ginger, the upper skin of ginger was peeled off and then sliced into small 2019, IJCRCPS. All Rights Reserved 2 pieces. The sliced pieces were dried in sunshade for two days. After complete drying 560 grams of dried ginger was taken and fried well in ghee and then powered.

50.4 grams of Purified Pepper, 33.6 grams of Thippili, 16.8 grams of Thipplimoolam, 42 grams of Kodiveliver, 35 grams of Moongil uppu, Lavangapathiri, Sandhana thool, Vilamichu-ver, Lavanga Pattai, Adhikari, Seeragam, Kirambu were taken and powered separately then mixed together with processed ginger powder. Finally, the mixture was ground well which favors the homogenous preparation. Then the mixture powder was sieved through the thin clean white cloth. After that twice the weight of sugar was added to the mixture and again it was ground well. Finally, the end product was obtained, which was kept in an air tight container and labeled as Siringipaerathi Chooranam (SPC) [5]. Purification of the Chooranam: steaming process (Pittaviyal murai) The Siringipaerathi Chooranam was purified by pittaviyal method (steam cooking in milk) as per Siddha classical literature. A mud pot was taken and it was half filled by milk and mixed with equal quantity of pure water. The mouth of the pot was sealed by a cloth. This chooranam was placed over a clean dry cloth and tied firmly around the mouth of mud pot. The gap between mud pots was tied with a wet cloth to avoid evaporation. The mud pot was kept on fire and boiled until the cow s milk reduced in the lower pot. The same drug was later dried and powdered then sieved again. It was used for the further study [6]. Storage of the drug: The prepared test drug was stored in a clean, air tight glass container. Administration of the drug: Form of the medicine : Chooranam Route of Administration : Enteral Dose : 2 gm twice a day depending on the severity Adjuvant : honey Indication: Kamaalai, Marbuvali, Kirani, Suram, Vaanthi, Peenisam. Experiment regarding details: Sophisticated instrumental analysis FT-IR (Fourier Transform Infra-Red) Fig: 1 FTIR-Instrument Fig: 2 FTIR-Mechanisms 2019, IJCRCPS. All Rights Reserved 3

Model : Spectrum one: FT-IR Spectrometer Scan Range : MIR 450-4000 cm-1 Resolution : 1.0 cm-1 Sample required : 50 mg, solid or liquid. FTIR analysis was done at SAIF, IIT Madras. IR data was acquired using Perkin elmer FT-IR spectrometer. For sampling techniques, KBr method (Price, 1972) was followed. It is the preferred method of infrared spectroscopy. FT-IR is an important and more advanced technique. It is used to identify the functional group, to determine the quality and consistency of the sample material and can determine the amount of compounds present in the sample. It is an excellent tool for quantitative analysis. In FT-IR infrared is passed from a source through a sample. This infrared is absorbed by the sample according to the chemical properties and some are transmitted. The spectrum that appears denotes the molecular absorption and transmission. It forms the molecular fingerprint of the sample. Like the finger print there is no two unique molecular structures producing the same infrared spectrum. It is recorded as the wavelength and the peaks seen in the spectrum indicates the amount of material present. FT-IR is the most advanced and the major advantage is its Speed Sensitivity Mechanical Simplicity Internally Calibrated [7] Results and Discussion Instrumental analysis 100.0 95 90 85 80 Siringi PChoor 2354 2070 816 75 774 70 65 60 55 880 468 665 576 614 524 711 %T 50 45 40 35 30 25 20 15 10 5 3415 2923 2853 1635 1512 1324 1375 1245 1036 1454 0.0 4000.0 3600 3200 2800 2400 2000 1800 1600 1400 1200 1000 800 600 450.0 Cm-1 Fig: 3 FT-IR (Fourier Transform Infra Red spectroscopy) 2019, IJCRCPS. All Rights Reserved 4

FTIR Siringipaerathi Chooranam. Table: 2. FT-IR Absorption peak cm -1 Stretch Functional group 3415 O-H Stretch, bonded N-H Stretch Alcohol Amine 2923 C-H Stretch O-H Stretch Acid 2853 C-H Stretch O-H Stretch Acid 1635 N-H Bending C=C Stretch Amide 1512 C=C Stretch C-Br Stretch Aromatic Alkyl Halide 1454 C=C Stretch -C-H Bending Aromatic 1375 -C-H Bending C-F Stretch N-O Stretch Alkyl Halide Nitro 1324 C-F Stretch Nitro 1245 C=O Stretch C-N Stretch C-O Stretch Acid Amine Ether 1036 C-O Stretch C=O Stretch Ether Ester 880 ==C-H Bending Alkene 816 ==C-H Bending Alkene 774 C-Cl Stretch Alkyl Halide 711 C-Cl Stretch ==C-H Bending Alkyl Halide Alkene 665 C-Cl Stretch Alkyl Halide 614 C-Cl Stretch Alkyl Halide 576 C-Br Stretch Alkyl Halide 524 C-Br Stretch Alkyl Halide 468 C-Br Stretch Alkyl Halide Interpretation FTIR instrumental analysis was done. The test drug was identified to have 15 peaks. They are the functional groups present in the trial drug Siringipaerathi Chooranam. The above table shows the presence of amide, phenols, alkanes, alkyl halide, acid, aromatic, ester, ether and alcohol groups which represents the peak value. OH group has higher potential towards inhibitory activity against microorganisms. Amines enhance the drug effect against the disease [8]. Conclusion The data observed from the FTIR characterization helps to standardize the Siddha poly herbal formulation Siringipaerathi Chooranam with its functional group. The functional groups identified from FTIR will give a better solution for clinical trails. Phenols possess highly Anti-Oxidant property which enhances the drug effect against the disease. 2019, IJCRCPS. All Rights Reserved 5

References 1. Urmila Thatte, Clinical Research Ayurvedic Medicines. Pharma Times, 2005; 37(7): 9-12. 2. Yadav NP, Dixit VK. Int J Integr Biol 2008;2:195-203. 3. Sathiyarajeswaran P et al., Powder Diffraction fingerprints on cinnabar and its preparations. Journal of Siddha, 2009; 2(1): 29-33. 4. M.Shanmugavelu, Noinadal Noimudhal Nadal Thirattu, Department of Indian Medicine and Homoeopathy, 3rd edition, Chennai-106, Page no: 119. 5. S.Venkatrajan, Sarabendra Vaidhiya Muraigal, Soolai, Moola, Kusta, Pitharoga Muraigal, Saraswathi Mahal Noolagam, 2nd edition, 2000, page no: 194-195. 6. K.George Mathew and Praveen Aggarwal, Prep Manual for Undergraduates, Medicine, Elsevier, 2nd Edition; 2014; Page no: 349. 7. Fourier Transform Infrared Spectroscopy (FTIR) Analysis [INTERNET]; Available from http://www.intertek.com/analysis/ftir/ 8. J.M.O'Reilly, R.Mosher, Functional groups in carbon black by FTIR spectroscopy [INTERNET];1983; from http://www.sciencedirect.com/science/article/pii/000 8622383901550. Access this Article in Online Website: www.ijcrcps.com Subject: Siddha Medicine Quick Response Code DOI: 10.22192/ijcrcps.2019.06.02.001 How to cite this article: Vijaya Nirmala R, Abinaya R, Punithavalli V, Velpandian V. (2019). Standardization of Siddha poly herbal formulation Siringipaerathi Chooranam through a scientific method FTIR (Fourier Transform Infrared Spectroscopy). Int. J. Curr. Res. Chem. Pharm. Sci. 6(2): 1-6. DOI: http://dx.doi.org/10.22192/ijcrcps.2019.06.02.001 2019, IJCRCPS. All Rights Reserved 6