Screening of Phytochemistry and Secondary Metabolites: A Case Study on Nyctanthes arboritis

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Research Article Screening of Phytochemistry and Secondary Metabolites: A Case Study on Nyctanthes arboritis *B. Ramachandran, M. Kamaraj, V. Subramani, J. Jerome Jeyakumar PG and Research Department of Botany, Jamal Mohamed College (Autonomous), Thiruchirappalli 620020, Tamilnadu, India. ABSTRACT Medicinal plants are sources of important therapeutic aids for alleviating human ailments. In a survey to see the scientific understanding behind its medicinal value, an attempt is made in this study, to analyze major bioactive s present in the ethanol extract from Nyctanthes arbors by GC-MS. The phytochemical constituent of plant leaf ethanolic extract contains steroids, phenol, alkaloids, saponin, tannin and flavonoids. GC-MS analysis were reveals the presence of 5 s such as Ar-turmerone, Curlone, Dibutyl phthalate, Hexadecanoic acid, ethyl ester, 9-Octadecenioc acid, ethyl ester and 1, 2- Benzenedicarboxylic acid, disooctyl ester. The ethanolic extract of Nyctanthes arboritis possess various potent bioactive s and is recommended as a plant of phyto-pharmaceutical importance. Keywords: Nyctanthes arboritis, GC-MS, phytochemical constituents, ethanol extract Received 22 Feb 2014 Received in revised form 07 March 2014 Accepted 09 March 2014 *Address for correspondence: B. Ramachandran, PG and Research Department of Botany, Jamal Mohammed College, Tiruchirappalli, Tamil Nadu - 620 020, India. E-mail: san6061@gmail.com INTRODUCTION Natural remedies from medicinal plants are ground to be safe and efficacious. Many flora species have been used in folkloric medicine to care for several complaints. Granting to the World Health Organization (WHO) in 2008, more than 80% of the world's population rely on traditional medical specialty for their primary health maintenance needs. Higher plants as sources of bioactive s continue to take on a predominant part in the maintenance of human wellness. Accounts available on green plants represent a reservoir of effective chemotherapeutants; these are non-phytotoxic, more systemic and easily biodegradable. A cognition of the chemical elements of plants is suitable not only for the discovery of curative factors, but as well because such information may be of great value in revealing new sources of economic phytos for the synthesis of complex chemical substances and for identifying the genuine significance of folkloric remedies. Nyctanthes arboritis linn. (Division: Magnoliophyta; Class: Magndiopsida; Order: Lamiales; Family: Oleaceae) is normally known as night jasmine and is a common plant in India. It is distributed wild in sub-himalayan region and also found in Indian gardens as an ornamental plant. It is employed in traditional medicine as Stomachic, carminative, piles various skin diseases, hair tonic and used for treatment of cancer [1]. Several pharmacopoeia containing monographs of the plant materials describes only the physicochemical parameters. GC-MS is the best technique to identify the bioactive components of long chain hydrocarbons, alcohols, acid. Used in the analysis of the herbal medicines, there are at least two significant advantages for GC MS, that is: (1) with the capillary column, GC MS has in general very good separation ability, which can produce a chemical fingerprint of high quality; (2) with the coupled mass spectroscopy and the corresponding mass spectral database, the qualitative/quantitative composition information of the herb investigated could B Ramachandran et.al, IJPRR 2014; 3(3) 7

be provided by GC MS, which will be extremely useful for the further research for elucidating the relationship between chemical constituents in herbal medicine and its pharmacology in further research [2]. Thus, GC MS should be the most preferable tool for the analysis of the volatile chemical s in herbal medicines. Therefore, the present study was carried out to determine the phytochemical constituents from Nyctanthes arboritis leaves by GC-MS by using ethanolic extract. MATERIALS AND METHODS Plant material The plant materials (Nyctanthes arboritis) were collected from Karur district of Tamil Nadu in India during the period of October December 2013. The plant samples were pre-cleaned by double distilled water to remove solid and dust particles. Plant sample extraction Five grams of the powdered plant sample were soaked in 20 ml of absolute methanol overnight and then filtered through Whitman No. 1 filter paper along with 2 mg sodium sulfate to take out the sediments and traces of pee in the filtrate. The filtrate is then concentrated by bubbling nitrogen gas into the answer and was preconcentrated to 2 milliliter of the final content. The selection contains both polar and nonpolar Phyto-components. Qualitative/quantitative analysis of phytochemical constituents The solvent extracts were subjected to routine qualitative secondary metabolite analysis to distinguish the nature of phytochemical constituents present in the sample [3] and the quantitative analysis of secondary metabolites by [4]. Steroids: Three ml of test solution and a minimum amount of chloroform was added with 3-4 drops of acetic anhydride and one drop of concentrated H2SO4. Purple color, thus formed changes into blue or green color showing the presence of steroids. Alkaloids: A 3 ml of test solution was taken with 2N HCl. Aqueous layer formed was decanted and then appended with one or a few drops of Mayer s reagent. Establishment of white precipitate or turbidity indicates the presence of alkaloids. Phenols: A 3 ml of test solution in alcohol was added with one drop of neutral ferric chloride (5%) solution. Establishment of an intense blue color shows the presence of phenols.ls. Flavonoids: A 3 ml of test solution in alcohol was added with a bit of magnesium and one (or) two drops of concentrated HCl and heated. Formation of red or orange color shows the presence of flavonoids. Saponins: A 3 ml of test solution was added to water and shacked. Formation of foamy lather indicates the presence of Saponins. Tannins: A 3 ml of test solution was added with water and lead acetate. Formation of white precipitate indicates the presence of tannins. GC-MS analysis: GC-MS analysis was carried out on a GC Clarus 500 Perkin Elmer System and Gas Chromatography interfaced to a Mass Spectrometry (GC-MS) instrument employing the following conditions: column Elite-1 fused silica capillary column (30mm X 0.25mm IDx1 (micron) Mdf, composed of 100% Dimethyl poly Siloxane), Operating in electron impact mode at 70 e' V; Helium (99.999%) was used as carrier gas at a constant flow of 1ml/min and an injection Volume of 2 µl was employed (split ratio of 10:1); Injector temperature 250 0 C; Ionsource temperature 280 0 C. The oven temperature was programmed from 110 0 C (isothermal for 2min), with an increase of 10 0 C /min, 200 0 C, then 5 0 C/min to 280 0 C, ending with a 9 min isothermal at 280 0 C. Mass Spectra were taken at 70 ev., a scan fragments from 45 to 450 Da. Total GC running time was 36 min. RESULTS AND DISCUSSION Qualitative secondary metabolites screening The ethanolic extract of Nyctanthes arbors leaves contain some groups of secondary metabolites such as steroids, phenol, alkaloids, saponin, tannin and flavonoids are presented in (Table 1). Flavonoids have been demonstrated to have antibacterial, anti-inflammatory, anti-allergic, anti-viral activity [5]. Alkaloids often have pharmacological effects and are used as medication and recreational drugs [6]. The average value of steroids, phenol, alkaloids, saponin, tannin and flavonoids were 0.53, 0.36, 0.24, 0.34, 0.20 and 0.42, respectively are presented in (Table 2). Saponins have been covered to show B Ramachandran et.al, IJPRR 2014; 3(3) 8

hypercholesterolemia and tumor inhibiting activity in experimental animals [7]. Tannins and phenols, which together constitute the polyphenolic group, are known to have antioxidant, anticancer and antimicrobial activities [8]. Apart from that, the result of the ethanol extract of Nyctanthes arboritis were identified by GC-MS analysis (Fig. 1). Gas Chromatography-Mass Spectrometry (GC- MS) is a valuable for tool for reliable identification of Phyto s [9]. Therefore this type of GC-MS analyses are the initiatory step towards realizing the nature of active principles in this medicinal plant and this character of survey will be helpful for further detailed work. Further investigation into the pharmacology of Nyctanthes arbors and their variety and detailed Phytochemistry may add new knowledge to the information in the traditional medical systems. The active principles with their retention time (RT), molecular formula, molecular weight (MW) and concentration % in the ethanol extract of whole plant of Nyctanthes arboritis are presented in (Table 3). In the present survey, 5 s have been distinguished from the ethanol extract of the whole plant of Nyctanthes arbors by Gas Chromatography-Mass Spectrometry analysis. The five s were Artumerone, Curlone, Dibutylphthalate, Hexadelanoic acid Ethyl ester, 1, 2- Benzene dicarboxylic acid-diisooctyl ester. Table 1: Qualitative Phytochemical Constituent of Nyctanthes arboritis Phytochemical Constituents Results Phenol +++ Flavonoids +++ Alkaloids ++ Steroids +++ Saponin ++ Tannins ++ Table 2: Quantitative Phytochemical Constituent of Nyctanthes arboritis Table 3: Secondary Metabolites and their Applications from Nyctanthes arboritis S. Name of the Molecular Molecular Peak area Compound RT Applications No formula Weight % Nature 1 9.66 Ar-tumerone C15H20O 216 8.42 Ketone Anticancer 2 10.08 Curlone C15H22O 218 1.14 Ketone 3 12.81 Dibutyl phthalate C16H22O4 278 11.16 Plasticizer 4 13.14 Hexadecanoic acid, C18H36O2 284 0.85 Palmitic Ethyl ester acid ester 5 20.53 1,2- Benzenedicarboxyli c acid, Diisooctyl ester RT Retention time Phytochemical Study Results (mg/g) Phenol 0.36 Flavonoids 0.42 Alkaloids 0.24 Steroids 0.53 Saponin 0.34 Tannins 0.20 C24H38O4 390 76.73 Plasticizer insecticidal activity Anticancer insecticidal activity Antifouling activity Antioxidant activity Antifouling activity B Ramachandran et.al, IJPRR 2014; 3(3) 9

a. Curlone b. 1, 2-Benzene dicarboxylic acid, diisooctyl ester c. Dibutyl phthalate d. Hexadelanoic acid, ethyl ester e. Ar-tumerone Figure 1: Ethanol Extract of Nyctanthes arboritis were Identified by GC-MS Analysis CONCLUSION It was concluded that ethanolic extract of the leaves of Nyctanthes arbors possesses various potent bioactive s and is recommended as a plant of Phytopharmaceutical importance. Further subjects are required to explore the potential s responsible for the biological activity from Nyctanthes arbors for application in drug delivery, nutritional or pharmaceutical studies. B Ramachandran et.al, IJPRR 2014; 3(3) 10

ACKNOWLEDGEMENT The authors thank the Biospark Biotechnological Research Center (BBRC), Tiruchirappalli, Tamil Nadu, India for GC- MS studies. REFERENCES 1. Abhishekkumar Sah and Vinodkumar Verma, Phytochemicals and pharmacological potential of Nyctanthes arbortristis: A comprehensive, www.ijrpbsonline,3, 2012:420-426. 2. Sermakkani and Thangapandian. GC-MS analysis of cassia italica leaf methanol extract, asian journal of pharmaceutical and clinical research, 5, 2012:90-94. 3. Koperuncholan M and Ahmed John S, Antimicrobial and Phytochemical Screening in Myristica dactyloides Gaertn. Journal of Pharmacy Research, 4, 2011:398-400. 4. Harborne JB, Phytochemical methods: A guide to modern technique of plant analysis. Charpman and Hall, London, 1973:1-30. 5. Alan LQ and Miller ND. Antioxidant. Flavonoids: Structure, function and chemical usage. Alt Med Rev, 1,1996:103-111. 6. Roger MF and Wink M. Alkaloids, Biochemistry, ecology and medicinal applications, Plennum press, 1998: 2-3. 7. John T. Phytochemicals as evolutionary mediators of Human nutritional physiology Int. J. Pharmacol (USA), 134, 1996:327-334. 8. Rice EC, Miller NJ and Paganga G. Structure and antioxidant activity, relationships of flavonoids and Phenolic acids. Free Radical Biol Med, 20, 1996:933-956. 9. Sampath Kumar S and Rama Krishnan N. Chromatographic fingerprint analysis of Naringi crenulata by HPTLC technique. Asian Pal. J. Trop. Biomedicine, 1, 2011:195-198. B Ramachandran et.al, IJPRR 2014; 3(3) 11