Phytochemical Profile of Andrographis paniculata Extract from Solvent Partition and Precipitation

References

• Shoji, T. (2014). Chapter Six - ATP-binding cassette and multidrug and toxic compound extrusion transporters in plants: A common theme among diverse detoxification mechanisms. Int. Rev. Cell Mol. Biol. 309: 303–346. doi: 10.1016/B978-0-12-800255-1.00006-5
   PubMed Web of Science ®Google Scholar
• Pandeti, S., Sonkar, R., Shukla, A., Bhatia, G. and Tadigoppula, N. (2013). Synthesis of new andrographolide derivatives and evaluation of their antidyslipidemic, LDL-oxidation and antioxidant activity. Eur. J. Med. Chem. 69: 439–448. doi: 10.1016/j.ejmech.2013.09.002
   PubMed Web of Science ®Google Scholar
• Zhu, Z., Duan, H., Jing, M., Xu, L. and Yu, P. (2018). Synthesis and biological evaluation of andrographolide derivatives as anti-inflammatory agent. Curr. Pharm. Des. 24: 3529–3533. doi: 10.2174/1381612824666180724130014
   PubMed Web of Science ®Google Scholar
• Chua, L.S. (2014). Review on liver inflammation and antiinflammatory activity of Andrographis paniculata for hepatoprotection. Phytother. Res. 28: 1589–1598. doi: 10.1002/ptr.5193
   PubMed Web of Science ®Google Scholar
• Chua, L.S., Yap, K.C., Jaganath, I.B. (2013). Comparison of total phenolic content, scavenging activity and HPLC-ESI-MS/MS profiles of both young and mature leaves and stems of Andrographis paniculate. Nat. Prod. Comm. 8: 1725–1729.
   PubMed Web of Science ®Google Scholar
• Okhuarobo, A., Falodun, J.E., Erharuyi, O., Imieje, V., Falodun, A., Langer, P. (2014). Harnessing the medicinal properties of Andrographis paniculata for diseases and beyond: a review of its phytochemistry and pharmacology. Asian Pac. J. Trop. Dis. 4(3): 213–222. doi: 10.1016/S2222-1808(14)60509-0
   Google Scholar
• Hossain, M.S., Urbi, Z., Sule, A., Hafizur Rahman, K.M. (2014). Andrographis paniculata (Burm. f.) Wall. ex Nees: A review of ethnobotany, phytochemistry, and pharmacology. Sci. World J. Article ID 274905, 28 pages.
   Google Scholar
• Jayakumar, T., Hsieh, C.Y., Lee, J.J. and Sheu, J.R. (2013). Experimental and clinical pharmacology of Andrographis paniculata and its major bioactive phytoconstituent andrographolide. Evid. Based Complement. Alternat. Med. 846740.
   Google Scholar
• Samy, R.P., Thwin, M.M., Gopalakrishnakone, P. and Ignacimuthu, S. (2008). Ethnobotanical survey of folk plants for the treatment of snakebites in Southern part of Tamilnadu, India. J. Ethnopharmacol. 115: 302–312. doi: 10.1016/j.jep.2007.10.006
   PubMed Web of Science ®Google Scholar
• Mishra, U.S., Mishra, A., Kumari, R., Murthy, P.N. and Naik, B.S. (2009). Antibacterial activity of ethanol extract of Andrographis paniculata. Indian J. Pharm. Sci. 71: 436–438. doi: 10.4103/0250-474X.57294
   PubMed Web of Science ®Google Scholar
• Abubakar, S., Ahmed, Q.U., Samah, O.A. and Omar, M.N. (2011). Bacteriostatic and bactericidal activity of the polar and non-polar extracts of Andrographis paniculata against skin disease causing pathogenic bacteria. J. Medicinal Plants Res. 5: 7–14.
   Google Scholar
• Wiart, C., Kumar, K., Yusof, M.Y., Hamimah, H., Fauzi, Z.M. and Sulaiman, M. (2005). Antiviral properties of ent-labdene diterpenes of Andrographis paniculata nees, inhibitors of herpes simplex virus type 1. Phytother. Res. 19: 1069–1070. doi: 10.1002/ptr.1765
   PubMed Web of Science ®Google Scholar
• Wen, W.C., Yueh, K.H. and Fong, L.B. (2010). Anti-inflammatory activity of new compounds from Andrographis paniculata by NF-êB transactivation inhibition. J. Agric. Food Chem. 58: 2505–2512. doi: 10.1021/jf903629j
   PubMed Web of Science ®Google Scholar
• Iruretagoyena, M.I., Tobar, J.A., González, P.A., Sepúlveda, S.E., Figueroa, C.A., Burgos, R.A., Hancke, J.L. and Kalergis, A.M. (2005). Andrographolide interferes with T cell activation and reduces experimental autoimmune encephalomyelitis in the mouse. J Pharmacol. Exp. Ther. 312: 366–372. doi: 10.1124/jpet.104.072512
   PubMed Web of Science ®Google Scholar
• Li, W., Xu, X., Zhang, H., Ma, C., Fong, H., van Breemen, R. and Fitzloff, J. (2007). Secondary metabolites from Andrographis paniculata. Chem. Pharm. Bull. (Tokyo). 55: 455–458. doi: 10.1248/cpb.55.455
   PubMed Web of Science ®Google Scholar
• Geethangili, M., Rao, Y.K., Fang, S.H. and Tzeng, Y.M. (2008). Cytotoxic constituents from Andrographis paniculata induce cell cycle arrest in jurkat cells. Phytother. Res. 22: 1336–1341. doi: 10.1002/ptr.2493
   PubMed Web of Science ®Google Scholar
• Bothiraja, C., Shinde, M.B., Rajalakshmi, S., Pawar, A.P. (2009). Evaluation of molecular pharmaceutical and in-vivo properties of spray-dried isolated andrographolide-PVP. J. Pharm. Phamarcol. 61: 1465–1472. doi: 10.1211/jpp.61.11.0005
   PubMed Web of Science ®Google Scholar
• Fuchs, H., Niesler, N., Trautner, A., Sama, S., Jerz, G., Panjideh, H., Weng, A. (2017). Glycosylated triterpenoids as endosomal escape enhancers in targeted tumor therapies. Biomed. 5(2): 14.
   Google Scholar
• Zacchino, S.A., Butassi, E., Liberto, M.D., Raimondi, M., Postigo, A. and Sortino, M. (2017). Plant phenolics and terpenoids as adjuvants of antibacterial and antifungal drugs. Phytomed. 37: 27–48. doi: 10.1016/j.phymed.2017.10.018
   PubMed Web of Science ®Google Scholar
• Jiang, Z., Kempinski, C. and Chappell, J. (2016). Extraction and analysis of terpenes/terpenoids. Curr. Protoc. Plant Biol. 1: 345–358. doi: 10.1002/cppb.20024
   PubMedGoogle Scholar
• Chua, L.S., Lau, C.H., Chew, C.Y., Dawood, D.A.S. (2019). Solvent fractionation and acetone precipitation for crude saponins from Eurycoma longifolia extract. Molecules. 24: 1416. doi: 10.3390/molecules24071416
   Web of Science ®Google Scholar
• Chua, L.S., Mohd Amin, N.A., Neo, J.C.H., Lee, T.H., Lee, C.T., Sarmidi, M.R., Abdul Aziz, R. (2011). LC-MS/MS-based metabolites of Eurycoma longifolia (Tongkat Ali) in Malaysia (Perak and Pahang). J. Chrom. B. 879(32): 3909–3919. doi: 10.1016/j.jchromb.2011.11.002
   PubMed Web of Science ®Google Scholar
• Makkar, H.P.S., Siddhuraju, P. and Becker, K. (2007). In: The Book Series of Methods in Molecular Biology; Chapter 16. Saponins, plant secondary metabolites; Humana Press: New Jersey. 393: 93–100. doi: 10.1007/978-1-59745-425-4_16
   Google Scholar
• Chang, C.L., Lin, C.S. and Lai, G.H. (2012). Phytochemical characteristics, free radical scavenging activities, and neuroprotection of five medicinal plant extracts. Evid. Based Complement. Alternat. Med. 984295.
   Web of Science ®Google Scholar
• Dartora, N., de Souza, L.M., Santana-Filho, A.P., Iacomini, M., Valduga, A.T., Gorin, P.A.J. and Sassaki, G.L. (2011). UPLC-PDA–MS evaluation of bioactive compounds from leaves of Ilex paraguariensis with different growth conditions, treatments and ageing. Food Chem. 129: 1453-1461. doi: 10.1016/j.foodchem.2011.05.112
   Web of Science ®Google Scholar
• Zhang, Y.D., Huang, X., Zhao, F.L., Tang, Y.L. and Yin, L. (2015). Study on the chemical markers of Caulis Lonicerae japonicae for quality control by HPLC-QTOF/MS/MS and chromatographic fingerprints combined with chemometrics methods. Anal. Methods. 7: 2064–2076. doi: 10.1039/C4AY02744B
   Web of Science ®Google Scholar
• Yuan, Y., Hou, W., Tang, M., Luo, H., Chen, L.J., Guan, Y.H. and Sutherland, I.A. (2008). Separation of flavonoids from the leaves of Oroxylum indicum by HSCCC. Chromatographia. 68: 885–892. doi: 10.1365/s10337-008-0859-0
   Web of Science ®Google Scholar
• Zhu, Y., Nomura, T., Xu, Y., Zhang, Y., Peng, Y., Mao, B., Hanada, A., Zhou, H., Wang, R., Li, P., Zhu, X., Mander, L.N., Kamiya, Y., Yamaguchi, S. and He, Z. (2006). Elongated uppermost internode encodes a cytochrome P450 monooxygenase that epoxidizes gibberellins in a novel deactivation reaction in rice. Plant Cell. 18: 442–456. doi: 10.1105/tpc.105.038455
   PubMed Web of Science ®Google Scholar
• Urbanová, T., Tarkowská, D., Novák, O., Hedden, P. and Strnad, M. (2013). Analysis of gibberellins as free acids by ultra performance liquid chromatography-tandem mass spectrometry. Talanta. 112: 85–94. doi: 10.1016/j.talanta.2013.03.068
   PubMed Web of Science ®Google Scholar
• Yang, T., Xu, C., Wang, Z.T. and Wang, C.H. (2013). Comparative pharmacokinetic studies of andrographolide and its metabolite of 14-deoxy-12-hydroxy-andrographolide in rat by ultra-performance liquid chromatography-mass spectrometry. Biomed. Chromatogr. 27: 931–937. doi: 10.1002/bmc.2884
   PubMed Web of Science ®Google Scholar
• https://massbank.eu/MassBank/RecordDisplay.jsp?id=PR020023&dsn=RIKEN (PR020023) assessed on 23 December 2018
   Google Scholar
• Altemimi, A., Lakhssassi, N., Baharlouei, A., Watson, D.G. and Lightfoot, D.A. (2017). Phytochemicals: extraction, isolation, and identification of bioactive compounds from plant Extracts. Plants. 6: 42. doi: 10.3390/plants6040042
   Web of Science ®Google Scholar
• Gupta, N., Sonambekar, A.A., Daksh, S.K. and Tomar, L. (2013). A rare presentation of methanol toxicity. Ann. Indian Acad. Neurol. 16(2): 249–251. doi: 10.4103/0972-2327.112484
   PubMed Web of Science ®Google Scholar
• Wei, L., Zhang, W., Yin, L., Yan, F., Xu, Y. and Chen, F. (2015). Extraction optimization of total triterpenoids from Jatropha curcas leaves using response surface methodology and evaluations of their antimicrobial and antioxidant capacities. Electronic J. Biotechnol. 18(2): 88–95. doi: 10.1016/j.ejbt.2014.12.005
   Web of Science ®Google Scholar
• Bishayee, A., Ahmed, S., Brankov, N. and Perloff, M. (2011). Triterpenoids as potential agents for the chemoprevention and therapy of breast cancer. Front Biosci. 16: 980–996. doi: 10.2741/3730
   PubMed Web of Science ®Google Scholar
• Le, A.V., Parks, S.E., Nguyen, M.H. and Roach, P.D. (2018). Improving the vanillin-sulphuric acid method for quantifying total saponins. Technol. 6: 84.
   Google Scholar
• Li, X.E., Wang, Y.X., Sun, P., Liao, D.Q. (2016). Determination of saponin content in Hang Maidong and Chuan Maidong via HPLC-ELSD analysis. J. Anal. Methods Chem. Article ID 7214607, 5 pages.
   Web of Science ®Google Scholar