Extraction of Artemisinin, an Active Antimalarial Phytopharmaceutical from Dried Leaves of Artemisia annua L., Using Microwaves and a Validated HPTLC-Visible Method for Its Quantitative Determination
A simple, rapid, precise, and accurate high-performance thin-layer chromatographic method coupled with visible densitometric detection of artemisinin is developed and validated. Samples of the dried Artemisia annua leaves were extracted via microwaves using different solvents. This method shows the advantage of shorter extraction time of artemisinin from leaves under the influence of electromagnetic radiations. Results obtained from microwave-assisted extraction (MAE) were compared with hot soxhlet extraction. Chromatographic separation of artemisinin from plant extract was performed over silica gel 60 F254 HPTLC plate using n-hexane?:?ethyl acetate as mobile phase in the ratio of 75?:?25, v/v. The plate was developed at room temperature 25?±?2.0°C. Artemisinin separation over thin-layer plate was visualized after postchromatographic derivatization with anisaldehyde-sulphuric acid reagent. HPTLC plate was scanned in a CAMAG’s TLC scanner 3 at 540?nm. Artemisinin responses were found to be linear over a range of 400–2800?ng spot?1 with a correlation coefficient 0.99754. Limits of detection and quantification were 40 and 80?ng spot?1, respectively. The HPTLC method was validated in terms of system suitability, precision, accuracy, sensitivity (LOD and LOQ), and robustness. Additionally, calculation of plate efficiency and flow constant were included as components of validation. Extracts prepared from different parts of the plant (leaves, branches, main stem, and roots) were analyzed for artemisinin content, in which, artemisinin content was found higher in the leaf extract with respect to branches and main stem extracts; however, no artemisinin was detected in root extract. The developed HPTLC-visible method of artemisinin determination will be very useful for pharmaceutical industries, which are involved in monitoring of artemisinin content during different growth stages (in vitro and in vivo) of A. annua for qualitative and quantitative assessment of final produce prior to commercial-scale processing for assessment of cost-benefit ratio. 1. Introduction Malaria is a vector-borne infectious disease, which affects approximately 400 million people every year, especially in Africa. The parasite responsible for fatal malarial infections is Plasmodium falciparum. The first effective antimalarial drug to treat this dangerous infection was quinine; since then, malaria has been treated with quinoline-based drugs like chloroquine, mefloquine, and pyrimethamine, but malaria parasite developed resistance to these drugs [1–3]. Artemisinin (Figure 1) is a natural
References
[1]
W. H. Wernsdorfer, “Epidemiology of drug resistance in malaria,” Acta Tropica, vol. 56, no. 2-3, pp. 143–156, 1994.
[2]
P. J. De Vries and T. K. Dien, “Clinical pharmacology and therapeutic potential of artemisinin and its derivatives in the treatment of malaria,” Drugs, vol. 52, no. 6, pp. 818–836, 1996.
[3]
E. Gkrania-Klotsas and M. L. Lever, “An update on malaria prevention, diagnosis and treatment for the returning traveller,” Blood Reviews, vol. 21, no. 2, pp. 73–87, 2007.
[4]
A. Singh, V. K. Kaul, V. P. Mahajan, A. Singh, L. N. Misra, and R. S. Thakur, “Introduction of Artemisia annua in India and isolation of artemisinin, a promising antimalarial drug,” Indian Journal of Pharmaceutical Sciences, vol. 48, no. 5, pp. 137–138, 1986.
[5]
CIMAP, “Development of Agro-technologies for Artemisia annua for antimalarial drug artemisinin,” Annual Project Report 1986-87, Central Institute for Medicinal and Aromatic Plants, Lucknow, India.
[6]
CIMAP, “Development of Agro-technologies for Artemisia annua for antimalarial drug artemisinin,” Annual Project Report 1988-89, Central Institute for Medicinal and Aromatic Plants, Lucknow, India.
[7]
S. K. Gupta, P. Singh, P. Bajpai, et al., “Morphogenetic variation for artemisinin and volatile oil in Artemisia annua,” Industrial Crops and Products, vol. 16, no. 3, pp. 217–224, 2002.
[8]
S. Kumar, S. K. Gupta, M. M. Gupta et al., “Method for maximization of artemisinin production of the plant Artemisia annua L,” Indian Patent No. NF-122/2000, US 09/538, 892, 2000, 6,393,763, 2002.
[9]
P. C. Allen, J. Lydon, and H. D. Danforth, “Effects of components of Artemisia annua on Coccidia infections in Chickens,” Poultry Science, vol. 76, no. 8, pp. 1156–1163, 1997.
[10]
H. A. Arab, S. Rahbari, A. Rassouli, M. H. Moslemi, and F. Khosravirad, “Determination of artemisinin in Artemisia sieberi and anticoccidial effects of the plant extract in broiler chickens,” Tropical Animal Health and Production, vol. 38, no. 6, pp. 497–503, 2006.
[11]
R. S. Bhakuni, D. C. Jain, R. P. Sharma, and S. Kumar, “Secondary metabolites of Artemisia annua and their biological activity,” Current Science, vol. 80, no. 1, pp. 35–48, 2001.
[12]
T. Efferth, M. R. Romero, D. G. Wolf, T. Stamminger, J. J. G. Marin, and M. Marschall, “The antiviral activities of artemisinin and artesunate,” Clinical Infectious Diseases, vol. 47, no. 6, pp. 804–811, 2008.
[13]
A. C. Beekman, P. K. Wierenga, H. J. Woerdenbag, et al., “Artemisinin-derived sesquiterpene lactones as potential antitumour compounds: cytotoxic action against bone marrow and tumour cells,” Planta Medica, vol. 64, no. 7, pp. 615–619, 1998.
[14]
S. Oh, B. J. Kim, N. P. Singh, H. Lai, and T. Sasaki, “Synthesis and anti-cancer activity of covalent conjugates of artemisinin and a transferrin-receptor targeting peptide,” Cancer Letters, vol. 274, no. 1, pp. 33–39, 2009.
[15]
J. A. Levy, L. F. Marins, and A. Sanchez, “Gene transfer technology in aquaculture,” Hydrobiologia, vol. 420, no. 1–3, pp. 91–94, 2000.
[16]
A. Mannan, N. Shaheen, W. Arshad, R. A. Qureshi, M. Zia, and B. Mirza, “Hairy roots induction and artemisinin analysis in Artemisia dubia and Artemisia indica,” African Journal of Biotechnology, vol. 7, no. 18, pp. 3288–3292, 2008.
[17]
X. C. He, M. Y. Zeng, G. F. Li, and Z. Liang, “Callus induction and regeneration of plantlets from Artemisia annua and changes of Qinghaosu contents,” Acta Botanica Sinica, vol. 25, no. 1, pp. 87–90, 1983.
[18]
D. P. Fulzele, A. T. Sipahimalani, and M. R. Heble, “Tissue cultures of Artemisia annua: organogenesis and artemisinin production,” Phytotherapy Research, vol. 5, no. 4, pp. 149–153, 1991.
[19]
M. B. Qin, G. Z. Li, H. C. Ye, and G. F. Li, “Induction of hairy root from Artemisia annua with Agrobacterium rhizogenes and its culture in vitro,” Acta Botanica Sinica, vol. 36, pp. 165–170, 1994.
[20]
A. Giri, S. T. Ravindra, V. Dhingra, and M. L. Narasu, “Influence of different strains of Agrobacterium rhizogenes on induction of hairy roots and artemisinin production in Artemisia annua,” Current Science, vol. 81, no. 4, pp. 378–382, 2001.
[21]
B. M. Aryanti, T. M. Ermayanti, and I. Mariska, “Production of antileukemic agent in untransformed and transformed root cultures of Artemisia cina,” Annales Bogorienses, vol. 8, pp. 11–16, 2001.
[22]
M. Zia and M. F. Chaudhary, “Effect of growth regulators and amino acids on artemisinin production in the callus of Artemisia absinthium,” Pakistan Journal of Botany, vol. 39, no. 3, pp. 799–805, 2007.
[23]
R. X. Tan, W. F. Zheng, and H. Q. Tang, “Biologically active substances from the genus Artemisia,” Planta Medica, vol. 64, no. 4, pp. 295–302, 1998.
[24]
E. Hsu, “The history of qing hao in the Chinese material medica,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 100, no. 6, pp. 505–508, 2006.
[25]
A. Mannan, I. Ahmed, W. Arshad et al., “Survey of artemisinin production by diverse Artemisia species in northern Pakistan,” Malaria Journal, vol. 9, no. 1, article 310, 2010.
[26]
J. Suresh, K. Mruthunjaya, N. Paramakrishnan, and M. N. Naganandhini, “Determination of artemisinin in Artemisia abrotanum and Artemisia pallens by LC/MS method,” International Journal of Current Pharmaceutical Research, vol. 3, no. 1, pp. 49–52, 2011.
[27]
A. G. Namdeo, K. R. Mahadik, and S. S. Kadam, “Antimalarial drug-Artemisia annua,” Pharmacognosy Magazine, vol. 2, no. 6, pp. 106–111, 2006.
[28]
E.-M. B. El-Naggar, M. Azazi, E. ?vajdlenka, and M. ?emli?ka, “Artemisinin from minor to major ingredient in Artemisia annua cultivated in Egypt,” Journal of Applied Pharmaceutical Science, vol. 3, no. 8, pp. 116–123, 2013.
[29]
D. L. Klayman, A. J. Lin, N. Acton, et al., “Isolation of artemisinin (qinghaosu) from Artemisia annua growing in the United States,” Journal of Natural Products, vol. 47, no. 4, pp. 715–717, 1984.
[30]
M. Gabri?ls and J. Plaizier-Vercammen, “Development of a reversed-phase thin-layer chromatographic method for artemisinin and its derivatives,” Journal of Chromatographic Science, vol. 42, no. 7, pp. 341–347, 2004.
[31]
M. M. Gupta, D. C. Jain, R. K. Verma, and A. P. Gupta, “A rapid analytical method for the estimation of artemisinin in Artemisia annua,” Journal of Medicinal and Aromatic plant sciences, vol. 18, no. 1, pp. 5–6, 1996.
[32]
J. A. Marchese, V. L. G. Rehder, and A. Sartoratto, “Quantification of artemisinin in Artemisia annua L A comparison of thin layer chromatography with densitometric detection and high performance liquid chromatography with UV detection,” Revista Brasileira de Plantas Medicinais, vol. 4, pp. 81–87, 2001.
[33]
M. Gabri?ls and J. A. Plaizier-Vercammen, “Densitometric thin-layer chromatographic determination of artemisinin and its lipophilic derivatives, artemether and arteether,” Journal of Chromatographic Science, vol. 41, no. 7, pp. 359–366, 2003.
[34]
P. Bhandari, A. P. Gupta, B. Singh, and V. K. Kaul, “Simultaneous densitometric determination of artemisinin, artemisinic acid and arteannuin-B in Artemisia annua using reversed-phase thin layer chromatography,” Journal of Separation Science, vol. 28, no. 17, pp. 2288–2292, 2005.
[35]
H. N. ElSohly, E. M. Croom, and M. A. ElSohly, “Analysis of the antimalarial sesquiterpene artemisinin in Artemisia annua by high-performance liquid chromatography (HPLC) with postcolumn derivatization and ultraviolet detection,” Pharmaceutical Research, vol. 4, no. 3, pp. 258–260, 1987.
[36]
B. L. Singh, D. V. Singh, R. K. Verma, M. M. Gupta, D. C. Jain, and S. Kumar, “Simultaneous determination of antimalarial drugs using reversed phase high-performance liquid chromatography diode-array detection,” Journal of Medicinal and Aromatic Plant Sciences, vol. 22-23, no. 4A-1A, pp. 17–20, 2000.
[37]
G.-P. Qian, Y.-W. Yang, and Q.-L. Ren, “Determination of artemisinin in Artemisia annua L. by reversed phase HPLC,” Journal of Liquid Chromatography & Related Technologies, vol. 28, no. 5, pp. 705–712, 2005.
[38]
N. Erdemoglu, I. Orhan, M. Kartal, N. Adygüzel, and B. Bani, “Determination of artemisinin in selected Artemisia L. species of Turkey by reversed phase HPLC,” Records of Natural Products, vol. 1, no. 2-3, pp. 36–43, 2007.
[39]
N. Acton, D. L. Klayman, and I. J. Rollman, “Reductive electrochemical HPLC assay for artemisinin (Qinghaosu),” Planta Medica, vol. 51, no. 5, pp. 445–446, 1985.
[40]
J. F. S. Ferreira, D. J. Charles, K. Wood, J. Janick, and J. E. Simon, “A comparison of gas chromatography and high performance liquid chromatography for artemisinin analyses,” Phytochemical Analysis, vol. 5, no. 3, pp. 116–120, 1994.
[41]
B. A. Avery, K. K. Venkatesh, and M. A. Avery, “Rapid determination of artemisinin and related analogues using high-performance liquid chromatography and an evaporative light scattering detector,” Journal of Chromatography B: Biomedical Sciences and Applications, vol. 730, no. 1, pp. 71–80, 1999.
[42]
X.-R. Hu and F.-H. She, “Determination of artemisinin content in Artemisia annua from different regions by HPLC-evaporative light scattering detection,” Xiandai Shipin Yu Yaopin Zazhi, vol. 16, pp. 34–36, 2006.
[43]
C. A. Peng, J. F. S. Ferreira, and A. J. Wood, “Direct analysis of artemisinin from Artemisia annua L. using high-performance liquid chromatography with evaporative light scattering detector, and gas chromatography with flame ionization detector,” Journal of Chromatography A, vol. 1133, no. 1-2, pp. 254–258, 2006.
[44]
C.-Z. Liu, H.-Y. Zhou, and Y. Zhao, “An effective method for fast determination of artemisinin in Artemisia annua L. by high performance liquid chromatography with evaporative light scattering detection,” Analytica Chimica Acta, vol. 581, no. 2, pp. 298–302, 2007.
[45]
A. Amponsaa-Karikari, N. Kishikawa, Y. Ohba, K. Nakashim, and N. Kuroda, “Determination of artemisinin in human serum by high-performance liquid chromatography with on-line UV irradiation and peroxyoxalate chemiluminescence detection,” Biomedical Chromatography, vol. 20, no. 11, pp. 1157–1162, 2006.
[46]
J. Xing, H. Yan, S. Zhang, G. Ren, and Y. Gao, “A high-performance liquid chromatography/tandem mass spectrometry method for the determination of artemisinin in rat plasma,” Rapid Communications in Mass Spectrometry, vol. 20, no. 9, pp. 1463–1468, 2006.
[47]
M. Wang, C. Park, Q. Wu, and J. E. Simon, “Analysis of artemisinin in Artemisia annua L. by LC-MS with selected ion monitoring,” Journal of Agricultural and Food Chemistry, vol. 53, no. 18, pp. 7010–7013, 2005.
[48]
B. Huang and C. Yao, “Determination of artemisinin by capillary electrophoresis with conductivity detection,” Fenxi Ceshi Xuebao, vol. 25, pp. 109–111, 2006.
[49]
H. J. Woerdenbag, N. Pras, R. Bos, J. F. Visser, H. Hendriks, and T. M. Malingre, “Analysis of artemisinin and related sesquiterpenoids from Artemisia annua by combined gas chromatography-mass spectrometry,” Phytochemical Analysis, vol. 2, no. 5, pp. 215–219, 1991.
[50]
A. T. Sipahimalani, D. P. Fulzele, and M. R. Heble, “Rapid method for the detection and determination of artemisinin by gas chromatography,” Journal of Chromatography A, vol. 538, no. 2, pp. 452–455, 1991.
[51]
J. F. S. Ferreira and J. Janick, “Immunoquantitative analysis of artemisinin from Artemisia annua using polyclonal antibodies,” Phytochemistry, vol. 41, no. 1, pp. 97–104, 1996.
[52]
T. V. Sreevidya and B. Narayana, “Spectrophotometric determination of artemisinin and dihydroartemisinin,” Indian Journal of Chemical Technology, vol. 15, no. 1, pp. 59–62, 2008.
[53]
P. Christen and J.-L. Veuthey, “New trends in extraction, identification and quantification of artemisinin and its derivatives,” Current Medicinal Chemistry, vol. 8, no. 15, pp. 1827–1839, 2001.
[54]
J.-Y. Hao, W. Han, S.-D. Huang, B.-Y. Xue, and X. Deng, “Microwave-assisted extraction of artemisinin from Artemisia annua L,” Separation and Purification Technology, vol. 28, no. 3, pp. 191–196, 2002.
[55]
S. Kumar, S. Banerjee, S. Dwivedi et al., “Registration of Jeevanraksha and suraksha varieties of the antimalarial medicinal plant Artemisia annua,” Journal of Medicinal and Aromatic Plant Sciences, vol. 21, no. 1, pp. 47–48, 1999.
[56]
Per Diemer (FAO consultant), WHO and EcoPort version by Peter Griffee (FAO), and Contributor: Peter Griffee, QA and TEM, “Artemisia annua; the plant, production and processing and medicinal applications,” 2013, http://www.mmv.org/sites/default/files/uploads/docs/artemisinin/2007_event/12_Diemer-Griffee_Artemisia_annuapaper.pdf.
[57]
E. Hahn-Deinstrop, Applied Thin-Layer Chromatography: Best Practice and Avoidance of Mistakes, Wiley-VCH Verlag GmbH & Co. KgaA, Weinheim, Germany, 2nd edition, 2007.
[58]
H. Misra, B. K. Mehta, and D. C. Jain, “Comparison of extraction conditions and HPTLC–UV method for determination of quinine in different extracts of Cinchona Species bark,” Records of Natural Products, vol. 2, no. 4, pp. 107–115, 2008.
[59]
H. Misra, D. Mehta, B. K. Mehta, M. Soni, and D. C. Jain, “Study of extraction and HPTLC - UV method for estimation of caffeine in marketed tea (Camellia sinensis) granules,” International Journal of Green Pharmacy, vol. 3, no. 1, pp. 47–51, 2009.
[60]
T. Kowalska, K. Kaczmarski, and W. Prus, “Handbook of thin-layer chromatography,” in Theory and Mechanism of Thin-Layer Chromatography, J. Sherma and B. Fried, Eds., chapter 2, pp. 47–80, Marcel Dekker, New York, NY, USA, 3rd edition, 2003.
[61]
T. Halkina and J. Sherma, “Comparative evaluation of the performance of silica gel TLC plates and irregular and spherical-particle HPTLC plates,” Acta Chromatographica, no. 17, pp. 261–271, 2006.
[62]
Martindale, The Extra Pharmacopoeia, The Pharmaceutical Press, London, UK, 30th edition, 1993.
[63]
E. Turk, “Phosgene from chloroform,” Chemical & Engineering News, vol. 76, no. 9, p. 6, 1998.
[64]
K. E. Maudens, S. M. R. Wille, and W. E. Lambert, “Traces of phosgene in chloroform: consequences for extraction of anthracyclines,” Journal of Chromatography B, vol. 848, no. 2, pp. 384–390, 2007.
[65]
X. Jiang, H. Zhang, M. Wang, and L. Zhang, “Comparison analysis of different parts and geographical origins from southwestern China on artemisinin content of Artemisia annua L,” Current Trends in Technology and Science, vol. 2, no. 4, pp. 293–297, 2013.
[66]
N. Delabays, X. Simonnet, and M. Gaudin, “The genetics of artemisinin content in Artemisia annua L. and the breeding of high yielding cultivars,” Current Medicinal Chemistry, vol. 8, no. 15, pp. 1795–1801, 2001.