Copyright (c) 2016 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Solvent Role in Molecular Recognition of Patchouli Extraction Process
Corresponding Author(s) : F. Adam
Asian Journal of Chemistry,
Vol. 28 No. 6 (2016): Vol 28 Issue 6
Abstract
Patchouli or Pogostemon cablin Benth is an aromatic plant of importance to the fragrant and cosmetic industries. Its secondary metabolites present interesting pharmacological benefits such as antioxidant and antimutagenic properties. This work is an extended study of the published work in ethanol and water solvents using Ewald summation method and mass spectra characterization of patchouli essential oil extracted with three different polar and non-polar solvents. Ewald summation method has reproduced a better radical distribution function (rdf) intensity in the polar ethanol and water solvents using COMPASS force-field. This work concludes that the complex molecular interaction particularly hydrogen bonding play a significant role to affect the solubility of patchoulol solute either in polar or non-polar solvents during the extraction process.
Keywords
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX
- T.-C. Lu, J.-C. Liao, T.-H. Huang, Y.-C. Lin, C.-Y. Liu, Y.-J. Chiu and W.-H. Peng, Evid. Based Complem. Altern. Med., Article ID 671741 (2009); doi:10.1093/ecam/nep183.
- Y. Yang, K. Kinoshita, K. Koyama, K. Takahashi, T. Tai, Y. Nunoura and K. Watanabe, Phytomedicine, 6, 89 (1999); doi:10.1016/S0944-7113(99)80041-5.
- F. Adam, A.B. Siti Hana, M.M. Yusoff and S.N. Tajuddin, J. Chem. Eng. Data, 59, 183 (2014); doi:10.1021/je3013292.
- J.T. Reilly, A. Thomas, A.R. Gibson, C.Y. Luebehusen and M.D. Donohue, Ind. Eng. Chem. Res., 52, 14456 (2013); doi:10.1021/ie302174r.
- M.C. MacMaster, GC/MS, A Practical User’s Guide, John Wiley & Sons Inc., New Jersey, p. 101 (2008).
- J.A. Masucci and G.W. Caldwell, in eds.: R.L. Grob and E.P. Barry, Techniques for Gas Chromatography/Mass Sepctrometry, Modern Practice of Gas Chromatography, John Wiley & Sons Inc., New Jersey, p. 124 (2004).
- H. Sun, J. Phys. Chem. B, 102, 7338 (1998); doi:10.1021/jp980939v.
- M.P. Allen and D.J. Tildesley, Computer Simulation of Liquids, Oxford University Press, Oxford, p. 58 (1987).
- C.L. Yaws, Thermophysical Properties of Chemicals and Hydrocarbon, William Andrew Inc., New York, p. 238 (2008).
- A.Y. Toukmaji and J.A. Board Jr., Comput. Phys. Commun., 95, 73 (1996); doi:10.1016/0010-4655(96)00016-1.
- L. Saiz, J.A. Padro and E. Guàrdia, J. Phys. Chem. B, 101, 78 (1997); doi:10.1021/jp961786j.
- P. Mark and L. Nilsson, J. Phys. Chem. B, 106, 9440 (2002); doi:10.1021/jp025965e.
- V. Sundaresan, S.P. Singh, A.N. Mishra, A.K. Shasany, M.P. Darokar, A. Kalra and A.A. Naqvi, J. Essent. Oil Res., 21, 220 (2009); doi:10.1080/10412905.2009.9700152.
- S.K. Abdul Mudalip, M.R. Abu Bakar, P. Jamal and F. Adam, J. Chem. Eng. Data, 58, 3447 (2013); doi:10.1021/je400714f.
- A.G. Carr, R. Mammucari and N.R. Foster, Chem. Eng. J., 172, 1 (2011); doi:10.1016/j.cej.2011.06.007.
- M.M. Jiménez-Carmona, J.L. Ubera and M.D. Luque de Castro, J. Chromatogr. A, 855, 625 (1999); doi:10.1016/S0021-9673(99)00703-7.
- T. Kondo and C. Sawatari, Polymer, 37, 393 (1996); doi:10.1016/0032-3861(96)82908-9.
- S. Kubo and J.F. Kadla, Biomacromolecules, 6, 2815 (2005); doi:10.1021/bm050288q.
- L. Fan, R. Jin, Y. Liu, M. An and S. Chen, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 879, 3653 (2011); doi:10.1016/j.jchromb.2011.09.035.
- A. Nikiforov, L. Jirovetz, G. Buchbauer and V. Raverdino, Mikrochim. Acta, 95, 193 (1988); doi:10.1007/BF01349751.
- A. Yahya and R.M. Yunus, Proceedia Eng., 53, 1 (2013); doi:10.1016/j.proeng.2013.02.001.
- N.X. Dung, P.A. Leclercq, T.H. Thai and L.D. Moi, J. Essent. Oil Res., 1, 99 (8989); doi:10.1080/10412905.1989.9697758.
- A. Donelian, L.H.C. Carlson, T.J. Lopes and R.A.F. Machado, J. Supercrit. Fluids, 48, 15 (2009); doi:10.1016/j.supflu.2008.09.020.
- L.F. Hu, S.P. Li, H. Cao, J.J. Liu, J.L. Gao, F.Q. Yang and Y.T. Wang, J. Pharm. Biomed. Anal., 42, 200 (2006); doi:10.1016/j.jpba.2005.09.015.
- J. Wu, X. Lu, W. Tang, H. Kong, S. Zhou and G. Xu, J. Chromatogr. A, 1034, 199 (2004); doi:10.1016/j.chroma.2004.02.028.
- G.A. Akowuah and I. Zhari, J. Herbs Spices Med. Plants, 16, 160 (2010); doi:10.1080/10496475.2010.509652.
References
T.-C. Lu, J.-C. Liao, T.-H. Huang, Y.-C. Lin, C.-Y. Liu, Y.-J. Chiu and W.-H. Peng, Evid. Based Complem. Altern. Med., Article ID 671741 (2009); doi:10.1093/ecam/nep183.
Y. Yang, K. Kinoshita, K. Koyama, K. Takahashi, T. Tai, Y. Nunoura and K. Watanabe, Phytomedicine, 6, 89 (1999); doi:10.1016/S0944-7113(99)80041-5.
F. Adam, A.B. Siti Hana, M.M. Yusoff and S.N. Tajuddin, J. Chem. Eng. Data, 59, 183 (2014); doi:10.1021/je3013292.
J.T. Reilly, A. Thomas, A.R. Gibson, C.Y. Luebehusen and M.D. Donohue, Ind. Eng. Chem. Res., 52, 14456 (2013); doi:10.1021/ie302174r.
M.C. MacMaster, GC/MS, A Practical User’s Guide, John Wiley & Sons Inc., New Jersey, p. 101 (2008).
J.A. Masucci and G.W. Caldwell, in eds.: R.L. Grob and E.P. Barry, Techniques for Gas Chromatography/Mass Sepctrometry, Modern Practice of Gas Chromatography, John Wiley & Sons Inc., New Jersey, p. 124 (2004).
H. Sun, J. Phys. Chem. B, 102, 7338 (1998); doi:10.1021/jp980939v.
M.P. Allen and D.J. Tildesley, Computer Simulation of Liquids, Oxford University Press, Oxford, p. 58 (1987).
C.L. Yaws, Thermophysical Properties of Chemicals and Hydrocarbon, William Andrew Inc., New York, p. 238 (2008).
A.Y. Toukmaji and J.A. Board Jr., Comput. Phys. Commun., 95, 73 (1996); doi:10.1016/0010-4655(96)00016-1.
L. Saiz, J.A. Padro and E. Guàrdia, J. Phys. Chem. B, 101, 78 (1997); doi:10.1021/jp961786j.
P. Mark and L. Nilsson, J. Phys. Chem. B, 106, 9440 (2002); doi:10.1021/jp025965e.
V. Sundaresan, S.P. Singh, A.N. Mishra, A.K. Shasany, M.P. Darokar, A. Kalra and A.A. Naqvi, J. Essent. Oil Res., 21, 220 (2009); doi:10.1080/10412905.2009.9700152.
S.K. Abdul Mudalip, M.R. Abu Bakar, P. Jamal and F. Adam, J. Chem. Eng. Data, 58, 3447 (2013); doi:10.1021/je400714f.
A.G. Carr, R. Mammucari and N.R. Foster, Chem. Eng. J., 172, 1 (2011); doi:10.1016/j.cej.2011.06.007.
M.M. Jiménez-Carmona, J.L. Ubera and M.D. Luque de Castro, J. Chromatogr. A, 855, 625 (1999); doi:10.1016/S0021-9673(99)00703-7.
T. Kondo and C. Sawatari, Polymer, 37, 393 (1996); doi:10.1016/0032-3861(96)82908-9.
S. Kubo and J.F. Kadla, Biomacromolecules, 6, 2815 (2005); doi:10.1021/bm050288q.
L. Fan, R. Jin, Y. Liu, M. An and S. Chen, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 879, 3653 (2011); doi:10.1016/j.jchromb.2011.09.035.
A. Nikiforov, L. Jirovetz, G. Buchbauer and V. Raverdino, Mikrochim. Acta, 95, 193 (1988); doi:10.1007/BF01349751.
A. Yahya and R.M. Yunus, Proceedia Eng., 53, 1 (2013); doi:10.1016/j.proeng.2013.02.001.
N.X. Dung, P.A. Leclercq, T.H. Thai and L.D. Moi, J. Essent. Oil Res., 1, 99 (8989); doi:10.1080/10412905.1989.9697758.
A. Donelian, L.H.C. Carlson, T.J. Lopes and R.A.F. Machado, J. Supercrit. Fluids, 48, 15 (2009); doi:10.1016/j.supflu.2008.09.020.
L.F. Hu, S.P. Li, H. Cao, J.J. Liu, J.L. Gao, F.Q. Yang and Y.T. Wang, J. Pharm. Biomed. Anal., 42, 200 (2006); doi:10.1016/j.jpba.2005.09.015.
J. Wu, X. Lu, W. Tang, H. Kong, S. Zhou and G. Xu, J. Chromatogr. A, 1034, 199 (2004); doi:10.1016/j.chroma.2004.02.028.
G.A. Akowuah and I. Zhari, J. Herbs Spices Med. Plants, 16, 160 (2010); doi:10.1080/10496475.2010.509652.