This study evaluates the ability of obtaining and of analysis of the binary systems of juglone with β-cyclodextrin using the simplest method of complexation - the kneading method. The purpose of this paper is to obtain and to investigate the binary systems of juglone with β-cyclodextrin. The obtained systems were analyzed with the spectrometric method in IR. In its turn, the given purpose gave the formulation of the following research objectives: a) the creation of a binary system that could reduce the toxic properties of juglone and enhance its antiseptic properties; b) the analysis of the influence of the quantity of water in the obtaining of the complex compounds by the method of kneading; c) the applying of the spectrometric method in IR in order to evaluate the efficiency of the research. Thus, it was found that the complexation process of juglone with β-cyclodextrin is more efficient with the use of water acting as facilitator of the formation of the proposed complex system, both substances being hydrophobic they tend to form a common complex.
Published in | World Journal of Applied Chemistry (Volume 2, Issue 3) |
DOI | 10.11648/j.wjac.20170203.17 |
Page(s) | 116-119 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2017. Published by Science Publishing Group |
Analysis, Binary Systems, β-Cyclodextrin, Complexation Reaction, Juglone
[1] | K. Aithal, S. Kumar, “Juglone, a naphthoquinone from walnut, exerts cytotoxic and genotoxic effects against cultured melanoma tumor cells,” J. Cell Biology International, 33: 1039-1049, 2009. |
[2] | V. Boldescu, I. Bratu, Gh. Borodi, I. Kasco, A. Bende, Gh. Duca, F. Macaev, S. Pogrebnoi, Z. Ribkovskaia, “Study of binary systems of -cyclodextrin with a highly potential anti-mycobacterial drug,” J. Incl. Phenom. Macrocycl. Chem., 74(1-4): 129-135, 2012. |
[3] | S. Chao, A. Greenleaf, D. Price, “Juglone, an inhibitor of the peptidyl-prolyl isomerase Pin 1, also directly blocks transcription,” J. Oxford. Nucleic Acids Research, 29 (3): 767-773, 2001. |
[4] | B. Evrard, P. Chiap, P. DeTullio, “Oral bioavailability in sheep of albendazole from a suspension and from a solution containing β-cyclodextrin,” J. Control Release, 85: 45-50, 2002. |
[5] | A. Hejl, F. Einhellig, J. Rasmussen, “Effects of juglone on growth, photosynthesis and respiration,” J. Chemical Ecology, 559-568, 2003. |
[6] | Xu Hua-Li, Yu Xiao-Feng, “Anti-proliferative effect of juglone on human leukemia cell HL-60 by inducing apoptosis through the mitochondria-dependent pathway,” J. European Journal of Pharmacology, 645: 14-22, 2010. |
[7] | F. Macaev, V. Boldescu, A. Geronikaki, N. Sucman, “Recent advances in the use of cyclodextrins in antifungal formulations,” J. Curr. Top. Med. Chem., 13 (21): 2677-2683, 2013. |
[8] | G. Junghietu, L. Vlad, “Juglone and the homologues of 1,4-naftaquinone,” ed. Science, Chișinău, 19‐57, 1978. |
[9] | Ji Yu-Bin, Qu Zhong-Yuan, “Juglone – induced apoptosis in human gastric cancer SGC-7901 cells via mitochondrial pathway,” J. Experimental and Toxicologic Pathology, 63: 69-78, 2011. |
[10] | https://ibn.idsi.md/sites/default/files/imag_file/Compusi%20complecsi%20de%20incluziune%20ai%20amantadinelor_0.pdf, accessed 2016. |
[11] | http://14.139.47.15/bitstream/123456789/15483/1/IJCA%2039A%288%29%20889-895.pdf, accessed 2016. |
[12] | http://www.washingtoncitypaper.com/articles/47564/if-juglone-can-induce-cell-death-in-humans-how-are, accessed 2016. |
APA Style
Ion Castravet. (2017). Obtaining & Analysis of the Binary Systems of Juglone with β-Cyclodextrin. World Journal of Applied Chemistry, 2(3), 116-119. https://doi.org/10.11648/j.wjac.20170203.17
ACS Style
Ion Castravet. Obtaining & Analysis of the Binary Systems of Juglone with β-Cyclodextrin. World J. Appl. Chem. 2017, 2(3), 116-119. doi: 10.11648/j.wjac.20170203.17
@article{10.11648/j.wjac.20170203.17, author = {Ion Castravet}, title = {Obtaining & Analysis of the Binary Systems of Juglone with β-Cyclodextrin}, journal = {World Journal of Applied Chemistry}, volume = {2}, number = {3}, pages = {116-119}, doi = {10.11648/j.wjac.20170203.17}, url = {https://doi.org/10.11648/j.wjac.20170203.17}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.wjac.20170203.17}, abstract = {This study evaluates the ability of obtaining and of analysis of the binary systems of juglone with β-cyclodextrin using the simplest method of complexation - the kneading method. The purpose of this paper is to obtain and to investigate the binary systems of juglone with β-cyclodextrin. The obtained systems were analyzed with the spectrometric method in IR. In its turn, the given purpose gave the formulation of the following research objectives: a) the creation of a binary system that could reduce the toxic properties of juglone and enhance its antiseptic properties; b) the analysis of the influence of the quantity of water in the obtaining of the complex compounds by the method of kneading; c) the applying of the spectrometric method in IR in order to evaluate the efficiency of the research. Thus, it was found that the complexation process of juglone with β-cyclodextrin is more efficient with the use of water acting as facilitator of the formation of the proposed complex system, both substances being hydrophobic they tend to form a common complex.}, year = {2017} }
TY - JOUR T1 - Obtaining & Analysis of the Binary Systems of Juglone with β-Cyclodextrin AU - Ion Castravet Y1 - 2017/09/04 PY - 2017 N1 - https://doi.org/10.11648/j.wjac.20170203.17 DO - 10.11648/j.wjac.20170203.17 T2 - World Journal of Applied Chemistry JF - World Journal of Applied Chemistry JO - World Journal of Applied Chemistry SP - 116 EP - 119 PB - Science Publishing Group SN - 2637-5982 UR - https://doi.org/10.11648/j.wjac.20170203.17 AB - This study evaluates the ability of obtaining and of analysis of the binary systems of juglone with β-cyclodextrin using the simplest method of complexation - the kneading method. The purpose of this paper is to obtain and to investigate the binary systems of juglone with β-cyclodextrin. The obtained systems were analyzed with the spectrometric method in IR. In its turn, the given purpose gave the formulation of the following research objectives: a) the creation of a binary system that could reduce the toxic properties of juglone and enhance its antiseptic properties; b) the analysis of the influence of the quantity of water in the obtaining of the complex compounds by the method of kneading; c) the applying of the spectrometric method in IR in order to evaluate the efficiency of the research. Thus, it was found that the complexation process of juglone with β-cyclodextrin is more efficient with the use of water acting as facilitator of the formation of the proposed complex system, both substances being hydrophobic they tend to form a common complex. VL - 2 IS - 3 ER -