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Anti-Infective Agents

Editor-in-Chief

ISSN (Print): 2211-3525
ISSN (Online): 2211-3533

Research Article

Enhancing Antibacterial Activity by Combination of Chloramphenicol with Constituents from Dracaena cochinchinensis (Lour.) S.C.Chen

Author(s): Ritbey Ruga and Warinthorn Chavasiri*

Volume 17, Issue 1, 2019

Page: [74 - 80] Pages: 7

DOI: 10.2174/2211352516666180730115216

Price: $65

Abstract

Background: Seven compounds were isolated from Dracaena cochinchinensis and elucidated their structure by NMR spectroscopic analysis and determined the optical rotation for certain compounds.

Methods: These compounds were screened for antibacterial activity by using agar well diffusion and determination of minimum inhibitory concentration (MIC) was conducted by the broth micro-dilution method using resazurin colorimetric assay. Further investigation on combination effect between each compound with chloramphenicol was conducted by agar well diffusion method. Among the seven compounds, compound 4 displayed the highest antibacterial activity against P. acnes and S. aureus with the inhibition zone of 17.3 and 16.7 mm, respectively. The MIC value of 1 and 4 against all tested bacteria was 62.5 µM, whereas those of other compounds were 62.5-250 µM. The combination of 4 and chloramphenicol exhibited the most synergistic effect against P. acnes with the rate in increasing antibacterial activity of 4 in combination as 1,250 folds. This compound also enhanced the antibacterial activity of chloramphenicol at 50 µM with an inhibition zone of 16.3 mm comparing to its activity alone (8.7 mm).

Results & Conclusion: The results revealed compound 4 displayed the highest antibacterial activity alone and in combination with chloramphenicol against P. acnes and S. aureus.

Keywords: Dracaena cochinchinensis, antibacterial activity, zone of inhibition, minimum inhibitory concentration, combination. effect, chloramphenicol.

Graphical Abstract

[1]
Kubo, I.; Muroi, H.; Kubo, A. Naturally occurring antiacne agents. J. Nat. Prod., 1994, 57, 9-17.
[2]
Tran, T.D.; Do, T.H.; Tran, N.C.; Ngo, T.D.; Huynh, T.N.P.; Tran, C.D. Synthesis and methicillin resistant Staphylococcus aureus activity of substituted chalcones alone and in combination with non-beta-lactam antibiotics. Bioorg. Med. Chem. Lett., 2012, 22, 4555-4560.
[3]
Zuo, G.Y.; Li, Y.; Wang, T.; Han, J.; Wang, G.C.; Zhang, Y.L. Synergistic antibacterial and antibiotic effects of bisbenzylisoquinoneline alkaloids on clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA). Molecules, 2011, 16, 9819-9828.
[4]
Reuk-ngam, N.; Chimnoi, N.; Khunnawutmanotham, N. Techasakul. Antimicrobial activity of coronarin D and its synergistic potential with antibiotics. Biomed Res. Int., 2014.
[http://dx.doi.org/10.1155/2014581985]
[5]
Hu, Z.Q.; Zhao, W.H.; Asano, N.; Yoda, Y.; Hara, Y.; Shimamura, T. Epigallocatechin gallate synergistically enhances the activity of carbapenems against methicillin-resistant Staphylococcus aureus. Antimicrob. Agents Chemother., 2000, 46, 558-560.
[6]
Yoshida, H.; Bogaki, M.; Nakamura, S.; Ubukata, K.; Konno, M. Nucleotide sequence and characterization of the Staphylococcus aureus norA gene, which confers resistance to quinolones. J. Bacteriol., 1990, 172, 6942-6949.
[7]
Sakagami, Y.; Iinuma, H.; Piyasena, K.; Dharmaratne, H. Antibacterial activity of α-mangostin against vancomycin resistant Enterococci (VRE) and synergism with antibiotics. Phytomedicine, 2005, 12, 203-208.
[8]
Sato, M.; Tanaka, H.; Oh-Uchi, T.; Fukai, T.; Etoh, H.; Yamaguchi, R. Antibacterial activity of phytochemicals isolated from Eerythrina zeyheri against vancomycin-resistant Enterococci and their combination with vancomycin. Phytother. Res., 2004, 18, 906-910.
[9]
Verpoorte, R.; Choi, Y.M.; Kim, H.K. Ethnopharmacology and systems biology: A perfect holistic match. J. Ethnopharmacol., 2005, 100, 53-56.
[10]
Hemaiswarya, S.; Kruthiventi, A.K.; Mukesh, D. Synergism between natural products and antibiotics against infection diseases. Phytomedicine, 2008, 15, 639-652.
[11]
Atta-ur-Rahman.; Choudhari, M.I.; Thomsen, W.J. Bioassay Techniques for Drug Development; Hardwood Academic Publisher: The Netherland, 2001, Vol. 16, .
[12]
Clinical and Laboratory Standards Institutes. Methods for Dilution Antimicrobial Susceptibility Test for bacteria that Grow aerobically; Approved Standard. 19th Edition, M07-M09, Wayne. PA., 2012, p. 32.
[13]
Sarker, S.D.; Nahar, L.; Kumarasamy, Y. Microtitre plate-based antibacterial assay incorporating resazurin as an indicator of cell growth, and its application in the in vitro antibacterial screening of phytochemicals. Methods, 2007, 42, 321-324.
[14]
Chuah, E.; Zakaria, Z.; Suhaili, Z. bakar, S.A.; Desa, M.N.M. Antimicrobial activities of plant extracts against methicillin-susceptibility and methillin-resistant Staphylococcus aureus. J. Microbial Res, 2014, 4, 6-13.
[15]
Fernandes, L.; Daruliza, K.; Sudhakaran, S.; Jegathambigai, R. Antimicrobial activity of crude extract of Piper sarmentosam against methillin-resistant Staphylococcus aureus, Escherichia coli, Vibrio cholera and Streptomyces pnemoniae. Eur. Rev. Med. Pharmacol. Sci., 2012, 16, 105-111.
[16]
Meksuriyen, D.; Cordell, G.A.; Ruangrungsi, N.; Tantivatana, P. Traditional medicinal plants of Thailand, IX. 10-hydroxy-11-methoxydracaenone and 7,10-dihydroxy-11-methoxydracaenone from Dracaena loureiri. J. Nat. Prod., 1987, 50, 1118-1125.
[17]
Zheng, Q.A.; Zhang, Y.J.; Yang, C.R. A new-meta homoisoflavane from the fresh stems of Dracaena cochinchinensis. J. Asian Nat. Prod. Res., 2006, 8, 571-577. b
[18]
Ichikawa, K.; Kitaoka, M.; Taki, M. Retrodihydrochalcones and homoisoflavonones isolated from Thai medicinal plant Dracaena loureiri and their estrogen agonist activity. Planta Med., 1997, 63, 540-543.
[19]
Yi, T.; Chen, H.B.; Zhao, Z.Z.; Yu, Z.L.; Jiang, Z.H. Comparison of the chemical profiles and antiplatelet aggregation effects of two “Dragon’s blood” drug used in traditional Chinese medicine. J. Ethnopharmacol., 2011, 133, 796-802.
[20]
Li, N.; Ma, Z.; Li, M.; Xing, Y. hou, Y. Natural potential therapeutic agents of neurodegenerative diseases from the traditional herbal medicine Chinese Dragon’s blood. J. Ethnopharmacol., 2014, 152, 508-521.
[21]
Heller, W.; Andermatt, P.; Schaad, W.A.; Tamn, C.; Homoisoflavanone, I.V. Neue inhaltsstoffe der eucomin-reihe von Eucomis bicolar. Helv. Chim. Acta, 1976, 59, 212-213.
[22]
Dai, Y.; Harinantenaina, L.; Brodie, P.J. Antiproliferative homoisoflavanoids and bufatrienolides from Urginea depressa. J. Nat. Prod., 2013, 76, 865-872.
[23]
Palombo, E.A. Traditional medicinal plant extracts and natural products with activity against oral bacteria: potential application in the prevention and treatment of oral diseases. J. Evid. Based Complementary Altern. Med., 2011.
[http://dx.doi.org/10.1093/ecam/nep067]
[24]
Jenkinson, H.F.; Lamont, R.J. Oral microbial communities in sickness and in health. Trends Microbiol., 2015, 13, 589-595.
[25]
Donel, M.R.O.; Saukkonen, J.J. Antimicrobial agents. New York, USA. MCGraw-Hill: 2012.
[26]
Mayaud, L.; Carricajo, A.; Aubert, G. Comparison of bacteriostatic and bactericidal activity of 13 essential oils against strains with varying sensitivity to antibiotics. Lett. Appl. Microbiol., 2008, 47, 167-173.
[27]
Bernatov, S.; Samek, O.; Pilat, Z. Following the mechanisms of bacteriostatic versus bactericidal action using Raman spectroscopy. Molecules, 2013, 18, 13188-13199.

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