Synthesis and study of anti-bacterial activity of complexes of diallyldisulphide from garlic
DOI:
https://doi.org/10.22377/ijgp.v6i3.257Abstract
Background: The development of bacterial resistance to available antibiotics and increasing incidence of multiresistant bacterial infections in hospitals and in the community has necessitated the search for new antibacterial agents to treat the bacterial infection. It has long been known that metal ions are involved in biological processes of life through bonding to the heteroatoms of the heterocyclic residues of biological molecules i.e., proteins, enzymes and nucleic acids etc. The behavior of the disulfide group as a donor in transition metal complexes has not been subjected to such detailed study as a number of other donor groups. Aim: The Diallyldisulphide is oneof the main constituents of Allium sativum (Garlic). The antibacterial and antifungal activity of the Garlic is due to the presence of sulphur containing compounds. The aim of the present work was to synthesize metal complexes with Diallyldisulphide. Materials and Methods: Complexation reactions between the Diallyldisulphide and the metal ions were carried out at three different pH i.e. acidic (pH 3), neutral (pH 7) and alkaline (pH 10) using three different ratios of metal ligand namely 1:1, 1:2, 1:3, respectively. Complex formation with the ligand and all the metals took place at pH 10, indicating that complexes were stable at this pH. Studies with different metal: ligand ratio showed that in case of silver the complexation took place at 1:1 ratio. In case of divalent metals, the appropriate ratio of metal: ligand was 1:2. The structures of the new complexes obtained were determined by spectroscopic
methods. Results and Discussion: Synthesized complexes were investigated for antimicrobial activity against Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae and E.coli. Diallyldisulphide-silver complex exhibited significant antibacterial activity (MIC 100 μg/ mL), and was found to be effective against selected organisms. The results concluded that the metal complexes are better antibacterial agents as compared to the silversulphadiazine.
Key words: Antibacterial activity, complexes, diallyldisulphide, garlic, minimum inhibitory concentration
Downloads
References
Ernst E. Cardiovascular effects of garlic (Allium sativum): A review.
Pharmatherapeutics 1987;5:83-9.
Tsao SM, Yin MC. In-vitro antimicrobial activity of four diallyl
sulphides occurring naturally in garlic and Chinese leek oils. J Med
Microbiol 2001;50:646-9.
Tan JT, Bardwell JC. Key Players Involved in Bacterial Disulfide-
Bond Formation. Chem Bio Chem 2004;5:1479-87.
Kang YJ. Metallothionein redox cycle and function. Exp Biol Med
;231:1459-67.
Matsumoto K, Sugiyama H. Organometallic-like CH bond
activation and CS bond. Acc Chem Res 2002;35:915-26.
Bianchini C, Meli A, Vizza FJ. Role of single-site catalysts in the
hydrogenation of thiophenes: From models systems to effective
HDS catalyst. Organomet Chem 2004;689:4277-90.
Natile G, Bor G. Studies of Differences in Ligand Transfer, Stability,
and Fragmentation on Electron-Impact of Some Organosulfur
Derivatives of Cobalt and Iron Carbonyls. J Organomet Chem
;35:185-93.
Roesky HW, Gries T, Jones PG, Weber KL, Sheldrick GM.
Synthesis and x-ray structure of tetrakis (diphenyl disulfide
or diselenide) disilver bis (hexafluoroarsenate) six-membered
silver-sulfur and silver-selenium rings. J Chem Soc Dalton Trans
;1781-4.
Louvain N, Mercier N, Kurmoo M, CuI–Br. Oligomers and
Polymers Involving Cu–S (cystamine) Bonds. Eur J Inorg Chem
;1654-60.
Adams RD, Long JW, Perrin JL. A New Route to Dihydrodithiins
by a Catalytic Reaction of Vinylthiiranes with W (CO)5(NCMe).
J Am Chem Soc 1998;120:1922-8.
Adams RD, Perrin JL. Catalytic Transformations of Vinylthiiranes
by Tungsten Carbonyl Complexes. A New Route to 3, 6-Dihydro-1,
-dithiins. J Am Chem Soc 1999;121:3984-91.
McKarns PJ, Heeg MJ, Winter CH. Synthesis, Structure,
Hydrolysis, and Film Deposition Studies of Complexes of
the Formula [NbCl(4)(S(2)R(2))(2)][NbCl(6)]. Inorg Chem
;37:4743-7.