Title of article :
Synthesis and Determination of Partition Coefficients of Zinc Complexes with Clinical Potential application
Author/Authors :
Saghaie, Lotfollah Departmen of Medicinal Chemistry - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan , Houshfar, Gholamali Departmen of Medicinal Chemistry - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan , Neishabor, Mostafa Departmen of Medicinal Chemistry - Faculty of Pharmacy and Pharmaceutical Sciences - Isfahan University of Medical Sciences, Isfahan
Pages :
11
From page :
179
To page :
189
Abstract :
Zinc sulphate is currently used for treatment of zinc deficiency. Its uptake by the body is poor, necessitating the administration of high doses. This leads to a range of unpleasant side effects. In order to increase the bioavailability of zinc, several zinc complexes have been designed and synthesized using bidentate ligands of hydroxypyranones and hydroxypyridinones. Elemental analysis in each zinc complex was consistent with the formulations of ZnL2 species L: bidentate ligand) with 1.5 or 7 water molecules per zinc and the water molecules were removed by heating in a vacuum oven to yield anhydrous zinc complexes. The partition coefficients (Kpart)of the complexes were also determined in 1-octanol/buffer (at pH 7.40) system by using shake-flask method. It was found that, the complexes with hydroxypyranone ligands possess higher Kpart values than those with hydroxypyidinone ligands. Therefore, the comparison of the complexes highlights the hydroxypyranone zinc complexes as the most promising candidates for using in zinc deficiency. Since it was anticipated that this type of complexes probably possesses suitable lipophilicity to facilitate their penetration into the gastrointestinal tract.
Keywords :
Zinc complexes , Zinc deficiency , Hydroxypyranones , Hydroxypyridinones , Zinc sulfate
Journal title :
Astroparticle Physics
Serial Year :
2006
Record number :
2481232
Link To Document :
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