2017
DOI: 10.4314/tjpr.v16i5.23
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Synthesis, characterization and pharmacological evaluation of mixed ligand-metal complexes containing omeprazole and 8-hydroxyquinoline

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Cited by 27 publications
(14 citation statements)
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“…First, plant seeds were washed to remove dust; after that, they were shade dried at a temperature of 25-30 °C [12]. With the help of a commercial blender (FTA-788, West point, Germany), seeds were pulverized and then sieved (150 mesh sieve (0.065 mm)) [13]. The resultant seed powder material was stored in an airtight container.…”
Section: Sample and Extract Preparationmentioning
confidence: 99%
“…First, plant seeds were washed to remove dust; after that, they were shade dried at a temperature of 25-30 °C [12]. With the help of a commercial blender (FTA-788, West point, Germany), seeds were pulverized and then sieved (150 mesh sieve (0.065 mm)) [13]. The resultant seed powder material was stored in an airtight container.…”
Section: Sample and Extract Preparationmentioning
confidence: 99%
“…The antimycotic propensity of the synthesized metal complex formazans (S1-S6) were evaluated against different mycological strains such as Trichophyton mentagrophytes (ATCC 9533), Candida albicans (ATCC 10231), Aspergillus niger (ATCC 16404), Saccharomyces cerevisiae (ATCC 9763) and Candida glabrata (ATCC 90030) adopting the standard protocol described by. [56,57] The employed fungal microorganisms were acquired from the microbiology laboratory of University of Veterinary and Animal Science Lahore, Pakistan. Terbinafine and Fluconazole were served as standard antimycotic drugs (positive control) for the comparative study of antimycotic propensity against different fungal strains.…”
Section: Antimycotic Activitymentioning
confidence: 99%
“…(8) Taking into account the total concentration of dissolved acid and the Ka 1 and Ka 2 acid constants of HQx, the equilibrium concentrations of the H 2 Qx +, HQx and Qxspecies can be deduced, depending on the concentration of hydrogen ions, respectively, depending on pH, equations (9)(10)(11). (11) Correlating concentrations suggested by the relationships (4-11) with the constants for studied ions complexes formation with 8-hydroxyquinoline [31,34] it (4) can be illustrated which ions will be separated depending on the pH of the receiving phase ( fig. 6).…”
Section: Determination Of Ph and Optimal Working Timementioning
confidence: 99%