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The Genoprotective Activity of Aqueous Green Tea extract against Metronidazole and Tinidazole Genotoxic Effect
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Aim: The study designed to evaluate the Geno-protective effect of green tea extract against genotoxicity induced by metronidazole and tinidazole. Methods: Thirty-six mice were used, For each experiment, The animals divided into 6 groups: Group I- Negative control administered distilled water; Group II-Healthy mice treated with metronidazole alone, Group III- Healthy mice treated with tinidazole alone; Group IV- Healthy mice administered green tea extract alone Group V- Healthy mice treated with metronidazole, followed by green tea extract administration, Group VI- Healthy mice treated with tinidazole, followed by administration of green tea extract. Results: treatment with Tinidazole significantly increase total chromosomal aberration (0.185± 0.0039, 0.167±0.0049) as compared to negative control group (0.116±0.004, 0.103±0.004) in bone marrow and spleen cells respectively. In addition results showed significant change in total chromosomal aberration between the groups (II, IV, V) (0.122±0.012, 0.079±0.005, 0.101±0.0077) (0.121±0.005, 0.067±0.002, 0.087±0.004) in bone marrow cells and spleen cells respectively. In addition, the results shown that there are significant changes in total chromosomal aberration between the groups (III, IV, VI) (0.185±0.0039, 0.079±0.005, 0.133±0.0135) (0.167±0.0049, 0.067±0.002, 0.11±0.012) in bone marrow cells and spleen cells respectively. Conclusion: Tinidazole has greater effect than metronidazole on total chromosomal aberration and the aqueous extract of green tea confers Geno-protective effect against the metronidazole or tinidazole induced genotoxicity in mice.

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Publication Date
Thu Nov 19 2020
Journal Name
Indonesian Journal Of Chemistry
Determination of Eugenol in Personal-Care Products by Dispersive Liquid-Liquid Microextraction Followed by Spectrophotometry Using <i>p</i>-Amino-<i>N,N</i>-dimethylaniline as a Derivatizing Agent
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Two simple methods for the determination of eugenol were developed. The first depends on the oxidative coupling of eugenol with p-amino-N,N-dimethylaniline (PADA) in the presence of K3[Fe(CN)6]. A linear regression calibration plot for eugenol was constructed at 600 nm, within a concentration range of 0.25-2.50 μg.mL–1 and a correlation coefficient (r) value of 0.9988. The limits of detection (LOD) and quantitation (LOQ) were 0.086 and 0.284 μg.mL–1, respectively. The second method is based on the dispersive liquid-liquid microextraction of the derivatized oxidative coupling product of eugenol with PADA. Under the optimized extraction procedure, the extracted colored product was determined spectrophotometrically at 618 nm. A l

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