ABSTRACT
In this research,we chiefly explored a new fast test method--microtox technology to evaluate the comprehensive toxicity of Shen Mai injection.We investigated characteristic parameters of vibrio fischeri (CS234) under different conditions in the pursuit of the optimum test parameters of the reliable method;and then locked the best parameters for Shen Mai injection assay with the products from different manufacturers by microtox fast test.As a result,the optimum reaction condition included 0.9 mL recovery liquid in each freeze-dried vial and 50 μL bacteria suspension of each sample within 2 mL solution in aggregate with 10-mins detection after adding bacteria suspension which pH value ranging from 5 to 10 and luminous intensity from 0.8 to 1.2 million in 10 mins.The relative standard deviation values of replication experiment and precision test were all below 15％.Under this optimum detection condition,it was found that the EC50 values were 35.60％,92.34％ and 146.57％,differing among the samples from three representative drug manufacturers,respectively (P ＜ 0.01).In conclusion,the concentration-effect relationship of Shen Mai injection existed in the toxicity assessment of vibrio fischeri with various ECs0 values from the three manufacturers.These results suggested that biological detection standards of Shen Mai injection presented great growth potential.Microtox-based fast test in the evaluation of comprehensive toxicity of ShenMai injection showed favorable application prospects over controlling the quality of different sources of products.
ABSTRACT
This study aimed at exploring the application of microtox technology to the evaluation of comprehensive toxicity of Sheng Mai injections.Characteristic parameters of vibrio fischeri (CS234) were measured by methodology inspection under different conditions to optimize the reaction condition with reliable technology.It was the first experiment to accomplish the comprehensive toxicity of Sheng Mai injections from various manufacturers using vibrio fischeri under the target condition.It was found that parameters of the optimum condition contained 0.9 mL recovery liquid volume in each freeze-dried vial and 50 μ L bacteria suspension of each sample,being included in 2 mL solution in aggregate under 10 mins' detection time after adding bacteria suspension with the favorable pH value ranging from 5 to 10 and luminous intensity from 0.8 to 1.2 million within 10 mins.The relative standard deviation values of replication experiment and precision test were all below 15％.Under this optimum detection condition,it was found that the EC50 values were 22.10％,34.10％ and 46.04％,respectively,presenting significant statistical differences (P＜0.05).These results demonstrated that the growth of biological detection standards of Sheng Mai injection was highlighted a long way to go.Besides,the microtox-based fast test for the evaluation of the comprehensive toxicity of Sheng Mai injection showed a prospective application to controlling the quality of different products from manufacturers.
ABSTRACT
Aims: The current study was aimed at evaluating the phytochemical profile and in vitro bacteria growth inhibitory potential of different solvent leaf extracts of V. amygdalina from northern Ghana. Study Design: Different solvent extracts of the plant were quantitatively and qualitatively evaluated for phytochemicals. In vitro bacteria sensitivity assay of the extracts was evaluated using some beta-lactamase producing bacteria as test microbes. Methodology: Ethanolic, methanolic, petroleum ether and aqueous leaf extracts of Vernonia amygdalina were studied in vitro for growth inhibition against beta-lactamase producing bacteria such as Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae and Pseudomonas aeruginosa using agar well diffusion method. Saponins, flavonoids, glycosides, alkaloids, tannins, phenolics, reducing sugars, anthracenosides, terpenes and phytosteroids were determined qualitatively and quantified. Results: All the phytochemicals tested were found to be present in both the methanolic and ethanolic leaf extracts. The aqueous extract showed the presence of saponins, reducing sugars and anthracenosides. Glycosides, flavonoids, saponins and alkaloids were the only groups of phytochemicals found in the petroleum ether extract. The methanolic extract showed the greatest amount of saponins (14.23%), flavonoids (2.15%), alkaloids (7.49%), tannins (5.4%), terpenes (10.20%) and phenolics (8.24%). The methanolic extract at concentration of 4 mg/ml showed growth inhibitory activities against all the test organisms with zone of inhibitions ranging from 16.00±0.50 (against E. coli) to 20.50±0.03 mm (against S. aureus). The ethanolic extract showed activity against only two of the test organisms viz. 23.00±0.33 mm against P. aeruginosa and 12.00±0.00 mm against S. aureus at similar concentration. All test organisms were resistant to both aqueous and pet ether extracts. Conclusion: The antibacterial activities of the methanolic and ethanolic extracts were significant (P < 0.05) and may be mediated by the presence of saponins, flavonoids, tannins, terpenes and alkaloids. Results from present study corroborate previous findings and also presents methanolic leaf extract of the plant as a credible candidate for the discovery of new phytotherapeutic agents against the beta-lactamase producing bacteria tested.