黑皮籽醇提物对阴道毛滴虫体外治疗作用的研究

M. S. J. Al-Ammash
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引用次数: 3

摘要

本研究采用甲硝唑类药物和黑穗槐种子酒精提取物对在i T上培养的阴道绦虫的影响进行了实验。结果表明,24-48 h后寄生虫数量开始增加,72-96 h后开始减少,因此从生长开始的72 h可以认为是阴道绦虫生长的对数期。本研究通过观察在生长周期(24、48、72和96)h内,随着提取物浓度的增加,滋养体数量逐渐减少,结果表明,实验室制备和进口浓度分别为450、550、650和750 mg/ml的苜蓿醇提物对阴道绦虫的毒性作用。不同浓度的甲硝哒唑被用作化学治疗和控制模型,每日药物效果,术后随访的结果,在当前结果显示浓度增加(24小时后)高数量的减少和活动的寄生虫的药物浓度,p ci增加150 200μg / l, th寄生虫96小时后完全消失,也抑制concentration50 (IC50) parasit w 100μg / l(英国《金融时报》48 h r孵化)。结果表明,苜蓿醇提物浓度为450和550 mg/ml时对寄生虫卵数量和活性的抑制作用较为接近,而浓度为650和750 mg/ml时对寄生虫卵生长的抑制作用最强。在培养中造成50%死亡的浓度(IC50)为550 mg/ml(加浓度72小时后)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study the Effect of Alcoholic Extract of Nigella sativa Seeds on Trichomomas vaginalis In Vitro
The present study included experimental effect of Metronidazole drug and Alcoholic extract of Nigella sativa seeds on T. vaginalis that cultivated on i T i Results showed that the numbers of parasite began increasing during a period after 24-48 hrs then began decreasing after 72-96 hrs, so that 72 hrs from growth considered logarithmic phase of T. vaginalis growth. Present results showed poisonous effect of N. sativa alcoholic extract that was prepared in laboratory and imported at concentrations (450, 550, 650 and 750) mg/ml on T. vaginalis by observing gradual decrease of trophozoite numbers with concentrate increase of extracts during growth periods (24, 48, 72 and 96) hrs. Different concentrations of Metronidazole were used as chemical therapy and control model, the results of the drug effects were followed-up daily, where current results showed (after 24 hours of concentration added) a high reduction in number and activity of the parasites at all concentrations of the drug were , p ci lly 150 200 μg/ l, th parasites disappeared completely after 96 hours, also the inhibitory concentration50 (IC50) of the parasit w 100 μg/ l ( ft r 48 h r incubation). The inhibitory effect of N. sativa alcoholic extract on the number and activity of T. vaginalis parasite was noted that the concentrations (450 and 550 mg/ml) were approximated in their effect on parasite growth, while the concentrations 650 and 750 mg/ml were the best in their inhibitory activity for parasite growth after 96 hours of addition. The concentration that causes 50% of death inculture (IC50) was 550 mg/ml (after 72 hours of concentration addition).
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