评估不同系列合成化合物的致癌/致突变潜力

Faisal Tasleem, Ayesha Bintay Farooq, Ijaz Ahmad, Abu Bakar Siddique, Rabia Tabassum, Farah Liaqat, Ambar Nadeem Muhammad, Adnan Hafiz, Rashed Rahman
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引用次数: 0

摘要

新药研究通常以合成药物为基础。长期以来,这些药物的使用给人类带来了耐受性等问题,由于抗感染的合法使用,微生物对品牌药物的防御也在不断增强。艾姆斯在 20 世纪 70 年代初进行的一项突变研究,在全球范围内被药品和化学品公司用于诊断突变致癌物,使其有可能被检测到,并被添加到诱变合成部分或辐射源中,引发不可逆的变化,以及从父代传递的遗传物质。脱氧核糖核酸(DNA)。本研究的目的是通过溶血、Ames 和损伤 DNA 保护试验评估合成化合物系列的致癌性。细胞毒性通过溶血试验和 DNA 损伤保护试验来确定,诱变性则通过鼠伤寒杆菌 TA100 和 TA98 菌株来确定。结论是,溶血性较低的化合物适合用于药物。经测定,合成化合物不具有诱变性。应用方差分析(ANOVA)比较了不同浓度之间的溶血率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Carcinogenic/Mutagenic Potential of Different Series of Synthetic Compounds
The new drug research is usually based on synthesis medicine. The use of these medications has created problems such as tolerance in humans, for a long time and due to legitimate use of anti-infection, microbial defense against branded medication is growing. A mutagensis study by Ames in the early 1970's, used worldwide by drug and chemicals companies to diagnose mutagens carcinogenes, making it possible for them to be detected, and to be added to the mutagenic synthesis portion or radiation source triggering irreversible changes, and to the genetic material transmitted from the parent. deoxyribonucleic acid (DNA). The purpose of this study was to assessment of carcinogenicity of synthetic compounds series by hemolytic, Ames and Damaged DNA protection assay. The cytotoxicity was determined with hemolytic assay and DNA Damage protection assay while mutagenicity was resolute by using S. typhimurium TA100 and TA98 strains. It is concluded that the compounds with less hemolytic compounds are good for uses in drugs. Synthetic compounds were determined to be non- mutagenic in nature. Analysis of variance (ANOVA) was applied to compare the hemolysis percent between different concentrations.
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