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Stopped-flow kinetic method for the fluorimetric determination of DNA traces in biological samples based on the interaction long-wavelength fluorophor, surfactant and nucleic acid

机译:基于长波荧光团,表面活性剂和核酸相互作用的停止流动力学方法荧光测定生物样品中的痕量DNA

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摘要

A simple and rapid method for the determination of DNA, involving the interaction between a surfactant, a long-wavelength fluorophor (LWF) and the nucleic acid, is presented. Different chemical systems based on the local effective charge of the surfactant/LWF system with DNA were tested, choosing cetyltrimethyl ammonium bromide (CTAB) and indocyanine green (ICG) for the development of the method. The fluorescence of ICG increases in the presence of CTAB, but it rapidly decreases in the presence of deoxyribonucleic acid. The initial reaction-rate (v0) and signal at a prefixed-time (Δ/F_(20)) are monitored at 780 and 802 nm as excitation and emission wavelengths, respectively, using stopped-flow mixing technique, which makes the method applicable to automate routine analysis. Each measurement was obtained in about 30 s, being the integration time 0.1 s. The dynamic range of the calibration graph was 10-1500 ng mL~(-1), with a detection limit of 5 ng mL~(-1). The precision of the method, expressed as relative standard deviation, ranged between 2.1% and 4.5%. After a sample treatment consisting on a conventional extraction, the method was applied to the determination of DNA in several samples from different biological materials.
机译:提出了一种简单,快速的DNA测定方法,该方法涉及表面活性剂,长波荧光团(LWF)和核酸之间的相互作用。测试了基于表面活性剂/ LWF系统带有DNA的局部有效电荷的不同化学系统,选择了十六烷基三甲基溴化铵(CTAB)和吲哚菁绿(ICG)来开发该方法。在CTAB存在下,ICG的荧光增加,但在脱氧核糖核酸存在下,ICG的荧光迅速下降。使用停止流混合技术,分别在780和802 nm处监测初始反应速率(v0)和预定时间的信号(Δ/ F_(20))作为激发和发射波长,这使该方法适用自动化常规分析。每次测量大约在30 s内完成,积分时间为0.1 s。校正图的动态范围为10-1500 ng mL〜(-1),检出限为5 ng mL〜(-1)。用相对标准偏差表示的方法精度在2.1%至4.5%之间。经过常规提取的样品处理后,该方法可用于测定来自不同生物材料的多个样品中的DNA。

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