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Determination of Trace Tetracycline Using Phase-Separation Sublation and Ultraviolet Detection

机译:相分离浮选-紫外检测法测定痕量四环素

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摘要

A novel analytical method was proposed to determine trace tetracycline (TC) by phase-separation sublation using Mg(II) as a ligand. When pH is 7.0, tetracycline and Mg(II) can combine to a stable complex (Mg-TC). Under certain conditions, the complex can be separated from a solution by phase-separation sublation, because it has better hydrophobicity, this procedure estimated by HPLC was good. The optimum phase-separation floatation was performed. 3.5 mol L~(-1) sodium chloride as ion intensity regulator, caustic soda solution as acidity regulator and tetrahydrofuran as extraction solvent. The detection wavelength is 380 nm, linear regression equation is A = 1.912 x 10~5C + 0.011, linear range is from 1.7 x 10~(-7) to 1.02 x 10~(-5) mol L~(-1), floating rate is 89 %, enrichment multiple is 26.7. The recoveries of tetracycline in water was 96.1 to 98.2 %.
机译:提出了一种新的分析方法,以Mg(II)为配体,通过相分离衍生法测定痕量四环素(TC)。当pH为7.0时,四环素和Mg(II)可以结合成稳定的络合物(Mg-TC)。在某些条件下,可以通过相分离转移将配合物从溶液中分离出来,因为它具有更好的疏水性,通过HPLC估算的这一程序很好。进行了最佳的相分离浮选。 3.5 mol L〜(-1)氯化钠作为离子强度调节剂,苛性钠溶液作为酸度调节剂,四氢呋喃作为萃取溶剂。检测波长为380 nm,线性回归方程为A = 1.912 x 10〜5C + 0.011,线性范围为1.7 x 10〜(-7)至1.02 x 10〜(-5)mol L〜(-1),浮动率为89%,富集倍数为26.7。水中四环素的回收率为96.1%至98.2%。

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