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Collaborative study of an liquid chromatographic method for the determination of R-timolol and other related substances in S-timolol maleate

机译:液相色谱法测定马来酸S-噻吗洛尔中R-噻吗洛尔及其他相关物质的合作研究

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A collaborative study applying an enantiomeric liquid chromatographic (LC) method was carried out to determine the content of the enantiomeric impurity R-timolol and other related substances in three different S-timolol maleate samples. Eight laboratories, all located in Europe, participated in the study. The quantitative results obtained were used to estimate the uncertainty on the content of the different impurities. For that purpose, a set-up was adapted from the ISO guidelines 5725-2, which allowed the estimation of the different variances, i.e. the between-laboratories (s(laboratories)(2)), the between-days (s(days)(2)) and the between-replicates (s(replicates)(2)), The variances of repeatability (s(r)(2)) and reproducibility (s(R)(2)) were then calculated using the equations s(r)(2) = s(replicates)(2) and s(R)(2) = s(replicates)(2) + s(days)(2) + s(laboratories)(2). For the timolol impurities, it was found that the estimated uncertainty seem to be concentration-dependent. Since the LC method which combines the compendial ones for enantiomeric purity and related substances testing was applied to evaluate uncertainty in this collaborative study, it was shown how a laboratory can evaluate the uncertainty of its results when applying the method in the future. (c) 2005 Elsevier B.V. All rights reserved.
机译:进行了一项使用对映体液相色谱(LC)方法的合作研究,以确定三种不同S-噻吗洛尔马来酸酯样品中对映体杂质R-噻吗洛尔和其他相关物质的含量。全部位于欧洲的八个实验室参加了这项研究。获得的定量结果用于估计不同杂质含量的不确定性。为此,根据ISO指南5725-2对设置进行了调整,该设置允许估算不同的方差,即实验室之间(s(laboratories)(2)),工作日之间(s(days) )(2))和复制品之间(s(复制品)(2)),然后使用等式计算可重复性(s(r)(2))和再现性(s(R)(2))的方差s(r)(2)= s(重复项)(2)和s(R)(2)= s(重复项)(2)+ s(天)(2)+ s(实验室)(2)。对于噻吗洛尔杂质,发现估计的不确定度似乎与浓度有关。由于在这项合作研究中,LC方法结合了对映体纯度和相关物质测试的补充方法来评估不确定性,因此表明了实验室在将来应用该方法时如何评估其结果的不确定性。 (c)2005 Elsevier B.V.保留所有权利。

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