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Quantitative HPLC Analysis of Active Pharmaceutical Ingredients in Syrup Vehicle Using Centrifugal Filter Devices and Determination of Xanthan Gum in Syrup Vehicle Using Rheometry

机译:离心过滤装置定量分析糖浆车中活性药物成分的HPLC和流变法测定糖浆车中黄原胶的含量

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摘要

Using rapid centrifugal filtration (≤ 30 min) of diluted samples, the filter membrane prevented compounds with molecular weight higher than the nominal molecular weight limit (NMWL) from transporting through the membrane, thus separating them from compounds with molecular weight smaller than NMWL, which would pass through the membrane. The purpose of this study aims to remove high molecular weight matrix (such as xanthan gum) interferences while achieving a quantitative analysis of the active pharmaceutical ingradients of interest. Two model active pharmaceutical ingredients, L-arginine and amphotericin B, were quantitatively recovered from the diluted syrup vehicle after centrifugation with the filter devices. The reproducibility [% relative standard deviation (RSD), peak area] of the filtered samples was less than 0.5%. For amphotericin B samples. The linear range was 0.28 μg/mL to 28.2 μg/mL. The limit of detection was 0.06μg/mL. The limit of quantification was 0.28 μg/mL. The viscosity of a syrup vehicle changed linearly with the concentration of xanthan gum. A method was thus developed to determine xanthan gum in the syrup vehicle. The accuracy was within 95.0% to 105.0% at different concentration levels.
机译:使用稀释样品的快速离心过滤(≤30分钟),滤膜可防止分子量高于标称分子量极限(NMWL)的化合物通过膜传输,从而将它们与分子量小于NMWL的化合物分离。会穿过膜。这项研究的目的是消除高分子量基质(如黄原胶)的干扰,同时对感兴趣的活性药物成分进行定量分析。用过滤装置离心后,从稀释的糖浆中定量回收两种模型活性药物成分L-精氨酸和两性霉素B。过滤后的样品的重现性[相对标准偏差%(RSD),峰面积]小于0.5%。用于两性霉素B样品。线性范围为0.28μg/ mL至28.2μg/ mL。检测限为0.06μg/ mL。定量限为0.28μg/ mL。糖浆媒介物的粘度随黄原胶的浓度线性变化。因此开发了一种确定糖浆媒介物中黄原胶的方法。在不同浓度水平下,准确度在95.0%至105.0%之内。

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