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Improved solid-state NMR quantifications of active principles in pharmaceutical formulations.

机译:改进了药物制剂中活性成分的固态NMR定量。

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摘要

The facility of implementation reached by solid-state nuclear magnetic resonance (ssNMR) spectroscopy makes this technique increasingly popular in pharmaceutical sciences, and more specifically for the dosage of active principles in pharmaceutical formulations, since about 80% of the formulations currently available on the market are present in the solid form. In this case, analysis by MAS NMR allows faster and simplified protocols, as a solubilization step is not required. However, the specificity of the ssNMR experiments should be explicitly taken into account when designing an accurate measurement procedure. In this work we show that, by using a combination of external concentration referencing and a properly designed sample preparation optimized for quantitative determinations, quantification of active principles in pharmaceutical formulations can be performed with both speed and precision. The method is illustrated by reinvestigating the dosage of Meprobamate, an anxiolytic agent typically prescribed in case of anxiety or muscular soreness, present in a commercial formulation (Equanil). Specifically, with respect to previously proposed analytical protocols, the procedure outlined here allows fast quantification with excellent precision.
机译:固态核磁共振(ssNMR)光谱学实现的便利性使得该技术在制药科学中越来越受欢迎,尤其是在药物制剂中有效成分的剂量方面,因为目前市场上约有80%的制剂可用以固体形式存在。在这种情况下,由于不需要增溶步骤,因此通过MAS NMR进行分析可以实现更快,更简单的方案。但是,在设计精确的测量程序时,应明确考虑ssNMR实验的特异性。在这项工作中,我们表明,通过结合使用外部浓度参考和为定量测定而优化的适当设计的样品前处理,可以快速而精确地对药物制剂中的有效成分进行定量。通过对商业配方(Equanil)中存在的丙氨酯(一种通常在焦虑或肌肉酸痛的情况下开出的抗焦虑药)的剂量进行重新研究来说明该方法。具体而言,相对于先前提出的分析方案,此处概述的过程可实现具有极高精确度的快速定量。

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