[Application of qNMR in Standard Materials Used for the Crude Drugs].

IF 0.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Azusa Suzuki
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引用次数: 0

Abstract

Crude drugs and Kampo formulations derived from natural materials such as plants, animals, and minerals are multicomponent medicines that contain numerous chemical constituents. Quantitative determination of characteristic constituents for quality control is crucial for the standardization and quality assurance of natural medicines. Quantitative assays to determine marker compound contents are commonly performed using HPLC systems. In order to achieve accurate quantitative determination, it is essential to use standard materials with well-defined purities corresponding to the target analytes. Many marker compounds used as standard materials must be purified and isolated from natural products while ensuring sufficient purity. However, the composition of impurities in the standard material differs among different batches due to differences in the raw materials and their extraction, separation, and purification processes. Therefore, controlling the purity of standard materials derived from natural products is more complex than that of synthetic substances. Quantitative NMR (qNMR), which has become widely used as an absolute quantitative method for low-molecule organic compounds, makes it possible to solve these issues. qNMR has been introduced into the crude drug section of the Japanese Pharmacopoeia (JP) for evaluating the purity of standard materials used for the assay. This review outlines an example of quantitative determination using relative molar sensitivity (RMS) based on qNMR adopted in the JP and introduces the latest efforts toward the application of qNMR to standard materials used for crude drugs in this context.

[qNMR 在粗制药物标准材料中的应用]。
从植物、动物和矿物等天然材料中提取的原药和康普制剂是多成分药物,含有多种化学成分。定量测定特征成分以进行质量控制对于天然药物的标准化和质量保证至关重要。测定标记化合物含量的定量检测通常使用 HPLC 系统。为了实现准确的定量测定,必须使用与目标分析物相对应的纯度明确的标准物质。许多用作标准物质的标记化合物必须从天然产物中纯化和分离出来,同时确保足够的纯度。然而,由于原材料及其提取、分离和纯化过程的不同,不同批次标准物质中的杂质成分也不尽相同。因此,控制天然产品标准物质的纯度比控制合成物质的纯度更为复杂。定量核磁共振(qNMR)作为一种低分子有机化合物的绝对定量方法已被广泛应用,使解决这些问题成为可能。本综述概述了日本药典中采用的基于 qNMR 的相对摩尔灵敏度 (RMS) 进行定量测定的实例,并介绍了在此背景下将 qNMR 应用于粗制药物标准材料的最新努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
169
审稿时长
1 months
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