Improving the efficiency of quantitative 1H NMR: An innovative external standard-internal reference approach

被引:18
作者
Huang, Yande [1 ]
Su, Bao-Ning [1 ]
Ye, Qingmei [1 ]
Palaniswamy, Venkatapuram A. [1 ]
Bolgar, Mark S. [1 ]
Raglione, Thomas V. [1 ]
机构
[1] Bristol Myers Squibb Co, Analyt & Bioanalyt Dev, New Brunswick, NJ 08903 USA
关键词
Quantitative NMR; External standard; Internal reference substance; qNMR method; Internal standard; NATURAL-PRODUCTS; NMR-SPECTROSCOPY; ERETIC METHOD; VALIDATION;
D O I
10.1016/j.jpba.2013.07.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The classical internal standard quantitative NMR (qNMR) method determines the purity of an analyte by the determination of a solution containing the analyte and a standard. Therefore, the standard must meet the requirements of chemical compatibility and lack of resonance interference with the analyte as well as a known purity. The identification of such a standard can be time consuming and must be repeated for each analyte. In contrast, the external standard qNMR method utilizes a standard with a known purity to calibrate the NMR instrument. The external standard and the analyte are measured separately, thereby eliminating the matter of chemical compatibility and resonance interference between the standard and the analyte. However, the instrumental factors, including the quality of NMR tubes, must be kept the same. Any deviations will compromise the accuracy of the results. An innovative qNMR method reported herein utilizes an internal reference substance along with an external standard to assume the role of the standard used in the traditional internal standard qNMR method. In this new method, the internal reference substance must only be chemically compatible and be free of resonance-interference with the analyte or external standard whereas the external standard must only be of a known purity. The exact purity or concentration of the internal reference substance is not required as long as the same quantity is added to the external standard and the analyte. The new method reduces the burden of searching for an appropriate standard for each analyte significantly. Therefore the efficiency of the qNMR purity assay increases while the precision of the internal standard method is retained. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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