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药物中不可紫外检测有机杂质研究中液相色谱检测方法的比较

Comparison of LC detection methods in the investigation of non-UV detectable organic impurities in a drug substance.

作者信息

McCrossen S D, Bryant D K, Cook B R, Richards J J

机构信息

SmithKline Beecham Pharmaceuticals, Tonbridge, Kent, UK.

出版信息

J Pharm Biomed Anal. 1998 Jul;17(3):455-71. doi: 10.1016/s0731-7085(97)00235-5.

Abstract

HPLC Analysis with different detection methods was shown to be essential in the separation and identification of unknown organic impurities in a drug substance. The impurities were found to exhibit very weak or no response to standard ultraviolet (UV) absorption detection. LC-MS, LC-NMR, indirect, refractive index and evaporative light-scattering detection were used to quantify and identify the impurities in this specific case. The drug substance studied was found to be an ideal analyte for demonstrating the advantages and limitations of several chromatographic detection systems for impurity profile analysis.

摘要

结果表明,采用不同检测方法的高效液相色谱分析对于原料药中未知有机杂质的分离和鉴定至关重要。发现这些杂质对标准紫外(UV)吸收检测表现出非常弱的响应或无响应。在这种特定情况下,使用液相色谱 - 质谱联用(LC-MS)、液相色谱 - 核磁共振联用(LC-NMR)、示差折光检测、间接检测和蒸发光散射检测来定量和鉴定杂质。所研究的原料药被发现是一种理想的分析物,可用于证明几种色谱检测系统在杂质谱分析中的优缺点。

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