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首页> 外文期刊>Journal of the Brazilian Chemical Society >Preparative Separation and Structural Identification of Impurities of a New ?± 2 -Adrenoceptor Agonist Using Stacking Injection, LC-MS n and LC-SPE-NMR
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Preparative Separation and Structural Identification of Impurities of a New ?± 2 -Adrenoceptor Agonist Using Stacking Injection, LC-MS n and LC-SPE-NMR

机译:LC-MS n和LC-SPE-NMR叠加注射法制备新型α±2-肾上腺素受体激动剂的杂质的制备分离和结构鉴定

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Identifying impurities in drug substances has become one of the most important issues in pharmaceutical analysis since it can have a significant impact on the efficacy of new pharmaceutical products. Due to the purity requirements, in this paper a new synthetic ?± 2 -adrenoceptor agonist, called LPSF-PT-31, was purified and its impurities were characterized by liquid chromatography-multistage mass spectrometry (LC-MS n ) and liquid chromatography-solid phase extraction-nuclear magnetic resonance (LC-SPE-NMR). The purification step was conducted using a semi-preparative liquid chromatography and stacked injections as a new approach to drug purification. As a result, a total yield of 75% of the pure LPSF-PT-31 and 2.9 L day -1 in solvent reduction was obtained. The combination of semi-preparative stacking injection, LC-MS n , and LC-SPE-NMR, demonstrated to be efficient to purify active drugs and unambiguously identify its impurities. In addition, isolation and identification of drug impurities in the early stages of development can improve the synthetic pathway, preventing the formation of impurities or minimizing this formation to minimum levels.
机译:鉴定原料药中的杂质已成为药物分析中最重要的问题之一,因为它会对新药物的功效产生重大影响。由于纯度的要求,本文纯化了一种新的合成的α±2-肾上腺素受体激动剂LPSF-PT-31,并通过液相色谱-多级质谱(LC-MS n)和液相色谱-固相萃取-核磁共振(LC-SPE-NMR)。纯化步骤使用半制备液相色谱法和堆叠式进样法进行,是药物纯化的新方法。结果,获得了纯LPSF-PT-31和2.9L第-1天的溶剂减少的总产率。半制备型堆叠进样,LC-MS n和LC-SPE-NMR的结合被证明可有效纯化活性药物并明确鉴定其杂质。此外,在开发的早期阶段对药物杂质进行分离和鉴定可以改善合成途径,防止杂质的形成或将这种形成的程度降至最低。

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