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采用混合模式色谱柱通过高效液相色谱法对L-蛋氨酸进行杂质剖析。

Impurity profiling of L-methionine by HPLC on a mixed mode column.

作者信息

Kühnreich Raphael, Holzgrabe Ulrike

机构信息

University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany.

University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany.

出版信息

J Pharm Biomed Anal. 2016 Apr 15;122:118-25. doi: 10.1016/j.jpba.2016.01.057. Epub 2016 Feb 2.

Abstract

Methionine is mostly produced synthetically. Thus, impurities are synthesis by-products in addition to oxidation and dimerization products. Here, a sensitive HPLC method for the determination of impurities in L-methionine was developed and validated using a SIELC(®) Primesep 100 column. Impurities were separated on the mixed mode column by reversed phase and cationic exchange mechanism. The limit of detection was in the range of 0.06-0.30 μg/ml (0.0004-0.002%), limit of quantification in the range of 0.30-0.75 μg/ml (0.002-0.005%) and linearity was shown in the range of 0.3-30.0 μg/ml (0.002-0.200%). The method was found to be precise (intermediate precision RS <5%; n=2) and accurate (recovery 96.0-121.4%, n=3). The method is also suitable for the purity assessment of DL-methionine and D-methionine. The amount of impurities found in batches was very low. Only L-methionine-sulfoxide and N-acetyl-DL-methionine could be detected in levels less than 0.05%.

摘要

蛋氨酸大多通过合成生产。因此,杂质除了氧化产物和二聚产物外,还有合成副产物。在此,开发了一种灵敏的高效液相色谱法,用于测定L-蛋氨酸中的杂质,并使用SIELC(®) Primesep 100柱进行了验证。杂质在混合模式柱上通过反相和阳离子交换机制进行分离。检测限在0.06 - 0.30μg/ml(0.0004 - 0.002%)范围内,定量限在0.30 - 0.75μg/ml(0.002 - 0.005%)范围内,线性范围在0.3 - 30.0μg/ml(0.002 - 0.200%)内。该方法被发现具有精密度(中间精密度RSD <5%;n = 2)和准确度(回收率96.0 - 121.4%,n = 3)。该方法也适用于DL-蛋氨酸和D-蛋氨酸的纯度评估。批次中发现的杂质量非常低。仅检测到L-蛋氨酸亚砜和N-乙酰-DL-蛋氨酸的含量低于0.05%。

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