Development and validation of a capillary electrophoresis-indirect photometric detection method for the determination of the non-UV-absorbing 1,4-dideoxy-1,4-imino-D-arabinitol in active pharmaceutical ingredients, solutions and tablets using an internal standard

被引:2
|
作者
Jamali, B
Nielsen, HM
机构
[1] Novo Nordisk AS, R&D, CMC Dev, Dept Analyt Dev, DK-2760 Malov, Denmark
[2] Novo Nordisk AS, Diabet Bulk Prod, Purificat Insulin Analogues, DK-2760 Malov, Denmark
关键词
pharmaceutical analysis; indirect detection; validation; dideoxyiminoarabinitol; piperidine;
D O I
10.1016/S0021-9673(03)00605-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high speed, selective, and robust capillary electrophoresis (CE) method with high capacity was developed and validated for determination of assay of 1,4-dideoxy-1,4-iminow-D-arabinitol in active pharmaceutical ingredients, solutions, and tablets during the development work at preclinical and Phase I and 11 clinical studies. 1,4-Dideoxy-1,4-imino-D-arabinitol, tartrate has (almost) no UV absorption. Therefore, the developed CE method for quantification was based on indirect UV detection. A cation CE principle was chosen using an electrolyte at pH 4.0 containing dimethyldiphenylphosphonium hydroxide, which has a strong UV absorbance. The quantification was performed using internal standard technique, by which piperidine was used as internal standard. The method was validated. The validation results showed that the CE method was suitable for the assay (and dissolution) analysis. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:213 / 223
页数:11
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