Defining a system suitability limit to decide on column deterioration and to facilitate column transfers in chiral supercritical fluid chromatography

被引:3
作者
Declerck, Sven [1 ]
Vander Heyden, Yvan [1 ]
Mangelings, Debby [1 ]
机构
[1] Vrije Univ Brussel, Dept Analyt Chem, Appl Chemometr & Mol Modelling FABI, Laarbeeklaan 103, B-1090 Brussels, Belgium
关键词
Supercritical fluid chromatography; Enantioseparations; Intermediate-precision study; System suitability; Transfer; NORMAL-PHASE LIQUID; ENANTIOSELECTIVE CHROMATOGRAPHY; SEPARATION; HPLC; PHARMACEUTICALS; TOOL;
D O I
10.1007/s00216-019-02173-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The separation of enantiomers is an important requirement during the entire drug life cycle in the pharmaceutical industry. High-performance liquid chromatography and supercritical fluid chromatography (SFC) are the main chromatographic techniques used to separate enantiomers. Since chiral stationary phases are often extensively used once a method has been developed, columns will age and must be replaced after a certain period. However, no practical guidelines exist to determine when a column is deteriorated or to decide whether a transfer to another column (with the same chiral selector) is successful. In this study, a system suitability limit for resolution was defined, based on an intermediate (time-different) precision study in SFC on four immobilized polysaccharide-based columns that only differed in manufacturer or particle size. This system suitability limit could be used to decide on column deterioration or as a requirement to evaluate whether a separation transfer was successful. Some method adaptations may be necessary to obtain successful transfers. An approach was proposed, which helped the analyst to make successful transfers.
引用
收藏
页码:6221 / 6230
页数:10
相关论文
共 36 条
[1]  
[Anonymous], 2005, Guideline on the environmental risk assessment of medicinal products for human use, P1
[2]   Chiral stationary phases for HPLC - Choosing the right stationary phase can be daunting. [J].
Armstrong, DW ;
Zhang, B .
ANALYTICAL CHEMISTRY, 2001, 73 (19) :557A-561A
[3]   Fast generic chiral separation strategies using electrophoretic and liquid chromatographic techniques [J].
Ates, Hasret ;
Mangelings, Debby ;
Heyden, Yvan Vander .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 48 (02) :288-294
[4]   The development of a semi-preparatory scale supercritical-fluid chromatograph for high-throughput purification of 'combi-chem' libraries [J].
Berger, TA ;
Fogleman, K ;
Staats, T ;
Bente, P ;
Crocket, I ;
Farrell, W ;
Osonubi, M .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2000, 43 (1-3) :87-111
[5]  
Bonner WA, 2000, CHIRALITY, V12, P114
[6]   The market of chiral drugs: Chiral switches versus de novo enantiomerically pure compounds [J].
Calcaterra, Andrea ;
D'Acquarica, Ilaria .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2018, 147 :323-340
[7]   Chromatographic classification of commercially available reverse-phase HPLC columns [J].
Cruz, E ;
Euerby, MR ;
Johnson, CM ;
Hackett, CA .
CHROMATOGRAPHIA, 1997, 44 (3-4) :151-161
[8]   Generic chiral method development in supercritical fluid chromatography and ultra-performance supercritical fluid chromatography [J].
De Klerck, Katrijn ;
Heyden, Yvan Vander ;
Mangelings, Debby .
JOURNAL OF CHROMATOGRAPHY A, 2014, 1363 :311-322
[9]   Exploratory data analysis as a tool for similarity assessment and clustering of chiral polysaccharide-based systems used to separate pharmaceuticals in supercritical fluid chromatography [J].
De Klerck, Katrijn ;
Vander Heyden, Yvan ;
Mangelings, Debby .
JOURNAL OF CHROMATOGRAPHY A, 2014, 1326 :110-124
[10]   Supercritical fluid chromatography for the enantioseparation of pharmaceuticals [J].
De Klerck, Katrijn ;
Mangelings, Debby ;
Vander Heyden, Yvan .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2012, 69 :77-92