Current State of Oligonucleotide Characterization Using Liquid Chromatography-Mass Spectrometry: Insight into Critical Issues

被引:50
|
作者
Sutton, J. Michael [1 ]
Guimaraes, Guilherme J. [1 ]
Annavarapu, Vidya [1 ]
van Dongen, William D. [2 ]
Bartlett, Michael G. [1 ]
机构
[1] Univ Georgia, Dept Pharmaceut & Biomed Sci, Coll Pharm, Athens, GA 30602 USA
[2] Anabiotec, B-9940 Evergem, Belgium
关键词
ELECTROSPRAY-IONIZATION; CHARGED DROPLETS; PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES; LC-MS; IDENTIFICATION; THERAPEUTICS; SENSITIVITY; SEPARATION; MODIFIERS; IMPURITY;
D O I
10.1021/jasms.0c00179
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As interests increase in oligonucleotide therapeutics, there has been a greater need for analytical techniques to properly analyze and quantitate these biomolecules. This article looks into some of the existing chromatographic approaches for oligonucleotide analysis, including anion exchange, hydrophilic interaction liquid chromatography, and ion pair chromatography. Some of the key advantages and challenges of these chromatographic techniques are discussed. Colloid formation in mobile phases of alkylamines and fluorinated alcohols, a recently discovered analytical challenge, is discussed. Mass spectrometry is the method of choice to directly obtain structural information about oligonucleotide therapeutics. Mass spectrometry sensitivity challenges are reviewed, including comparison to other oligonucleotide techniques, salt adduction, and the multiple charge state envelope. Ionization of oligonucleotides through the charge residue model, ion evaporation model, and chain ejection model are analyzed. Therapeutic oligonucleotides have to undergo approval from major regulatory agencies, and the impurities and degradation products must be well-characterized to be approved. Current accepted thresholds for oligonucleotide impurities are reported. Aspects of the impurities and degradation products from these types of molecules are discussed as well as optimal analytical strategies to determine oligonucleotide related substances. Finally, ideas are proposed on how the field of oligonucleotide therapeutics may improve to aid in future analysis.
引用
收藏
页码:1775 / 1782
页数:8
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