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核苷、核苷酸和寡核苷酸的亲水作用色谱(HILIC)分离:最新进展综述。

Separation of nucleobases, nucleosides, nucleotides and oligonucleotides by hydrophilic interaction liquid chromatography (HILIC): A state-of-the-art review.

机构信息

School of Pharmacy and Health Sciences, Fairleigh Dickinson University, 230 Park Ave. Florham Park, New Jersey 07932, USA.

出版信息

J Chromatogr A. 2024 Dec 6;1738:465467. doi: 10.1016/j.chroma.2024.465467. Epub 2024 Oct 22.

Abstract

The polar nature of nucleobases, nucleosides and nucleotides makes hydrophilic interaction chromatography (HILIC) a good choice of technology for separation. Both naturally occurring and modified nucleosides and nucleotides have been successfully separated in HILIC. A wide range of stationary phases with different retention and selectivity are suitable for the separation of nucleobases, nucleosides and nucleotides; and a sufficient knowledge base is also available to guide method development. Although oligonucleotides are significantly different from nucleotides in terms of polarity and charges, HILIC has been shown to be a viable alternative to ion-pairing reversed-phase liquid chromatography (IP-RPLC). Only a few polar stationary phases have been shown to provide satisfactory performance; however, the requirements for the mobile phase composition including organic solvent, mobile phase pH and salt concentration are sufficiently understood. This review provides a comprehensive evaluation of the chromatographic conditions with a historical perspective on adopting and developing HILIC for the separation of nucleobases, nucleosides, nucleotides and oligonucleotides. The areas for more research and potential directions for future development activities are identified and discussed.

摘要

碱基、核苷和核苷酸的极性使得亲水性相互作用色谱(HILIC)成为分离的理想技术选择。天然存在的和修饰的核苷和核苷酸都已成功地在 HILIC 中分离。具有不同保留和选择性的广泛的固定相适用于碱基、核苷和核苷酸的分离;并且也有足够的知识库来指导方法开发。尽管寡核苷酸在极性和电荷方面与核苷酸有很大的不同,但 HILIC 已被证明是离子对反相液相色谱(IP-RPLC)的可行替代方法。只有少数几个极性固定相被证明具有令人满意的性能;然而,对包括有机溶剂、流动相 pH 值和盐浓度在内的流动相组成的要求已经有了充分的了解。本综述从历史角度全面评估了采用和发展 HILIC 用于分离碱基、核苷、核苷酸和寡核苷酸的色谱条件,并确定和讨论了进一步研究的领域和未来发展活动的潜在方向。

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