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使用热调谐串联柱通过反相和离子交换色谱法分离选定的碱性药物。

Separation of selected basic pharmaceuticals by reversed-phase and ion-exchange chromatography using thermally tuned tandem columns.

作者信息

Mao Y, Carr P W

机构信息

Department of Chemistry, University of Minnesota, Minneapolis 55455, USA.

出版信息

Anal Chem. 2001 Sep 15;73(18):4478-85. doi: 10.1021/ac010353w.

Abstract

The separation of basic pharmaceuticals is usually performed on C8 or C18 bonded silica supports. Silanolphilic interactions between basic analytes and surface silanol groups often lead to tailed peaks, poor efficiency, and irreproducible retention times. To solve these problems, many new types of silica-, zirconia-, and polymer-based columns, which provide unique selectivities, improved stability at high pH, or both, have been developed for the analysis of basic compounds. The essence of method development for the chromatographic analysis of basic compounds is to choose a system in which the band spacing can be varied dramatically, quickly, and conveniently while minimizing the tailing due to silanolphilic interactions. The thermally tuned tandem column (T3C) approach has been shown to provide an effective way to adjust stationary-phase selectivity for nonionic compounds. In this study, a tandem combination of an octadecylsilane (ODS) and a polybutadiene-coated zirconia (PBD-ZrO2) phase was used to separate nine antihistamines. Selectivity is tuned by independently adjusting the isothermal temperatures of the two columns. We found dramatic differences in the retention factors, elution sequences, and band spacing for the above set of basic drugs on the two types of columns. The T3C model has been used successfully to locate the optimal temperatures based on only four exploratory runs. The nine antihistamines were baseline separated on the tandem column combination even though they could not be separated on the individual phases. The effect of the buffer concentration on retention of the basic antihistamines was also studied. We conclude that cation-exchange interactions predominate on the PBD-ZrO2 phase, while reversed-phase interactions are more important on the ODS phase. Interestingly, an increase in column temperature causes a significant increase in the retention on the ODS column and a decrease of retention on the PBD-ZrO2 column. This can be explained by the change in the analyte's degree of ionization with temperature. The T3C combination of silica- and zirconia-based RPLC columns is demonstrated to be a powerful approach for the separation of this mixture of basic analytes.

摘要

碱性药物的分离通常在C8或C18键合硅胶载体上进行。碱性分析物与表面硅醇基团之间的硅醇亲合相互作用常常导致峰拖尾、效率低下以及保留时间不可重现。为了解决这些问题,人们开发了许多新型的基于硅胶、氧化锆和聚合物的色谱柱,这些色谱柱具有独特的选择性,在高pH值下稳定性提高,或两者兼具,用于碱性化合物的分析。碱性化合物色谱分析方法开发的关键在于选择一个系统,在该系统中,谱带间距能够快速、方便地显著变化,同时尽量减少硅醇亲合相互作用导致的拖尾现象。热调谐串联柱(T3C)方法已被证明是一种调节非离子化合物固定相选择性的有效方法。在本研究中,使用十八烷基硅烷(ODS)和聚丁二烯涂层氧化锆(PBD-ZrO2)相的串联组合来分离九种抗组胺药。通过独立调节两根色谱柱的等温温度来调整选择性。我们发现,上述一组碱性药物在两种类型的色谱柱上的保留因子、洗脱顺序和谱带间距存在显著差异。T3C模型仅通过四次探索性运行就成功地确定了最佳温度。即使这九种抗组胺药在单独的固定相上无法分离,但在串联柱组合上实现了基线分离。还研究了缓冲液浓度对碱性抗组胺药保留的影响。我们得出结论,阳离子交换相互作用在PBD-ZrO2相上占主导地位,而反相相互作用在ODS相上更为重要。有趣的是,柱温升高会导致ODS柱上的保留显著增加,而在PBD-ZrO2柱上的保留减少。这可以通过分析物的电离程度随温度的变化来解释。基于硅胶和氧化锆的反相液相色谱柱的T3C组合被证明是分离这种碱性分析物混合物的有效方法。

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