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

机译:使用热调谐串联色谱柱通过反相和离子交换色谱分离特定的基础药物

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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 ((TC)-C-3) 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 (TC)-C-3 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 (TC)-C-3 combination of silica- and zirconia-based RPLC columns is demonstrated to be a powerful approach for the separation of this mixture of basic analytes.
机译:碱性药物的分离通常在C8或C18键合的二氧化硅载体上进行。碱性分析物与表面硅烷醇基团之间的亲硅相互作用通常会导致峰拖尾,效率低和保留时间无法重现。为解决这些问题,已开发出许多新型的硅胶,氧化锆和聚合物基色谱柱,它们可提供独特的选择性,在高pH下可提高稳定性,或同时提供这两种色谱柱,用于分析碱性化合物。碱性化合物色谱分析方法开发的实质是选择一种系统,在该系统中,带隙可以显着,快速和方便地变化,同时最小化由于亲硅相互作用引起的拖尾。热调谐串联色谱柱((TC)-C-3)方法已显示出为调整非离子化合物固定相选择性提供了一种有效方法。在这项研究中,十八烷基硅烷(ODS)和聚丁二烯涂层氧化锆(PBD-ZrO2)相的串联组合用于分离9种抗组胺药。通过独立调节两根色谱柱的等温温度来调节选择性。我们发现在两种类型的色谱柱上,以上一组基本药物的保留因子,洗脱序列和谱带间距存在显着差异。 (TC)-C-3模型已成功用于仅基于四个探索性运行来确定最佳温度的位置。即使无法在各个相上将九种抗组胺药在串联色谱柱组合上进行基线分离。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,色谱柱温度的升高会导致ODS色谱柱的保留率显着增加,而PBD-ZrO2色谱柱的保留率下降。这可以通过分析物的电离度随温度的变化来解释。硅胶和氧化锆基RPLC色谱柱的(TC)-C-3组合被证明是分离碱性分析物混合物的有效方法。

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