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使用同时混合模式(离子交换/反相)和亲水相互作用液相色谱法对药品进行综合分析。

Comprehensive analysis of pharmaceutical products using simultaneous mixed-mode (ion-exchange/reversed-phase) and hydrophilic interaction liquid chromatography.

作者信息

Kazarian Artaches A, Nesterenko Pavel N, Soisungnoen Phimpha, Burakham Rodjana, Srijaranai Supalax, Paull Brett

机构信息

Australian Centre for Research on Separation Science, School of Chemistry, University of Tasmania, Hobart, Tasmania, Australia.

出版信息

J Sep Sci. 2014 Aug;37(16):2138-44. doi: 10.1002/jssc.201400411. Epub 2014 Jun 30.

DOI:10.1002/jssc.201400411
PMID:24890905
Abstract

Liquid chromatographic assays were developed using a mixed-mode column coupled in sequence with a hydrophilic interaction liquid chromatography column to allow the simultaneous comprehensive analysis of inorganic/organic anions and cations, active pharmaceutical ingredients, and excipients (carbohydrates). The approach utilized dual sample injection and valve-mediated column switching and was based upon a single high-performance liquid chromatography gradient pump. The separation consisted of three distinct sequential separation mechanisms, namely, (i) ion-exchange, (ii) mixed-mode interactions under an applied dual gradient (reversed-phase/ion-exchange), and (iii) hydrophilic interaction chromatography. Upon first injection, the Scherzo SS C18 column (Imtakt) provided resolution of inorganic anions and cations under isocratic conditions, followed by a dual organic/salt gradient to elute active pharmaceutical ingredients and their respective organic counterions and potential degradants. At the top of the mixed-mode gradient (high acetonitrile content), the mobile phase flow was switched to a preconditioned hydrophilic interaction liquid chromatography column, and the standard/sample was reinjected for the separation of hydrophilic carbohydrates, some of which are commonly known excipients in drug formulations. The approach afforded reproducible separation and resolution of up to 23 chemically diverse solutes in a single run. The method was applied to investigate the composition of commercial cough syrups (Robitussin®), allowing resolution and determination of inorganic ions, active pharmaceutical ingredients, excipients, and numerous well-resolved unknown peaks.

摘要

液相色谱分析方法的开发采用了混合模式柱与亲水作用液相色谱柱串联的方式,以便同时对无机/有机阴离子和阳离子、活性药物成分及辅料(碳水化合物)进行全面分析。该方法采用双进样和阀介导的柱切换,基于一台高效液相色谱梯度泵。分离过程包括三种不同的连续分离机制,即:(i)离子交换,(ii)在施加的双梯度(反相/离子交换)下的混合模式相互作用,以及(iii)亲水作用色谱。首次进样时,Scherzo SS C18柱(Imtakt)在等度条件下实现无机阴离子和阳离子的分离,随后采用双有机/盐梯度洗脱活性药物成分及其相应的有机抗衡离子和潜在降解产物。在混合模式梯度的顶部(高乙腈含量),流动相切换至预平衡的亲水作用液相色谱柱,重新进样标准品/样品以分离亲水性碳水化合物,其中一些是药物制剂中常见的辅料。该方法在一次运行中可实现多达23种化学性质不同的溶质的可重现分离和拆分。该方法用于研究市售止咳糖浆(Robitussin®)的成分,可实现无机离子、活性药物成分、辅料及众多分离良好的未知峰的拆分和测定。

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