Department of Food Science and Technology, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, United States.
Waters Corporation, Waters Mid-Atlantic Office, Suite 103, 5565 Sterrett Place, Columbia, MD 21044, United States.
J Chromatogr A. 2019 Jun 7;1594:54-64. doi: 10.1016/j.chroma.2019.02.007. Epub 2019 Feb 4.
Cocoa flavanols (catechins and procyanidins) can exist in various polymerization states and are commonly classified by their degree of polymerization (DP). There is increasing evidence that flavanols of distinct DP possess different biological activities, but separation and quantification of the higher DP procyanidins is challenging and has thus created the need for new methodologies that utilize advancements in columns and LC-MS/MS systems. An aqueous normal phase (hydrophilic interaction liquid chromatography, HILIC), UPLC method with post-column ESI adjuvant infusion was developed to reduce the total analysis time, increase peak separation, and increase detection specificity (compared to traditional fluorescence methods) by coupling with mass spectrometry detection. The total elution time was reduced from 70 to 90 min (typically used for normal phase and HILIC HPLC separation of procyanidins) down to 9 min by employing UPLC. Results indicate that by using a post-column 0.04 M ammonium formate infusion (5 μL/min), ionization of procyanidins was significantly enhanced. Lower limits of detection ranged from 3.19 × 10 to 4.56 pmol-on-column, and lower limits of quantification ranged from 2.79 × 10 to 1.17 × 10 pmol-on-column across compounds DP 1-9. This method builds upon the foundation set by existing analytical methods and employs new technologies to dramatically increase sample throughput and enhance detection limits and specificity, facilitating improved analysis for procyanidins.
可可黄烷醇(儿茶素和原花青素)可以存在于不同的聚合状态,通常根据聚合度(DP)进行分类。越来越多的证据表明,具有不同 DP 的黄烷醇具有不同的生物活性,但分离和定量高 DP 的原花青素具有挑战性,因此需要利用柱和 LC-MS/MS 系统的进步开发新的方法。开发了一种水相正相(亲水相互作用液相色谱,HILIC)、UPLC 方法,并在后柱 ESI 添加剂输注,以减少总分析时间,增加峰分离,并通过与质谱检测相结合增加检测特异性(与传统荧光方法相比)。通过采用 UPLC,将总洗脱时间从 70 分钟到 90 分钟(通常用于正相和 HILIC HPLC 分离原花青素)缩短到 9 分钟。结果表明,通过在后柱 0.04 M 甲酸铵输注(5 μL/min),原花青素的离子化显著增强。在化合物 DP 1-9 中,检测限范围从 3.19×10 到 4.56 pmol-on-column,定量限范围从 2.79×10 到 1.17×10 pmol-on-column。该方法建立在现有分析方法的基础上,并采用新技术,显著提高样品通量,增强检测限和特异性,为原花青素的分析提供了更好的条件。