Discovery and Development Technologies (DDTech), Merck KGaA, Frankfurter Strasse 250, 64293 Darmstadt, Germany; Department of Drug Design and Optimization (DDOP), Helmholtz-Institute for Pharmaceutical Research Saarland (HIPS) - Helmholtz Centre for Infection Research (HZI), Campus E8.1, 66123 Saarbrücken, Germany; Department of Pharmacy, Saarland University, Campus E8.1, 66123 Saarbrücken, Germany.
Innovation Center, Merck KGaA, Frankfurter Strasse 250, 64293 Darmstadt, Germany.
Eur J Pharm Sci. 2021 Sep 1;164:105884. doi: 10.1016/j.ejps.2021.105884. Epub 2021 Jun 20.
Structural elucidation of small molecules only available in low quantity (nanogram) is one of the big advantages of the crystalline sponge method. The optimization of various soaking parameters is crucial for effective analyte absorption and repetitive positioning in the pores of the crystal. Time-consuming X-ray diffraction measurements are necessary for data collection and confirmation of successful guest inclusion. In this work, we report a screening method to select optimal soaking conditions without the need of single-crystal X-ray diffraction analysis for individual compounds and mixtures. 14 substances were chosen as test compounds. Parallel guest soaking of individual compounds and mixtures was conducted using various soaking conditions. After evaporation of solvent, excessive material was removed, and guest molecules released through dissolution of the framework. Liquid chromatography-tandem mass spectrometry allowed the estimation of analyte trapped in the pores and the selection of optimal soaking condition dependent on the highest amount of analyte to crystal size (affinity factor). The tool allowed subsequent crystallographic analysis of ten compounds with minimal experiment time. Additionally, a study to examine the lower limit of detection of the crystalline sponge method was conducted. Determination of two target analytes was possible using only 5 ng of sample. Our study shows the potential of an affinity screening to prioritize soaking parameters by estimation of the guest concentration in a single crystal for one or multiple target compounds within a short period of time.
对于仅可获得少量(纳克级)的小分子结构解析而言,晶体海绵法是一个巨大的优势。优化各种浸泡参数对于有效吸收分析物并在晶体孔中重复定位至关重要。耗时的 X 射线衍射测量对于数据收集和成功包含客体的确认是必要的。在这项工作中,我们报告了一种筛选方法,无需对单个化合物和混合物进行单晶 X 射线衍射分析,即可选择最佳的浸泡条件。选择了 14 种物质作为测试化合物。对单个化合物和混合物进行平行客体浸泡,并采用各种浸泡条件。蒸发溶剂后,除去多余的材料,并通过溶解骨架释放出客体分子。液相色谱-串联质谱允许估计被困在孔中的分析物,并根据分析物与晶体尺寸的最高量(亲和力因子)选择最佳浸泡条件。该工具允许随后对十种化合物进行结晶学分析,实验时间最短。此外,还进行了研究以检查晶体海绵法的最低检测限。仅使用 5ng 的样品即可测定两种目标分析物。我们的研究表明,通过在短时间内估计单个晶体中客体的浓度,可以优先考虑浸泡参数的亲和力筛选,从而对一个或多个目标化合物进行筛选。