Department of Pharmaceutical Analysis, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Department of Analytical Chemistry, School of Science, China Pharmaceutical University, Nanjing 211198, China.
J Chromatogr A. 2022 Jun 21;1673:463199. doi: 10.1016/j.chroma.2022.463199. Epub 2022 Jun 5.
Compound structure change of the template molecule from rutin samples might affect the selectivity and adsorption of molecularly imprinted polymers based on magnetic halloysite nanotubes (MHNTs@MIPs). In the present study, not only MHNTs@MIPs were successfully characterized by TEM, SEM, EDS, FT-IR, TGA and VSM, but related compounds and potential degradation factors of template molecule rutin were also investigated in the polymerization and elution process of MHNTs@MIPs by high-performance liquid chromatography together with photodiode array and tandem mass spectrometry (HPLC-PDA-MS/MS) in negative ion mode. Nine flavonol components were detected in rutin active pharmaceutical ingredient samples, such as rutin, isoquercetrin, kaempferol-3-O-rutoside, isorhamnetin-3-O-rutoside, quercetin, kaempferol, isorhamnetin and two unknown triglycosides. Under acidic, basic, oxidative and solvent conditions, two common degradants with negative ESI-MS ions at m/z 317 and 349 were found. Meanwhile, protocatechuic acid and methyl ester were also observed as two characteristic oxidative degradants. Compared to above degradation results, rutin-dimethylsulfoxide adduct and oxidative degradant were observed in the synthesis supernatant, which demonstrated that appropriate solvents and strict control of the oxygen level were critical in the synthesis process. Therefore, degradation studies provide a solid foundation for the optimization of MHNT@MIP synthesis with rutin as a template, which can be potentially applied to other templates for further material performance investigation.
模板分子的化合物结构变化可能会影响基于磁性埃洛石纳米管(MHNTs@MIPs)的分子印迹聚合物的选择性和吸附性。在本研究中,不仅通过 TEM、SEM、EDS、FT-IR、TGA 和 VSM 成功地对 MHNTs@MIPs 进行了表征,而且还通过高效液相色谱法与光电二极管阵列和串联质谱(HPLC-PDA-MS/MS)在聚合和洗脱过程中研究了模板分子芦丁的相关化合物和潜在的降解因素。在芦丁原料药样品中检测到 9 种黄酮醇成分,如芦丁、异槲皮苷、山奈酚-3-O-芦丁苷、异鼠李素-3-O-芦丁苷、槲皮素、山奈酚、异鼠李素和两种未知的三糖苷。在酸性、碱性、氧化和溶剂条件下,发现两种常见的降解产物在 m/z 317 和 349 处具有负 ESI-MS 离子。同时,还观察到原儿茶酸和甲酯作为两种特征氧化降解产物。与上述降解结果相比,在合成上清液中观察到芦丁-二甲亚砜加合物和氧化降解产物,这表明在合成过程中适当的溶剂和严格控制氧气水平至关重要。因此,降解研究为优化以芦丁为模板的 MHNT@MIP 合成提供了坚实的基础,这可能会潜在应用于其他模板进行进一步的材料性能研究。