球形c18功能化有序介孔二氧化硅填充微固相萃取筒,用于同时测定花提取物中23种生物碱

IF 6.5 Q1 CHEMISTRY, ANALYTICAL
Begoña Fernández-Pintor , Judith Gañán , Damián Pérez-Quintanilla , Sonia Morante-Zarcero , Isabel Sierra
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引用次数: 0

摘要

成功合成了十八烷基硅烷配体功能化的球形有序介孔二氧化硅(SM-C18),其比表面积为647 m2/g,孔径为45 Å,粒径为4 ~ 6 μm,功能化度为0.37 mmol/g。将1.5 mg SM-C18装进EPREP微固相萃取(µSPEed)盒中,与手持式可编程数字分析注射器(digiVOL®)一起使用,以制定样品制备方案,用于分析两种tropane (TAs)和21种pyrrolizidine (PAs)生物碱。与商用C18/亲水无定形二氧化硅吸附剂相比,SM-C18表现出更大的保留容量。优化的提取条件为:100µL甲醇(2个循环)和100µL H2O(2个循环),100µL水重构样品(10个循环),共装样1ml, 100µL甲醇(2个循环)洗脱,UHPLC-MS/MS分析。结果表明,该方法回收率在91% ~ 97%之间,定量限低,不存在基质效应。此外,与商业材料相比,SM-C18材料包装的墨盒具有更好的可重复使用性,因为已经证明它们可以用于至少75次提取。这大大提高了该方法的可持续性。最后,将其应用于25个花提取物补充剂(FES)样品。对两批旋花FES4a和FES4b样品中阿托品和东莨菪碱进行定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spherical C18-functionalized ordered mesoporous silica packed on micro-solid phase extraction cartridges for simultaneous determination of twenty-three alkaloids in flower extract supplements

Spherical C18-functionalized ordered mesoporous silica packed on micro-solid phase extraction cartridges for simultaneous determination of twenty-three alkaloids in flower extract supplements
A spherical ordered mesoporous silica functionalized with octadecylsilane ligand (SM-C18) was successfully synthesized and characterized, showing 647 m2/g of surface area, 45 Å of pore size, 4–6 μm of particle diameter and 0.37 mmol/g of functionalization degree. 1.5 mg of SM-C18 were packed into EPREP micro-solid phase extraction (µSPEed) cartridges for use with a handheld programmable digital analytical syringe (digiVOL®) to develop a sample preparation protocol for the analysis of two tropane (TAs) and twenty-one pyrrolizidine (PAs) alkaloids. The SM-C18 demonstrated greater retention capacity compared with commercial C18/hydrophilic amorphous silica sorbent. The optimized extraction conditions were as follows: 100 µL of methanol (2 cycles) and 100 µL of H2O (2 cycles) for conditioning, 100 µL of H2O-reconstituted sample (10 cycles), for a total of 1 mL of sample loaded, and 100 µL of methanol (2 cycles) for elution, followed by subsequent analysis by UHPLC-MS/MS. The method was successfully validated, showing good recoveries ranging between 91 and 97 %, low quantification limits and absence of matrix effect for the twenty-tree alkaloids. Additionally, cartridges packed with SM-C18 material allow for better reusability compared to the commercial material, as it has been demonstrated that they can be used for at least 75 extractions. This significantly enhances the method's sustainability. Finally, it was applied to 25 samples of flower extract supplements (FES). In two different batches of the sample obtained from Convolvulus arvensis flowers (FES4a and FES4b), atropine and scopolamine were quantified.
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