超高效液相色谱-手性柱前衍生化串联质谱法特异性测定植物油中的(-)-和(+)-苔藓酚。

Mimi Guo, Yameng Wang, Yalin Xue, Zhangqun Duan, Qiaoying Chang
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引用次数: 0

摘要

背景:棉酚是棉籽油的独特成分,具有毒性,其对映体之间存在差异。虽然已经对棉花或棉籽中的(-)-和(+)-棉酚进行了测定,但有关植物油中棉酚对映体的检测却鲜有报道:方法:在超高效液相色谱(UPLC)系统上,采用ACQUITY C18反相柱(100 mm × 2.1 mm, 1.7 μm)分离(-)-和(+)-棉酚。流动相为甲醇(溶剂 A)和含 0.1% 甲酸的水(溶剂 B)。分析物在正离子模式下用电子喷雾电离源检测。采用多重反应监测对(-)-和(+)-苔藓酚标准衍生物的含量进行定量,定量离子对的跃迁为 m/z 633/483,定性离子对的跃迁为 m/z 633/558:结果表明,定量分析可在 12.5 分钟内完成,(-)- 和 (+)-gossypol 的检出限分别为 25.55 μg/kg 和 14.67 μg/kg。将该方法应用于添加了棉酚标准品的橄榄油中,获得了良好的回收率((-)-棉酚为 95.37%-105.84%,(+)-棉酚为 98.96%-105.14%)和 RSD((-)-棉酚为 3.41%-6.02%,(+)-棉酚为 4.50%-6.94%):本研究证实了测定棉酚对映体的可行性,并实现了植物油中(-)-和(+)-棉酚的痕量测定。这些结果使该方法更适用于定性鉴定植物油中是否混有棉籽油:亮点:实现了植物油中(-)-和(+)-棉酚的痕量测定。该方法为进一步鉴定市售植物油中是否混有棉籽油提供了技术支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Specific Determination of (-)- and (+)-Gossypol in Vegetable Oil by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry with Chiral Pre-Column Derivatization.

Background: As the unique ingredient of cottonseed oil, gossypol is toxic and there are differences between the enantiomers. Although the determination of (-)- and (+)-gossypol in cotton plants or cottonseed has been performed, the detection of the gossypol enantiomers in vegetable oil has rarely been reported.

Objective: To develop a specific inspection method for (-)- and (+)-gossypol in vegetable oil by ultra-performance liquid chromatography (UPLC)-tandem mass spectrometry with chiral pre-column derivatization.

Methods: (-)- and (+)-Gossypol were separated on an ACQUITY C18 reverse-phase column (100 mm × 2.1 mm, 1.7 μm) maintained at 40°C on an UPLC system with gradient elution. The mobile phases were composed of methanol (solvent A) and water containing 0.1% formic acid (solvent B). Analytes were detected using an electrospray ionization (ESI) source in positive mode. The contents of (-)- and (+)-gossypol standard derivatives were quantified by multiple reaction monitoring (MRM) with the transitions of m/z 633/483 for quantitative ion pairs and m/z 633/558 for qualitative ion pairs.

Results: The results indicated that the quantitative analysis could be accomplished within 12.5 min and the LODs of (-)- and (+)-gossypol were 25.55 and 14.67 μg/kg, respectively. When this method was applied to olive oil spiked with gossypol standards, good recoveries [95.37-105.84% for (-)-gossypol and 98.96-105.14% for (+)-gossypol] and RSDs [3.41-6.02% for (-)-gossypol and 4.50-6.94% for (+)-gossypol)] were achieved.

Conclusion: The present study confirms the feasibility of determining gossypol enantiomers and achieves trace determination of (-)- and (+)-gossypol in vegetable oil. These results make this method more suitable for the qualitative identification of whether the vegetable oil has been mixed with cottonseed oil.

Highlights: The trace determination of (-)- and (+)-gossypol in vegetable oils has been achieved. This method provides technical support for further identification of whether commercially available vegetable oil has been mixed with cottonseed oil.

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