李婷, 王珏, 袁铭, 孙会敏. 聚氧乙烯35蓖麻油的UPCC-Q-TOF-MS成分分析与安全性初探J. 药学学报, 2020,55(11): 2688-2694. doi: 10.16438/j.0513-4870.2020-0670
引用本文: 李婷, 王珏, 袁铭, 孙会敏. 聚氧乙烯35蓖麻油的UPCC-Q-TOF-MS成分分析与安全性初探J. 药学学报, 2020,55(11): 2688-2694. doi: 10.16438/j.0513-4870.2020-0670
LI Ting, WANG Jue, YUAN Ming, SUN Hui-min. Safety study and compositional analysis of polyoxyethylene 35 castor oil by UPCC-Q-TOF-MSJ. Acta Pharmaceutica Sinica, 2020,55(11): 2688-2694. doi: 10.16438/j.0513-4870.2020-0670
Citation: LI Ting, WANG Jue, YUAN Ming, SUN Hui-min. Safety study and compositional analysis of polyoxyethylene 35 castor oil by UPCC-Q-TOF-MSJ. Acta Pharmaceutica Sinica, 2020,55(11): 2688-2694. doi: 10.16438/j.0513-4870.2020-0670

聚氧乙烯35蓖麻油的UPCC-Q-TOF-MS成分分析与安全性初探

Safety study and compositional analysis of polyoxyethylene 35 castor oil by UPCC-Q-TOF-MS

  • 摘要: 建立UPCC-Q-TOF-MS法分析聚氧乙烯35蓖麻油(polyoxyethylene 35 castor oil,CrEL)成分,并初探样品的安全性。采用Acquity UPCC Torus Diol色谱柱(3.0 mm×100 mm,1.7 μm),以CO2和甲醇-乙腈(50:50)为流动相,梯度洗脱,柱温50℃,流速1.0 mL·min-1,背压2 000 psi,以含2.5 mmol·L-1甲酸铵的甲醇为离子化试剂,离子化试剂流速0.2 mL·min-1,电喷雾正离子电离连同MSE技术,结合Progenesis QI软件进行快速结构确证及建立主成分分析(PCA)模型。以L-02细胞和RBL-2H3细胞作为细胞模型考察样品的细胞毒性和组胺释放。得到分离良好的13类成分,共255个化合物;以归一化法计算,所有样品中定义成分聚氧乙烯甘油三蓖麻油酸酯(polyoxyethylene glycerol tri-ricinoleate,PGTri-蓖麻油酸酯)仅占0.36%~2.80%,主要成分为聚乙二醇、乙氧基化甘油和聚氧乙烯甘油单蓖麻油酸酯。所有样品均存在不同程度的细胞毒性和组胺释放,与PGTri-蓖麻油酸酯含量负相关,与聚氧乙烯脂肪酸酯含量正相关。UPCC-Q-TOF-MS法简单快速、分离能力强且准确性高,适用于分析CrEL成分;建议对注射用CrEL标准补充脂肪酸组成检查项,提高PGTri-蓖麻油酸酯含量和降低聚氧乙烯脂肪酸酯含量,从而提高产品安全性。

     

    Abstract: A UPCC-Q-TOF-MS method was established to analyze the components of polyoxyethylene 35 castor oil. The separation was performed at 50℃ on a Waters Acquity UPCC system by an Torus Diol column (3.0 mm×100 mm, 1.7 μm) with gradient elution of CO2 and methanol-acetonitrile (50:50); the flow rate was 1.0 mL·min-1, the back pressure was 2 000 psi, and methanol containing 2.5 mmol·L-1 ammonium formate was used as ionization reagent, whose flow rate was 0.2 mL·min-1. Positive ion electrospray ionization (ESI) mode and MSE technology were used. The qualitative analyses were carried out by using precise mass information of the parent and product ions and a PCA model was established by UPCC-Q-TOF-MS. L-02 cells and RBL-2H3 cells were used to study the cytotoxicity and histamine release of CrEL samples in vitro. A total of 13 kinds of CrEL components were obtained and their structures were identified by UPCC-Q-TOF-MS, with 255 compounds in total. The percentage content of 13 types of components was calculated by the normalization method. The content of polyoxyethylene glycerol tri-ricinoleate (PGTri-ricinoleate) in all samples was 0.36%-2.80% and the main components were polyethylene glycol, polyethylene glycerol and polyoxyethylene glycerol mono-ricinoleate. All samples have different degrees of cytotoxicity and histamine release, which is negatively correlated with the content of PGTri-ricinoleate and positively correlated with the content of polyoxyethylene glycol fatty acid esters. The UPCC-Q-TOF-MS method is simple and rapid, has strong separation ability and high accuracy. It is suitable for the analysis of CrEL components. It is suggested that the fatty acid composition should be included in the monograph of CrEL for injection to increase the content of PGTri-ricinoleate and decrease the content of polyoxyethylene glycol fatty acid esters, so as to improve the product safety.

     

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